Section 72

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Hopkins, R.H.; Jelinek, B. 1949: Action of beta-amylase on amylose. Nature 164(4179): 955
Raoul, Y.; Gautheret, R.J. 1947: Action of beta-naphthoxyacetic acid and 2-4-dichlorophenoxyacetic acid on the development of carrot and Jerusalem artichoke tissue cultivated in vitro. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 129-131
Cull-Candy, S.G.; Neal, H.; Usherwood, P.N. 1973: Action of black widow spider venom on an aminergic synapse. Nature 241(5388): 353-354
Bastin, R. 1948: Action of blood serum and whole blood on the departure of cultures of the tuberculous bacillus. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(1-2): 11
Pezzi, A.R. 1945: Action of blood transfusion in Brucellosis patients. Revista Medica de Cordoba 33: 635
Ktistakis, N.T.; Linder, M.E.; Roth, M.G. 1992: Action of brefeldin A blocked by activation of a pertussis-toxin-sensitive G protein. Nature 356(6367): 344-346
Ottaviano, G. 1947: Action of bulbocapnine on the isolated toad heart and on the isolated rabbit intestine. Bollettino della Societa Italiana di Biologia Sperimentale 23(12): 1125
Granjon, A.; Vassy, S. 1947: Action of caffeine and adrenaline on the uterus of the spleen. Gynecologie et Obstetrique 40(1): 115-119
Vignes, H. 1949: Action of camphor on the female genital organs. Journal des Praticiens; Revue Generale de Clinique et de Therapeutique 63(6): 63
Legrand, R.; Warembourg, H. 1945: Action of carbohydrate overload and insulin on endogenous oxycarbonemia. Le Progres Medical 73(9-10): 147-149
Rondoni, P.; Bassi, M. 1948: Action of carcinogens on proteolytic enzymes. La Ricerca Scientifica 18(8-9): 1038-1043
Alanis, R.J. 1948: Action of cardiac glycosides and inhibitory reagents of sulfhydryl enzymes on smooth muscle. Archivos del Instituto de Cardiologia de Mexico 18(3): 410-424
Sweet, H.C.; Falk, O.P.J.; Agar, D. 1948: Action of caronamide in penicillin treatment. America Clinica 13(3): 205-208
Bertrand, D.; Polonovski, J. 1948: Action of cationic soaps on certain oxidasic systems (laccase, catechoxidase, cytochromeoxydase). ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(13-14): 926
Banderet, A.; Ranby, B. 1947: Action of caustic soda on cellulose in an oxygen-free atmosphere. Helvetica Chimica Acta 30(5): 1190-1200
Pochon, J.; Lajudie, J. 1948: Action of certain antiseptics on the normal soil microflora. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(25): 2091
Prevot, A.R.; Taffanel, J. 1946: Action of certain bodies on the fermentation of some anaerobic bacteria; dyes; vitamins; metal. Annales de l'Institut Pasteur 72: 450-453
Benard, H.; Gajdos, A.; Gajdos-Torok, M. 1955: Action of certain inhibitors and activators on the metabolism of porphobilinogen in vitro. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(3-4): 312-314
Desnuelle, P.; Constantin, M.J.; Sarda, L. 1956: Action of certain organophosphoric derivatives on lipase and esterase of the pancreas. Bulletin de la Societe de Chimie Biologique 38(4): 625-631
Michaelis, M.; Hashimoto, S. 1962: Action of chloretone on reduced cozymaze oxidation by cytochrome c. Nature 194: 680-681
Lepine, P.; Marcenac, F. 1948: Action of chlorine on fecal matter with a view to the destruction of the poliomyelitis virus. Bulletin de l'Academie Nationale de Medecine 132(13-14): 262-266
Normant, H. 1948: Action of chlorine on tetrahydrofuran. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(2): 185-187
Heuschem, C.; Firket, J.; Bacq, Z.M. 1947: Action of chloropicrin on the germination of peas. Bulletin de la Societe de Chimie Biologique 29(4-6): 453-459
de Waart, C.; Sietsma, J.H.; Ferwerda, W.; Brogt, T.M. 1966: Action of chlorpromazine on non-specific phosphatase bound to membranes in brain tissue of the rat. Nature 212(5064): 848-849
Warembourg, H.; Lekieffre, J. 1956: Action of chlorpromazine on plasma volume. Therapie 11(6): 1178-1181
Robey, M.; Simon, P.; Simonnet, H. 1955: Action of chlorpromazine on rat gonads. Bulletin de la Federation des Societes de Gynecologie et Dobstetrique de Langue Francaise 7(2): 127-129
Furtado, D. 1956: Action of chlorpromazine on the state of epilepticus. L'Encephale 45(4): 727-729
Bachrach, E.; Guillot, N. 1955: Action of chlorterytracycline (aureomycin) on Lactobacillus acidophilus. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(3-4): 300-302
Sfowzini, P. 1948: Action of choline and methionine on blood crase. Il Policlinico. Sezione Pratica 55(40): 1201-1206
Frommel, E. 1949: Action of cholinesterase on acetylcholine chloromanganate. Schweizerische Medizinische Wochenschrift 79(28): 646
Valdecases, F.G.; Casellas Boix, J.A. 1949: Action of cholinesterase on acetylcholine chloromanganate. Schweizerische Medizinische Wochenschrift 79(19): 433
Caujolle, F.; Franck, C.; Grandpierre, R. 1945: Action of cobalt chloride on hypogastric hypertensive reflex. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 1158
Feissly, R.; Ludin, H. 1949: Action of cocaine on blood platelets. Helvetica Physiologica et Pharmacologica Acta 7(2): C 9
David, M. 1945: Action of colchicine and acenaphthene on the spermatogenesis of orthoptera of the genus Stauroderus Boh. ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences 221(6-9): 185
Buvat, R.; Tuchmann-Duplessis, H. 1947: Action of colchicine and some substances deemed toxic on the living cell. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(19): 1377-1379
Garofalo, F. 1947: Action of colchicine on the respiration of some bacterial species. Giornale di Batteriologia e Immunologia 35(2): 102-104
Zambruno, D. 1946: Action of colchicine, narcotin, and androstendione on the multiplication of Staphylococcus aureus. Giornale di Batteriologia e Immunologia 34(1): 55-57
Laigret, J.; March, H.N.; Kessel, J.F. 1957: Action of cortisone and prednisone on elephantiasis. Medecine Tropicale: Revue du Corps de Sante Colonial 17(6): 891-898
Linquette, M.; Rabache, R. 1955: Action of cortisone on 4 cases of myotonia. Annales d'Endocrinologie 16(1): 88-96
Zizine, L. 1955: Action of cortisone on gonadotropic hormones in rats. Annales d'Endocrinologie 16(4): 708-713
Meunier, J.M.; Duluc, A.J.; Mayer, G. 1955: Action of cortisone on the hormonal balance of progestin and gestation. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(3-4): 366-370
Cattan, R.; Mazloum, A.W. 1955: Action of cortisone, hydrocortisone and metacortandracin on diarrhea. Archives des Maladies de l'Appareil Digestif et des Maladies de la Nutrition 44(11): 1113-1125
Fernet, P.; Collart; Daguet 1947: Action of current therapeutics on serological reactions during recent syphilis. Journal des Praticiens; Revue Generale de Clinique et de Therapeutique 61(45): 497
Bacq, Z.M.; Cuypers, Y.; Evrard, E.; Soetens, R. 1955: Action of cystamine on the resistance of the rat to barometric depression. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149: 2014-2017
Goffart, M.; Paton, W.D. 1955: Action of cysteamine and cystamine on a sympathetic ganglion. Archives Internationales de Physiologie et de Biochimie 63(4): 477-499
Vescia, A.; Bertolini, A. 1947: Action of cystine and thiamine on the activity of some enzyme systems in rats on a glycidic diet. Bollettino della Societa Italiana di Biologia Sperimentale 23(12): 1166-1168
Smith, G.F.; Ridler, M.A.; Faunch, J.A. 1967: Action of cytochalasin B on cultured human lymphocytes. Nature 216(5120): 1134-1135
Del Castillo, E.B.; Rapela, C.E. 1945: Action of deoxycorticosterone acetate on the adrenal glands. Revista de la Sociedad Argentina de Biologia 21: 338-359
Callan, H.G.; Macgregor, H.C. 1958: Action of deoxyribonuclease on lampbrush chromosomes. Nature 181(4621): 1479-1480
Balatre, P.H.; Merlen, J.F. 1956: Action of derivatives of theophylline in experimental pink arteriosclerosis. Therapie 11(6): 1080-1083
Parodi; Proust; Talarmin 1956: Action of dexyxybenzoins (1183 TH) on intestinal bilharziasis. Bulletin de la Societe de Pathologie Exotique et de Ses Filiales 49(4): 654-657
Urrets Zavalia, A.H. 1949: Action of diaminodiphenyl sulfones on ocular complications of leprosy. Archivos de la Sociedad Oftalmologica Hispano-Americana 9(2): 160-175
Facquet, J.; Sassier, R.; Kisch, R. 1945: Action of dicoumarin (3-3'-methylene-bis-4-hydroxycoumarin) on prothrombinemia and plasma coagulation in normal adults. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 262
SIMOES de MENEZES, R. 1945: Action of diestro donor fish hypophyses on estrus breeding fish. Revista Brasileira de Biologia 5: 535-539
Mahaux, J.; Kowalewski, K. 1949: Action of diethylaminoethyl-N-thiodiphenylamine hydrochloride on basal metabolism and metabolism after exertion of hyperthyroid and normothyroid subjects. Archives Internationales de Pharmacodynamie et de Therapie 80(4): 464-469
Benoit, J.; Gros, G.; Clavert, J. 1945: Action of diethylstilboestrol in birds. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 723
Drutel, P.; Olivier, H.R. 1947: Action of different strains of bacillus subtilis on carbohydrates. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(7-8): 374-377
Bairati, A. 1947: Action of digestive ferments on the elements of human glia. Bollettino della Societa Italiana di Biologia Sperimentale 23(5): 543-545
Bertrand, G.; Silberstein, L. 1949: Action of dilute alkaline solutions on wood. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 228(8): 621-624
Lepine, P.; Pavilanis, V. 1947: Action of dimethylbenzoylsulfamide on the inguinal lymphogranulomatosis virus in mice. Annales de l'Institut Pasteur 73(7): 693
Gley, P.; Fournier, P.; Touchard, T. 1945: Action of diphenylhydantoin and ethylphenylmalonyluree on subcortical epilepsy. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 298
Bourgeois, P.; Genevrier, R.; Vic-Dupont 1949: Action of directed intrabranchic injections of streptomycin on tuberculous caves. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 25(7): 285-288
Badaró, M.M.; Bueno, F.L.; Makrakis, L.R.; Araújo, C.B.; Oliveira, V.d.C.ás.; Macedo, A.P.; Paranhos, H.d.F.O.; Watanabe, E.; Silva-Lovato, C.áu.H. 2021: Action of disinfectant solutions on adaptive capacity and virulence factors of the Candida spp. biofilms formed on acrylic resin. Journal of Applied Oral Science: Revista Fob 29: E20210024
Hartley, E.G. 1967: Action of disinfectants on experimental mouse scrapie. Nature 213(5081): 1135
Huguenin, A. 1947: Action of dry diet in acute nephritis. Algerie Medicale 50(6): 506-509
Vijayaraghavan, P.K.; Narasinga Rao, B.S. 1953: Action of duck's egg white ovomucoid on tryptic hydrolysis of casein in vitro. Nature 172(4390): 1152-1153
Bonnet, V.; Bremer, F. 1948: Action of eserin and prostigmine on central synaptic potentials. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142: 1442-1444
Lipschutz, A. 1947: Action of estrogen hormones. Archives Hospitalieres 19(6): 202
Coste, F.; Galmiche, P. 1950: Action of estrogens on metastases of breast cancer in postmenopausal women. Revue du Rhumatisme et des Maladies Osteo-Articulaires 17(2): 69-71
Comsa, J. 1945: Action of estrone on the guinea pig urine creatine. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 1033
Vilagines, R.; Atanasiu 1967: Action of ethidium bromide on growth of herpes virus in cell cultures. Nature 215(5096): 87-88
Olomucki, E. 1957: Action of ethylene dibromide on hen gonadotrophic hormones. Nature 180(4598): 1358-1359
Bouisset, L.; Harant, H.; Ruffie, J. 1956: Action of experimental hibernation on the evolution of Trypanosoma equiperdum (Doflein 1901) in the white rat. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 150(6): 1277-1280
Waysbaum-Moschkowski 1945: Action of extracts from the pineal gland on the ovaries of guinea pigs and rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 1069
Savary, P. 1948: Action of fatty acid salts on the halohydrins of polyalcohols. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(1): 89
Remlinger, P.; Bailly, J. 1947: Action of fig latex on the rabies virus. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(21): 1467
Irving, J.T. 1946: Action of fluorine on the teeth of rachitic rats. Nature 158(4026): 949
Chauchard, P.; Mazoue, H.; Lecoc, R. 1947: Action of folic acid and ascorbic acid on the chronaxic syndrome of carbohydrate imbalances. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(3-4): 101
Bousser, J.; Robineaux, R. 1949: Action of folic acid and hepatic extracts in sprue. Le Sang 20(7): 472-475
Lourau, M.; Marinone, G. 1947: Action of folic acid on hematopolysis in normal animals. Experientia 3(5): 190
Cazzola, D. 1948: Action of follicle, stilbenes and methylthiouracil on the X zone of the mouse adrenal cortex; experimental research. Folia Gynaecologica 43(3): 207-248
Clavert, J.; Duval, M. 1945: Action of folliculin on the level of hepatic and muscular glycogen in the pigeon. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 1119
Clavert, J. 1945: Action of folliculin on the pigeon's liver; histological changes. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 106-108
Flandin, C.; Flandin, F.; Millot, J. 1945: Action of fontarsol on blood formula. Annales de Dermatologie et de Syphiligraphie 5: 75
Nelis, P.; Lafontaine, A. 1948: Action of formalin on the germs of the glycerinated vaccine pulp. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(11-12): 859
Metayer, M.; De Bievre-Gallin, G. 1947: Action of formamide and methylformamide on aldehydes. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 225(15): 635-637
Evans, P.D.; Gee, J.D. 1980: Action of formamidine pesticides on octopamine receptors. Nature 287(5777): 60-62
Valdecasas, F.G.; Vilanova, X. 1949: Action of gammahexane on yeasts of dermatological interest; hypothesis about its anti-tabolic activity on inositol. Archives Internationales de Pharmacodynamie et de Therapie 80(1): 28-34
Giacobini, E.; Cordone, M. 1949: Action of gastro-duodenal mucosa extracts in ulcerative disease. L'Attualita Medica 14(2): 15-17
Shiells, R.A.; Falk, G.; Naghshineh, S. 1981: Action of glutamate and aspartate analogues on rod horizontal and bipolar cells. Nature 294(5841): 592-594
Gardner, L.R.; Stewart, P.S. 2002: Action of glutaraldehyde and nitrite against sulfate-reducing bacterial biofilms. Journal of Industrial Microbiology and Biotechnology 29(6): 354-360
Duhamel, J. 1960: Action of glycyrrhetinic acid in suppositories in anorectal diseases. La Semaine des Hopitaux: Therapeutique 36: 928-932
Trabucco, A.; Bottini, H.E.B. 1948: Action of gonadorophins on oligozoospermia. Revista Argentina de Urologia 17(7-8): 127-132
Thieblot, L.; Berthelay, J.; Vannier, J. 1955: Action of gonadotropic hormones on vascular tone and sympathetic reflex excitability. Journal de Physiologie 47(1): 290-291
Mouriquand, G.; Edel, V.; Chighizola, R. 1947: Action of group B vitamins on the vestibular chronological index. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141: 943-945
Cocking, E.C. 1962: Action of growth substances, chelating agents and antibiotics on isolated root protoplasts. Nature 193: 998-999
Jayle, M.F.; Said Ishak; Gillard, P. 1946: Action of haptoglobin on the peroxidase catalysis of hemoglobin; new theory on the constitution of enzymes. Bulletin de la Societe de Chimie Biologique 28: 63-80
Solomides, J. 1946: Action of heat on the tuberculicidal power of cod liver oil. Revue de la Tuberculose 10(5-6): 314-316
Hawkins, R.I. 1971: Action of heparin on platelet electrophoretic mobility. Nature: new Biology 233(37): 92-93
Dreyfus, G.; Fischgold, H.; Weissenbach, R. 1949: Action of heterologous sexual hormone therapy on the radiographic evolution of bone metastases during prostate and breast cancers. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 25(51): 2192-2196
Morquer, R.; Nysterakis, F. 1948: Action of heterosine on the dimorphism of Candida albicans. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(11): 950
Moretti, G.P.; Testolin, M. 1948: Action of hexachlorocyclohexane on the sarcopte of human scabies (Sarcoptes scabiei V. Hominis). Minerva Medica 39(44 Part 2): 483
Cordonnier, V. 1946: Action of histamine and antihistamine substances on the experimental eczema. Annales de Dermatologie et de Syphiligraphie 6(9): 498
Halpern, B.N.; Guillaumat, L.; Cruchaud, S. 1948: Action of histamine and synthetic antihistamines on the capillary permeability of the blood-brain barrier. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 24(80): 2564
Cabrera, G.; Thompson, J.E. 1950: Action of histamine on procaine nerve block. Nature 165(4200): 681
Bennati, D.; Bacq, Z.M. 1946: Action of histamine, acetylcholine and peptone in sympathectomized dogs. Archives Internationales de Pharmacodynamie et de Therapie 72(3-4): 397-404
Pignatelli, G. 1945: Action of hormonal substances on the healing process of tendon wounds. Il Progresso Medico 1(7): 186-189
Vasconcelos, K.át.d.; Oliveira, A.S.B.; Fuchs, L.F.P.; Simões, R.S.; Simoes, M.d.J.; Girão, M.J.ão.B.C.; Soares Júnior, J.M.; Baracat, E.C. 2020: Action of hormonal therapy in amyotrophic lateral sclerosis: a systematic review. Revista da Associacao Medica Brasileira 66(11): 1589-1594
Legrand, J.C.; Gonnard, P. 1959: Action of human serum on the oxidation of D-L-dihydroxyphenylalanine and L-tyrosine. Bulletin de la Societe de Chimie Biologique 41(2-3): 353-361
Drouhet, E.; Segretain, G. 1949: Action of hyaluronidase on the capsule of Torula histolytica. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 228(5): 424
Schmitt, H.; Gicquel, J. 1956: Action of hydrazinophthalazine (C5968) and dihydrazino-1-4 phthalazine (C7441) on the vasomotor centers. Archives Internationales de Pharmacodynamie et de Therapie 105(3-4): 269-278
Grossfeld, H. 1958: Action of hydrocortisone on respiration of human cancer cells in tissue culture. Nature 182(4627): 35-37
Bell, W.C.; Maassab, H.F. 1968: Action of hydroxyurea on multiplication of influenza virus in mammalian cells. Nature 217(5129): 646-647
Bacq, Z.M.; Charlier, R.; Philippot, E. 1948: Action of hyperitis and its derivatives by intravenous injection on the dog's cardiac output. Archives Internationales de Pharmacodynamie et de Therapie 77(1): 123-126
Franck, C.; Grandpierre, R. 1948: Action of hyperoxia on adrenalin hypertension and hyperglycemia. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(5-6): 372-376
Dumont, L.; Verniory, A.; Bacq, Z.M. 1945: Action of hypertensive dog blood by renal ischemia and action of renin on the cat's nictitating membrane. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 775-777
Conard, V.; Kowalewski, K.; Van Geertruyden, J. 1949: Action of increasing doses of histamine on gastric secretion in patients protected by antistin. ActaGastro-EnterologicaBelgica 12(2): 97
Raoul, Y.; Marnay, C. 1948: Action of indol-3-acetic acid and 2,4-dichloro-phenoxy-acetic acid on the growing rat. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(12): 1043-1045
Raoul, Y. 1947: Action of indol-3-acetic acid on Escherichia coli demonstrated by the antagonism of substances of analogous structure. Bulletin de la Societe de Chimie Biologique 29(1-3): 183-192
Gautheret, R. 1947: Action of indole-acetic acid on the development of normal tissues and crown-gall tissues of Jerusalem artichoke cultivated in vitro. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(24): 1728-1730
Gautheret, R. 1948: Action of indole-acetic acid on the development of three types of scorzonera tissue; normal tissues, crown-gall tissues and tissues accustomed to hetero-auxin. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(11-12): 774
Siliprandi, N.; Boffi, V.; Lucarelli, A. 1955: Action of insulin on thiamine phosphorylation in vitro. Nature 176(4474): 219-220
Sudaka; Gardel; Klingler 1948: Action of intramuscular thrombase in the preparation of tonsillectomies. Algerie Medicale 51(8): 447-451
Calma, I.; Wright, S. 1947: Action of intrathecally injected eserine on the spinal cord of the cat. Journal of Physiology 106(1): 80-94
Lecoq, R. 1945: Action of intravenous injections of vitamins on the alkaline reserve. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 139(11-12): 582
Mayer, G.; Levy, A. 1949: Action of intravenous novocaain in a case of heart failure. Strasbourg Medical 109(6): 75
Benda, R.; Galby, R. 1945: Action of intravenous novocaine on inert or bloated caves. Revue de la Tuberculose 9(11-12): 359-361
Cavalleri, A.; Modena, L. 1948: Action of intravenous para-aminobenzoyldiethylaminoethanol hydrochloride on gastric secretion curves. Minerva Medica 39(14): 359
Notter, A.; Burnod, A. 1947: Action of intravenous spasmalgine on uterine contraction. Lyon Medical 178(45): 745-751
Parrot, J.L.; Cotereau, H. 1945: Action of iodadrenochrome on the resistance of capillaries. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 902-904
Sendrail, M.; Bazex, A.; Gleize, E. 1948: Action of iodine on the cytological formula of the insular pancreas. Toulouse Medical 49(1): 1-3
Tuchmann-Duplessis, H. 1948: Action of iodoproteins on the thyroid and metamorphosis of amphibians (rana temporaria) biometric and histological study. Bulletin d'Histologie Appliquee et de Technique Microscopique 25(7): 123-136
Nakao, Y. 1953: Action of irradiated cytoplasm on untreated chromosomes of the silkworm. Nature 172(4379): 625-626
Viallier, J.; Cayre, R.M. 1956: Action of isonicotyl hydrazide para-amino salicylate on mycobacteria. I. Bacteriostatic action exerted in vitro. Annales de l'Institut Pasteur 90(1): 114-117
Lees, A.D. 1977: Action of juvenile hormone mimics on the regulation of larval-adult and alary polymorphism in aphids. Nature 267(5606): 46-48
Desmarez, J.J. 1955: Action of khelline on experimental gastric ulcer in rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(11-12): 1291-1292
Soulairac, A. 1948: Action of lactoflavin on alkaline phosphatase in the intestine and kidney of the adrenalectomized rat. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(11-12): 778
Troupin, G. 1946: Action of light and temperature on the growth and sexuality of males and females of Mercurialis annua L. Growth 10(4): 343-359
Baschieri, L.; Ferri, F. 1949: Action of lipotropic and vitamin factors on the histological picture of experimental diphtheria intoxication. Lo Sperimentale 99(9-10): 417-434
Albrieux, A.S.; Rodriguez, M.L. 1945: Action of liver extracts on the content of sterols and vitamin a in the liver. ANALES. Asociacion de Quimica y Farmacia del Uruguay 47(1): 27-30
Steen, A.S. 1951: Action of living cells on cortisone acetate crystals. Nature 168(4276): 652-653
Swan, H.J.C. 1950: Action of local hormones. Proceedings of the Royal Society of London. Series B Biological Sciences 137(888): 315
Ambache, N. 1950: Action of local hormones. Proceedings of the Royal Society of London. Series B Biological Sciences 137(888): 315-317
Saltonstall, H.; Walker, J. 1945: Action of local treatment of burns on liver function. Anales de Cirugia 4: 296-305
Wurmser, L. 1947: Action of low doses of butellin on the isolated rat intestine. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(1-2): 15-17
Hoffmann, J. 1945: Action of lysocithin on red blood cells in a case of ovalocytosis. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 426
Chabbert, B.; Habrant, A.; Herbaut, Mël.; Foulon, L.; Aguié-Béghin, Véronique.; Garajova, S.; Grisel, S.; Bennati-Granier, Cé.; Gimbert-Herpoël, I.; Jamme, Fédéric.; Réfrégiers, M.; Sandt, C.; Berrin, J-Guy.; Paës, G. 2017: Action of lytic polysaccharide monooxygenase on plant tissue is governed by cellular type. Scientific Reports 7(1): 17792
Mordelet-Dambrine, M.; Parrot, J.L. 1966: Action of magnesium on serum histaminopexy in the adrenalectomized and castrated rat. Journal de Physiologie 58(3): 303-308
Cohen, S.; Butcher, G.A.; Crandall, R.B. 1969: Action of malarial antibody in vitro. Nature 223(5204): 368-371
Darlington, C.D.; McLENH, J. 1951: Action of maleic hydrazide on the cell. Nature 167(4245): 407-408
Lallier, R. 1955: Action of malononitrile on the embryonic development of Ambystoma mexicanum and Rana temporaria. Revue Canadienne de Biologie 14(2): 123-128
Schoysman, R. 1956: Action of massive doses of androstanolone benzoate on the genital tract of the adult spleen. Bruxelles Medical 36(32): 1562-1573
Kozák, J.; Rusnák, A. 1966: Action of mecholyl on the respiration of cardiac muscle in vitro. Nature 210(5036): 636-637
Dumazert, C.; Levy, M.; Marszak, I. 1945: Action of metal complex formers on blood glycolysis and probable nature of weakly combined sugar in blood. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139(3-4): 219-221
Olivier, H.R.; Blanchon, E. 1946: Action of metal salts of dehydrocholalic acid on experimental tuberculosis of rabbits. Revue de Tuberculose et de Pneumologie 10(1-2): 52-54
Adeshara, K.A.; Bangar, N.S.; Doshi, P.R.; Diwan, A.; Tupe, R.S. 2020: Action of metformin therapy against advanced glycation, oxidative stress and inflammation in type 2 diabetes patients: 3 months follow-up study. Diabetes and Metabolic Syndrome 14(5): 1449-1458
Lacassagne, A.; Latarjet, R. 1945: Action of methylcholanthrene on the skin previously subjected to strong violet irradiation, in adult mice. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 4-6
Morando, G.G. 1948: Action of methylthiouracil on the carbohydrate intermediate metabolism in experimental hyperthyroidism. Archivio Per le Scienze Mediche 85(5): 247-254
Gallois, J. 1946: Action of minimal electro vasodilation on the retina. Archives des Maladies du Coeur et des Vaisseaux 39(3-4): 77-80
Bossard, M. 1947: Action of molybdates on various enzymes. Bulletin de la Societe de Chimie Biologique 29(1-3): 218-221
Allard, J. 1947: Action of monochloromethyl ether on some terpene carbides. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(13): 1020-1022
Sarzana, G.; Bevilotti, V. 1947: Action of monoiodoacetic acid on cardiac activity; electrocardiographic research. Bollettino della Societa Italiana di Biologia Sperimentale 23(5): 494-497
Dixit, S.; Kumar Biswal, A.; Min, A.; Henry, A.; Oane, R.H.; Raorane, M.L.; Longkumer, T.; Pabuayon, I.M.; Mutte, S.K.; Vardarajan, A.R.; Miro, B.; Govindan, G.; Albano-Enriquez, B.; Pueffeld, M.; Sreenivasulu, N.; Slamet-Loedin, I.; Sundarvelpandian, K.; Tsai, Y-Ching.; Raghuvanshi, S.; Hsing, Y-Ie.C.; Kumar, A.; Kohli, A. 2015: Action of multiple intra-QTL genes concerted around a co-localized transcription factor underpins a large effect QTL. Scientific Reports 5: 15183
Bacq, Z.M.; Charlier, R.; Philippot, E. 1948: Action of mustard and its derivatives on the heart and respiratory exchanges in anesthetized dogs. Archives Internationales de Pharmacodynamie et de Therapie 77(4): 353-368
Alcalay, W. 1947: Action of naphthoquinonic compounds on the growth of acid-resistant bacteria and others. Schweizerische Zeitschrift für Pathologie und Bakteriologie. Revue Suisse de Pathologie et de Bacteriologie 10(3): 229-244
Posternak, J.; Mangold, R. 1949: Action of narcotics on conduction by nerve fibers and their membrane potential. Helvetica Physiologica et Pharmacologica Acta 7(4): C 55
Bessou, P.; Laporte, Y. 1956: Action of nembutal on sympathetic tonic activity. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 150(7): 1467-1470
Butterworth, P.J.; Moss, D.W. 1966: Action of neuraminidase on human kidney alkaline phosphatase. Nature 209(5025): 805-806
Pellerat, J.; Murat; Sauvageot, G. 1948: Action of new synthetic antihistamines (3,015 R.P. and 3,277 R.P.) on histamine. Lyon Medical 179(26): 441
Sposito, M.; Giannico, O. 1949: Action of nicotamide and nicotinic acid on the prothrombin rate. La Riforma Medica 63(26): 606-609
D'ambrosio, L. 1948: Action of nicotinic acid amide on some immune indices in tifica and paratifica B. infections. La Riforma Medica 62(9-10): 133-135
Gallois 1946: Action of nicotinic amide in the case of ocular hypertension. Annales d'Oculistique 179(1): 51
Merlen, J.F.; Dubrulle, P.; Grandjean, L. 1948: Action of nitrated esters on capillary fragility. L'Echo Medical du Nord 19(4): 101-103
Merlen, J.F.; Dubrulle, P.; Grandjean, L. 1948: Action of nitrated esters on capillary fragility. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(5-6):Unknown
Amal, H. 1949: Action of nitric acid on products with a pyrazolinic nucleus. Pharmaceutica Acta Helvetiae 24(9): 311-314
Bentley, H.R.; McDERMOTT, E.E. 1949: Action of nitrogen trichloride (agene) on proteins; isolation of crystalline toxic factor. Nature 164(4167): 438
Bentley, H.R.; Booth, R.G. 1948: Action of nitrogen trichloride on proteins; production of toxic derivative. Nature 161(4082): 126
Bentley, H.R.; McDERMOTT, E.E. 1949: Action of nitrogen trichloride on proteins; progress in the isolation of the toxic factor. Nature 163(4148): 675
Betz, H.; Heusghem, C.; Lecomte, J. 1949: Action of nitrogen yperite, methyl-bis-chloroethylamine, and alarm syndrome. Revue Belge de Pathologie et de Medecine Experimentale 19(5): 251-266; 4 Pl
Viscontini, M. 1945: Action of nitrous acid on glycine and on glycine polypeptides. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 220(23): 832-834
Cristol, P.; Crastes De Paulet, A.; Cristol, P. 1956: Action of nitrous acid, chloramine T and ninhydrin on glycyl, alanyl, leucyl peptides. Bulletin de la Societe de Chimie Biologique 38(4): 639-647
Radouco-Thomas, S.; Radouco-Thomas, C.; Le Breton, E. 1957: Action of noradrenaline and reserpine on experimental analgesia. Naunyn-Schmiedebergs Archiv für Experimentelle Pathologie und Pharmakologie 232(1): 279-281
Caselli, P.; Cavallo, G. 1947: Action of normal urinary constituents on lysozyme bacteriolysis. Bollettino della Societa Italiana di Biologia Sperimentale 23(5): 566
Krause, G.; Patz, M.; Isaeva, P.; Wigger, M.; Baki, I.; Vondey, V.; Kerwien, S.; Kuckertz, M.; Brinker, R.; Claasen, J.; Frenzel, L.P.; Wendtner, C-M.; Heider, K-H.; Hallek, M. 2012: Action of novel CD37 antibodies on chronic lymphocytic leukemia cells. Leukemia 26(3): 546-549
Liesch, E. 1947: Action of novocaine on tendon reflexes and muscle tone in humans in normal and pathological conditions; plaque sclerosis. Archivio di Fisiologia 46(3-4): 147-170
Gurriarán-Rodríguez, Uía.; Santos-Zas, Iía.; González-Sánchez, J.; Beiroa, D.; Moresi, V.; Mosteiro, C.S.; Lin, W.; Viñuela, J.E.; Señarís, Jé.; García-Caballero, Tás.; Casanueva, F.F.; Nogueiras, Rén.; Gallego, Ría.; Renaud, J-Marc.; Adamo, S.; Pazos, Y.; Camiña, Jús.P. 2015: Action of obestatin in skeletal muscle repair: stem cell expansion, muscle growth, and microenvironment remodeling. Molecular Therapy: the Journal of the American Society of Gene Therapy 23(6): 1003-1021
Ciaccio, C. 1953: Action of oxidizing agents in histochemistry; specific demonstration of carbonyl group. Bollettino della Societa Italiana di Biologia Sperimentale 29(12)
Aubel, E.; Perdigon, E. 1945: Action of oxygen on strict anaerobes; study of the action of oxygen on the production of bodies in C2 and C4 by C1. saccharobutyricum. Revue Canadienne de Biologie 4(4): 498-501
Aubel, E.; Rosenberg, A.J.; Szulmajster, J. 1947: Action of oxygenated water on a strict anaerobic. Experientia 3(3): 107
De Vita, P.; Ramunni, M. 1949: Action of p-amino-benzoic acid on the development of some germs in the blood. Bollettino Dell'istituto Sieroterapico Milanese 28(7-8): 145-149
Wahl, R.; Blum-Emerique, L. 1947: Action of pH on bacteriophages C16 and S13. Annales de l'Institut Pasteur 73(8): 741-748
Velu, H.; Penau, H.; Benoist, D. 1946: Action of pH on the bacteriostatic activity of penicillin. Bulletindel'AcademiedeMedecine 130(6-8): 141
Gautheret, R.J. 1947: Action of pH on the development of carrot tissue cultures. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(1-2): 25-29
Magee, D.F.; Nakamura, N. 1966: Action of pancreozymin preparations on gastric secretion. Nature 212(5069): 1487-1488
Dumont, M. 1950: Action of panthenol on the muscle cramps of pregnant women. La Presse Medicale 58(1): 3
Meyer, J.; Malgras, J.; Ponnelle, J. 1956: Action of pantothenic acid in specific immunization. Revue d'Immunologie et de Therapie Antimicrobienne 20(1-2): 55-57
Moran, D.; Rice, R.W. 1976: Action of papaverine and ionophore A23187 on neurulation. Nature 261(5560): 497-499
Sanchez-Calvo, R.; Diaz, M. 1948: Action of para-aminobenzoic acid on intestinal motility. Revista Clinica Espanola 29(1): 21-23
Lamy, L. 1946: Action of para-aminophenylsulfamide (1162 F) on the start of Entamoeba-dysenteriae cultures. Annales de l'Institut Pasteur 72: 295-297
Olivier, H.R. 1949: Action of para-aminosalicylic acid in progressive deforming rheumatism. France Medecine 12(6): 6
Picard, J. 1955: Action of parathormone in the calcium-calcium metabolism. La Presse Medicale 63(65): 1320-1324
Di Bella, S. 1949: Action of parenteral high-dose synthetic estrogens on serum cholinesterase. Archivio Per le Scienze Mediche 88(2): 174-185
Puig Muset, P.; Ramia, J.; Martín-Esteve, J. 1967: Action of pemoline on RNA metabolism in the brain. Nature 215(5100): 522-523
Scarzella, M. 1948: Action of penicillin aerosols in the treatment of diphtheria germ carriers. LaPediatriadelMedicoPratico 23(5-6): 106
Gros, F.; Rybak, B. 1948: Action of penicillin and streptomycin on the catabolism of ribonucleic acid. Helvetica Chimica Acta 31(6): 1855-1863
Gros, F.; Macheboeuf, M. 1947: Action of penicillin and tyrothricin on the adenylpyrophosphatase activity of extracts of muscles. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(24): 1736-1738
Delay, J.; Dreyfus-Moreau; Stevenin, L. 1946: Action of penicillin in a general juvenile paralysis. Annales Medico-Psychologiques 104: 152-156
Legros, J. 1946: Action of penicillin in aerosols on the diphtheria bacillus. Acta Paediatrica Belgica 1(1-2): 80-82
Pautrier, L.M.; Wasmer 1947: Action of penicillin in local applications in the treatment of suppurative dermatoses. Annales de Dermatologie et de Syphiligraphie 7(4): 152
Lemierre, A.; Reilly, J. 1946: Action of penicillin in some septicemia with anaerobic microbes. La Presse Medicale 54: 49
Gourmont, P.; Gardere, H. 1947: Action of penicillin on Koch's bacillus and on tuberculosis. Revue de la Tuberculose 11(5-6): 350-356
Gros, F.; Macheboeuf, M. 1947: Action of penicillin on the carbohydrate metabolism of Clostridium sporogenes. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(11): 858-860
Citarda, A. 1947: Action of penicillin on the glycemic rate and on the glycidic metabolism in animals (rabbits) and humans; action of penicillin on the glycemic rate in rabbits. Bollettino della Societa Italiana di Biologia Sperimentale 23(5): 503
Nelis, P. 1948: Action of penicillin on the glycerine vaccine pulp. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(7-8): 566
Bonet-Maury, P.; Deysine, A. 1947: Action of penicillin on the homogeneous tuberculosis bacillus of arloing-courmont. Annales de l'Institut Pasteur 73(8): 816-819
Gorini, L.; Torriani, A. 1948: Action of penicillin on the protein-olytic activity of acid-protein-olytic bacteria. Biochimica et Biophysica Acta 2(3): 226-238
Sureau, B.; Boyer, F.; Saviard, M. 1948: Action of penicillinase in vivo; Study of the concentration of penicillin in the blood of rabbits having received penicillinase. Annales de l'Institut Pasteur 75(2): 177-180
Pick, F. 1947: Action of peptone solutions on various combinations of iodine. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(5-6): 240
Thelin, F.; Bonstein, I. 1949: Action of peritoneal dialysis in the uremia; about a recent sighting. Revue Medicale de la Suisse Romande 69(11): 848-851
Marnay, C. 1949: Action of phenylalaline on the growth of colibacillus inhibited by indolacrylic acid. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 229(20): 1036-1038
Somerville, P.J.; Kaye, M. 1982: Action of phosphorus on calcium release in isolated perfused rat tails. Kidney International 22(4): 348-354
Sabet, K.A.; Dowson, W.J. 1951: Action of phytopathogenic bacteria on pectate gel. Nature 168(4275): 605
Guo, Q.; Li, T.; Qu, Y.; Wang, X.; Liu, L.; Liu, H.; Wang, Q. 2021: Action of phytosterols on thermally induced trans fatty acids in peanut oil. Food Chemistry 344: 128637
Soulairac, A.; Soulairac, M.L.; Teysseyre, J. 1955: Action of pituitary corticostimulin, cortisone and dexyxycorticosterone on the testis and the vas deferens of normal adult rats. Annales d'Endocrinologie 16(2): 229-235
Stutinsky, F. 1947: Action of pituitary extracts associated with subtosan on Brunn's reaction in the toad. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(9-10): 477-479
Hinglais, H.; Hinglais, M. 1948: Action of pituitary or chorionic gonadotropins on the adult native male toad (Bufo vulgaris and Bufo calamita); application to the biological diagnosis of gestation. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(7-8): 460
Gautheret, R. 1947: Action of plant tissues on the pH of the media in which they are grown. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(6): 410-412
Legrand, R.; Desruelles, J.; Gerard, A.; Wache, F. 1956: Action of potassium chloride on certain heart rhythm disorders. Therapie 11(6): 1190-1198
Wellers, G. 1949: Action of potassium cyanide on the raw cobra venom. Revue Canadienne de Biologie 8(2): 139-156
Barraud, J.; Derremaux, P.; Roy, J. 1947: Action of powdery aluminum on sluggish wounds. La Presse Medicale 55(2): 25
Kuperman, A.S.; Altura, B.T.; Chezar, J.A. 1968: Action of procaine on calcium efflux from frog nerve and muscle. Nature 217(5129): 673-675
Nordmann, M. 1948: Action of progesterone on childbirth. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 24(90): 2925
Desclin, L. 1948: Action of prolactin on the structure of the ovary of the normal and hypophysectomized rat. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142: 1436-1438
De Gennes, J.L.; Truffert, J. 1955: Action of protamine sulfate on lipids of human serum in vivo. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(7-8): 648-651
Villela, G.G.; Mello, M.I. 1948: Action of pteroalglutamic acid on kidney weight and alkaline phosphatase. Memorias do Instituto Oswaldo Cruz 46(4): 795-801
Neukomm, S.; Thompson, C.B.; Boissonnaz, A. 1949: Action of pure arginase on the growth of transplanted mouse cancer. Experientia 5(6): 239-241
Roig Tarin, M. 1949: Action of pure soda perborate, due to its chemical properties, in particular the production of nascent oxygen, in oral and dental disinfection. Odontoiatria; Revista Ibero-Americana de Medicina de la Boca 6(62): 65-79
Vincent, D.; Segonzac, G.; Issandoucarles, R. 1954: Action of purine alkaloids and caffeine drugs on hyaluronidase. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 148(11-12): 1075-1078
Andre, R. 1946: Action of pyridoxine hydrochloride (vitamin B6) on the central nervous system. Concours Medical 68: 731
Gallagher, C.H.; Koch, J.H. 1959: Action of pyrrolizidine alkaloids on the neuromuscular junction. Nature 183(4668): 1124-1125
Lobato Guimaraes, J. 1949: Action of quinine camphosulfonate on cardiac work in the frog. Archives Internationales de Pharmacodynamie et de Therapie 80(2-3): 125-136
Ludwig, F. 1954: Action of radioactive phosphorus on tumor cells labeled with this element. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 239(5): 453-454
Dechaume, M.; Cauhepe, J.; Goudaert, M. 1949: Action of radiotherapy on the development of the maxillae, dental germs and salivary glands. La Presse Medicale 57(20): 262
Terroine, T. 1946: Action of redox dyes on nitrogenous metabolism. Archives Internationales de Pharmacodynamie et de Therapie 72: 206-223
Pulitano, E. 1948: Action of repeated blood transfusions on gastric secretion. Minerva Medica 39(24): 591-593
Matha, J.; Segonzac, G.; Vincent, D. 1956: Action of reserpine and serpentine on cholinesterases. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 150(7): 1462-1464
Maggi, A.L.; Meeroff, M.; Cosen, J.N. 1957: Action of reserpine on gastric secretion. Prensa Medica Argentina 44(11): 770-777
Baruk, H.; Berges, J.; Launay, S. 1956: Action of reserpine on psychomotricity and experimental catatonia. Revue Neurologique (Paris) 95(1): 62-63
Tuchmann-Duplessis, H.; Mercier-Parot, L. 1956: Action of reserpine on the reproductive system of the adult rat. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 242(9): 1233-1235
Tuchmann-Duplessis, H. 1956: Action of reserpine on the testis and the rat's genital tract. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 242(12): 1651-1653
Kourilsky, R.; Drilhon, A. 1945: Action of riboflavin on experimental staphylococcal infection in guinea pigs. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 139(3-4): 171
Ledoux, L. 1955: Action of ribonuclease on two solid tumours in vivo. Nature 176(4470): 36-37
Cristini, G. 1947: Action of roentgenterapy on the medullary sympathetic centers in glaucoma; Especially in relation to perimetric alterations and optic atrophy. Rivista Oto-Neuro-Oftalmologica 22(2): 124-147
Hazard, R.; Renier-Cornec, A. 1955: Action of rubidium on the isolated intestine of the rat; comparison with potassium. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(3-4): 292-293
Garcha, R.S.; Hughes, A.D. 1997: Action of ryanodine on neurogenic responses in rat isolated mesenteric small arteries. British Journal of Pharmacology 122(1): 142-148
Mazurek, C.; Tardieux, P. 1956: Action of saliva in certain experimental infections. Annales de l'Institut Pasteur 91(5): 774-778
O'brien, R.D.; Spencer, E.Y. 1957: Action of schradan in the cockroach. Nature 179(4549): 52-53
Shah, S.V.; Northrup, T.E.; Hui, Y.S.; Dousa, T.P. 1979: Action of serotonin (5-hydroxytryptamine) on cyclic nucleotides in glomeruli of rat renal cortex. Kidney International 15(5): 463-472
Corazzi, E.S.; Bidoggia, H.; Anselmo, A. 1945: Action of serum gonadotrophins on male and female gonads; experimental work. Prensa Medica Argentina 32: 1861-1865
Mery, J. 1949: Action of several factors on the growth and pigmentation of rhodotorulaceae. Annales de Parasitologie Humaine et Comparee 24(1-2): 180-185
Raynaud, A. 1947: Action of sex hormones on the embryonic development of the mouse mammary gland. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 225(2): 150-152
Rey, M.P. 1947: Action of sex hormones on the muscles of the forelimbs of anuran amphibians; different characteristics of this musculature in the male and female of Bufo vulgaris, Laur. Annales d'Endocrinologie 8(1): 35-41
Sánchez García, J.A.; Santiago Laguna, D. 1981: Action of silymarin on the fatty acid composition of the hepatic lipids of estrogenized chickens. Archivos de Farmacologia y Toxicologia 7(1): 143-150
Sue, P.; Melander, L. 1947: Action of slow neutrons on bromine ions in solution. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 225(9): 413-415
Braganca, B.M.; Quastel, J.H. 1952: Action of snake venom on acetylcholine synthesis in brain. Nature 169(4304): 695-697
Aubel, E.; Szulmajster, J. 1947: Action of sodium azide N3Na on Esch respiration and fermentation. coli. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(9): 680
Gengou, O.; Gregoire, P.E. 1950: Action of sodium citrate on sparingly soluble calcium and barium compounds. Archives Internationales de Pharmacodynamie et de Therapie 81(1): 61-84
Warembourg, H.; Niquet, G.; Lekieffre, J. 1955: Action of sodium dehydrocholate on the lipidogram in normal and atherosclerotic subjects. Therapie 10(6): 931-935
Camelin, A.; Accoyer, P. 1949: Action of sodium gentisate in Bouillaud's disease; first clinical trials. Bulletins et Memoires de la Societe Medicale des Hopitaux de Paris 65(21-22): 826-832
LOEPER Jacques; LOEPER Jacqueline 1954: Action of sodium hyposulfite and mercaptopyruvic acid on the development of methylcholanthrene tumors in rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 148: 1800-1802
Loeper, J. 1955: Action of sodium hyposulfite on the bile elimination of methylcholanthrene. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(1-2): 74-76
Previtera, G.; Condorelli, V. 1949: Action of sodium salicylate and paraminobenzoic acid on the development of the Koch bacillus. Giornale di Batteriologia e Immunologia 40(2): 113-124
Tayeau, F.; Neuzil, E. 1947: Action of sodium salicylate on blood serum in vitro and in vivo. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(1-2): 79
Gajatto, S. 1947: Action of sodium silicate on the isolated toad heart and contributions to the study of the activity carried out by perfusion fluids with various hydrogenion concentration. Rassegna Medica Sarda 49(1-2): 18-21
Heymans, C.; Jacob, J. 1947: Action of sodium succinate on respiration. Experientia 3(7): 294
Masset, J.L. 1947: Action of some antiseptics on molds. Pharmaceutica Acta Helvetiae 22(6): 316-319
Warembourg, H.; Niquet, G.; Lekieffre, J. 1956: Action of some bile acids on the lipoprotein balance of serum. Therapie 11(6): 1094-1100
Binet, L.; Burstein, M. 1948: Action of some cations on the tone of the peripheral vessels. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142: 1363-1366
Bocca, E. 1949: Action of some drugs on the clinical and radiological picture of cardiospasm; diagnostic and therapeutic etiopathogenetic considerations. Minerva Medica 40(23): 684-690
Dumazet, C.; Levy, M.; Marszak, I. 1945: Action of some formers of metal complexes on various phosphoesterases and pyrophosphatases. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 99-101
Becquerel, P.; Rousseau, J. 1947: Action of some growth substances on the germination and productivity of the seeds of pisum sativum. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(10): 700-702
Becquerel, P.; Rousseau, J. 1947: Action of some growth substances, added, either of urane nitrate, or of manganese sulfate, on the germination and the productivity of Pisum sativum. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(11): 773-775
Chauchard, B.; Chauchard, P. 1948: Action of some hormones on the crab's nervous system. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(21-22): 1342
Beretta Anguissola, A.; Lajolo Di Cossano, D.; Pecco, P.; Bert, G. 1970: Action of some immunosuppressive substances on the lymphocytic membrane. Minerva Medica 61(55): 3028-3031
Aubel, E.; Szulmejster, J. 1947: Action of some inhibitory substances on the respiration and the fermentation of Esch. coli. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(22): 1592
Nelis, P. 1945: Action of some microbial filtrates on bacterial toxins. Revue Belge des Sciences Medicales 16: 373-377
Alcalay, W. 1947: Action of some naphthoquinonic compounds on experimental tuberculosis. Schweizerische Zeitschrift für Pathologie und Bakteriologie. Revue Suisse de Pathologie et de Bacteriologie 10(5): 501-516
Parant, M.; Raymond-Hamet; Vincent, D. 1956: Action of some sympathicosthenic alkaloids on cholinesterases. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 150(7): 1384-1386
Monro, R.E.; Celma, M.L.; Vazquez, D. 1969: Action of sparsomycin on ribosome-catalysed peptidyl transfer. Nature 222(5191): 356-358
Franck, C.; Grandpierre, R.; Lemaire, R. 1947: Action of sparteine sulfate on hypogastric hypertensive reflex. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(3-4): 179
Hazard, R.; Beauvallet, M.; Guidicelli, R. 1947: Action of spartine on the vascular effects of diphenolic amino alcohols related to adrenaline. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(5-6): 219
Vallejos, R.H.; Stoppani, A.O. 1965: Action of steroids on mitochondrial respiration. Revista de la Sociedad Argentina de Biologia 41(5): 214-223
Vallejos, R.H.; Stoppani, A.O. 1965: Action of steroids on the oxidation of ascorbate-TMPD by mitochondria. Revista de la Sociedad Argentina de Biologia 41(5): 236-244
Nasio, J. 1946: Action of stilbestrol by parenteral route on the development of experimental zinc peptic ulcer. Prensa Medica Argentina 33: 859-862
Leone, R. 1949: Action of streptomycin and penicillin on Sabouraud's microbacillus. Giornale Italiano di Dermatologia 90(2): 101-105
Christiaens 1948: Action of streptomycin on Koch's bacillus; the clinical point of view. Journal des Sciences Medicales de Lille 66(23): 515-518
Spaas, G. 1949: Action of streptomycin on hearing. Acta Oto-Rhino-Laryngologica Belgica 3(3): 429-439
De Ropp, R.S. 1948: Action of streptomycin on plant tumours. Nature 162(4116): 459
Gernez 1948: Action of streptomycin on the bacillus of Koch. Journal des Sciences Medicales de Lille 66(23): 514
Ezes, H.; Laffargue, P. 1948: Action of streptomycin on the follicular formations of the endometrium during granulia. Comptes Rendus de la Societe Francaise de Gynecologie 18(6): 177
Tisca; Weil 1948: Action of streptomycin on tuberculous caves. Journal de Medecine de Lyon 29(695): 915
Quaranta, L. 1949: Action of streptomycin on tuberculous lesions in different stages of evolution in the same subject. Accademia Medica 64(11): 369-371
De Angeli, W.; Barsantini, J.C. 1955: Action of stress on the activity of hepatic arginase in rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149: 1711-1712
De Angelis, W.; Vignolo, W.H.; Barsantini, J.C. 1956: Action of stress on the activity of hepatic arginase in rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 150(8-9): 1655-1657
Olivier, H.R.; De Saint-Rat, L. 1946: Action of subtle bacillus and endo-subtilysin on Koch's bacillus (Arloing and Courmont strain) and in experimental tuberculosis. Revue de Tuberculose et de Pneumologie 10(1-2): 50-52
Dureuil, M.; Rakoto Ratsimananga, A. 1948: Action of sudden temperature variations on the capacity of forced labor of the normal rat. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(11-12): 720-723
Mouzon; Nemours-Auguste 1947: Action of sugar on the evacuation of the dolicho-megaoesophagus. ArchivesdesMaladiesdel'AppareilDigestifetdesMaladiesdelaNutrition 36(3-4): 204
De Allende, I.L.D.; Astrada, J.J.; Orias, O. 1948: Action of sulfa drugs on ovulation and sperm release in the Bufo arenarum Hensel toad. Revista de la Sociedad Argentina de Biologia 24(3): 218-224
Lenti, G. 1948: Action of sulfamicides on the anaphylactic shock of the guinea pig. Il Policlinico. Sezione Pratica 55(15): 468
De Almeida, F.; Da Silva Lacaz, C.; Forattini, O.P. 1946: Action of sulfanilamide and its derivatives, in vitro, on Paracoccidioides brasiliensis. Resenha Clinico-Cientifica 15: 113-117
Kayser, F.; Besson, S. 1948: Action of sulfonamides and colchicine on the development of the Pisum root. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(1-2): 84-86
Lozac'h, N. 1947: Action of sulfur on eugenol and isoeugenol. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 225(16): 686-688
Martini, M.T. 1947: Action of sulphonamides on leukocytes grown in vitro. Clinica Odontoiatrica; Revista Mensile di Operativa Dentaria Chirurgia Orale Ortodontia e Protesi 2(4): 87
Town, B.W.; Wills, E.D.; Wormall, A. 1949: Action of suramin and antrycide on enzymes. Nature 164(4162): 233
Mazzella, H.; Garcia Mullin, R. 1956: Action of sympathomimetic amines on the sympathectomized carotid sinus. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 150(8-9): 1660
Hugues, J. 1946: Action of sympathomimimetic amines on human glycemia: therapeutic conclusions. Acta Clinica Belgica 1(5): 429-435
Nemours-Auguste 1947: Action of syncope on the evacuation of the dolicho-megaoesophagus. ArchivesdesMaladiesdel'AppareilDigestifetdesMaladiesdelaNutrition 36(3-4): 202
Quagliariello, E.; Auricchio, S.; Barone, B. 1956: Action of synkavit on conversion of 3-hydroxyanthranilic acid to quinolinic acid. Bollettino della Societa Italiana di Biologia Sperimentale 32(12): 1575-1577
Boucher, H.; Lafuma, J.; Grenaut, J. 1949: Action of synthetic antihistamines on certain syndromes of early or late pleural intolerance during collapsotherapy. Lyon Medical 181(3): 33-37
Halpern, B.; Reuse, J. 1949: Action of synthetic antihistamines on the imbibition of the striated muscle. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 228(6): 514-516
Mayer, G. 1949: Action of synthetic curarisants during epigastric colors of ulcerative or non-ulcerative digestive origin. Gazette Medicale de France 56(24): 943
Thiers, H.; Racouchot, J.; Traeger 1948: Action of synthetic estrogens in gonococcal prostatitis. Lyon Medical 179(17): 291
Laroche, G.; Hochfeld, M. 1947: Action of synthetic estrogens on sedimentation rate and haptoglobin index. Annales d'Endocrinologie 8(1): 92-95
Lepage, F. 1947: Action of synthetic estrogens on the milky rise. Bulletin Medical 61(21): 309
Chaudhury, R.R.; Chaudhury, M.R. 1962: Action of synthetic oxytocin on the crop gland of the pigeon. Nature 193: 179-180
Vincent, D.; De Prat, J. 1945: Action of tannin toxin and diphtheria toxin risk on serum cholinesterase. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 1146-1148
Daviault, L. 1947: Action of temperature and humidity on the biology of Pristiphora geniculata Htg. (Hymenoptera, Tenthredinidae). Revue Canadienne de Biologie 6(2): 366-368
Boquien, Y.; Trichereau, R. 1954: Action of terramycin on carriers of diphtheria germs. Bulletins et Memoires de la Societe Medicale des Hopitaux de Paris 70(21-23): 807-809
Gross, A. 1954: Action of testosterone on experimental white asthma. Therapie 9(6): 752-755
Jost, A. 1947: Action of testosterone on the castrated rabbit embryo. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(5-6): 275
Hamon, M. 1945: Action of testosterone on the morphology of Gambusia holbrooki Gir male. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 108
Herve, A.; Lecomte, J. 1949: Action of the Adrenochromic Semicarbazone on Petechiae Caused by X-radiation. Archives Internationales de Pharmacodynamie et de Therapie 79(1): 109-112
Likerman, J.E.; Viegas Aurelio, J.I. 1947: Action of the D.D.T. on the Argas persicus. Revista de Medicina Veterinaria 29: 550-556
Nunes, Jão.M.; Mayer-Hartl, M.; Hartl, F.Ulrich.; Müller, D.J. 2015: Action of the Hsp70 chaperone system observed with single proteins. Nature Communications 6: 6307
Bugnard, L.; Planques, J. 1946: Action of the Lobeline on the electroencephalogram of epileptics. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 22: 1225
Vauthey, P.; Vauthey, M. 1946: Action of the Vichy cure on ascorbic metabolism in hepatobiliary. Journal Mediterranee Medical 14: 406-413
Desgrez, P.; Delbarre, F.; Chevrolle, J. 1946: Action of the adrenochromic semicarbazone on the glycemia of normal humans. Annales de Biologie Clinique 4(9): 272
Nasio, J. 1946: Action of the antitoxic principle in liver diseases; influence in the pre and postoperative period of the biliary tract. CONGRESO. Sociedad de Cirujanos de Chile 8: 244-267
Chauchard, B.; Chauchard, P. 1947: Action of the centers on the local sensitivity of the nerves. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 149-152
Mariat, F. 1948: Action of the components of aneurine on the development of orchid embryos. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(11-12): 840
Dureuil, M.; Prost, M.; Rakoto Ratsimananga, A. 1948: Action of the cortical hormone on the work of the rat stimulated by heat. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(11-12): 723-726
Mercier, J. 1948: Action of the cupric ion on the isolated intestine of rabbits and dogs. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(5-6): 362
Pitous, P. 1949: Action of the cure of Barbotan on the functions of elimination. LaPresseThermaleetClimatique 86(3-4): 100
Jorge, C. 1949: Action of the diatragma on the last ribs; experimental study. Clinica Contemporanea; Revista de Medicina e Cirurgia 3(28): 1589-1594
Mahaux, J.; Kowalewski, K. 1948: Action of the diethylaminoethyl ester of phenyl-cyclopentane-carboxylic acid (parpanit) on basal metabolism and metabolism after the effort of hyperthyroid, hypothyroid and normothyroid subjects. Archives Internationales de Pharmacodynamie et de Therapie 77(3): 289-299
Genevois, L.; Paynaud, E.; Ribereau-Gayon, J. 1948: Action of the environment on the secondary products of alcoholic fermentation of elliptical yeasts. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 226(1): 126-128
Rahandraha, T.; Ratsimamanga, A.R. 1955: Action of the enzymatic system of the normal and scurvy adrenal gland on neutral cholesterol oxidation products. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149(11-12): 1206-1209
Caujolle, F.; Franck, C. 1945: Action of the essence of marjoram (Origanum majorana L.) of the terpenes of the essence of marjoram and the essence of detergpen marjoram on intestinal motility. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139(3-4): 210-212
Parvis, D.; Ceppelini, R. 1948: Action of the filtrate of Aspergillus fumigatus on the acid-resistance of the B. paratuberculars and tuberculars. Giornale di Batteriologia e Immunologia 39(1): 3-10
Remlinger, P.; Bailly, J. 1946: Action of the filtrate of bacillus subtilis cultures on the equine encephalomyelitis virus. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 223(6): 267
Junod, J.M. 1947: Action of the gonadotropic antihormone on cancer growth. Schweizerische Medizinische Wochenschrift 77(5): 191
Flores, N.A. 1948: Action of the gravid urine in hypophysectomized male toads. Revista de la Sociedad Argentina de Biologia 24(3): 307-310
Hamon, M. 1945: Action of the hormone estrogen on the external morphology of Gambusia holbrooki (Girard). Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 740-742
Hamon, M. 1945: Action of the hormone estrogen on the germline male of Gambusia holbrooki (Gir.). Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 762-763
Mussio-Fournier, J.C.; Conti, O. 1949: Action of the hormone melanophore on the visual disturbances of diabetic retinosis. Bulletin de l'Academie Nationale de Medecine 133(23-24): 485-489
Irving, J.T. 1956: Action of the hypophysis and of dietary protein on the calcifying tissues. Nature 178(4544): 1231
Warter, J.; Fitzenkam, A. 1948: Action of the infiltration of the pneumogastric nerves on the pains of peptic ulcers. Strasbourg Medical 108(12): 127
Capretti, G.; Bonaconza, E. 1949: Action of the infusion and the decoction of olive leaves (Olea europea) on some physical constants of the blood (viscosity and surface tension) and on some components of the exchange (uric acid, chlorides, Na, K, cholesterin). Giornale di Clinica Medica 30(8): 630-642
Longo, O.F.; Sosa Gallardo, C. 1949: Action of the intravenous novocaine in acute pancreatic diseases. Prensa Medica Argentina 36(4): 179-184
Desnuelle, P.; Rovery, M. 1947: Action of the ketene on protein thiol groups. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(3): 235-237
Dumont, L. 1945: Action of the liver and the kidneys on arterial hypertension by renal ischemia. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 318
Gley, P.; Benard, R.; Goossens, R. 1948: Action of the pancreas on the healing process. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 142(21-22): 1375
Makhlouf, G.M.; McManus, J.P.; Card, W.I. 1968: Action of the pentapeptide (ICi 50123) on gastric secretion in man. Gastroenterology 54(4 Suppl): 727-728
Schlechter, P. 1947: Action of the pituitary gonadotropic hormones on the breathing of the gonads. Bollettino della Societa Italiana di Biologia Sperimentale 23(12): 1289
Pavlovsky, A.; Castellanos, H. 1948: Action of the routine on the fragility and capillary permeability. Revista de la Asociacion Medica Argentina 62: 631-632
Cingolini, P. 1949: Action of the réntgenterapia of the bony epiphyses on the water, lipoid and protidic exchange; treatment of diabetes insipidus and lipoid nephrosis. Radiologia; Rassegna Internazionale Trimestrale di Radiobiologia Radioterapia Radiodiagnostica Terapia Fisica e Fisica Applicata Alla Medicina 5(1): 25-34
Wahl, R. 1946: Action of the sublimated on bacteriophages. Annales de l'Institut Pasteur 72: 287-289
Perello, J.M.; Serrano, M. 1948: Action of the sulfa drugs on the germination and growth of Ricinus communis. Farmacognosia; Anales del Instituto Jose Celestino Mutis 7(12): 35-45
Castex, M.R.; Capdehourat, E.L.; Rechniewski, C. 1947: Action of the transthoracically injected streptomycin on the microbial flora of the expectoration of chronic pulmonary suppurations; On the subject of two observations. Prensa Medica Argentina 34(40): 1885-1890
Cachera, R.; Lamotte, M. 1949: Action of the treatment of hyperthyroidism on extra-cellular fluids. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 25(39): 1666-1672
Cachera, R.; Lamotte, M. 1949: Action of the treatment of hyperthyroidism on extra-cellular fluids. Bulletins et Memoires de la Societe Medicale des Hopitaux de Paris 65(15-16): 635-643
Truhaut, R.; Delsol, M. 1947: Action of the unsaponifiable matter of the liver of cancerous subjects on tissue cultures in vitro. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 136-138
Vidal Breard, J.J. 1946: Action of the venom of Bothrops neuwiedii meridionalis on Staphylococcus aureus. Archivos de Bioquimica Quimica y Farmacia Tucuman 3(1): 127-135
Boquet, P.; Lehoult, Y. 1948: Action of the venom of Naja tripudians, Vipera aspis and Vipers russellii (Daboïa) on the cytoplasm of bacteria. Annales de l'Institut Pasteur 74(4): Unknown
De Allende, I.L.C.; De Caligaris, L.S.; Orias, O. 1948: Action of thiamine, ascorbic acid and tocopherols on the secretion of the glands of the oviduct in the toad Bufo arenarum Hensel. Revista de la Sociedad Argentina de Biologia 24(3): 301-306
Eley, S.L.; Allen, C.M.; Williams, C.L.; Bukoski, R.D.; Pointer, M.A. 2008: Action of thiazide on renal interstitial calcium. American Journal of Hypertension 21(7): 814-819
Martinez Aparicio, A. 1949: Action of thio-barbiturates on the electrocardiogram. Revista Cubana de Cardiologia 10(1): 41-48
Human, J.P.E.; Mills, J.A. 1946: Action of thionyl chloride on carboxylic acids in presence of pyridine. Nature 158(4024): 877
Tinacci, F. 1947: Action of thiouracil and methylthiouracil on the gaseous exchanges of fertilized sea urchin eggs. Bollettino della Societa Italiana di Biologia Sperimentale 23(12): 1101
Delsol, M. 1948: Action of thiouracil on the metamorphosis of Discoglossus pictus Otth. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(7-8): 458-460
Florentin, P.; Martin, R.; Sadoul, P. 1947: Action of thiourea on the adrenal cortex. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 177-179
Ritchie, J.C.; Davis, T.P.; Nemeroff, C.B. 2003: Action of three ectopeptidases on corticotropin-releasing factor: metabolism and functional aspects. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology 28(1): 22-33
Bailey, K.; Bettelheim, F.R.; Lorand, L.; Middlebrook, W.R. 1951: Action of thrombin in the clotting of fibrinogen. Nature 167(4241): 233-234
Comsa, J. 1947: Action of thymus extract on guinea pig urine creatine. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(16): 1185-1187
Louw, G.N.; Sutton, W.W.; Kenny, A.D. 1967: Action of thyrocalcitonin in the teleost fish Ictalurus melas. Nature 215(5103): 888-889
Wase, A.W.; Solewski, J.; Rickes, E.; Seidenberg, J. 1967: Action of thyrocalcitonin on bone. Nature 214(5086): 388-389
Michel, R.; Michel, O.; Raoul, B. 1968: Action of thyroid hormones on the oxidoreduction state of respiratory coenzymes. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences. Serie D: Sciences Naturelles 267(10): 969-971
Begg, D.J.; Munro, H.N. 1965: Action of thyroid-stimulating hormone on ribonucleic acid synthesis in thyroid slices and in isolated thyroid nuclei. Nature 207(996): 483-485
Peczenik, O. 1946: Action of thyroxin and the response of the thyroid to treatment with sulpha drugs. Nature 157: 771
Wright, M.R.; Lerner, A.B. 1960: Action of thyroxine analogues on frog melanocytes. Nature 185: 169-170
Masson, G. 1947: Action of thyroxine on the testoid effect of testosterone. Revue Canadienne de Biologie 6(2): 355-358
Baranger, P.; Thomas, P.; Filer, M.K. 1947: Action of total alkaloids extracted from quinquinas in Madagascar on P. relictum and P. gallinaceum. Annales de l'Institut Pasteur 73(8): 764-776
Bourguignon, G. 1945: Action of transceereal calcium electrolysis on the ovary, before and after hypophysectomy in rats. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139(11-12): 568-570
Truhaut, R.; Deysson, G. 1955: Action of triethylenamine on the seedlings of Pisum sativum L .; beta-mercaptoethlamine protection tests. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 240(10): 1123-1125
Ramanamanjary, W. 1947: Action of trimethylammonium propanediol ethylal (2268 F.) on the dog's heart rate. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(3-4): 110
Brochier, A. 1956: Action of two antibiotics on a Salmonella paratyphi B toxin. Revue d'Immunologie et de Therapie Antimicrobienne 20(5-6): 404-412
Mercier, J. 1947: Action of two organic lithium salts on the diuresis and the elimination of uric acid in rabbits. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(9-10): 491-494
De Seguin, L.; Castelain, G. 1947: Action of ultra-high frequency waves (wavelength 21 cm) on the temperature of small laboratory animals. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(23): 1662
Consden, R.; Kirrane, J.A. 1967: Action of ultra-violet light on soluble collagens. Nature 215(5097): 165-166
Denier, A. 1949: Action of ultrasound on gastrointestinal motility. JournaldeRadiologied'ElectrologieandArchivesd'ElectriciteMedicale 30(5-6): 349
Violle, H. 1948: Action of ultrasound on pertussis bacillus. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 227(18): 922-924
Mastagli, P.; Mahoux, A.P. 1947: Action of ultrasound on the properties of simple bodies and composite bodies. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(4): 276
Loza, J. 1949: Action of ultrasound on the seeds and seedlings of higher plants. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 228(7): 595
Perrault, M.; Vignalou, J.; Baillet, J. 1948: Action of urethra in a case of chronic myeloid leukemia in acute flare-up. Therapie 3(2): 49-52
Maragliano, G.; Petrina, N. 1948: Action of urotropin on human isoemagglutinins. Giornale di Batteriologia e Immunologia 39(1): 69-76
Chauchard, P. 1945: Action of vagotonin on the pre- and post-ganglionic sympathetic fibers. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 238
Gagnier, M. 1949: Action of vanilla tincture on uterine contraction. La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 25(55): 2361-2363
Vetulani, J.; Sulser, F. 1975: Action of various antidepressant treatments reduces reactivity of noradrenergic cyclic AMP-generating system in limbic forebrain. Nature 257(5526): 495-496
Pontieri, G.; Chaumont, L. 1954: Action of various antiseptics on the shope fibroma virus. Annales de l'Institut Pasteur 86(4): 532-534
Halpern, B.N.; Gaudin, O. 1948: Action of various cholera drugs on the composition of bile in dogs with a permanent bile fistula. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(11-12): 779-783
Mouriquand, G.; Coisnard, J. 1946: Action of various drugs on vestibular chronaxy. Bulletin de l'Academie de Medecine 130(9-11): 172-178
Mouriquand, G.; Coisnard, J. 1946: Action of various drugs on vestibular chronaxy; subjects at rest or in a state of sporting activity. Journal de Medecine de Lyon 27(636): 487-490
Sentein, P. 1949: Action of various substances, caffeine, urethra, cacodylate, trypaflavin, on mitosis. Schweizerische Medizinische Wochenschrift 79(23): 528
Jagues, S. 1946: Action of verrine on muscular excitability. Revue Canadienne de Biologie 5(5): 511-546
Castellanos, F.J. 1948: Action of vibrations on the body. Revista de Sanidad de Aeronautica 1(3): 121-124
Tropeano, L. 1948: Action of vitamin e on blood clotting. Il Progresso Medico 4(6): 169
Parrot, J.L.; Galmiche, P. 1945: Action of vitamin P on bleeding time. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 948-950
Lecoq, R.; Chauchard, P.; Mazoue, H. 1947: Action of vitamin P on neuromuscular disorders of scurvy. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(1-2): 52
Pegni, U. 1949: Action of vitamin PP introduced intravenously on the blood and bone marrow in some anemias. Haematologica 33(4): 369-377
Bacq, Z.M.; Desreux, V. 1948: Action of war veterans and toxicants on proteins and enzymes. Exposes Annuels de Biochimie Medicale 2(8 Ser): 67-82
Solomides, J. 1945: Action of water and rabbit serum on the toxic and antigenic properties of glycerin. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139: 10-12
Delga, J.; Hazard, R. 1955: Action of yohimbine on noradrenal hyperkalemia; comparison with its action on adrenal hyperkalemia. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 149: 1756-1759
Hazard, R.; Beauvallet, M.; Giudicelli, R. 1947: Action of yohimbine on the cardiovascular effects of diphenolic amino alcohols apparent to adrenaline. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 123-125
Amoaku, W.; Blakeney, S.; Freeman, M.; Gale, R.; Johnston, R.; Kelly, S.P.; McLaughlan, B.; Sahu, D.; Varma, D.; Amoaku, W.; Blakeney, S.; Freeman, M.; Gale, R.; Johnsto, R.; Kelly, S.P.; McLaughlan, B.; Sahu, D.; Varma, M.Deepali. 2012: Action on AMD. Optimising patient management: act now to ensure current and continual delivery of best possible patient care. Eye 26 Suppl. 1: S2-21
Raoul, Y.; Chopin, J.; Ayrault, A. 1947: Action on Bacillus coli of the naphthalene isostere of tryptophan and action of anthranillic acid. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(18): 1309-1311
Roche, J.; Nguyen-Van Thoai; Dziri, A. 1945: Action on amino acid amylases associated with metal ions. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 139(11-12): 519-522
Flandin, C.; Flandin, F.; Millot, J. 1945: Action on blood coagulation in vitro of fontarsan and fontarsol. Annales de Dermatologie et de Syphiligraphie 5: 75
Gale, R.; Scanlon, P.H.; Evans, M.; Ghanchi, F.; Yang, Y.; Silvestri, G.; Freeman, M.; Maisey, A.; Napier, J. 2017: Action on diabetic macular oedema: achieving optimal patient management in treating visual impairment due to diabetic eye disease. Eye 31(S1): S1-S20
Hele, J. 1993: Action on food labelling. South African Medical Journal 83(2): 134
Feissly, R. 1949: Action on hemophiliac plasma of a thromboplastin co-factor existing in normal plasma. Schweizerische Medizinische Wochenschrift 79(36): 829
Collins, P.Y.; Saxena, S. 2016: Action on mental health needs global cooperation. Nature 532(7597): 25-27
Sautet, J.; Audouin, A. 1947: Action on mosquito larvae, a pure suspension of D.D.T. obtained by ultrasound. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences 224(1): 66
Loeb, J. 2021: Action on pet primates falls short of a ban. Veterinary Record 189(4): 132
Mills, G. 2021: Action on puppy smuggling announced. Veterinary Record 189(5): 180
Watt, R.G.; Johnson, N.W.; Warnakulasuriya, K.A. 2000: Action on smoking--opportunities for the dental team. British Dental Journal 189(7): 357-360
Faccini, L.; Arduini, M. 1948: Action on the bladder of albino rats and guinea pigs of synthetic estrogens administered by injection and subcutaneous grafting. Annali Italiani di Chirurgia 25(9): 577-602
Martin, R.; Sureau, B.; Joyeux, Y. 1945: Action on the body of p-aminophenylsulfamido-2-pyrimidine and methyldiazine. Annales de l'Institut Pasteur 71: 210-216
Pisanty, J. 1949: Action on the cardiac and skeletal muscle of some substances that interrupt the intermediate metabolism of glucose. Archivos del Instituto de Cardiologia de Mexico 19(1): 110-116
Theodorides, J. 1949: Action on the mushrooms of mineral essence and carmine in solution in oil. Annales de Parasitologie Humaine et Comparee 24(1-2): 116-123
Luteraan, P.J.; Mery, J. 1949: Action on the mushrooms of miners spirits and carmine In solution in petroleum. AnnalesdeParasitologieHumaineetComparee 24(1-2): 191
Rousset, J.; Soeur Marie-Suzanne 1949: Action on the underlying injections of hydrogenated chaulmoogra oil. Lyon Medical 182(47): 328
Hestrin, S. 1948: Action pattern of crystalline muscle phosphorylase. Biological Bulletin 95(2): 238
Sano, M.; Yamaguchi, K.; Fukatsu, R.; Hoshiyama, M. 2019: Action performance in children with autism spectrum disorder at preschool age: a pilot study. International Journal of Developmental Disabilities 66(4): 289-295
Gallivan, J.P.; Barton, K.S.; Chapman, C.S.; Wolpert, D.M.; Flanagan, J.Randall. 2015: Action plan co-optimization reveals the parallel encoding of competing reach movements. Nature Communications 6: 7428
Walgate, R. 2005: Action plan peps up Europe's mental health. Nature Medicine 11(3): 239
Bahadori, M.; Barumerli, R.; Geronazzo, M.; Cesari, P. 2021: Action planning and affective states within the auditory peripersonal space in normal hearing and cochlear-implanted listeners. Neuropsychologia 155: 107790
Enachescu, V.; Schrater, P.; Schaal, S.; Christopoulos, V. 2021: Action planning and control under uncertainty emerge through a desirability-driven competition between parallel encoding motor plans. Plos Computational Biology 17(10): E1009429
Elliman, M.G.; Sloman, P.; South, M.; Cheng, D.R. 2020: Action plans into action - An electronic action plan generation tool at a paediatric centre. International Journal of Medical Informatics 141: 104219
Flanagan, J.Randall.; Johansson, R.S. 2003: Action plans used in action observation. Nature 424(6950): 769-771
Begum, R.; Bakiri, Y.; Volynski, K.E.; Kullmann, D.M. 2016: Action potential broadening in a presynaptic channelopathy. Nature Communications 7: 12102
Macianskiene, R.; Bito, V.; Raeymaekers, L.; Brandts, B.; Sipido, K.R.; Mubagwa, K. 2003: Action potential changes associated with a slowed inactivation of cardiac voltage-gated sodium channels by KB130015. British Journal of Pharmacology 139(8): 1469-1479
Kole, M.H.P.; Ilschner, S.U.; Kampa, Börn.M.; Williams, S.R.; Ruben, P.C.; Stuart, G.J. 2008: Action potential generation requires a high sodium channel density in the axon initial segment. Nature Neuroscience 11(2): 178-186
Yi, G.; Wang, J.; Wei, X.; Deng, B. 2017: Action potential initiation in a two-compartment model of pyramidal neuron mediated by dendritic Ca 2+ spike. Scientific Reports 7: 45684
Weiss, D.E. 1969: Action potential model based on a lipophosphoprotein. Nature 223(5206): 634-635
Kyriacou, C.P.; Hall, J.C. 1985: Action potential mutations stop a biological clock in Drosophila. Nature 314(6007): 171-173
Engelhorn, R. 1957: Action potential of kidney nerves. Naunyn-Schmiedebergs Archiv für Experimentelle Pathologie und Pharmakologie 232(1): 251-252
Mueller, P.; Rudin, D.O. 1967: Action potential phenomena in experimental bimolecular lipid membranes. Nature 213(5076): 603-604
Mortensen, P.; Gao, H.; Smith, G.; Simitev, R.D. 2021: Action potential propagation and block in a model of atrial tissue with myocyte-fibroblast coupling. Mathematical Medicine and Biology: a Journal of the Ima 38(1): 106-131
Lowe, M.D.; Grace, A.A.; Vandenberg, J.I.; Kaumann, A.J. 1998: Action potential shortening through the putative beta4-adrenoceptor in ferret ventricle: comparison with beta1- and beta2-adrenoceptor-mediated effects. British Journal of Pharmacology 124(7): 1341-1344
Klassen, S.A.; Shoemaker, J.K. 2021: Action potential subpopulations within human muscle sympathetic nerve activity: Discharge properties and governing mechanisms. Autonomic Neuroscience: Basic and Clinical 230: 102743
Fabricant, A.; Iwata, G.Z.; Scherzer, Sönke.; Bougas, L.; Rolfs, K.; Jodko-Władzińska, A.; Voigt, J.; Hedrich, R.; Budker, D. 2021: Action potentials induce biomagnetic fields in carnivorous Venus flytrap plants. Scientific Reports 11(1): 1438
Mueller, P.; Rudin, D.O. 1968: Action potentials induced in biomolecular lipid membranes. Nature 217(5130): 713-719
Schalow, G.; Schmidt, H. 1975: Action potentials induced in slow muscle fibres by partial denervation. Nature 253(5487): 122-123
Mulkey, R.M.; Zucker, R.S. 1991: Action potentials must admit calcium to evoke transmitter release. Nature 350(6314): 153-155
Miyajima, Y.; Tsugu, Y.; Tatsu, R.; Ozawa, T.; Shibata, Y. 1974: Action potentials of the stomach during vagotomy. Nihon Heikatsukin Gakkai Zasshi 10(3): 232
Ward, E.K.; Braukmann, R.; Weiland, R.F.; Bekkering, H.; Buitelaar, J.K.; Hunnius, S. 2021: Action predictability is reflected in beta power attenuation and predictive eye movements in adolescents with and without autism. Neuropsychologia 157: 107859
Monroy, C.; Chen, C.-H.; Houston, D.; Yu, C. 2021: Action prediction during real-time parent-infant interactions. Developmental Science 24(3): E13042
Strassburg, S.; Pfluger, P.T.; Chaudhary, N.; Tso, P.; Tschöp, M.H.; Anker, S.D.; Nogueiras, R.; Perez-Tilve, D. 2010: Action profile of the antiobesity drug candidate oleoyl-estrone in rats. Obesity 18(12): 2260-2267
Steensgaard, R.; Kolbaek, R.; Jensen, J.B.; Angel, S. 2021: Action research as a catalyst for change: Empowered nurses facilitating patient participation in rehabilitation. Nursing Inquiry 28(1): E12370
Bjurling-Sjöberg, P.; Pöder, U.; Jansson, I.; Wadensten, B.; Nordgren, L. 2021: Action research improved general prerequisites for evidence-based practice. Heliyon 7(4): E06814
Lee, H-Tzu.Sophie.; Chen, T-Ru.; Yang, C-Ling.; Chiu, T-Yuan.; Hu, W-Yu. 2019: Action research study on advance care planning for residents and their families in the long-term care facility. Bmc Palliative Care 18(1): 95
Wilson, C.; Heinrich, L.; Heidari, P.; Adams, K. 2020: Action research to implement an Indigenous health curriculum framework. Nurse Education Today 91: 104464
Palmér, T.; Ek, F.; Enqvist, O.; Olsson, R.; Åström, K.; Petersson, P. 2017: Action sequencing in the spontaneous swimming behavior of zebrafish larvae - implications for drug development. Scientific Reports 7(1): 3191
Margiotoudi, K.; Pulvermüller, F. 2020: Action sound-shape congruencies explain sound symbolism. Scientific Reports 10(1): 12706
Barran, P. 2020: Action spectra of chiral secondary structure. Science 368(6498): 1426-1427
Coughlan, N.J.A.; Stockett, M.H.; Kjær, C.; Ashworth, E.K.; Bulman Page, P.C.; Meech, S.R.; Brøndsted Nielsen, S.; Blancafort, L.ís.; Hopkins, W.S.; Bull, J.N. 2021: Action spectroscopy of the isolated red Kaede fluorescent protein chromophore. Journal of Chemical Physics 155(12): 124304
Ikehata, H.; Higashi, S.; Nakamura, S.; Daigaku, Y.; Furusawa, Y.; Kamei, Y.; Watanabe, M.; Yamamoto, K.; Hieda, K.; Munakata, N.; Ono, T. 2013: Action spectrum analysis of UVR genotoxicity for skin: the border wavelengths between UVA and UVB can bring serious mutation loads to skin. Journal of Investigative Dermatology 133(7): 1850-1856
Carr, R.E.; Siegel, I.M. 1970: Action spectrum of the human early receptor potential. Nature 225(5227): 88-89
Mattila, H.; Khorobrykh, S.; Hakala-Yatkin, M.; Havurinne, V.; Kuusisto, I.; Antal, T.; Tyystjärvi, T.; Tyystjärvi, E. 2020: Action spectrum of the redox state of the plastoquinone pool defines its function in plant acclimation. Plant Journal: for Cell and Molecular Biology 104(4): 1088-1104
Padma, T.V. 2011: Action urged on foreign takeovers of Indian drugmakers. Nature Medicine 17(2): 141
Dalton, R. 2001: Action urged to combat killer algae. Nature 412(6844): 260
Klepp, A.; van Dijk, H.; Niccolai, V.; Schnitzler, A.; Biermann-Ruben, K. 2019: Action verb processing specifically modulates motor behaviour and sensorimotor neuronal oscillations. Scientific Reports 9(1): 15985
Frak, V.; Labrecque, D.; Cohen, H. 2021: Action verbs drive motor activity in adolescents but not in children. Brain and Cognition 148: 105673
Green, C.Shawn.; Bavelier, D. 2003: Action video game modifies visual selective attention. Nature 423(6939): 534-537
Zhang, R-Yuan.; Chopin, A.; Shibata, K.; Lu, Z-Lin.; Jaeggi, S.M.; Buschkuehl, M.; Green, C.Shawn.; Bavelier, D. 2021: Action video game play facilitates "learning to learn". Communications Biology 4(1): 1154
Peters, J.L.; Crewther, S.G.; Murphy, M.J.; Bavin, E.L. 2021: Action video game training improves text reading accuracy, rate and comprehension in children with dyslexia: a randomized controlled trial. Scientific Reports 11(1): 18584
Franceschini, S.; Trevisan, P.; Ronconi, L.; Bertoni, S.; Colmar, S.; Double, K.; Facoetti, A.; Gori, S. 2017: Action video games improve reading abilities and visual-to-auditory attentional shifting in English-speaking children with dyslexia. Scientific Reports 7(1): 5863
Aron, M.; Aron, C. 1947: Action, on the guinea pig thyrold, of the thyroxine directly introduced into the gland, compared with its action by subcutaneous injection. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(3-4):Unknown
Aron, M.; Aron, C. 1947: Action, on the thyroid gland, in the guinea pig, of iodine, of certain iodized compounds and of thyroid extract, directly introduced into the organ; Test of interpretation of thyroid functioning. ComptesRendusdesSeancesdelaSocietedeBiologieetdeSesFiliales 141(11-12): 670
Urbanik, P.ł; Svennevig, J. 2021: Action-Depicting Gestures and Morphosyntax: the Function of Gesture-Speech Alignment in the Conversational Turn. Frontiers in Psychology 12: 689292
Gould, S.J. 2020: Action-Observation in Fine Motor Learning Applying Neuropsychology Principles to Enhance Academic Teaching in the Field of Rheumatology a Pilot Study. Bulletin of the Hospital for Joint Disease 78(2): 144-145
Arora, V.; Ventresca, M. 2017: Action-based Modeling of Complex Networks. Scientific Reports 7(1): 6673
Heiney, S.A.; Wojaczynski, G.J.; Medina, J.F. 2021: Action-based organization of a cerebellar module specialized for predictive control of multiple body parts. Neuron 109(18): 2981-2994.E5
Horváth, János.; Bíró, B.; Neszmélyi, B. 2018: Action-effect related motor adaptation in interactions with everyday devices. Scientific Reports 8(1): 6592
Debanne, D.; Guérineau, N.C.; Gähwiler, B.H.; Thompson, S.M. 1997: Action-potential propagation gated by an axonal I(A)-like K+ conductance in hippocampus. Nature 389(6648): 286-289
Neszmélyi, B.; Horváth, J.án. 2021: Action-related auditory ERP attenuation is not modulated by action effect relevance. Biological Psychology 161: 108029
Ciardo, F.; Lugli, L.; Nicoletti, R.; Rubichi, S.; Iani, C. 2016: Action-space coding in social contexts. Scientific Reports 6: 22673
Leem, J.; Kim, H.Y. 2020: Action-specialized expert ensemble trading system with extended discrete action space using deep reinforcement learning. Plos one 15(7): E0236178
Morris, R.W.; Dezfouli, A.; Griffiths, K.R.; Balleine, B.W. 2014: Action-value comparisons in the dorsolateral prefrontal cortex control choice between goal-directed actions. Nature Communications 5: 4390
Edwards, C.; Bolling-Walker, K.; Deupree, J. 2020: Actionability and Usability of a Fever Management Tool for Pediatric Caregivers. Journal of Continuing Education in Nursing 51(7): 338-344
Zimmermann, B.; Starke, G.; Shaw, D.; Elger, B.; Koné, I. 2020: Actionability and scope should determine the extent of counselling for presymptomatic genetic testing. Swiss Medical Weekly 150: W20274
Okawa, Y.; Ebata, N.; Kim, N.K.D.; Fujita, M.; Maejima, K.; Sasagawa, S.; Nakamura, T.; Park, W.-Y.; Hirano, S.; Nakagawa, H. 2021: Actionability evaluation of biliary tract cancer by genome transcriptome analysis and Asian cancer knowledgebase. Oncotarget 12(15): 1540-1552
DeCristo, D.M.; Milko, L.V.; O'Daniel, J.M.; Foreman, A.K.M.; Mollison, L.F.; Powell, B.C.; Powell, C.M.; Berg, J.S. 2021: Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making. Genome Medicine 13(1): 50
Hekman, R.M.; Hume, A.J.; Goel, R.K.; Abo, K.M.; Huang, J.; Blum, B.C.; Werder, R.B.; Suder, E.L.; Paul, I.; Phanse, S.; Youssef, A.; Alysandratos, K.D.; Padhorny, D.; Ojha, S.; Mora-Martin, A.; Kretov, D.; Ash, P.E.A.; Verma, M.; Zhao, J.; Patten, J.J.; Villacorta-Martin, C.; Bolzan, D.; Perea-Resa, C.; Bullitt, E.; Hinds, A.; Tilston-Lunel, A.; Varelas, X.; Farhangmehr, S.; Braunschweig, U.; Kwan, J.H.; McComb, M.; Basu, A.; Saeed, M.; Perissi, V.; Burks, E.J.; Layne, M.D.; Connor, J.H.; Davey, R.; Cheng, J.-X.; Wolozin, B.L.; Blencowe, B.J.; Wuchty, S.; Lyons, S.M.; Kozakov, D.; Cifuentes, D.; Blower, M.; Kotton, D.N.; Wilson, A.A.; Mühlberger, E.; Emili, A. 2021: Actionable Cytopathogenic Host Responses of Human Alveolar Type 2 Cells to SARS-CoV-2. Molecular Cell 81(1): 212
Dang, A-Thu.Huynh.; Tran, V-Uyen.; Tran, T-Truong.; Thi Pham, H-Anh.; Le, D-Thong.; Nguyen, L.; Nguyen, N-Vu.; Thi Nguyen, T-Hoa.; Nguyen, C.Van.; Le, H.Thu.; Thi Nguyen, M-Lan.; Le, V.Thuong.; Nguyen, P.Huu.; Vo, B.Thanh.; Thi Dao, H-Thuy.; Nguyen, L.Thanh.; Van Nguyen, T-Chi.; Bui, Q-Tram.Nguyen.; Nguyen, L.Hung.; Nguyen, N.Huu.; Thi Nguyen, Q-Tho.; Le, T.Xuan.; Do, T-Thuy.Thi.; Dinh, K.Truong.; Do, H.Ngoc.; Phan, M-Duy.; Nguyen, H-Nghia.; Tran, L.Son.; Giang, H. 2020: Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population. Scientific Reports 10(1): 2707
Stix, C. 2021: Actionable Principles for Artificial Intelligence Policy: Three Pathways. Science and Engineering Ethics 27(1): 15
Manni, S.; Fregnani, A.; Barilà, G.; Zambello, R.; Semenzato, G.; Piazza, F. 2020: Actionable Strategies to Target Multiple Myeloma Plasma Cell Resistance/Resilience to Stress: Insights from "Omics" Research. Frontiers in Oncology 10: 802
Myers, L.; Ho, M-Lan.; Cauvet, E.; Lundin, K.; Carlsson, T.; Kuja-Halkola, R.; Tammimies, K.; Bölte, S. 2020: Actionable and incidental neuroradiological findings in twins with neurodevelopmental disorders. Scientific Reports 10(1): 22417
Heeke, A.L.; Xiu, J.; Elliott, A.; Korn, W.M.; Lynce, F.; Pohlmann, P.R.; Isaacs, C.; Swain, S.M.; Vidal, G.; Schwartzberg, L.S.; Tan, A.R. 2020: Actionable co-alterations in breast tumors with pathogenic mutations in the homologous recombination DNA damage repair pathway. Breast Cancer Research and Treatment 184(2): 265-275
Tempini, N.ò; Leonelli, S. 2021: Actionable data for precision oncology: Framing trustworthy evidence for exploratory research and clinical diagnostics. Social Science and Medicine 272: 113760
Lagan, S.; Aquino, P.; Emerson, M.R.; Fortuna, K.; Walker, R.; Torous, J. 2020: Actionable health app evaluation: translating expert frameworks into objective metrics. Npj Digital Medicine 3: 100
Lagan, S.; Aquino, P.; Emerson, M.R.; Fortuna, K.; Walker, R.; Torous, J. 2020: Actionable health app evaluation: translating expert frameworks into objective metrics. Npj Digital Medicine 3(1): 100
Schrader, A.; Crispatzu, G.; Oberbeck, S.; Mayer, P.; Pützer, S.; von Jan, J.; Vasyutina, E.; Warner, K.; Weit, N.; Pflug, N.; Braun, T.; Andersson, E.I.; Yadav, B.; Riabinska, A.; Maurer, B.; Ventura Ferreira, M.S.; Beier, F.; Altmüller, J.; Lanasa, M.; Herling, C.D.; Haferlach, T.; Stilgenbauer, S.; Hopfinger, G.; Peifer, M.; Brümmendorf, T.H.; Nürnberg, P.; Elenitoba-Johnson, K.S.J.; Zha, S.; Hallek, M.; Moriggl, R.; Reinhardt, H.C.; Stern, M-H.; Mustjoki, S.; Newrzela, S.; Frommolt, P.; Herling, M. 2018: Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL. Nature Communications 9(1): 697
Yu, M.H.C.; Chan, M.C.Y.; Chung, C.C.Y.; Li, A.W.T.; Yip, C.Y.W.; Mak, C.C.Y.; Chau, J.F.T.; Lee, M.; Fung, J.L.F.; Tsang, M.H.Y.; Chan, J.C.K.; Wong, W.H.S.; Yang, J.; Chui, W.C.M.; Chung, P.H.Y.; Yang, W.; Lee, S.L.; Chan, G.C.F.; Tam, P.K.H.; Lau, Y.L.; Tang, C.S.M.; Yeung, K.S.; Chung, B.H.Y. 2021: Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population. Plos Genetics 17(2): E1009323
Abicht, A.; Schön, U.; Laner, A.; Holinski-Feder, E.; Diebold, I. 2021: Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counseling. Cardiovascular Diagnosis and Therapy 11(2): 637-649
Russo, G.C.; Bernardes, N.; Baraldi, N.ál.R.; Saraiva, D.J.B.; Angelis, K.át.D.; Lantieri, C.J.B.; Saraiva, J.é F. 2020: Actions Against Covid-19 in the down Syndrome Population. Arquivos Brasileiros de Cardiologia 115(5): 939-941
Willgerodt, M.A.; Maughan, E.; Jameson, B.; Johnson, K.H. 2021: Actions Speak Louder than Words: Social Justice Is Integral to School Nursing Practice. Journal of School Nursing: the Official Publication of the National Association of School Nurses 37(4): 226-227
Van der Put, A.C.; Mandemakers, J.J.; de Wit, J.B.F.; van der Lippe, T. 2021: Actions Speak Louder than Words: Workplace Social Relations and Worksite Health Promotion use. Journal of Occupational and Environmental Medicine 63(7): 614-621
De Lucas Ramos, P.; García-Botella, A.; García-Lledó, A.; Gómez-Pavón, J.; González Del Castillo, J.; Hernández-Sampelayo, T.; Martín-Delgado, M.C.; Martín Sánchez, F.J.; Martínez-Sellés, M.; Molero García, J.M.; Moreno Guillén, S.; Rodríguez-Artalejo, F.J.; Ruiz-Galiana, J.; Cantón, R.; Bouza, E. 2022: Actions and attitudes on the immunized patients against SARS-CoV-2. Revista Espanola de Quimioterapia: Publicacion Oficial de la Sociedad Espanola de Quimioterapia 35(1): 7-15
van den Brenk, H.A.; Stone, M.G. 1974: Actions and interactions of colchicine and cytochalasin B on contraction of granulation tissue and on mitosis. Nature 251(5473): 327-329
Sedor, J.R.; Abboud, H.E. 1984: Actions and metabolism of histamine in glomeruli and tubules of the human kidney. Kidney International 26(2): 144-152
Bacq, Z.M.; Renson, J. 1960: Actions and physiological importance of metanephrine and normetanephrine. Bulletin de l'Academie Royale de Medecine de Belgique 25: 755-779
Regner, T.; Matthey, A. 2021: Actions and the Self: i Give, Therefore i am?. Frontiers in Psychology 12: 684078
Camilleri, M.; Papathanasopoulos, A.; Odunsi, S.T. 2009: Actions and therapeutic pathways of ghrelin for gastrointestinal disorders. Nature Reviews. Gastroenterology and Hepatology 6(6): 343-352
Carreira, E.M.; Chirik, P.J.; Miller, S.J. 2020: Actions at J. Org. Chem., Org. Lett., and Organometallics to Combat Discrimination and Bias. Journal of Organic Chemistry 85(16): 10285-10286
Carreira, E.M.; Chirik, P.J.; Miller, S.J. 2020: Actions at J. Org. Chem., Org. Lett., and Organometallics to Combat Discrimination and Bias. Organic Letters 22(16): 6221-6222
Wenzel, L.; Dörrenberg, S.; Proft, M.; Liszkowski, U.; Rakoczy, H. 2020: Actions do not speak louder than words in an interactive false belief task. Royal Society Open Science 7(10): 191998
Silva, M.S.B.d.; Gutiérrez, M.G.R.d.; Figueiredo, E.N.íg.d.; Barbieri, M.ár.; Ramos, C.F.V.; Gabrielloni, M.C. 2021: Actions for early detection of breast cancer in two municipalities in the Western Amazon. Revista Brasileira de Enfermagem 74(2): E20200165
Santos, L.ís.K.d.P.ão.D.; Santana, C.áu.d.C.; Souza, M.V.O.d. 2020: Actions for enhancing resilience among adolescents. Ciencia and Saude Coletiva 25(10): 3933-3943
King, Régine.Uwibereyeho.; Este, D.Clarence.; Yohani, S.; Duhaney, P.; McFarlane, C.; Liu, J.Ka.Kei. 2021: Actions needed to promote health equity and the mental health of Canada's Black refugees. Ethnicity and Health 2021: 1-19
Hosie, A.M.; Akagi, H.; Ishida, M.; Shinozaki, H. 1999: Actions of 3-[2-phosphonomethyl[1,1-biphenyl]-3-yl]alanine (PMBA) on cloned glycine receptors. British Journal of Pharmacology 126(5): 1230-1236
Low, A.M.; Sormaz, L.; Kwan, C.Y.; Daniel, E.E. 1997: Actions of 4-chloro-3-ethyl phenol on internal Ca2+ stores in vascular smooth muscle and endothelial cells. British Journal of Pharmacology 122(3): 504-510
Howson, P.A.; Jane, D.E. 2003: Actions of LY341495 on metabotropic glutamate receptor-mediated responses in the neonatal rat spinal cord. British Journal of Pharmacology 139(1): 147-155
Mousa, S.A.; Hercbergs, A.; Lin, H.-Y.; Keating, K.A.; Davis, P.J. 2021: Actions of Thyroid Hormones on Thyroid Cancers. Frontiers in Endocrinology 12: 691736
Aishima, M.; Tomoda, T.; Yunoki, T.; Nakano, T.; Seki, N.; Yonemitsu, Y.; Sueishi, K.; Naito, S.; Ito, Y.; Teramoto, N. 2006: Actions of ZD0947, a novel ATP-sensitive K+ channel opener, on membrane currents in human detrusor myocytes. British Journal of Pharmacology 149(5): 542-550
House, C.R.; Ginsborg, B.L. 1976: Actions of a dopamine analogue and a neuroleptic at a neuroglandular synapse. Nature 261(5558): 332-333
Cahalan, S.M.; Gonzalez-Cabrera, P.J.; Sarkisyan, G.; Nguyen, N.; Schaeffer, M-Therese.; Huang, L.; Yeager, A.; Clemons, B.; Scott, F.; Rosen, H. 2011: Actions of a picomolar short-acting S1P₁ agonist in S1P₁-eGFP knock-in mice. Nature Chemical Biology 7(5): 254-256
Steele, T.H.; Gottstein, J.H.; Challoner-Hue, L.; Underwood, J.L. 1982: Actions of angiotensin II on the isolated spontaneously hypertensive rat kidney. Kidney International 21(3): 466-470
Hu, H-Zhen.; Liu, S.; Gao, N.; Xia, Y.; Mostafa, R.; Ren, J.; Zafirov, D.H.; Wood, J.D. 2003: Actions of bradykinin on electrical and synaptic behavior of neurones in the myenteric plexus of guinea-pig small intestine. British Journal of Pharmacology 138(7): 1221-1232
Barker, H.; Isles, T.E. 1978: Actions of cyclic AMP, its butyryl derivatives and Na butyrate on the HCG output of malignant trophoblast cells in vitro. British Journal of Cancer 38(1): 158-162
Rodríguez-Puyol, D.; Lamas, S.; Olivera, A.; López-Farré, A.; Ortega, G.; Hernando, L.; López-Novoa, J.M. 1989: Actions of cyclosporin A on cultured rat mesangial cells. Kidney International 35(2): 632-637
Gault, V.A.; Porter, W.D.; Flatt, P.R.; Hölscher, C. 2010: Actions of exendin-4 therapy on cognitive function and hippocampal synaptic plasticity in mice fed a high-fat diet. International Journal of Obesity 34(8): 1341-1344
Clements-Jewery, H.; Kanaganayagam, G.Sunthar.; Kabra, R.; Curtis, M.J. 2006: Actions of flecainide on susceptibility to phase-2 ventricular arrhythmias during infarct evolution in rat isolated perfused hearts. British Journal of Pharmacology 147(5): 468-475
Lopes, C.M.; Franks, N.P.; Lieb, W.R. 1998: Actions of general anaesthetics and arachidonic pathway inhibitors on K+ currents activated by volatile anaesthetics and FMRFamide in molluscan neurones. British Journal of Pharmacology 125(2): 309-318
Cong, Y.; Shay, J.W. 2008: Actions of human telomerase beyond telomeres. Cell Research 18(7): 725-732
Lu, X.; Crowley, S.D. 2020: Actions of immune cells in the hypertensive kidney. Current Opinion in Nephrology and Hypertension 29(5): 515-522
Reggianini, O. 1947: Actions of monochromatic lights on the development of Bacillus subtilis. Giornale di Batteriologia e Immunologia 36(1): 17-21
Arakawa, K.; Ishihara, T.; Aoto, M.; Inamasu, M.; Saito, A.; Ikezawa, K. 1998: Actions of novel antidiabetic thiazolidinedione, T-174, in animal models of non-insulin-dependent diabetes mellitus (NIDDM) and in cultured muscle cells. British Journal of Pharmacology 125(3): 429-436
Auclair, Aès.L.; Kleven, M.S.; Besnard, Jël.; Depoortère, R.; Newman-Tancredi, A. 2006: Actions of novel antipsychotic agents on apomorphine-induced PPI disruption: influence of combined serotonin 5-HT1A receptor activation and dopamine D2 receptor blockade. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology 31(9): 1900-1909
Zheng, F.; Grandy, D.K.; Johnson, S.W. 2002: Actions of orphanin FQ/nociceptin on rat ventral tegmental area neurons in vitro. British Journal of Pharmacology 136(7): 1065-1071
Uski, T.K.; Reinstrup, P. 1990: Actions of platelet-activating factor on isolated feline and human cerebral arteries. Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism 10(3): 428-431
Dognon, A.; Biancani, H. 1948: Actions of radiation on cells and tissues. Tabulae Biologicae 19(3): 72-99
Heymans, C.; Delaunois, A.L.; Jacob, J. 1948: Actions of soda succinate on dog breathing and metabolism. Archives Internationales de Pharmacodynamie et de Therapie 75(3-4): 392-401
Davey, M.G.; Lüscher, E.F. 1965: Actions of some coagulant snake venoms on blood platelets. Nature 207(998): 730-732
Wawra, E.; Klein, W.; Kocsis, F.; Weniger, P. 1975: Actions of some drugs on enzymes involved in DNA repair and semi-conservative DNA synthesis. British Journal of Cancer 32(6): 759-760
Stoll, R. 1948: Actions of some sex hormones on the development of the Müller channels of the chicken embryo. Archives d'Anatomie Microscopique et de Morphologie Experimentale 37(2): 118-135
Dantchakoff, V. 1947: Actions of testosterone on the overall energies of the organism. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 141(3-4): 114-116
Jayamanne, A.; Greenwood, R.; Mitchell, V.A.; Aslan, S.; Piomelli, D.; Vaughan, C.W. 2006: Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models. British Journal of Pharmacology 147(3): 281-288
Alippe, Y.; Kress, D.; Ricci, B.; Sun, K.; Yang, T.; Wang, C.; Xiao, J.; Abu-Amer, Y.; Mbalaviele, G. 2021: Actions of the NLRP3 and NLRC4 inflammasomes overlap in bone resorption. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 35(9): e21837
Nolan, M.F.; Gibson, I.C.; Logan, S.D. 1997: Actions of the anaesthetic Saffan on rat sympathetic preganglionic neurones in vitro. British Journal of Pharmacology 121(2): 324-330
Davey, M.G.; Lüscher, E.F. 1967: Actions of thrombin and other coagulant and proteolytic enzymes on blood platelets. Nature 216(5118): 857-858
Siegel, E.; Tobias, C.A. 1966: Actions of thyroid hormones on cultured human cells. Nature 212(5068): 1318-1321
Pandita, R.Kumar.; Pehrson, R.; Christoph, T.; Friderichs, E.; Andersson, K-Erik. 2003: Actions of tramadol on micturition in awake, freely moving rats. British Journal of Pharmacology 139(4): 741-748
De Petrocellis, L.; Chu, C.J.; Moriello, A.Schiano.; Kellner, J.C.; Walker, J.Michael.; Di Marzo, V. 2004: Actions of two naturally occurring saturated N-acyldopamines on transient receptor potential vanilloid 1 (TRPV1) channels. British Journal of Pharmacology 143(2): 251-256
Huguenin, R.; Truhaut, R.C. 1954: Actions of various chemotherapies in the treatment of human cancers. Acta Radiologica. Supplementum 116: 417-422
Casier, H. 1948: Actions of various substances on blood cholinesterases. Archives Internationales de Pharmacodynamie et de Therapie 77(1): 58
Mandavilli, A. 2006: Actions speak louder than images. Nature 444(7120): 664-665
Barr, R.; Rusnak, S.N.; Brito, N.H.; Nugent, C. 2020: Actions speak louder than words: Differences in memory flexibility between monolingual and bilingual 18-month-olds. Developmental science 23(2): e12881
Twizelimana, D.; Muula, A.S. 2020: Actions taken by female sex workers (FSWs) after condom failure in semi urban Blantyre, Malawi. Bmc Women's Health 20(1): 273
Tuma, F.; Malgor, R.D.; Nassar, A.K. 2021: Actions to enhance interactive learning in surgery. Annals of Medicine and Surgery 64: 102256
Yang, Y.; Yue, S.; Qiao, Y.; Zhang, P.; Jiang, N.; Ning, Z.; Liu, C.; Hou, Y. 2020: Activable Multi-Modal Nanoprobes for Imaging Diagnosis and Therapy of Tumors. Frontiers in Chemistry 8: 572471
Lin, H.; Tang, X.; Li, A.; Gao, J. 2021: Activatable 19 F MRi Nanoprobes for Visualization of Biological Targets in Living Subjects. Advanced Materials 33(50): E2005657
Wang, X.; Zhao, Y.; Hu, Y.; Fei, Y.; Zhao, Y.; Xue, C.; Cai, K.; Li, M.; Luo, Z. 2021: Activatable Biomineralized Nanoplatform Remodels the Intracellular Environment of Multidrug-Resistant Tumors for Enhanced Ferroptosis/Apoptosis Therapy. Small 17(47): E2102269
Chen, F.; Teng, L.; Lu, C.; Zhang, C.; Rong, Q.; Zhao, Y.; Yang, Y.; Wang, Y.; Song, G.; Zhang, X. 2020: Activatable Magnetic/Photoacoustic Nanoplatform for Redox-Unlocked Deep-Tissue Molecular Imaging in Vivo via Prussian Blue Nanoprobe. Analytical Chemistry 92(19): 13452-13461
Zhou, C.; Zhang, L.; Sun, T.; Zhang, Y.; Liu, Y.; Gong, M.; Xu, Z.; Du, M.; Liu, Y.; Liu, G.; Zhang, D. 2021: Activatable NIR-Ii Plasmonic Nanotheranostics for Efficient Photoacoustic Imaging and Photothermal Cancer Therapy. Advanced Materials 33(3): E2006532
Chen, X.; Bian, Y.; Li, M.; Zhang, Y.; Gao, X.; Su, D. 2020: Activatable Off-on Near-Infrared QCy7-based Fluorogenic Probes for Bioimaging. Chemistry An Asian Journal 15(23): 3983-3994
Zeng, Z.; Zhang, C.; Li, J.; Cui, D.; Jiang, Y.; Pu, K. 2021: Activatable Polymer Nanoenzymes for Photodynamic Immunometabolic Cancer Therapy. Advanced Materials 33(4): E2007247
Wang, W.; Xiong, J.; Song, X.; Wang, Z.; Zhang, F.; Mao, Z. 2020: Activatable Two-Photon Near-Infrared Fluorescent Probe Tailored toward Peroxynitrite in Vivo Imaging in Tumors. Analytical Chemistry 92(19): 13305-13312
Zhao, M.; Li, B.; Zhang, H.; Zhang, F. 2020: Activatable fluorescence sensors for in vivo bio-detection in the second near-infrared window. Chemical Science 12(10): 3448-3459
Xu, L.; Sun, L.; Zeng, F.; Wu, S. 2020: Activatable fluorescent probe based on aggregation-induced emission for detecting hypoxia-related pathological conditions. Analytica Chimica Acta 1125: 152-161
Zhang, J.; Ning, L.; Huang, J.; Zhang, C.; Pu, K. 2019: Activatable molecular agents for cancer theranostics. Chemical Science 11(3): 618-630
Fu, J.; Li, T.; Yang, Y.; Jiang, L.; Wang, W.; Fu, L.; Zhu, Y.; Hao, Y. 2021: Activatable nanomedicine for overcoming hypoxia-induced resistance to chemotherapy and inhibiting tumor growth by inducing collaborative apoptosis and ferroptosis in solid tumors. Biomaterials 268: 120537
Jiang, Y.; Huang, J.; Xu, C.; Pu, K. 2021: Activatable polymer nanoagonist for second near-infrared photothermal immunotherapy of cancer. Nature Communications 12(1): 742
Wu, Y.; Huang, S.; Wang, J.; Sun, L.; Zeng, F.; Wu, S. 2018: Activatable probes for diagnosing and positioning liver injury and metastatic tumors by multispectral optoacoustic tomography. Nature Communications 9(1): 3983
Kang, S.H.; Chung, B.Y.; Park, J.E.; Jeon, J.; Park, Y.D. 2020: Activatable red emitting fluorescent probe for rapid and sensitive detection of intracellular peroxynitrite. Talanta 217: 121053
Giamarellos-Bourboulis, E.J.; Tsilika, M.; Moorlag, S.; Antonakos, N.; Kotsaki, A.; Domínguez-Andrés, J.; Kyriazopoulou, E.; Gkavogianni, T.; Adami, M.-E.; Damoraki, G.; Koufargyris, P.; Karageorgos, A.; Bolanou, A.; Koenen, H.; van Crevel, R.; Droggiti, D.-I.; Renieris, G.; Papadopoulos, A.; Netea, M.G. 2020: Activate: Randomized Clinical Trial of BCG Vaccination against Infection in the Elderly. Cell 183(2): 315-323.E9
Li, H.L.; Hancock, W.W.; Dowling, J.P.; Atkins, R.C. 1991: Activated (IL-2R+) intraglomerular mononuclear cells in crescentic glomerulonephritis. Kidney International 39(4): 793-798
Jacobson, B.A.; De, A.; Kratzke, M.G.; Patel, M.R.; Jay-Dixon, J.; Whitson, B.A.; Sadiq, A.A.; Bitterman, P.B.; Polunovsky, V.A.; Kratzke, R.A. 2009: Activated 4E-BP1 represses tumourigenesis and IGF-I-mediated activation of the eIF4F complex in mesothelioma. British Journal of Cancer 101(3): 424-431
Jeong, S-Jin.; Pise-Masison, C.A.; Radonovich, M.F.; Park, H.Ung.; Brady, J.N. 2005: Activated AKT regulates NF-kappaB activation, p53 inhibition and cell survival in HTLV-1-transformed cells. Oncogene 24(44): 6719-6728
Lopez-Delisle, L.; Pierre-Eugène, Cécile.; Louis-Brennetot, C.; Surdez, D.; Raynal, V.; Baulande, S.; Boeva, V.; Grossetête-Lalami, S.; Combaret, Vérie.; Peuchmaur, M.; Delattre, O.; Janoueix-Lerosey, I. 2018: Activated ALK signals through the ERK-ETV5-RET pathway to drive neuroblastoma oncogenesis. Oncogene 37(11): 1417-1429
Gu, X.; Han, Y.-Y.; Yang, C.-Y.; Ji, H.-M.; Lan, Y.-J.; Bi, Y.-Q.; Zheng, C.; Qu, J.; Cheng, M.-H.; Gao, J. 2021: Activated AMPK by metformin protects against fibroblast proliferation during pulmonary fibrosis by suppressing FOXM1. Pharmacological Research 173: 105844
Cai, P.; Feng, Z.; Feng, N.; Zou, H.; Gu, J.; Liu, X.; Liu, Z.; Yuan, Y.; Bian, J. 2021: Activated AMPK promoted the decrease of lactate production in rat Sertoli cells exposed to Zearalenone. Ecotoxicology and Environmental Safety 220: 112367
Anderton, S.M.; Fillatreau, S. 2008: Activated B cells in autoimmune diseases: the case for a regulatory role. Nature Clinical Practice. Rheumatology 4(12): 657-666
Oxley, K.L.; Hanson, B.M.; Zani, A.N.; Bishop, G.A. 2021: Activated B lymphocytes and tumor cell lysate as an effective cellular cancer vaccine. Cancer Immunology Immunotherapy: Cii 70(11): 3093-3103
Robinson, J.P.; VanBrocklin, M.W.; Guilbeault, A.R.; Signorelli, D.L.; Brandner, S.; Holmen, S.L. 2010: Activated BRAF induces gliomas in mice when combined with Ink4a/Arf loss or Akt activation. Oncogene 29(3): 335-344
Jung, S.; Myung, Y.; Kim, B.Na.; Kim, I.Gyoo.; You, I-Kyu.; Kim, T. 2018: Activated Biomass-derived Graphene-based Carbons for Supercapacitors with High Energy and Power Density. Scientific Reports 8(1): 1915
Yacyshyn, B.R. 1993: Activated CD19+ B cell lamina propria lymphocytes in ulcerative colitis. Immunology and Cell Biology 71: 265-274
Wong, S.-S.; Oshansky, C.M.; Guo, X.-Z.J.; Ralston, J.; Wood, T.; Reynolds, G.E.; Seeds, R.; Jelley, L.; Waite, B.; Jeevan, T.; Zanin, M.; Widdowson, M.-A.; Huang, Q.S.; Thomas, P.G.; Webby, R.J.; Turner, N.; Baker, M.; Grant, C.; McArthur, C.; Roberts, S.; Trenholmes, A.; Wong, C.; Taylor, S.; Thompson, M.; Gross, D.; Duque, J.; Haven, K.; Aley, D.; Muponisi, P.; Chand, B.; Chen, Y.; Plewes, L.; Sawtell, F.; Lawrence, S.; Cogcoy, R.; Smith, J.; Gravidez, F.; Ma, M.; Chamberlin, S.; Davey, K.; Knowles, T.; McLeish, J.-A.; Todd, A.; Bocacao, J.; Gunn, W.; Kawakami, P.; Walker, S.; Madge, R.; Moore, N.; Rahnama, F.; Qiao, H.; Tse, F.; Zibaei, M.; Korrapadu, T.; Optland, L.; Dela Cruz, C. 2021: Activated CD4+ T cells and CD14hiCD16+ monocytes correlate with antibody response following influenza virus infection in humans. Cell Reports. Medicine 2(4): 100237
Duizendstra, A.A.; de Knegt, R.J.; Mancham, S.; Klepper, M.; Roelen, D.L.; Brand-Schaaf, S.H.; Boor, P.P.; Doukas, M.; de Man, R.A.; Sprengers, D.; Peppelenbosch, M.P.; Betjes, M.G.H.; Kwekkeboom, J.; Litjens, N.H.R. 2022: Activated CD4+ T Cells and Highly Differentiated Alloreactive CD4+ T Cells Distinguish Operationally Tolerant Liver Transplantation Recipients. Liver Transplantation: Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 28(1): 98-112
Chapin, C.A.; Melin-Aldana, H.; Kreiger, P.A.; Burn, T.; Neighbors, K.; Taylor, S.A.; Ostilla, L.; Wechsler, J.B.; Horslen, S.P.; Leonis, M.A.; Loomes, K.M.; Behrens, E.M.; Squires, R.H.; Alonso, E.M. 2020: Activated CD8 T-cell Hepatitis in Children with Indeterminate Acute Liver Failure: Results from a Multicenter Cohort. Journal of Pediatric Gastroenterology and Nutrition 71(6): 713-719
O'Rourke, A.M.; Rogers, J.; Mescher, M.F. 1990: Activated CD8 binding to class I protein mediated by the T-cell receptor results in signalling. Nature 346(6280): 187-189
Patil, J.A.; Kshirsagar, M.S.; Patil, A.J. 2021: Activated Carbon Fabric Mask Reduces Lead Absorption and Improves the Heme Biosynthesis and Hematological Parameters of Battery Manufacturing Workers. Indian Journal of Clinical Biochemistry: Ijcb 36(1): 94-99
Alcaraz, L.; Adán-Más, A.; Arévalo-Cid, P.; Montemor, M.d.F.; López, F.él.A. 2020: Activated Carbons from Winemaking Biowastes for Electrochemical Double-Layer Capacitors. Frontiers in Chemistry 8: 686
Wehner, J.E.; Boehne, M.; David, S.; Brand, K.; Tiede, A.; Bikker, R. 2020: Activated Clotting time (ACT) for Monitoring of Low-Dose Heparin: Performance Characteristics in Healthy Adults and Critically Ill Patients. Clinical and Applied Thrombosis/Hemostasis: Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 26: 1076029620975494
Papageorgiou, C.; Synetos, A.; Tampakis, K.; Anninos, H.; Kontogiannis, C.; Kapelouzou, A.; Kanakakis, I.; Tousoulis, D.; Paraskevaidis, I.; Toutouzas, K. 2020: Activated Clotting time as a Marker of Inflammation in Hospitalized Patients. Clinical and Applied Thrombosis/Hemostasis: Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 26: 1076029620929090
Conlon, B.P.; Nakayasu, E.S.; Fleck, L.E.; LaFleur, M.D.; Isabella, V.M.; Coleman, K.; Leonard, S.N.; Smith, R.D.; Adkins, J.N.; Lewis, K. 2013: Activated ClpP kills persisters and eradicates a chronic biofilm infection. Nature 503(7476): 365-370
Jin, L.-Q.; John, B.H.; Hu, J.; Selzer, M.E. 2020: Activated Erk Is an Early Retrograde Signal After Spinal Cord Injury in the Lamprey. Frontiers in Neuroscience 14: 580692
Ichikawa, K.; Watanabe Miyano, S.; Minoshima, Y.; Matsui, J.; Funahashi, Y. 2020: Activated FGF2 signaling pathway in tumor vasculature is essential for acquired resistance to anti-VEGF therapy. Scientific Reports 10(1): 2939
Ma, W.; Liang, F.; Zhan, H.; Jiang, X.; Gao, C.; Zhang, X.; Zhang, K.; Sun, Q.; Hu, H.; Zhao, Z. 2020: Activated FMS-like tyrosine kinase 3 ameliorates angiotensin II-induced cardiac remodelling. Acta Physiologica 230(2): E13519
Giordano, C.; Barone, I.; Vircillo, V.; Panza, S.; Malivindi, R.; Gelsomino, L.; Pellegrino, M.; Rago, V.; Mauro, L.; Lanzino, M.; Panno, M.Luisa.; Bonofiglio, D.; Catalano, S.; Andò, S. 2016: Activated FXR Inhibits Leptin Signaling and Counteracts Tumor-promoting Activities of Cancer-Associated Fibroblasts in Breast Malignancy. Scientific Reports 6: 21782
Sanada, F.; Taniyama, Y.; Muratsu, J.; Otsu, R.; Iwabayashi, M.; Carracedo, M.; Rakugi, H.; Morishita, R. 2016: Activated Factor X Induces Endothelial Cell Senescence Through IGFBP-5. Scientific Reports 6: 35580
Pang, N.; Alimu, X.; Chen, R.; Muhashi, M.; Ma, J.; Chen, G.; Zhao, F.; Wang, L.; Qu, J.; Ding, J. 2021: Activated Galectin-9/Tim3 promotes Treg and suppresses Th1 effector function in chronic lymphocytic leukemia. References 35(7): E21556
Xi, S.; Zheng, X.; Li, X.; Jiang, Y.; Wu, Y.; Gong, J.; Jie, Y.; Li, Z.; Cao, J.; Sha, L.; Zhang, M.; Chong, Y. 2021: Activated Hepatic Stellate Cells Induce Infiltration and Formation of CD163+ Macrophages via CCL2/CCR2 Pathway. Frontiers in Medicine 8: 627927
Nagy-Baló, Z.; Kiss, R.ár.; Menge, A.; Bödör, C.; Bajtay, Z.; Erdei, A. 2020: Activated Human Memory B Lymphocytes use CR4 (CD11c/CD18) for Adhesion, Migration, and Proliferation. Frontiers in Immunology 11: 565458
Tamai, H.; Miyake, K.; Takatori, M.; Miyake, N.; Yamaguchi, H.; Dan, K.; Shimada, T.; Inokuchi, K. 2011: Activated K-Ras protein accelerates human MLL/AF4-induced leukemo-lymphomogenicity in a transgenic mouse model. Leukemia 25(5): 888-891
Mukhopadhyay, A.; Krishnaswami, S.R.; Yu, B.D-Y. 2011: Activated Kras alters epidermal homeostasis of mouse skin, resulting in redundant skin and defective hair cycling. Journal of Investigative Dermatology 131(2): 311-319
Rachagani, S.; Senapati, S.; Chakraborty, S.; Ponnusamy, M.P.; Kumar, S.; Smith, L.M.; Jain, M.; Batra, S.K. 2011: Activated KrasG¹²D is associated with invasion and metastasis of pancreatic cancer cells through inhibition of E-cadherin. British Journal of Cancer 104(6): 1038-1048
Thorington, G.U.; Hessinger, D.A. 2020: Activated L-Type Calcium Channels Inhibit Chemosensitized Nematocyst Discharge from Sea Anemone Tentacles. Biological Bulletin 238(3): 180-192
Xia, X.; Wang, D.; Yu, L.; Wang, B.; Wang, W.; Jiao, C.; Chen, X.; Zhang, H.; Chen, F.; Feng, J. 2021: Activated M1 macrophages suppress c-kit expression via TNF-α-mediated upregulation of miR-222 in Neonatal Necrotizing Enterocolitis. Inflammation Research: Official Journal of the European Histamine Research Society . 70(3): 343-358
Yang, H.; Kircher, D.A.; Kim, K.H.; Grossmann, A.H.; VanBrocklin, M.W.; Holmen, S.L.; Robinson, J.P. 2017: Activated MEK cooperates with Cdkn2a and Pten loss to promote the development and maintenance of melanoma. Oncogene 36(27): 3842-3851
Robinson, J.P.; Vanbrocklin, M.W.; Lastwika, K.J.; McKinney, A.J.; Brandner, S.; Holmen, S.L. 2011: Activated MEK cooperates with Ink4a/Arf loss or Akt activation to induce gliomas in vivo. Oncogene 30(11): 1341-1350
Li, J.; Wang, R.; Hu, X.; Gao, Y.; Wang, Z.; Li, J.; Wong, J. 2019: Activated MEK/ERK Pathway Drives Widespread and Coordinated Overexpression of UHRF1 and DNMT1 in Cancer cells. Scientific Reports 9(1): 907
Zeng, Y.; Stokes, J.; Hahn, S.; Hoffman, E.; Katsanis, E. 2014: Activated MHC-mismatched T helper-1 lymphocyte infusion enhances GvL with limited GvHD. Bone Marrow Transplantation 49(8): 1076-1083
Johnson, V.; Webb, T.; Norman, A.; Coy, J.; Kurihara, J.; Regan, D.; Dow, S. 2017: Activated Mesenchymal Stem Cells Interact with Antibiotics and Host Innate Immune Responses to Control Chronic Bacterial Infections. Scientific Reports 7(1): 9575
Peshkova, A.D.; Le Minh, G.; Tutwiler, V.; Andrianova, I.A.; Weisel, J.W.; Litvinov, R.I. 2017: Activated Monocytes Enhance Platelet-Driven Contraction of Blood Clots via Tissue Factor Expression. Scientific Reports 7(1): 5149
Yougbaré, I.; Tai, W-She.; Zdravic, D.; Oswald, B.Elaine.; Lang, S.; Zhu, G.; Leong-Poi, H.; Qu, D.; Yu, L.; Dunk, C.; Zhang, J.; Sled, J.G.; Lye, S.J.; Brkić, J.; Peng, C.; Höglund, P.; Croy, B.Anne.; Adamson, S.Lee.; Wen, X-Yan.; Stewart, D.J.; Freedman, J.; Ni, H. 2017: Activated NK cells cause placental dysfunction and miscarriages in fetal alloimmune thrombocytopenia. Nature Communications 8(1): 224
Ehlers, F.A.I.; Mahaweni, N.M.; Olieslagers, T.I.; Bos, G.M.J.; Wieten, L. 2021: Activated Natural Killer Cells Withstand the Relatively Low Glucose Concentrations Found in the Bone Marrow of Multiple Myeloma Patients. Frontiers in Oncology 11: 622896
Witkowski, M.T.; Cimmino, L.; Hu, Y.; Trimarchi, T.; Tagoh, H.; McKenzie, M.D.; Best, S.A.; Tuohey, L.; Willson, T.A.; Nutt, S.L.; Busslinger, M.; Aifantis, I.; Smyth, G.K.; Dickins, R.A. 2015: Activated Notch counteracts Ikaros tumor suppression in mouse and human T-cell acute lymphoblastic leukemia. Leukemia 29(6): 1301-1311
Kim, S.B.; Chae, G.W.; Lee, J.; Park, J.; Tak, H.; Chung, J.H.; Park, T.G.; Ahn, J.K.; Joe, C.O. 2007: Activated Notch1 interacts with p53 to inhibit its phosphorylation and transactivation. Cell Death and Differentiation 14(5): 982-991
Chen, Z.; Long, L.; Xiao, J.; Liu, N.; Dong, R. 2020: Activated Oxytocin Neurons in the PVN-DVC Pathway in Asthmatic Rats. Frontiers in Neuroanatomy 14: 47
Rea, I.Maeve. 2019: Activated P13Kδ disrupts germinal center GC T(fh)/GC B cell cross talk and B cell antibody coding. Cellular and Molecular Immunology 16(11): 848-850
Thouenon, R.; Moreno-Corona, N.; Poggi, L.; Durandy, A.; Kracker, S. 2021: Activated PI3Kinase Delta Syndrome-A Multifaceted Disease. Frontiers in Pediatrics 9: 652405
Zeng, H.; Wang, L.; Zhang, J.; Pan, T.; Yu, Y.; Lu, J.; Zhou, P.; Yang, H.; Li, P. 2021: Activated PKB/GSK-3β synergizes with PKC-δ signaling in attenuating myocardial ischemia/reperfusion injury via potentiation of NRF2 activity: Therapeutic efficacy of dihydrotanshinone-i. Acta Pharmaceutica Sinica. B 11(1): 71-88
Moosecker, S.; Gomes, Pícia.; Dioli, C.; Yu, S.; Sotiropoulos, I.; Almeida, O.F.X. 2019: Activated PPARγ Abrogates Misprocessing of Amyloid Precursor Protein, Tau Missorting and Synaptotoxicity. Frontiers in Cellular Neuroscience 13: 239
Tao, Y.; Shao, F.; Cai, M.; Liu, Z.; Peng, Y.; Huang, Q.; Meng, F. 2021: Activated Pancreatic Stellate Cells Enhance the Warburg Effect to Cause the Malignant Development in Chronic Pancreatitis. Frontiers in Oncology 11: 714598
Kulig, C.E.; Schomer, K.J.; Black, H.B.; Dager, W.E. 2021: Activated Partial Thromboplastin time Versus Anti-Factor Xa Monitoring of Heparin Anticoagulation in Adult Venoarterial Extracorporeal Membrane Oxygenation Patients. Asaio Journal 67(4): 411-415
Komban, R.Joy.; Strömberg, A.; Biram, A.; Cervin, J.; Lebrero-Fernández, C.; Mabbott, N.; Yrlid, U.; Shulman, Z.; Bemark, M.; Lycke, N. 2019: Activated Peyer's patch B cells sample antigen directly from M cells in the subepithelial dome. Nature Communications 10(1): 2423
Klein-Goldberg, A.; Voloshin, T.; Zemer-Tov, E.; Paz, R.; Koren, L.; Wainer-Katsir, K.; Volodin, A.; Koltun, B.; Brant, B.; Giladi, M.; Weinberg, U.; Palti, Y. 2021: Activated Phosphoinositide 3-Kinase/AKT/mTOR Signaling Confers Resistance to Tumor Treating Fields (TTFields). International Journal of Radiation Oncology Biology Physics 111(3s): E252
Lee, S.J.; Yoon, B.R.; Kim, H.Y.; Yoo, S.-J.; Kang, S.W.; Lee, W.-W. 2020: Activated Platelets Convert CD14+CD16- into CD14+CD16+ Monocytes with Enhanced FcγR-Mediated Phagocytosis and Skewed M2 Polarization. Frontiers in Immunology 11: 611133
Tsai, H.H.C.; Moyers, J.T.; Moore, C.J.; Thinn, M. 2021: Activated Prothrombin Complex Concentrate-Induced Atypical Hemolytic Uremic Syndrome Treated with Eculizumab. American Journal of Case Reports 22: E929616
Hanashiro, K.; Brancaccio, M.; Fukasawa, K. 2011: Activated ROCK II by-passes the requirement of the CDK2 activity for centrosome duplication and amplification. Oncogene 30(19): 2188-2197
Muhammad, R.Nasser.; Sallam, N.; El-Abhar, H.Salah. 2020: Activated ROCK/Akt/eNOS and ET-1/ERK pathways in 5-fluorouracil-induced cardiotoxicity: modulation by simvastatin. Scientific Reports 10(1): 14693
Kim, S.Joo.; Yoon, S. 2016: Activated Rac1 regulates the degradation of IκBα and the nuclear translocation of STAT3-NFκB complexes in starved cancer cells. Experimental and Molecular Medicine 48: E231
Dorman, C.M.; Johnson, S.E. 1999: Activated Raf inhibits avian myogenesis through a MAPK-dependent mechanism. Oncogene 18(37): 5167-5176
Meadows, K.N.; Bryant, P.; Vincent, P.A.; Pumiglia, K.M. 2004: Activated Ras induces a proangiogenic phenotype in primary endothelial cells. Oncogene 23(1): 192-200
Shmulevitz, M.; Marcato, P.; Lee, P.W.K. 2010: Activated Ras signaling significantly enhances reovirus replication and spread. Cancer Gene Therapy 17(1): 69-70
Lombardo, G.; Dentelli, P.; Togliatto, G.; Rosso, A.; Gili, M.; Gallo, S.; Deregibus, M.Chiara.; Camussi, G.; Brizzi, M.Felice. 2016: Activated Stat5 trafficking Via Endothelial Cell-derived Extracellular Vesicles Controls IL-3 Pro-angiogenic Paracrine Action. Scientific Reports 6: 25689
Kong, Y.Y.; Feige, U.; Sarosi, I.; Bolon, B.; Tafuri, A.; Morony, S.; Capparelli, C.; Li, J.; Elliott, R.; McCabe, S.; Wong, T.; Campagnuolo, G.; Moran, E.; Bogoch, E.R.; Van, G.; Nguyen, L.T.; Ohashi, P.S.; Lacey, D.L.; Fish, E.; Boyle, W.J.; Penninger, J.M. 1999: Activated T cells regulate bone loss and joint destruction in adjuvant arthritis through osteoprotegerin ligand. Nature 402(6759): 304-309
Cárdeno, A.; Magnusson, M.K.; Quiding-Järbrink, M.; Lundgren, A. 2018: Activated T follicular helper-like cells are released into blood after oral vaccination and correlate with vaccine specific mucosal B-cell memory. Scientific Reports 8(1): 2729
Naparstek, Y.; Cohen, I.R.; Fuks, Z.; Vlodavsky, I. 1984: Activated T lymphocytes produce a matrix-degrading heparan sulphate endoglycosidase. Nature 310(5974): 241-244
Coombs, D.; Kalergis, A.M.; Nathenson, S.G.; Wofsy, C.; Goldstein, B. 2002: Activated TCRs remain marked for internalization after dissociation from pMHC. Nature Immunology 3(10): 926-931
Ni, B.; Cao, H.; Zhang, C.; Li, S.; Zhang, Q.; Tian, X.; Li, D.; Wu, J.; Tian, Y. 2020: Activated Type i and Type Ii Process for Two-Photon Promoted ROS Generation: the Coordinated Zn Matters. Inorganic Chemistry 59(18): 13671-13678
Xavier, G.M.; Patist, A.L.; Healy, C.; Pagrut, A.; Carreno, G.; Sharpe, P.T.; Martinez-Barbera, J.Pedro.; Thavaraj, S.; Cobourne, M.T.; Andoniadou, C.L. 2015: Activated WNT signaling in postnatal SOX2-positive dental stem cells can drive odontoma formation. Scientific Reports 5: 14479
Abriani, A.; Hamad, C. 2020: Activated antimicrobial peptides due to periodontal bacteria in synovial fluid - the link between psoriatic arthritis and periodontitis?. Medical Hypotheses 144: 109967
Yang, F.; Liu, Y.; Tu, J.; Wan, J.; Zhang, J.; Wu, B.; Chen, S.; Zhou, J.; Mu, Y.; Wang, L. 2014: Activated astrocytes enhance the dopaminergic differentiation of stem cells and promote brain repair through bFGF. Nature Communications 5: 5627
Liu, Y.; Zhang, Y.; Zhang, M.; Meng, J.; Ma, Q.; Hao, Z.; Zheng, M.; Zhang, L.; Chen, X.; Liang, C. 2021: Activated autophagy restored the impaired frequency and function of regulatory T cells in chronic prostatitis. Prostate 81(1): 29-40
Davidson, A.; Diamond, B. 2010: Activated basophils give lupus a booster shot. Nature Medicine 16(6): 635-636
Qiao, Y.; Zhang, C.; Kong, F.; Zhao, Q.; Kong, A.; Shan, Y. 2021: Activated biochar derived from peanut shells as the electrode materials with excellent performance in Zinc-air battery and supercapacitance. Waste Management 125: 257-267
Su, L.; Zhang, H.; Oh, K.; Liu, N.; Luo, Y.; Cheng, H.; Zhang, G.; He, X. 2021: Activated biochar derived from spent Auricularia auricula substrate for the efficient adsorption of cationic azo dyes from single and binary adsorptive systems. Water Science and Technology: a Journal of the International Association on Water Pollution Research 84(1): 101-121
Li, J.; Xiao, X.; Xu, X.; Lin, J.; Huang, Y.; Xue, Y.; Jin, P.; Zou, J.; Tang, C. 2013: Activated boron nitride as an effective adsorbent for metal ions and organic pollutants. Scientific Reports 3: 3208
Lin, J.; Arlinghaus, R. 2008: Activated c-Abl tyrosine kinase in malignant solid tumors. Oncogene 27(32): 4385-4391
Di Siena, S.; Gimmelli, R.; Nori, S.L.; Barbagallo, F.; Campolo, F.; Dolci, S.; Rossi, P.; Venneri, M.A.; Giannetta, E.; Gianfrilli, D.; Feigenbaum, L.; Lenzi, A.; Naro, F.; Cianflone, E.; Mancuso, T.; Torella, D.; Isidori, A.M.; Pellegrini, M. 2016: Activated c-Kit receptor in the heart promotes cardiac repair and regeneration after injury. Cell Death and Disease 7(7): E2317
Wilson, G.R.; Cramer, A.; Welman, A.; Knox, F.; Swindell, R.; Kawakatsu, H.; Clarke, R.B.; Dive, C.; Bundred, N.J. 2006: Activated c-SRC in ductal carcinoma in situ correlates with high tumour grade, high proliferation and HER2 positivity. British Journal of Cancer 95(10): 1410-1414
Makarov, A.V.; Safonov, A.V.; Konevnik, Y.V.; Teterin, Y.A.; Maslakov, K.I.; Teterin, A.Y.; Karaseva, Y.Y.; German, K.E.; Zakharova, E.V. 2021: Activated carbon additives for technetium immobilization in bentonite-based engineered barriers for radioactive waste repositories. Journal of Hazardous Materials 401: 123436
Erdem, C.U.; Ateia, M.; Liu, C.; Karanfil, T. 2020: Activated carbon and organic matter characteristics impact the adsorption of DBP precursors when chlorine is added prior to GAC contactors. Water Research 184: 116146
Cao, J.; Li, N.; Jiang, J.; Xu, Y.; Zhang, B.; Luo, X.; Hu, Y. 2022: Activated carbon as an insoluble electron shuttle to enhance the anaerobic ammonium oxidation coupled with Fe(III) reduction process. Environmental Research 204(Part A): 111972
Iwanow, M.; Gärtner, T.; Sieber, V.; König, B. 2020: Activated carbon as catalyst support: precursors, preparation, modification and characterization. Beilstein Journal of Organic Chemistry 16: 1188-1202
Gutiérrez, M.; Grillini, V.; Mutavdžić Pavlović, D.; Verlicchi, P. 2021: Activated carbon coupled with advanced biological wastewater treatment: a review of the enhancement in micropollutant removal. Science of the Total Environment 790: 148050
Al-Musawi, T.J.; Mengelizadeh, N.; Taghavi, M.; Mohebi, S.; Balarak, D. 2021: Activated carbon derived from Azolla filiculoides fern: a high-adsorption-capacity adsorbent for residual ampicillin in pharmaceutical wastewater. Biomass Conversion and Biorefinery 2021: 1-13
Ozcan, N.; Saloglu, D. 2020: Activated carbon embedded alginate beads for removing nonsteroidal anti-inflammatory drug naproxen from wastewater: equilibrium, kinetics, thermodynamics, desorption, and reusability. Water Science and Technology: a Journal of the International Association on Water Pollution Research 81(7): 1432-1444
Bai, B.Chol.; Lee, Y-Seak.; Im, J.Sun. 2019: Activated carbon fibers for toxic gas removal based on electrical investigation: Mechanistic study of p-type/n-type junction structures. Scientific Reports 9(1): 14458
Bao, K.; Li, F.; Liu, H.; Wang, Z.; Shen, Q.; Wang, J.; Zhang, W. 2015: Activated carbon for aerobic oxidation: Benign approach toward 2-benzoylbenzimidazoles and 2-benzoylbenzoxazoles synthesis. Scientific Reports 5: 10360
Che, L.; Xu, H.; Wei, Z.; Wei, R.; Yang, B. 2022: Activated carbon modified with nano manganese dioxide triggered electron transport pathway changes for boosted anaerobic treatment of dyeing wastewater. Environmental Research 203: 111944
Queiroz, L.S.; de Souza, L.K.C.; Thomaz, K.T.C.; Leite Lima, E.T.; da Rocha Filho, G.N.; do Nascimento, L.A.S.; de Oliveira Pires, L.H.; Faial, K.d.C.F.; da Costa, C.E.F. 2020: Activated carbon obtained from amazonian biomass tailings (acai seed): Modification, characterization, and use for removal of metal ions from water. Journal of Environmental Management 270: 110868
Mopoung, S.; Dejang, N. 2021: Activated carbon preparation from eucalyptus wood chips using continuous carbonization-steam activation process in a batch intermittent rotary kiln. Scientific Reports 11(1): 13948
Liu, Q.; Yang, J.; Li, H.; Ye, J.; Fei, Z.; Chen, X.; Zhang, Z.; Tang, J.; Cui, M.; Qiao, X. 2021: Activated carbon prepared from catechol distillation residue for efficient adsorption of aromatic organic compounds from aqueous solution. Chemosphere 269: 128750
Hara, T.; Nabei, H.; Kyuka, A. 2020: Activated carbon/titanium dioxide composite to adsorb volatile organic compounds associated with human body odor. Heliyon 6(11): E05455
Abuelnoor, N.; AlHajaj, A.; Khaleel, M.; Vega, L.F.; Abu-Zahra, M.R.M. 2021: Activated carbons from biomass-based sources for CO2 capture applications. Chemosphere 282: 131111
Theamwong, N.; Intarabumrung, W.; Sangon, S.; Aintharabunya, S.; Ngernyen, Y.; Hunt, A.J.; Supanchaiyamat, N. 2021: Activated carbons from waste Cassia bakeriana seed pods as high-performance adsorbents for toxic anionic dye and ciprofloxacin antibiotic remediation. Bioresource Technology 341: 125832
Hu, J.; Jia, Z.; Zhao, S.; Wang, W.; Zhang, Q.; Liu, R.; Huang, Z. 2021: Activated char supported Fe-Ni catalyst for syngas production from catalytic gasification of pine wood. Bioresource Technology 340: 125600
Holt, L.E.; Holz, P.H. 1962: Activated charcoal as an antidote for poisons. Bulletin 1962: 1-3
Viana, Ít.E.íd.L.; Weiss, G.S.; Sakae, L.íc.O.; Niemeyer, S.H.; Borges, A.B.üh.; Scaramucci, T.ís. 2021: Activated charcoal toothpastes do not increase erosive tooth wear. Journal of Dentistry 109: 103677
Li, Y.; Zhang, Y.; Xu, W.; Liang, J.; Luo, X.; Han, X.; Shi, X.; Jie, H.; Li, X.; He, Y.; Sun, E. 2020: Activated coagulation is associated with the disease activity of axial spondyloarthritis. International Immunopharmacology 88: 106979
Lockhart, C.E.H. 1943: Activated coals; first contribution to the study of the methods of determining its adsorbing power. Revista de la Facultad de Ciencias Quimicas . la Plata. Universidad Nacional. Facultad de Quimica y Farmacia 18: 23-34
Woo, J-A.A.; Liu, T.; Fang, C.C.; Cazzaro, S.; Kee, T.; LePochat, P.; Yrigoin, K.; Penn, C.; Zhao, X.; Wang, X.; Liggett, S.B.; Kang, D.E. 2019: Activated cofilin exacerbates tau pathology by impairing tau-mediated microtubule dynamics. Communications Biology 2: 112
Woo, J-A.A.; Liu, T.; Fang, C.C.; Cazzaro, S.; Kee, T.; LePochat, P.; Yrigoin, K.; Penn, C.; Zhao, X.; Wang, X.; Liggett, S.B.; Kang, D.E. 2019: Activated cofilin exacerbates tau pathology by impairing tau-mediated microtubule dynamics. Communications Biology 2(1): 112
Zheng, L.; Jin, J.; Karrar, E.; Wang, X.; Jin, Q. 2020: Activated complex theory is a classical theory suitable for food science with appropriate use. Food Chemistry 332: 127486
Yang, F.; Wei, Y.; Cai, Z.; Yu, L.; Jiang, L.; Zhang, C.; Yan, H.; Wang, Q.; Cao, X.; Liang, T.; Wang, J. 2015: Activated cytotoxic lymphocytes promote tumor progression by increasing the ability of 3LL tumor cells to mediate MDSC chemoattraction via Fas signaling. Cellular and Molecular Immunology 12(1): 66-76
Ladislau, L.; Portilho, Débora.M.; Courau, T.; Solares-Pérez, A.; Negroni, E.; Lainé, J.; Klatzmann, D.; Bonomo, A.; Allenbach, Y.; Benveniste, O.; Riederer, I.; Savino, W.; Mouly, V.; Butler-Browne, G.; Benjamim, C.F. 2018: Activated dendritic cells modulate proliferation and differentiation of human myoblasts. Cell Death and Disease 9(5): 551
Delgado Silva, J.; Almeida, J.-S.; Rodrigues-Santos, P.; Santos Rosa, M.; Gonçalves, L. 2020: Activated double-negative T cells (CD3+CD4-CD8-HLA-DR+) define response to renal denervation for resistant hypertension. Clinical Immunology 218: 108521
Cyranoski, D. 2007: Activated eggs offer route to stem cells. Nature 448(7150): 116
Xu, L.-J.; Gao, F.; Cheng, S.; Zhou, Z.-X.; Li, F.; Miao, Y.; Niu, W.-R.; Yuan, F.; Sun, X.-H.; Wang, Z. 2020: Activated ephrinA3/EphA4 forward signaling induces retinal ganglion cell apoptosis in experimental glaucoma. Neuropharmacology 178: 108228
Omori, S.; Kitagawa, H.; Koike, J.; Fujita, H.; Hida, M.; Pringle, K.C.; Awazu, M. 2008: Activated extracellular signal-regulated kinase correlates with cyst formation and transforming growth factor-beta expression in fetal obstructive uropathy. Kidney International 73(9): 1031-1037
Yaoi, H.; Shida, Y.; Kitazawa, T.; Shima, M.; Nogami, K. 2021: Activated factor VIII-mimicking effect by emicizumab on thrombus formation in type 2N von Willebrand disease under high shear flow conditions. Thrombosis Research 198: 7-16
Wang, D.; Shao, X.; Wang, Q.; Pan, X.; Dai, Y.; Yao, S.; Yin, T.; Wang, Z.; Zhu, J.; Xi, X.; Chen, Z.; Chen, S.; Zhang, G. 2021: Activated factor X targeted stored in platelets as an effective gene therapy strategy for both hemophilia a and B. Clinical and Translational Medicine 11(3): E375
Kobayashi, E.; Nakano, M.; Kubota, K.; Himuro, N.; Mizoguchi, S.; Chikenji, T.; Otani, M.; Mizue, Y.; Nagaishi, K.; Fujimiya, M. 2018: Activated forms of astrocytes with higher GLT-1 expression are associated with cognitive normal subjects with Alzheimer pathology in human brain. Scientific Reports 8(1): 1712
Sato, O.; Jung, H.Suk.; Komatsu, S.; Tsukasaki, Y.; Watanabe, T.M.; Homma, K.; Ikebe, M. 2017: Activated full-length myosin-X moves processively on filopodia with large steps toward diverse two-dimensional directions. Scientific Reports 7: 44237
Fernández-Bañares, F.; López-Palacios, N.; Corzo, M.ía.; Arau, B.; Rubio, M.; Fernández-Prieto, M.; Tristán, E.; Pujals, M.; Farrais, S.; Horta, S.úl.; Hernández, J.M.ía.; Gomez-Perosanz, M.; Reche, P.A.; Esteve, M.ía.; Núñez, C.ón. 2021: Activated gut-homing CD8+ T cells for coeliac disease diagnosis on a gluten-free diet. Bmc Medicine 19(1): 237
Shi, J.; Zhao, J.; Zhang, X.; Cheng, Y.; Hu, J.; Li, Y.; Zhao, X.; Shang, Q.; Sun, Y.; Tu, B.; Shi, L.; Gao, B.; Wang, F-Sheng.; Zhang, Z. 2017: Activated hepatic stellate cells impair NK cell anti-fibrosis capacity through a TGF-β-dependent emperipolesis in HBV cirrhotic patients. Scientific Reports 7: 44544
Song, Y.; Kim, S-Hyuk.; Kim, K.Mo.; Choi, E.Kyung.; Kim, J.; Seo, H.Ran. 2016: Activated hepatic stellate cells play pivotal roles in hepatocellular carcinoma cell chemoresistance and migration in multicellular tumor spheroids. Scientific Reports 6: 36750
Ma, H.; Xie, L.; Zhang, L.; Yin, X.; Jiang, H.; Xie, X.; Chen, R.; Lu, H.; Ren, Z. 2018: Activated hepatic stellate cells promote epithelial-to-mesenchymal transition in hepatocellular carcinoma through transglutaminase 2-induced pseudohypoxia. Communications Biology 1: 168
Zhang, R.; Yao, R-Rong.; Li, J-Huan.; Dong, G.; Ma, M.; Zheng, Q-Dan.; Gao, D-Mei.; Cui, J-Feng.; Ren, Z-Gang.; Chen, R-Xin. 2017: Activated hepatic stellate cells secrete periostin to induce stem cell-like phenotype of residual hepatocellular carcinoma cells after heat treatment. Scientific Reports 7(1): 2164
Levring, T.Bøegh.; Hansen, A.Kathrine.; Nielsen, B.Lisbeth.; Kongsbak, M.; von Essen, M.Rode.; Woetmann, A.; Odum, N.; Bonefeld, C.Menné.; Geisler, C. 2012: Activated human CD4+ T cells express transporters for both cysteine and cystine. Scientific Reports 2: 266
Walsh, N.C.; Alexander, K.A.; Manning, C.A.; Karmakar, S.; Karmakar, S.K.; Wang, J.F.; Weyand, C.M.; Pettit, A.R.; Gravallese, E.M. 2013: Activated human T cells express alternative mRNA transcripts encoding a secreted form of RANKL. Genes and Immunity 14(5): 336-345
Shaw, R.J.; Walsh, G.M.; Cromwell, O.; Moqbel, R.; Spry, C.J.; Kay, A.B. 1985: Activated human eosinophils generate SRS-A leukotrienes following IgG-dependent stimulation. Nature 316(6024): 150-152
Yoon, N.; Park, M.S.; Shigemoto, T.; Peltier, G.; Lee, R.H. 2016: Activated human mesenchymal stem/stromal cells suppress metastatic features of MDA-MB-231 cells by secreting IFN-β. Cell Death and Disease 7: E2191
Martinet, Y.; Bitterman, P.B.; Mornex, J.F.; Grotendorst, G.R.; Martin, G.R.; Crystal, R.G. 1986: Activated human monocytes express the c-sis proto-oncogene and release a mediator showing PDGF-like activity. Nature 319(6049): 158-160
Gao, Y.; Liu, Q.; Kong, W.; Wang, J.; He, L.; Guo, L.; Lin, H.; Fan, H.; Fan, Y.; Zhang, X. 2020: Activated hyaluronic acid/collagen composite hydrogel with tunable physical properties and improved biological properties. International Journal of Biological Macromolecules 164: 2186-2196
Cox, S.N.; Sallustio, F.; Serino, G.; Loverre, A.; Pesce, F.; Gigante, M.; Zaza, G.; Stifanelli, P.F.; Ancona, N.; Schena, F.P. 2012: Activated innate immunity and the involvement of CX3CR1-fractalkine in promoting hematuria in patients with IgA nephropathy. Kidney International 82(5): 548-560
Xie, S.; Zhang, H.; Wang, F.; Liu, Y.; Gao, K.; Zhang, J.; Fan, R.; Xie, S.; Xie, Z.; Jiang, W. 2020: Activated leukocyte cell adhesion molecule as a biomarker for disease severity and efficacy of sublingual immunotherapy in allergic rhinitis. International Immunopharmacology 88: 106975
Achiha, T.; Kijima, N.; Kodama, Y.; Kagawa, N.; Kinoshita, M.; Fujimoto, Y.; Nonaka, M.; Fukai, J.; Inoue, A.; Nishida, N.; Yamanaka, T.; Harada, A.; Mori, K.; Tsuyuguchi, N.; Uda, T.; Ishibashi, K.; Tomogane, Y.; Sakamoto, D.; Shofuda, T.; Yoshioka, E.; Kanematsu, D.; Mano, M.; Luu, B.; Taylor, M.D.; Kanemura, Y.; Kishima, H. 2020: Activated leukocyte cell adhesion molecule expression correlates with the WNT subgroup in medulloblastoma and is involved in regulating tumor cell proliferation and invasion. Plos one 15(12): E0243272
Cayrol, R.; Wosik, K.; Berard, J.L.; Dodelet-Devillers, A.; Ifergan, I.; Kebir, H.; Haqqani, A.S.; Kreymborg, K.; Krug, S.; Moumdjian, R.; Bouthillier, A.; Becher, B.; Arbour, N.; David, S.; Stanimirovic, D.; Prat, A. 2008: Activated leukocyte cell adhesion molecule promotes leukocyte trafficking into the central nervous system. Nature Immunology 9(2): 137-145
Shao, X.; Yao, H.; Cui, S.; Peng, Y.; Gao, X.; Yuan, C.; Chen, X.; Hu, Y.; Mao, X. 2021: Activated low-grade phosphate rocks for simultaneously reducing the phosphorus loss and cadmium uptake by rice in paddy soil. Science of the Total Environment 780: 146550
Savelli, G.; Bonacina, M.; Rizzo, A.; Zaniboni, A. 2020: Activated macrophages are the main inflammatory cell in COVID-19 interstitial pneumonia infiltrates. Is it possible to show their metabolic activity and thus the grade of inflammatory burden with 18F-Fluorocholine PET/CT?. Medical Hypotheses 144: 109885
Polverini, P.J.; Cotran, P.S.; Gimbrone, M.A.; Unanue, E.R. 1977: Activated macrophages induce vascular proliferation. Nature 269(5631): 804-806
Currie, G.A. 1978: Activated macrophages kill tumour cells by releasing arginase. Nature 273(5665): 758-759
Oguma, K.; Oshima, H.; Aoki, M.; Uchio, R.; Naka, K.; Nakamura, S.; Hirao, A.; Saya, H.; Taketo, M.Mark.; Oshima, M. 2008: Activated macrophages promote Wnt signalling through tumour necrosis factor-alpha in gastric tumour cells. EMBO Journal 27(12): 1671-1681
Palm, A-Karin.E.; Garcia-Faroldi, G.; Lundberg, M.; Pejler, G.; Kleinau, S. 2016: Activated mast cells promote differentiation of B cells into effector cells. Scientific Reports 6: 20531
Turunen, A.; Kuuliala, K.; Kuuliala, A.; Tervahartiala, T.; Mustonen, H.; Puolakkainen, P.; Kylänpää, L.; Sorsa, T. 2021: Activated matrix metalloproteinase 8 in serum predicts severity of acute pancreatitis. Pancreatology: Official Journal of the International Association of Pancreatology . 21(5): 862-869
Zhao, Y.; Fu, B.; Chen, P.; Li, Q.; Ouyang, Q.; Zhang, C.; Cai, G.; Wu, L.; Chen, X. 2021: Activated mesangial cells induce glomerular endothelial cells proliferation in rat anti-Thy-1 nephritis through VEGFA/VEGFR2 and Angpt2/Tie2 pathway. Cell proliferation 54(6): e13055
Park, G-Hoo.; Noh, H.; Shao, Z.; Ni, P.; Qin, Y.; Liu, D.; Beaudreault, C.P.; Park, J.S.; Abani, C.P.; Park, J.M.; Le, D.T.; Gonzalez, S.Z.; Guan, Y.; Cohen, B.M.; McPhie, D.L.; Coyle, J.T.; Lanz, T.A.; Xi, H.S.; Yin, C.; Huang, W.; Kim, H-Young.; Chung, S. 2020: Activated microglia cause metabolic disruptions in developmental cortical interneurons that persist in interneurons from individuals with schizophrenia. Nature Neuroscience 23(11): 1352-1364
Zheng, T.; Zhang, Z. 2021: Activated microglia facilitate the transmission of α-synuclein in Parkinson's disease. Neurochemistry International 148: 105094
Azevedo, E.P.; Ledo, J.H.; Barbosa, G.; Sobrinho, M.; Diniz, L.; Fonseca, A.C.C.; Gomes, F.; Romão, L.; Lima, F.R.S.; Palhano, F.L.; Ferreira, S.T.; Foguel, D. 2013: Activated microglia mediate synapse loss and short-term memory deficits in a mouse model of transthyretin-related oculoleptomeningeal amyloidosis. Cell Death and Disease 4: E789
Murata, Y.; Sugimoto, K.; Yang, C.; Harada, K.; Gono, R.; Harada, T.; Miyashita, Y.; Higashisaka, K.; Katada, R.; Tanaka, J.; Matsumoto, H. 2020: Activated microglia-derived macrophage-like cells exacerbate brain edema after ischemic stroke correlate with astrocytic expression of aquaporin-4 and interleukin-1 alpha release. Neurochemistry International 140: 104848
Zheng, T.; Zhou, X.; Guo, J.; Zhong, C.; Liu, Y. 2020: Activated mineral adsorbent for the efficient removal of Pb(II) and Cd(II) from aqueous solution: adsorption performance and mechanism studies. Water Science and Technology: a Journal of the International Association on Water Pollution Research 82(9): 1896-1911
Zhang, L.; Ma, L.; Yan, T.; Han, X.; Xu, J.; Xu, J.; Xu, X. 2018: Activated mitochondrial apoptosis in hESCs after dissociation involving the PKA/p-p53/Bax signaling pathway. Experimental Cell Research 369(2): 226-233
Wang, X.; Cui, Y.; Luo, G.; Wang, Q.; Hu, J.; He, W.; Yuan, J.; Zhou, J.; Wu, Y.; Sun, X.; Robson, S.C.; Li, X.; Tan, J.; Peng, Y.; Xue, G.; Lu, L.; Gao, W.; Wu, J. 2012: Activated mouse CD4(+)Foxp3(-) T cells facilitate melanoma metastasis via Qa-1-dependent suppression of NK-cell cytotoxicity. Cell Research 22(12): 1696-1706
Li, A.; Ma, Y.; Jin, M.; Mason, S.; Mort, R.L.; Blyth, K.; Larue, L.; Sansom, O.J.; Machesky, L.M. 2012: Activated mutant NRas(Q61K) drives aberrant melanocyte signaling, survival, and invasiveness via a Rac1-dependent mechanism. Journal of Investigative Dermatology 132(11): 2610-2621
Kim, A.; Noh, Y-Woock.; Kim, K.Dong.; Jang, Y-Suk.; Choe, Y-Kyung.; Lim, J-Seok. 2004: Activated natural killer cell-mediated immunity is required for the inhibition of tumor metastasis by dendritic cell vaccination. Experimental and Molecular Medicine 36(5): 428-443
Siegler, U.; Kalberer, C.P.; Nowbakht, P.; Sendelov, S.; Meyer-Monard, S.; Wodnar-Filipowicz, A. 2005: Activated natural killer cells from patients with acute myeloid leukemia are cytotoxic against autologous leukemic blasts in NOD/SCID mice. Leukemia 19(12): 2215-2222
Craven, T.H.; Walton, T.; Akram, A.R.; Scholefield, E.; McDonald, N.; Marshall, A.D.L.; Humphries, D.C.; Mills, B.; Campbell, T.A.; Bruce, A.; Mair, J.; Dear, J.W.; Newby, D.E.; Hill, A.T.; Walsh, T.S.; Haslett, C.; Dhaliwal, K. 2021: Activated neutrophil fluorescent imaging technique for human lungs. Scientific Reports 11(1): 976
Shan, Z.-G.; Chen, J.; Liu, J.-S.; Zhang, J.-Y.; Wang, T.-T.; Teng, Y.-S.; Mao, F.-Y.; Cheng, P.; Zou, Q.-M.; Zhou, W.-Y.; Peng, L.-S.; Zhao, Y.-L.; Zhuang, Y. 2021: Activated neutrophils polarize protumorigenic interleukin-17A-producing T helper subsets through TNF-α-B7-H2-dependent pathway in human gastric cancer. Clinical and Translational Medicine 11(6): E484
Shi, Y.; Lai, X.; Ye, L.; Chen, K.; Cao, Z.; Gong, W.; Jin, L.; Wang, C.; Liu, M.; Liao, Y.; Wang, J.Ming.; Zhou, N. 2017: Activated niacin receptor HCA2 inhibits chemoattractant-mediated macrophage migration via Gβγ/PKC/ERK1/2 pathway and heterologous receptor desensitization. Scientific Reports 7: 42279
Noguchi, T.; Adelaide, J.; Marics, I.; Raybaud, F.; de Lapeyrière, O.; Birnbaum, D. 1987: Activated oncogenes in human tumors. Bulletin du Cancer 74(6): 607-621
Sanchez, M.M.; Alagbe, O.; Felger, J.C.; Zhang, J.; Graff, A.E.; Grand, A.P.; Maestripieri, D.; Miller, A.H. 2007: Activated p38 MAPK is associated with decreased CSF 5-HIAA and increased maternal rejection during infancy in rhesus monkeys. Molecular Psychiatry 12(10): 895-897
Abdelwahab, E.M.M.; Bovari-Biri, J.; Smuk, G.; Fillinger, J.; McPhail, D.; Krymskaya, V.P.; Pongracz, J.E. 2021: Activated p53 in the anti-apoptotic milieu of tuberous sclerosis gene mutation induced diseases leads to cell death if thioredoxin reductase is inhibited. Apoptosis: An International Journal on Programmed Cell Death 26(5-6): 253-260
Tang, X.; Milyavsky, M.; Shats, I.; Erez, N.; Goldfinger, N.; Rotter, V. 2004: Activated p53 suppresses the histone methyltransferase EZH2 gene. Oncogene 23(34): 5759-5769
Huang, Q.; Huang, M.; Meng, F.; Sun, R. 2019: Activated pancreatic stellate cells inhibit NK cell function in the human pancreatic cancer microenvironment. Cellular and Molecular Immunology 16(1): 87-89
Bariéty, J.; Bruneval, P. 2006: Activated parietal epithelial cells or dedifferentiated podocytes in FSGS: can we make the difference?. Kidney International 69(1): 194
Fukuda, T.; Shimazu, C. 1999: Activated partial thromboplastin time (APTT), partial thromboplastin time (PTT). Nihon Rinsho. Japanese Journal of Clinical Medicine 57 Suppl: 548-550
Shimazu, C.; Fukuda, T. 2004: Activated partial thromboplastin time (APTT), partial thromboplastin time (PTT). Nihon Rinsho. Japanese Journal of Clinical Medicine 62(Suppl 12): 590-593
Katsanis, E.; Weisdorf, D.J.; Miller, J.S. 1998: Activated peripheral blood mononuclear cells from patients receiving subcutaneous interleukin-2 following autologous stem cell transplantation prolong survival of SCID mice bearing human lymphoma. Bone Marrow Transplantation 22(2): 185-191
Gao, Y.; Champagne, P.; Blair, D.; He, O.; Song, T. 2020: Activated persulfate by iron-based materials used for refractory organics degradation: a review. Water Science and Technology: a Journal of the International Association on Water Pollution Research 81(5): 853-875
Suzuki, Y.; Sano, H.; Mochizuki, L.; Honkura, N.; Urano, T. 2020: Activated platelet-based inhibition of fibrinolysis via thrombin-activatable fibrinolysis inhibitor activation system. Blood Advances 4(21): 5501-5511
Nakazawa, D.; Desai, J.; Steiger, S.; Müller, S.; Devarapu, S.Kumar.; Mulay, S.R.; Iwakura, T.; Anders, H-Joachim. 2018: Activated platelets induce MLKL-driven neutrophil necroptosis and release of neutrophil extracellular traps in venous thrombosis. Cell Death Discovery 4: 6
Au, A.E-L.; Sashindranath, M.; Borg, R.J.; Kleifeld, O.; Andrews, R.K.; Gardiner, E.E.; Medcalf, R.L.; Samson, A.L. 2014: Activated platelets rescue apoptotic cells via paracrine activation of EGFR and DNA-dependent protein kinase. Cell Death and Disease 5: E1410
Hudde, T.; Rayner, S.A.; Comer, R.M.; Weber, M.; Isaacs, J.D.; Waldmann, H.; Larkin, D.F.; George, A.J. 1999: Activated polyamidoamine dendrimers, a non-viral vector for gene transfer to the corneal endothelium. Gene Therapy 6(5): 939-943
Uchiba, M. 2011: Activated protein C. Rinsho Byori. Japanese Journal of Clinical Pathology Suppl 147: 171-176
Roberts, I. 1996: Activated protein C and pulmonary embolism. Lancet 347(9018): 1841
Bazzan, M.; Aluffi, E.; Vaccarino, A.; Schinco, P.; Montaruli, B. 1996: Activated protein C and pulmonary embolism. Lancet 347(9018): 1842
Cheng, T.; Liu, D.; Griffin, J.H.; Fernández, Jé.A.; Castellino, F.; Rosen, E.D.; Fukudome, K.; Zlokovic, B.V. 2003: Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective. Nature Medicine 9(3): 338-342
Lee, Y-Jin.; Jeong, J-Kyo.; Seol, J-Won.; Xue, M.; Jackson, C.; Park, S-Youel. 2013: Activated protein C differentially regulates both viability and differentiation of osteoblasts mediated by bisphosphonates. Experimental and Molecular Medicine 45: E9
Cheng, T.; Petraglia, A.L.; Li, Z.; Thiyagarajan, M.; Zhong, Z.; Wu, Z.; Liu, D.; Maggirwar, S.B.; Deane, R.; Fernández, Jé.A.; LaRue, B.; Griffin, J.H.; Chopp, M.; Zlokovic, B.V. 2006: Activated protein C inhibits tissue plasminogen activator-induced brain hemorrhage. Nature Medicine 12(11): 1278-1285
Yan, A.; Pan, X.; Wen, X.; Nie, X.; Li, Y. 2021: Activated protein C overexpression suppresses the pyroptosis of subarachnoid hemorrhage model cells by regulating the NLRP3 inflammasome pathway. Experimental and Therapeutic Medicine 22(6): 1391
Isermann, B.; Vinnikov, I.A.; Madhusudhan, T.; Herzog, S.; Kashif, M.; Blautzik, J.; Corat, M.A.F.; Zeier, M.; Blessing, E.; Oh, J.; Gerlitz, B.; Berg, D.T.; Grinnell, B.W.; Chavakis, T.; Esmon, C.T.; Weiler, H.; Bierhaus, A.; Nawroth, P.P. 2007: Activated protein C protects against diabetic nephropathy by inhibiting endothelial and podocyte apoptosis. Nature Medicine 13(11): 1349-1358
Ranjan, S.; Goihl, A.; Kohli, S.; Gadi, I.; Pierau, M.; Shahzad, K.; Gupta, D.; Bock, F.; Wang, H.; Shaikh, H.; Kähne, T.; Reinhold, D.; Bank, U.; Zenclussen, A.C.; Niemz, J.; Schnöder, T.M.; Brunner-Weinzierl, M.; Fischer, T.; Kalinski, T.; Schraven, B.; Luft, T.; Huehn, J.; Naumann, M.; Heidel, F.H.; Isermann, B. 2017: Activated protein C protects from GvHD via PAR2/PAR3 signalling in regulatory T-cells. Nature Communications 8(1): 311
Gohchi, K. 2004: Activated protein C resistance (APC resistance). Nihon Rinsho. Japanese Journal of Clinical Medicine 62(Suppl 12): 678-680
Shahzad, K.; Gadi, I.; Nazir, S.; Al-Dabet, M'd.Mohanad.; Kohli, S.; Bock, F.; Breitenstein, L.; Ranjan, S.; Fuchs, T.; Halloul, Z.; Nawroth, P.P.; Pelicci, P.Giuseppe.; Braun-Dullaeus, R.C.; Camerer, E.; Esmon, C.T.; Isermann, B. 2018: Activated protein C reverses epigenetically sustained p66 Shc expression in plaque-associated macrophages in diabetes. Communications Biology 1: 104
Van Zanten, A.R.; Bakker, J.; van den Berg, P.C.; Girbes, A.R.; van Leeuwen, S.J. 2001: Activated protein C, coagulation, inflammation and treatment of severe sepsis. Nederlands Tijdschrift Voor Geneeskunde 145(24): 1179
Ott, A. 2001: Activated protein C, coagulation, inflammation and treatment of severe sepsis. Nederlands Tijdschrift Voor Geneeskunde 145(45): 2196-2197
Bobby, L.; Westlake, E.; Esplin, N.; Young, S. 2021: Activated prothrombin complex concentrate for reversal of oral factor Xa inhibitors at a level 1 trauma center. Thrombosis Research 206: 33-35
Shaw, J.R.; Carrier, M.; Dowlatshahi, D.; Chakraborty, S.; Tokessy, M.; Buyukdere, H.; Castellucci, L.A. 2020: Activated prothrombin complex concentrates for direct oral anticoagulant-associated bleeding or urgent surgery: Hemostatic and thrombotic outcomes. Thrombosis Research 195: 21-28
Loebrich, S.; Bähring, R.; Katsuno, T.; Tsukita, S.; Kneussel, M. 2006: Activated radixin is essential for GABAA receptor alpha5 subunit anchoring at the actin cytoskeleton. EMBO Journal 25(5): 987-999
Ivan, M.; Bond, J.A.; Prat, M.; Comoglio, P.M.; Wynford-Thomas, D. 1997: Activated ras and ret oncogenes induce over-expression of c-met (hepatocyte growth factor receptor) in human thyroid epithelial cells. Oncogene 14(20): 2417-2423
Kim, Y.C.; Song, K.S.; Yoon, G.; Nam, M.J.; Ryu, W.S. 2001: Activated ras oncogene collaborates with HBx gene of hepatitis B virus to transform cells by suppressing HBx-mediated apoptosis. Oncogene 20(1): 16-23
Magalhães, E.R.B.; Costa Filho, Jé.D.B.; Padilha, C.E.A.; Silva, F.L.; Sousa, M.A.S.B.; Santos, E.S. 2020: Activated sludge treatment for promoting the reuse of a synthetic produced water in irrigation. Journal of Environmental Science and Health. Part. B Pesticides Food Contaminants and Agricultural Wastes 2020: 1-16
Park, S.; Oh, S. 2020: Activated sludge-degrading analgesic drug acetaminophen: Acclimation, microbial community dynamics, degradation characteristics, and bioaugmentation potential. Water Research 182: 115957
Imamura, S.; Washio, K.; Mizuno, M.; Oda, Y.; Fukunaga, A.; Nishigori, C. 2021: Activated steady status and distinctive FcεRI-mediated responsiveness in basophils of atopic dermatitis. Allergology International: Official Journal of the Japanese Society of Allergology 70(3): 327-334
Ni, R.; Neves, M.A.D.; Wu, C.; Cerroni, S.E.; Flick, M.J.; Ni, H.; Weitz, J.I.; Gross, P.L.; Kim, P.Y. 2020: Activated thrombin-activatable fibrinolysis inhibitor (TAFIa) attenuates fibrin-dependent plasmin generation on thrombin-activated platelets. Journal of Thrombosis and Haemostasis: Jth 18(9): 2364-2376
Muraoka-Cook, R.S.; Shin, I.; Yi, J.Y.; Easterly, E.; Barcellos-Hoff, M.H.; Yingling, J.M.; Zent, R.; Arteaga, C.L. 2006: Activated type I TGFbeta receptor kinase enhances the survival of mammary epithelial cells and accelerates tumor progression. Oncogene 25(24): 3408-3423
Granados, J.Z.; Ten Have, G.A.M.; Letsinger, A.C.; Thaden, J.J.; Engelen, M.P.K.J.; Lightfoot, J.T.; Deutz, N.E.P. 2020: Activated whole-body arginine pathway in high-active mice. Plos one 15(6): E0235095
Jaldín-Fincati, J.R.; Actis Dato, V.; Díaz, Nás.M.; Sánchez, Mía.C.; Barcelona, P.F.; Chiabrando, G.A. 2019: Activated α 2 -Macroglobulin Regulates LRP1 Levels at the Plasma Membrane through the Activation of a Rab10-dependent Exocytic Pathway in Retinal Müller Glial Cells. Scientific Reports 9(1): 13234
Bastida-Ruiz, D.; Wuillemin, C.; Pederencino, A.; Yaron, M.; Martinez de Tejada, Bña.; Pizzo, S.Vincent.; Cohen, M. 2020: Activated α 2 -macroglobulin binding to cell surface GRP78 induces trophoblastic cell fusion. Scientific Reports 10(1): 9666
Sumida, T.; Lincoln, M.R.; Ukeje, C.M.; Rodriguez, D.M.; Akazawa, H.; Noda, T.; Naito, A.T.; Komuro, I.; Dominguez-Villar, M.; Hafler, D.A. 2018: Activated β-catenin in Foxp3 + regulatory T cells links inflammatory environments to autoimmunity. Nature Immunology 19(12): 1391-1402
Yu, L.; Zhang, Y.; Xiong, J.; Liu, J.; Zha, Y.; Kang, Q.; Zhi, P.; Wang, Q.; Wang, H.; Zeng, W.; Huang, Y. 2021: Activated γδ T Cells with Higher CD107a Expression and Inflammatory Potential During Early Pregnancy in Patients with Recurrent Spontaneous Abortion. Frontiers in Immunology 12: 724662
Li, G.; Kolan, S.S.; Guo, S.; Marciniak, K.; Kolan, P.; Malachin, G.; Grimolizzi, F.; Haraldsen, G.; Skålhegg, B.ør.S. 2021: Activated, Pro-Inflammatory Th1, Th17, and Memory CD4+ T Cells and B Cells Are Involved in Delayed-Type Hypersensitivity Arthritis (DTHA) Inflammation and Paw Swelling in Mice. Frontiers in Immunology 12: 689057
Herberts, C.; Murtha, A.J.; Fu, S.; Wang, G.; Schönlau, E.; Xue, H.; Lin, D.; Gleave, A.; Yip, S.; Angeles, A.; Hotte, S.; Tran, B.; North, S.; Taavitsainen, S.; Beja, K.; Vandekerkhove, G.; Ritch, E.; Warner, E.; Saad, F.; Iqbal, N.; Nykter, M.; Gleave, M.E.; Wang, Y.; Annala, M.; Chi, K.N.; Wyatt, A.W. 2020: Activating AKT1 and PIK3CA Mutations in Metastatic Castration-Resistant Prostate Cancer. European Urology 78(6): 834-844
Niedzwiedz, W. 2016: Activating ATR, the devil's in the dETAA1l. Nature Cell Biology 18(11): 1120-1122
Qian, C.; Yang, C.; Lu, M.; Bao, J.; Shen, H.; Deng, B.; Li, S.; Li, W.; Zhang, M.; Cao, C. 2021: Activating AhR alleviates cognitive deficits of Alzheimer's disease model mice by upregulating endogenous Aβ catabolic enzyme Neprilysin. Theranostics 11(18): 8797-8812
Oeck, S.; Al-Refae, K.; Riffkin, H.; Wiel, G.; Handrick, R.; Klein, D.; Iliakis, G.; Jendrossek, V. 2017: Activating Akt1 mutations alter DNA double strand break repair and radiosensitivity. Scientific Reports 7: 42700
Kringle, E.A.; Terhorst, L.; Gibbs, B.B.; Campbell, G.; McCue, M.; Skidmore, E.R. 2020: Activating Behavior to Reduce Sedentary Behavior After Stroke: a Nonrandomized Pilot Feasibility Study. American Journal of Occupational Therapy: Official Publication of the American Occupational Therapy Association 74(6): 7406205030p1-7406205030p10
Yan, R.; Pham, R.; Chen, C.-L. 2020: Activating Bubble's Escape, Coalescence, and Departure under an Electric Field Effect. Langmuir: the Acs Journal of Surfaces and Colloids 36(51): 15558-15571
Dong, B.; Lee, J-Seog.; Park, Y-Yong.; Yang, F.; Xu, G.; Huang, W.; Finegold, M.J.; Moore, D.D. 2015: Activating CAR and β-catenin induces uncontrolled liver growth and tumorigenesis. Nature Communications 6: 5944
Berki, D.M.; Liu, L.; Choon, S-Eng.; David Burden, A.; Griffiths, C.E.M.; Navarini, A.A.; Tan, E.S.; Irvine, A.D.; Ranki, A.; Ogo, T.; Petrof, G.; Mahil, S.K.; Duckworth, M.; Allen, M.H.; Vito, P.; Trembath, R.C.; McGrath, J.; Smith, C.H.; Capon, F.; Barker, J.N. 2015: Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris. Journal of Investigative Dermatology 135(12): 2964-2970
Park, S.Hye.; Jeong, S.; Kim, B.Ram.; Jeong, Y.A.; Kim, J.Lim.; Na, Y.Jin.; Jo, M.Jee.; Yun, H.Kyeong.; Kim, D.Yeong.; Kim, B.Gyeom.; Lee, D-Hee.; Oh, S.Cheul. 2020: Activating CCT2 triggers Gli-1 activation during hypoxic condition in colorectal cancer. Oncogene 39(1): 136-150
Li, B.; Zhang, Y.; Yin, R.; Zhong, W.; Chen, R.; Yan, J. 2020: Activating CD137 Signaling Promotes Sprouting Angiogenesis via Increased VEGFA Secretion and the VEGFR2/Akt/eNOS Pathway. Mediators of Inflammation 2020: 1649453
Kurppa, K.J.; Denessiouk, K.; Johnson, M.S.; Elenius, K. 2016: Activating ERBB4 mutations in non-small cell lung cancer. Oncogene 35(10): 1283-1291
Robinson, D.R.; Wu, Y-Mi.; Vats, P.; Su, F.; Lonigro, R.J.; Cao, X.; Kalyana-Sundaram, S.; Wang, R.; Ning, Y.; Hodges, L.; Gursky, A.; Siddiqui, J.; Tomlins, S.A.; Roychowdhury, S.; Pienta, K.J.; Kim, S.Y.; Roberts, J.Scott.; Rae, J.M.; Van Poznak, C.H.; Hayes, D.F.; Chugh, R.; Kunju, L.P.; Talpaz, M.; Schott, A.F.; Chinnaiyan, A.M. 2013: Activating ESR1 mutations in hormone-resistant metastatic breast cancer. Nature Genetics 45(12): 1446-1451
Liang, H.; Liu, R.-P.; An, X.-Q.; Liu, H.-J. 2020: Activating Efficiency of Iron-copper Bimetallic Organic Framework MIL-101(Fe,Cu) Toward H2 O2 for Degradation of Dyes. Huan Jing Ke Xue= Huanjing Kexue 41(10): 4607-4614
Matsubara, A.; Ogawa, R.; Suzuki, H.; Oda, I.; Taniguchi, H.; Kanai, Y.; Kushima, R.; Sekine, S. 2015: Activating GNAS and KRAS mutations in gastric foveolar metaplasia, gastric heterotopia, and adenocarcinoma of the duodenum. British Journal of Cancer 112(8): 1398-1404
Sarin, K.Y.; McNiff, J.M.; Kwok, S.; Kim, J.; Khavari, P.A. 2014: Activating HRAS mutation in nevus spilus. Journal of Investigative Dermatology 134(6): 1766-1768
Yao, H.; Ma, Y.; Hong, Z.; Zhao, L.; Monaghan, S.A.; Hu, M-C.; Huang, L.J. 2017: Activating JAK2 mutants reveal cytokine receptor coupling differences that impact outcomes in myeloproliferative neoplasm. Leukemia 31(10): 2122-2131
Smith, G.; Bounds, R.; Wolf, H.; Steele, R.J.C.; Carey, F.A.; Wolf, C.R. 2010: Activating K-Ras mutations outwith 'hotspot' codons in sporadic colorectal tumours - implications for personalised cancer medicine. British Journal of Cancer 102(4): 693-703
Chen, C.; Busson, M.; Rocha, V.; Appert, M-L.; Lepage, V.; Dulphy, N.; Haas, P.; Socié, G.; Toubert, A.; Charron, D.; Loiseau, P. 2006: Activating KIR genes are associated with CMV reactivation and survival after non-T-cell depleted HLA-identical sibling bone marrow transplantation for malignant disorders. Bone Marrow Transplantation 38(6): 437-444
Shirazi, F.; Jones, R.J.; Singh, R.K.; Zou, J.; Kuiatse, I.; Berkova, Z.; Wang, H.; Lee, H.C.; Hong, S.; Dick, L.; Chattopadhyay, N.; Orlowski, R.Z. 2020: Activating KRAS, NRAS, and BRAF mutants enhance proteasome capacity and reduce endoplasmic reticulum stress in multiple myeloma. Proceedings of the National Academy of Sciences of the United States of America 117(33): 20004-20014
Malnati, M.S.; Ugolotti, E.; Monti, M.Cristina.; Battista, D.De.; Vanni, I.; Bordo, D.; Sironi, F.; Larghero, P.; Marco, E.Di.; Biswas, P.; Poli, G.; Vicenzi, E.; Riva, A.; Tarkowski, M.; Tambussi, G.; Nozza, S.; Tripodi, G.; Marras, F.; De Maria, A.; Pistorio, A.; Biassoni, R. 2017: Activating Killer Immunoglobulin Receptors and HLA-C: a successful combination providing HIV-1 control. Scientific Reports 7: 42470
Chen, H.; Lim, C.; Zhou, M.; He, Z.; Sun, X.; Li, X.; Ye, Y.; Tan, T.; Zhang, H.; Yang, C.; Han, J.W.; Chen, Y. 2021: Activating Lattice Oxygen in Perovskite Oxide by B-Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures. Advanced Science 8(22): E2102713
Zhou, Z.; Wang, X.; Zhang, H.; Huang, H.; Sun, L.; Ma, L.; Du, Y.; Pei, C.; Zhang, Q.; Li, H.; Ma, L.; Gu, L.; Liu, Z.; Cheng, L.; Tan, C. 2021: Activating Layered Metal Oxide Nanomaterials via Structural Engineering as Biodegradable Nanoagents for Photothermal Cancer Therapy. Small 17(12): E2007486
Yeh, I.; Botton, T.; Talevich, E.; Shain, A.Hunter.; Sparatta, A.J.; de la Fouchardiere, A.; Mully, T.W.; North, J.P.; Garrido, M.C.; Gagnon, A.; Vemula, S.S.; McCalmont, T.H.; LeBoit, P.E.; Bastian, B.C. 2015: Activating MET kinase rearrangements in melanoma and Spitz tumours. Nature Communications 6: 7174
Dong, L.; Han, D.; Meng, X.; Xu, M.; Zheng, C.; Xia, Q. 2021: Activating Mutation of SHP2 Establishes a Tumorigenic Phonotype Through Cell-Autonomous and Non-Cell-Autonomous Mechanisms. Frontiers in Cell and Developmental Biology 9: 630712
Jarahian, M.; Marstaller, K.; Banna, N.; Ahani, R.; Etemadzadeh, M.H.; Boller, L.K.; Azadmanesh, K.; Cid-Arregui, A.; Khezri, A.; Berger, M.R.; Momburg, F.; Watzl, C. 2022: Activating Natural Killer Cell Receptors, Selectins, and Inhibitory Siglecs Recognize Ebolavirus Glycoprotein. Journal of Innate Immunity 14(2): 135-147
Sun, B.; Jiang, Y.; Cui, H.; Fang, X.; Han, G.; Dai, X.; Zhou, S.; Mao, H.; Wang, B. 2020: Activating PIK3CA mutation promotes adipogenesis of adipose-derived stem cells in macrodactyly via up-regulation of E2F1. Cell Death and Disease 11(7): 600
Cui, H.; Han, G.; Sun, B.; Fang, X.; Dai, X.; Zhou, S.; Mao, H.; Wang, B. 2020: Activating PIK3CA mutation promotes osteogenesis of bone marrow mesenchymal stem cells in macrodactyly. Cell Death and Disease 11(7): 505
Wang, X.; Hawkins, B.T.; Miller, D.S. 2011: Activating PKC-β1 at the blood-brain barrier reverses induction of P-glycoprotein activity by dioxin and restores drug delivery to the CNS. Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism 31(6): 1371-1375
Hang, H.; Wang, L-Kun.; Ren, S-Ying.; Song, A-Jun.; Wu, G-Feng. 2020: Activating PPARγ Increases NQO1 and γ-GCS Expression via Nrf2 in Thrombin-activated Microglia. Current Medical Science 40(1): 55-62
Seow, H.; Winemaker, S. 2021: Activating Patients and Families to Improve Palliative Care: The Waiting Room Revolution. Healthcare Quarterly 24(1): 6-9
Lai, F.; Orom, U.A.; Cesaroni, M.; Beringer, M.; Taatjes, D.J.; Blobel, G.A.; Shiekhattar, R. 2013: Activating RNAs associate with Mediator to enhance chromatin architecture and transcription. Nature 494(7438): 497-501
Lochhead, P.A.; Wickman, G.; Mezna, M.; Olson, M.F. 2010: Activating ROCK1 somatic mutations in human cancer. Oncogene 29(17): 2591-2598
Irby, R.B.; Mao, W.; Coppola, D.; Kang, J.; Loubeau, J.M.; Trudeau, W.; Karl, R.; Fujita, D.J.; Jove, R.; Yeatman, T.J. 1999: Activating SRC mutation in a subset of advanced human colon cancers. Nature Genetics 21(2): 187-190
Xie, J.; Murone, M.; Luoh, S.M.; Ryan, A.; Gu, Q.; Zhang, C.; Bonifas, J.M.; Lam, C.W.; Hynes, M.; Goddard, A.; Rosenthal, A.; Epstein, E.H.; de Sauvage, F.J. 1998: Activating Smoothened mutations in sporadic basal-cell carcinoma. Nature 391(6662): 90-92
Pasini, S.; Liu, J.; Corona, C.; Peze-Heidsieck, E.; Shelanski, M.; Greene, L.A. 2016: Activating Transcription Factor 4 (ATF4) modulates Rho GTPase levels and function via regulation of RhoGDIα. Scientific Reports 6: 36952
Stengel, S.T.; Fazio, A.; Lipinski, S.; Jahn, M.T.; Aden, K.; Ito, G.; Wottawa, F.; Kuiper, J.W.P.; Coleman, O.I.; Tran, F.; Bordoni, D.; Bernardes, J.P.; Jentzsch, M.; Luzius, A.; Bierwirth, S.; Messner, B.; Henning, A.; Welz, L.; Kakavand, N.; Falk-Paulsen, M.; Imm, S.; Hinrichsen, F.; Zilbauer, M.; Schreiber, S.; Kaser, A.; Blumberg, R.; Haller, D.; Rosenstiel, P. 2020: Activating Transcription Factor 6 Mediates Inflammatory Signals in Intestinal Epithelial Cells Upon Endoplasmic Reticulum Stress. Gastroenterology 159(4): 1357-1374.E10
Gao, S.; Proekt, A.; Renier, N.; Calderon, D.P.; Pfaff, D.W. 2019: Activating an anterior nucleus gigantocellularis subpopulation triggers emergence from pharmacologically-induced coma in rodents. Nature Communications 10(1): 2897
Turnbull, I.R.; Colonna, M. 2007: Activating and inhibitory functions of DAP12. Nature Reviews. Immunology 7(2): 155-161
Pegram, H.J.; Andrews, D.M.; Smyth, M.J.; Darcy, P.K.; Kershaw, M.H. 2011: Activating and inhibitory receptors of natural killer cells. Immunology and Cell Biology 89(2): 216-224
Gazdar, A.F. 2009: Activating and resistance mutations of EGFR in non-small-cell lung cancer: role in clinical response to EGFR tyrosine kinase inhibitors. Oncogene 28 Suppl. 1: S24-S31
Orjatsalo, M.; Partinen, E.; Wallukat, G.; Alakuijala, A.; Partinen, M. 2021: Activating autoantibodies against G protein-coupled receptors in narcolepsy type 1. Sleep Medicine 77: 82-87
Galluzzi, L.; Bravo-San Pedro, Jé.Manuel.; Demaria, S.; Formenti, S.Chiara.; Kroemer, G. 2017: Activating autophagy to potentiate immunogenic chemotherapy and radiation therapy. Nature Reviews. Clinical Oncology 14(4): 247-258
Beau, M.; Jeannin, O.; Lee, S.; Barrière, F.éd.ér.; Fourmigué, M.; Jeon, I.-R. 2020: Activating both Halogen and Chalcogen Bonding Interactions in Cation Radical Salts of Iodinated Tetrathiafulavalene Derivatives. Chempluschem 85(9): 2136-2142
Wichmann, C.; Quagliano-Lo Coco, I.; Yildiz, Ö.; Chen-Wichmann, L.; Weber, H.; Syzonenko, T.; Döring, C.; Brendel, C.; Ponnusamy, K.; Kinner, A.; Brandts, C.; Henschler, R.; Grez, M. 2015: Activating c-KIT mutations confer oncogenic cooperativity and rescue RUNX1/ETO-induced DNA damage and apoptosis in human primary CD34+ hematopoietic progenitors. Leukemia 29(2): 279-289
Schirosi, L.; Nannini, N.; Nicoli, D.; Cavazza, A.; Valli, R.; Buti, S.; Garagnani, L.; Sartori, G.; Calabrese, F.; Marchetti, A.; Buttitta, F.; Felicioni, L.; Migaldi, M.; Rea, F.; Di Chiara, F.; Mengoli, M.C.; Rossi, G. 2012: Activating c-KIT mutations in a subset of thymic carcinoma and response to different c-KIT inhibitors. Annals of Oncology: Official Journal of the European Society for Medical Oncology 23(9): 2409-2414
Piermattei, A.; Karthikeyan, S.; Sijbesma, R.P. 2009: Activating catalysts with mechanical force. Nature Chemistry 1(2): 133-137
Ling, T.; Yan, D-Yang.; Wang, H.; Jiao, Y.; Hu, Z.; Zheng, Y.; Zheng, L.; Mao, J.; Liu, H.; Du, X-Wen.; Jaroniec, M.; Qiao, S-Zhang. 2017: Activating cobalt(II) oxide nanorods for efficient electrocatalysis by strain engineering. Nature Communications 8(1): 1509
Möller, I.; Murali, R.; Müller, H.; Wiesner, T.; Jackett, L.A.; Scholz, S.L.; Cosgarea, I.; van de Nes, J.Ap.; Sucker, A.; Hillen, U.; Schilling, B.; Paschen, A.; Kutzner, H.; Rütten, A.; Böckers, M.; Scolyer, R.A.; Schadendorf, D.; Griewank, K.G. 2017: Activating cysteinyl leukotriene receptor 2 (CYSLTR2) mutations in blue nevi. Modern Pathology: An Official Journal of the United States and Canadian Academy of Pathology Inc 30(3): 350-356
Stower, H. 2019: Activating cytokines in the brain. Nature Medicine 25(10): 1469
Huppke, P.; Weissbach, S.; Church, J.A.; Schnur, R.; Krusen, M.; Dreha-Kulaczewski, S.; Kühn-Velten, W.Nikolaus.; Wolf, A.; Huppke, B.; Millan, F.; Begtrup, A.; Almusafri, F.; Thiele, H.; Altmüller, J.; Nürnberg, P.; Müller, M.; Gärtner, J. 2017: Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder. Nature Communications 8(1): 818
Brizuela, M.; Antipov, A.; Blessing, W.W.; Ootsuka, Y. 2019: Activating dopamine D2 receptors reduces brown adipose tissue thermogenesis induced by psychological stress and by activation of the lateral habenula. Scientific Reports 9(1): 19512
Bolton, O.; Lee, K.; Kim, H-Jun.; Lin, K.Y.; Kim, J. 2011: Activating efficient phosphorescence from purely organic materials by crystal design. Nature Chemistry 3(3): 205-210
Cheng, H-Yi.; Hou, Y-Nan.; Zhang, X.; Yang, Z-Ni.; Xu, T.; Wang, A-Jie. 2017: Activating electrochemical catalytic activity of bio-palladium by hybridizing with carbon nanotube as "e - Bridge". Scientific Reports 7(1): 16588
Vollberg, M.C.; Gaesser, B.; Cikara, M. 2021: Activating episodic simulation increases affective empathy. Cognition 209: 104558
Li, L.; Matsui, M.; Corey, D.R. 2016: Activating frataxin expression by repeat-targeted nucleic acids. Nature Communications 7: 10606
Janowski, B.A.; Younger, S.T.; Hardy, D.B.; Ram, R.; Huffman, K.E.; Corey, D.R. 2007: Activating gene expression in mammalian cells with promoter-targeted duplex RNAs. Nature Chemical Biology 3(3): 166-173
Flanagan, S.E.; Haapaniemi, E.; Russell, M.A.; Caswell, R.; Allen, H.Lango.; De Franco, E.; McDonald, T.J.; Rajala, H.; Ramelius, A.; Barton, J.; Heiskanen, K.; Heiskanen-Kosma, T.; Kajosaari, M.; Murphy, N.P.; Milenkovic, T.; Seppänen, M.; Lernmark, Åke.; Mustjoki, S.; Otonkoski, T.; Kere, J.; Morgan, N.G.; Ellard, S.; Hattersley, A.T. 2014: Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease. Nature Genetics 46(8): 812-814
Hensel, I. 1989: Activating group work with residents of retirement and nursing homes. Zeitschrift für Arztliche Fortbildung 83(8): 411-413
Carranza, G.; Garcia, M.; Sanchez, B.ña. 2020: Activating inclusive growth in railway SMEs by workplace innovation. Transportation Research Interdisciplinary Perspectives 7: 100193
Lamandé, S.R.; North, K.N. 2014: Activating internal ribosome entry to treat Duchenne muscular dystrophy. Nature Medicine 20(9): 987-988
Carlotti, B.; Madu, I.K.; Kim, H.; Cai, Z.; Jiang, H.; Muthike, A.K.; Yu, L.; Zimmerman, P.M.; Goodson, T. 2020: Activating intramolecular singlet exciton fission by altering π-bridge flexibility in perylene diimide trimers for organic solar cells. Chemical Science 11(33): 8757-8770
Grimaud, A.; Diaz-Morales, O.; Han, B.; Hong, W.T.; Lee, Y-Lin.; Giordano, L.; Stoerzinger, K.A.; Koper, M.T.M.; Shao-Horn, Y. 2017: Activating lattice oxygen redox reactions in metal oxides to catalyse oxygen evolution. Nature Chemistry 9(5): 457-465
Hoang, S.; Guo, Y.; Binder, A.J.; Tang, W.; Wang, S.; Liu, J.Jimmy.; Tran, H.; Lu, X.; Wang, Y.; Ding, Y.; Kyriakidou, E.A.; Yang, J.; Toops, T.J.; Pauly, T.R.; Ramprasad, R.; Gao, P-Xian. 2020: Activating low-temperature diesel oxidation by single-atom Pt on TiO 2 nanowire array. Nature Communications 11(1): 1062
Strutt, R.; Hindley, J.W.; Gregg, J.; Booth, P.J.; Harling, J.D.; Law, R.V.; Friddin, M.S.; Ces, O. 2021: Activating mechanosensitive channels embedded in droplet interface bilayers using membrane asymmetry. Chemical Science 12(6): 2138-2145
Chapiro, E.; Russell, L.; Lainey, E.; Kaltenbach, S.; Ragu, C.; Della-Valle, V.; Hanssens, K.; Macintyre, E.A.; Radford-Weiss, I.; Delabesse, E.; Cavé, H.; Mercher, T.; Harrison, C.J.; Nguyen-Khac, F.; Dubreuil, P.; Bernard, O.A. 2010: Activating mutation in the TSLPR gene in B-cell precursor lymphoblastic leukemia. Leukemia 24(3): 642-645
George, R.E.; Sanda, T.; Hanna, M.; Fröhling, S.; Luther, W.; Zhang, J.; Ahn, Y.; Zhou, W.; London, W.B.; McGrady, P.; Xue, L.; Zozulya, S.; Gregor, V.E.; Webb, T.R.; Gray, N.S.; Gilliland, D.Gary.; Diller, L.; Greulich, H.; Morris, S.W.; Meyerson, M.; Look, A.Thomas. 2008: Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature 455(7215): 975-978
Durham, B.H.; Lopez Rodrigo, E.; Picarsic, J.; Abramson, D.; Rotemberg, V.; De Munck, S.; Pannecoucke, E.; Lu, S.X.; Pastore, A.; Yoshimi, A.; Mandelker, D.; Ceyhan-Birsoy, O.; Ulaner, G.A.; Walsh, M.; Yabe, M.; Petrova-Drus, K.; Arcila, M.E.; Ladanyi, M.; Solit, D.B.; Berger, M.F.; Hyman, D.M.; Lacouture, M.E.; Erickson, C.; Saganty, R.; Ki, M.; Dunkel, I.J.; Santa-María López, V.; Mora, J.; Haroche, J.; Emile, J-Francois.; Decaux, O.; Geissmann, F.; Savvides, S.N.; Drilon, A.; Diamond, E.L.; Abdel-Wahab, O. 2019: Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms. Nature Medicine 25(12): 1839-1842
Åkerström, T.; Maharjan, R.; Sven Willenberg, H.; Cupisti, K.; Ip, J.; Moser, A.; Stålberg, P.; Robinson, B.; Alexander Iwen, K.; Dralle, H.; Walz, M.K.; Lehnert, H.; Sidhu, S.; Gomez-Sanchez, C.; Hellman, P.; Björklund, P. 2016: Activating mutations in CTNNB1 in aldosterone producing adenomas. Scientific Reports 6: 19546
Goriely, A.; Hansen, R.M.S.; Taylor, I.B.; Olesen, I.A.; Jacobsen, G.Krag.; McGowan, S.J.; Pfeifer, S.P.; McVean, G.A.T.; Rajpert-De Meyts, E.; Wilkie, A.O.M. 2009: Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors. Nature Genetics 41(11): 1247-1252
Palomero, T.; McKenna, K.; O-Neil, J.; Galinsky, I.; Stone, R.; Suzukawa, K.; Stiakaki, E.; Kalmanti, M.; Fox, E.A.; Caligiuri, M.A.; Aster, J.C.; Look, A.T.; Ferrando, A.A. 2006: Activating mutations in NOTCH1 in acute myeloid leukemia and lineage switch leukemias. Leukemia 20(11): 1963-1966
Jeffers, M.F.; Vande Woude, G.F. 1999: Activating mutations in the Met receptor overcome the requirement for autophosphorylation of tyrosines crucial for wild type signaling. Oncogene 18(36): 5120-5125
Tzoneva, G.; Perez-Garcia, A.; Carpenter, Z.; Khiabanian, H.; Tosello, V.; Allegretta, M.; Paietta, E.; Racevskis, J.; Rowe, J.M.; Tallman, M.S.; Paganin, M.; Basso, G.; Hof, J.; Kirschner-Schwabe, R.; Palomero, T.; Rabadan, R.; Ferrando, A. 2013: Activating mutations in the NT5C2 nucleotidase gene drive chemotherapy resistance in relapsed ALL. Nature Medicine 19(3): 368-371
Desta, F.; Christiansen, D.H.; Andersen, M.K.; Pedersen-Bjergaard, J. 2006: Activating mutations of JAK2V617F are uncommon in t-MDS and t-AML and are only observed in atypic cases. Leukemia 20(3): 547-548
Gutiérrez, M. 2020: Activating mutations of STAT3: Impact on human growth. Molecular and Cellular Endocrinology 518: 110979
Küçük, C.; Jiang, B.; Hu, X.; Zhang, W.; Chan, J.K.C.; Xiao, W.; Lack, N.; Alkan, C.; Williams, J.C.; Avery, K.N.; Kavak, Pınar.; Scuto, A.; Sen, E.; Gaulard, P.; Staudt, L.; Iqbal, J.; Zhang, W.; Cornish, A.; Gong, Q.; Yang, Q.; Sun, H.; d'Amore, F.; Leppä, S.; Liu, W.; Fu, K.; de Leval, L.; McKeithan, T.; Chan, W.C. 2015: Activating mutations of STAT5B and STAT3 in lymphomas derived from γδ-T or NK cells. Nature Communications 6: 6025
Tunc-Ozcan, E.; Peng, C-Yu.; Zhu, Y.; Dunlop, S.R.; Contractor, A.; Kessler, J.A. 2019: Activating newborn neurons suppresses depression and anxiety-like behaviors. Nature Communications 10(1): 3768
Shen, Y-C.; Ou, D-L.; Hsu, C.; Lin, K-L.; Chang, C-Y.; Lin, C-Y.; Liu, S-H.; Cheng, A-L. 2013: Activating oxidative phosphorylation by a pyruvate dehydrogenase kinase inhibitor overcomes sorafenib resistance of hepatocellular carcinoma. British Journal of Cancer 108(1): 72-81
Singhal, S.S.; Horne, D.; Singhal, J.; Awasthi, S.; Salgia, R. 2021: Activating p53 function by targeting RLIP. Biochimica et Biophysica Acta. Reviews on Cancer 1875(2): 188512
Ramirez, S.; Liu, X.; MacDonald, C.J.; Moffa, A.; Zhou, J.; Redondo, R.L.; Tonegawa, S. 2015: Activating positive memory engrams suppresses depression-like behaviour. Nature 522(7556): 335-339
Ansari, S.; Hosseinzadeh, H.; Dennis, S.; Zwar, N. 2017: Activating primary care COPD patients with multi-morbidity (APCOM) pilot project: study protocol. Npj Primary Care Respiratory Medicine 27(1): 12
Ansari, S.; Hosseinzadeh, H.; Dennis, S.; Zwar, N. 2020: Activating primary care COPD patients with multi-morbidity through tailored self-management support. Npj Primary Care Respiratory Medicine 30(1): 12
Wu, C. 1984: Activating protein factor binds in vitro to upstream control sequences in heat shock gene chromatin. Nature 311(5981): 81-84
Rong, L.; Zheng, X.; Oba, B.T.; Shen, C.; Wang, X.; Wang, H.; Luo, Q.; Sun, L. 2021: Activating soil microbial community using bacillus and rhamnolipid to remediate TPH contaminated soil. Chemosphere 275: 130062
Andersson, E.; Kuusanmäki, H.; Bortoluzzi, S.; Lagström, S.; Parsons, A.; Rajala, H.; van Adrichem, A.; Eldfors, S.; Olson, T.; Clemente, M.J.; Laasonen, A.; Ellonen, P.; Heckman, C.; Loughran, T.P.; Maciejewski, J.P.; Mustjoki, S. 2016: Activating somatic mutations outside the SH2-domain of STAT3 in LGL leukemia. Leukemia 30(5): 1204-1208
Joshi, M.; Ansell, S.M. 2020: Activating the Antitumor Immune Response in Non-Hodgkin Lymphoma Using Immune Checkpoint Inhibitors. Journal of Immunology Research 2020: 8820377
Frimodt-Møller, J.; Koulouktsis, A.; Charbon, G.; Otterlei, M.; Nielsen, P.E.; Løbner-Olesen, A. 2021: Activating the Cpx response induces tolerance to antisense PNA delivered by an arginine-rich peptide in Escherichia coli. Molecular Therapy. Nucleic Acids 25: 444-454
Cai, X.; Sang, X.-G.; Song, Y.; Guo, D.; Liu, X.-X.; Sun, X. 2020: Activating the Highly Reversible Mo4+/Mo5+ Redox Couple in Amorphous Molybdenum Oxide for High-Performance Supercapacitors. Acs Applied Materials and Interfaces 12(43): 48565-48571
Yu, Y.; Xu, M.; Ding, X.; Chu, Z.; Liu, H. 2021: Activating the MYB51 and MYB122 to upregulate the transcription of glucosinolates biosynthesis genes by copper ions in Arabidopsis. Plant Physiology and Biochemistry: Ppb 162: 496-505
Li, K.; Xu, J.; Chen, C.; Xie, Z.; Liu, D.; Qu, D.; Tang, H.; Wei, Q.; Deng, Q.; Li, J.; Hu, N. 2021: Activating the hydrogen evolution activity of Pt electrode via synergistic interaction with NiS2. Journal of Colloid and Interface Science 582(Part B): 591-597
Chen, X.; Ma, R.; Zhou, H.; Zhou, X.; Che, L.; Yao, S.; Wang, Z. 2013: Activating the microscale edge effect in a hierarchical surface for frosting suppression and defrosting promotion. Scientific Reports 3: 2515
Cinchetti, M.; Dediu, V.Alek.; Hueso, L.E. 2017: Activating the molecular spinterface. Nature Materials 16(5): 507-515
Lee, S-H.; Bahn, J.H.; Whitlock, N.C.; Baek, S.J. 2010: Activating transcription factor 2 (ATF2) controls tolfenamic acid-induced ATF3 expression via MAP kinase pathways. Oncogene 29(37): 5182-5192
Zhang, C.; Zhang, R.; Dai, X.; Cao, X.; Wang, K.; Huang, X.; Ren, Q. 2020: Activating transcription factor 2 (ATF2) negatively regulates the expression of antimicrobial peptide genes through tumor necrosis factor (TNF) in Macrobrachium nipponense. Fish and Shellfish Immunology 107(Part A): 26-35
Yin, H.-M.; Yan, L.-F.; Liu, Q.; Peng, Z.; Zhang, C.-Y.; Xia, Y.; Su, D.; Gu, A.-H.; Zhou, Y. 2020: Activating transcription factor 3 coordinates differentiation of cardiac and hematopoietic progenitors by regulating glucose metabolism. Science Advances 6(19): Eaay 9466
Wang, F.; Li, J.; Wang, H.; Zhang, F.; Gao, J. 2020: Activating transcription factor 3 inhibits endometrial carcinoma aggressiveness via JunB suppression. International Journal of Oncology 57(3): 707-720
Zhao, Q.; Luo, Y.-F.; Tian, M.; Xiao, Y.-L.; Cai, H.-R.; Li, H. 2021: Activating transcription factor 3 involved in Pseudomonas aeruginosa PAO1-induced macrophage senescence. Molecular Immunology 133: 122-127
Kwon, J-Woong.; Kwon, H-Kwon.; Shin, H-Jun.; Choi, Y-Min.; Anwar, M.Ayaz.; Choi, S. 2015: Activating transcription factor 3 represses inflammatory responses by binding to the p65 subunit of NF-κB. Scientific Reports 5: 14470
Yan, C.; Lu, D.; Hai, T.; Boyd, D.D. 2005: Activating transcription factor 3, a stress sensor, activates p53 by blocking its ubiquitination. EMBO Journal 24(13): 2425-2435
Lorenz, N.I.; Sittig, A.C.M.; Urban, H.; Luger, A-Luisa.; Engel, A.L.; Münch, C.; Steinbach, J.P.; Ronellenfitsch, M.W. 2021: Activating transcription factor 4 mediates adaptation of human glioblastoma cells to hypoxia and temozolomide. Scientific Reports 11(1): 14161
Chen, L.; Liu, X.; Zhou, H.; Li, G.; Huang, F.; Zhang, J.; Xia, T.; Lei, W.; Zhao, J.; Li, C.; Chen, M. 2021: Activating transcription factor 4 regulates angiogenesis under lipid overload via methionine adenosyltransferase 2A-mediated endothelial epigenetic alteration. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 35(6): e21612
Niccoli, T.; Kerr, F.; Snoeren, I.; Fabian, D.; Aleyakpo, B.; Ivanov, D.; Sofola-Adesakin, O.; Cryar, A.; Adcott, J.; Thornton, J.; Partridge, L. 2021: Activating transcription factor 4-dependent lactate dehydrogenase activation as a protective response to amyloid beta toxicity. Brain Communications 3(2): Fcab 053
Tang, X.; Shen, H.; Chen, J.; Wang, X.; Zhang, Y.; Chen, L-li.; Rukachaisirikul, V.; Jiang, H-liang.; Shen, X. 2011: Activating transcription factor 6 protects insulin receptor from ER stress-stimulated desensitization via p42/44 ERK pathway. Acta Pharmacologica Sinica 32(9): 1138-1147
Giannoudis, A.; Malki, M.I.; Rudraraju, B.; Mohhamed, H.; Menon, S.; Liloglou, T.; Ali, S.; Carroll, J.S.; Palmieri, C. 2020: Activating transcription factor-2 (ATF2) is a key determinant of resistance to endocrine treatment in an in vitro model of breast cancer. Breast Cancer Research: Bcr 22(1): 126
Wenger, T.L.; Bly, R.A.; Wu, N.; Albert, C.M.; Park, J.; Shieh, J.; Chenbhanich, J.; Heike, C.L.; Adam, M.P.; Chang, I.; Sun, A.; Miller, D.E.; Beck, A.E.; Gupta, D.; Boos, M.D.; Zackai, E.H.; Everman, D.; Ganapathi, S.; Wilson, M.; Christodoulou, J.; Zarate, Y.A.; Curry, C.; Li, D.; Guimier, A.; Amiel, J.; Hakonarson, H.; Webster, R.; Bhoj, E.J.; Perkins, J.A.; Dahl, J.P.; Dobyns, W.B. 2020: Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy. American Journal of Medical Genetics. Part a 182(7): 1576-1591
Gualtieri, A.; Kyprianou, N.; Gregory, L.C.; Vignola, M.Lillina.; Nicholson, J.G.; Tan, R.; Inoue, S-Ichi.; Scagliotti, V.; Casado, P.; Blackburn, J.; Abollo-Jimenez, F.; Marinelli, E.; Besser, R.E.J.; Högler, W.; Karen Temple, I.; Davies, J.H.; Gagunashvili, A.; Robinson, I.C.A.F.; Camper, S.A.; Davis, S.W.; Cutillas, P.R.; Gevers, E.F.; Aoki, Y.; Dattani, M.T.; Gaston-Massuet, C. 2021: Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans. Nature Communications 12(1): 2028
Napoli, N.J.; Demas, M.; Stephens, C.L.; Kennedy, K.D.; Harrivel, A.R.; Barnes, L.E.; Pope, A.T. 2020: Activation Complexity: A Cognitive Impairment Tool for Characterizing Neuro-isolation. Scientific Reports 10(1): 3909
Maruyama, S. 2021: Activation Dynamics Analysis of Language-related Areas with High Temporal Resolution fMRi. Nihon Hoshasen Gijutsu Gakkai Zasshi 77(9): 941-946
Botello, L.E.; Feliu, J.M.; Climent, V. 2020: Activation Energy of Hydrogen Adsorption on Pt(111) in Alkaline Media: An Impedance Spectroscopy Study at Variable Temperatures. Acs Applied Materials and Interfaces 12(38): 42911-42917
Song, L.; Xu, W.; Huo, J.; Li, F.; Wang, L.-M.; Ediger, M.D.; Wang, J.-Q. 2020: Activation Entropy as a Key Factor Controlling the Memory Effect in Glasses. Physical Review Letters 125(13): 135501
Iverson, D.B.; Xiao, Y.; Jones, D.N.; Eisenmesser, E.Z.; Ahn, N.G. 2020: Activation Loop Dynamics Are Coupled to Core Motions in Extracellular Signal-Regulated Kinase-2. Biochemistry 59(29): 2698-2706
Morimoto, K. 2021: Activation Mechanism of Prostanoid Receptors -X-ray Crystallography of EP3 Receptor. Yakugaku Zasshi: Journal of the Pharmaceutical Society of Japan 141(4): 473-479
Ma, N.; Lee, S.; Vaidehi, N. 2020: Activation Microswitches in Adenosine Receptor A2A Function as Rheostats in the Cell Membrane. Biochemistry 59(42): 4059-4071
Wu, Y.; Qian, R.; Yang, Y.; Sheng, Y.; Li, W.; Wang, W. 2021: Activation Pathways and Free Energy Landscapes of the SARS-CoV-2 Spike Protein. Acs Omega 6(36): 23432-23441
Luo, Y.; Xue, Y.; Mao, L.; Lin, Q.; Tang, G.; Song, H.; Liu, W.; Tong, S.; Hou, H.; Huang, M.; Ouyang, R.; Wang, F.; Sun, Z. 2021: Activation Phenotype of Mycobacterium tuberculosis-Specific CD4+ T Cells Promoting the Discrimination Between Active Tuberculosis and Latent Tuberculosis Infection. Frontiers in Immunology 12: 721013
Ye, W.; Tu, Y-Hsiang.; Cooper, A.J.; Zhang, Z.; Katritch, V.; Liman, E.R. 2018: Activation Stoichiometry and Pore Architecture of TRPA1 Probed with Channel Concatemers. Scientific Reports 8(1): 17104
Danielsen, A.; Steinnes, E. 1968: Activation analysis in medicine. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 88(20): 1930-1933
Liu, F.; Li, Y.; Huang, Y.; Tsyrenova, A.; Miller, K.; Zhou, L.; Qin, H.; Jiang, S. 2020: Activation and Assembly of Plasmonic-Magnetic Nanosurfactants for Encapsulation and Triggered Release. Nano Letters 20(12): 8773-8780
Guo, Y.; Zhang, L.; Zhang, J.; Lv, S.-X.; Du, C.-X.; Wang, T.; Wang, H.-S.; Xie, W.; Liu, J. 2021: Activation and Blockade of Serotonin-4 Receptors in the Lateral Habenula Produce Antidepressant Effects in the Hemiparkinsonian Rat. Neuropsychobiology 80(1): 52-63
Liu, L.; Li, S.; Sun, R.; Qin, X.; Ju, J.; Zhang, C.; Duan, Y.; Huang, Y. 2020: Activation and Characterization of Bohemamine Biosynthetic Gene Cluster from Streptomyces sp. CB02009. Organic Letters 22(12): 4614-4619
Lees, A.; Zhou, J. 2021: Activation and Conjugation of Soluble Polysaccharides using 1-Cyano-4-Dimethylaminopyridine Tetrafluoroborate (CDAP). Journal of Visualized Experiments: Jove 2021(172)
Ahmetaj-Shala, B.; Marei, I.; Kawai, R.; Rothery, S.; Pericleous, C.; Mohamed, N.A.; Gashaw, H.; Bokea, K.; Samuel, J.; Vandenheste, A.; Shala, F.; Kirkby, N.S.; Mitchell, J.A. 2021: Activation and Contraction of Human "Vascular" Smooth Muscle Cells Grown from Circulating Blood Progenitors. Frontiers in Cell and Developmental Biology 9: 681347
Kong, R.Y.; Crimmin, M.R. 2020: Activation and Functionalization of C-C σ Bonds of Alkylidene Cyclopropanes at Main Group Centers. Journal of the American Chemical Society 142(28): 11967-11971
Choudhury, S.M.; Ma, X.; Abdullah, S.W.; Zheng, H. 2021: Activation and Inhibition of the NLRP3 Inflammasome by RNA Viruses. Journal of Inflammation Research 14: 1145-1163
Zhou, W.; Sonnenberg, G.F. 2020: Activation and Suppression of Group 3 Innate Lymphoid Cells in the Gut. Trends in Immunology 41(8): 721-733
Yan, M.; Wang, H.; Chan, B.; Roose-Girma, M.; Erickson, S.; Baker, T.; Tumas, D.; Grewal, I.S.; Dixit, V.M. 2001: Activation and accumulation of B cells in TACI-deficient mice. Nature Immunology 2(7): 638-643
Huang, C.-F. 2021: Activation and activity of STOP1 in aluminium resistance. Journal of Experimental Botany 72(7): 2269-2272
Kruse, A.C.; Ring, A.M.; Manglik, A.; Hu, J.; Hu, K.; Eitel, K.; Hübner, H.; Pardon, E.; Valant, C.; Sexton, P.M.; Christopoulos, A.; Felder, C.C.; Gmeiner, P.; Steyaert, J.; Weis, W.I.; Garcia, K.Christopher.; Wess, Jürgen.; Kobilka, B.K. 2013: Activation and allosteric modulation of a muscarinic acetylcholine receptor. Nature 504(7478): 101-106
Akk, G.; Steinbach, J.H. 2000: Activation and block of recombinant GABA(A) receptors by pentobarbitone: a single-channel study. British Journal of Pharmacology 130(2): 249-258
Wang, J.-W.; Gao, F.; Wang, Z.-L.; Wang, X.-C.; Yang, J.; Ma, B.-R.; Wang, H.-S.; Xie, W.; Guo, Y.; Zhang, L. 2021: Activation and blockade of dorsal hippocampal serotonin4 receptors produce antidepressant effects in the hemiparkinsonian rats. Brain Research 2021: 147426
Luo, Y.; Huang, H.; Liang, J.; Wang, M.; Lu, L.; Shao, Z.; Cobb, R.E.; Zhao, H. 2013: Activation and characterization of a cryptic polycyclic tetramate macrolactam biosynthetic gene cluster. Nature Communications 4: 2894
Scriven, P.; Coulson, S.; Haines, R.; Balasubramanian, S.; Cross, S.; Wyld, L. 2009: Activation and clinical significance of the unfolded protein response in breast cancer. British Journal of Cancer 101(10): 1692-1698
Salgado-Pineda, P.; Rodriguez-Jimenez, R.; Moreno-Ortega, M.; Dompablo, M.ón.; Martínez de Aragón, A.; Salvador, R.; McKenna, P.J.; Pomarol-Clotet, E.; Palomo, T.ás. 2021: Activation and deactivation patterns in schizophrenia during performance of an fMRi adapted version of the stroop task. Journal of Psychiatric Research 144: 1-7
Arteaga-Henriquez, G.; Burger, B.; Weidinger, E.; Grosse, L.; Moll, N.; Schuetze, G.; Schwarz, M.; Wijkhuijs, A.; Op de Beeck, G.; Berghmans, R.; Versnel, M.A.; Arolt, V.; Müller, N.; Drexhage, H.A. 2020: Activation and deactivation steps in the tryptophan breakdown pathway in major depressive disorder: A link to the monocyte inflammatory state of patients. ProgressinNeuro-PsychopharmacologyandBiologicalPsychiatry 2020: 110226
Dirar, Q.; Russell, T.; Liu, L.; Ahn, S.; Dotti, G.; Aravamudhan, S.; Conforti, L.; Yun, Y. 2020: Activation and degranulation of CAR-T cells using engineered antigen-presenting cell surfaces. Plos one 15(9): E0238819
Easson, M.L.A.E.; Malka, O.; Paetz, C.; Hojná, A.; Reichelt, M.; Stein, B.; van Brunschot, S.; Feldmesser, E.; Campbell, L.; Colvin, J.; Winter, S.; Morin, S.; Gershenzon, J.; Vassão, D.G. 2021: Activation and detoxification of cassava cyanogenic glucosides by the whitefly Bemisia tabaci. Scientific Reports 11(1): 13244
Xie, Y.; Chen, J.; Wang, B.; Chen, T.; Chen, J.; Zhang, Y.; Liu, X.; Chen, Q. 2020: Activation and enhancement of caerulomycin a biosynthesis in marine-derived Actinoalloteichus sp. AHMU CJ021 by combinatorial genome mining strategies. Microbial Cell Factories 19(1): 159
Lange, P.T.; White, M.C.; Damania, B. 2022: Activation and Evasion of Innate Immunity by Gammaherpesviruses. Journal of Molecular Biology 434(6): 167214
Lei, X.; Dong, X.; Ma, R.; Wang, W.; Xiao, X.; Tian, Z.; Wang, C.; Wang, Y.; Li, L.; Ren, L.; Guo, F.; Zhao, Z.; Zhou, Z.; Xiang, Z.; Wang, J. 2020: Activation and evasion of type I interferon responses by SARS-CoV-2. Nature Communications 11(1): 3810
Zhang, D.K.Y.; Cheung, A.S.; Mooney, D.J. 2020: Activation and expansion of human T cells using artificial antigen-presenting cell scaffolds. Nature Protocols 15(3): 773-798
Smith, L.I.F.; Zhao, Z.; Walker, J.; Lightman, S.; Spiga, F. 2021: Activation and expression of endogenous CREB-regulated transcription coactivators (CRTC) 1, 2 and 3 in the rat adrenal gland. Journal of Neuroendocrinology 33(1): E12920
Sano, M.; Abdellatif, M.; Oh, H.; Xie, M.; Bagella, L.; Giordano, A.; Michael, L.H.; DeMayo, F.J.; Schneider, M.D. 2002: Activation and function of cyclin T-Cdk9 (positive transcription elongation factor-b) in cardiac muscle-cell hypertrophy. Nature Medicine 8(11): 1310-1317
Rousseau, R.K.; Szadkowski, L.; Kovacs, C.M.; Saikali, M.F.; Nadeem, R.; Malazogu, F.; Huibner, S.; Cummins, C.L.; Kaul, R.; Walmsley, S.L. 2021: Activation and gut-homing of peripheral T cells in HIV immunologic non-responders despite long term viral suppression. Plos one 16(7): E0254149
Nakashima, H.; Nakashima, M.; Kinoshita, M.; Ikarashi, M.; Miyazaki, H.; Hanaka, H.; Imaki, J.; Seki, S. 2016: Activation and increase of radio-sensitive CD11b+ recruited Kupffer cells/macrophages in diet-induced steatohepatitis in FGF5 deficient mice. Scientific Reports 6: 34466
Lipski, W.J.; Grace, A.A. 2013: Activation and inhibition of neurons in the hippocampal ventral subiculum by norepinephrine and locus coeruleus stimulation. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology 38(2): 285-292
Kishor, A.; Fritz, S.E.; Haque, N.; Ge, Z.; Tunc, I.; Yang, W.; Zhu, J.; Hogg, J.R. 2020: Activation and inhibition of nonsense-mediated mRNA decay control the abundance of alternative polyadenylation products. Nucleic Acids Research 48(13): 7468-7482
Papke, R.L.; Thinschmidt, J.S.; Moulton, B.A.; Meyer, E.M.; Poirier, A. 1997: Activation and inhibition of rat neuronal nicotinic receptors by ABT-418. British Journal of Pharmacology 120(3): 429-438
Pegu, A.; Asokan, M.; Wu, L.; Wang, K.; Hataye, J.; Casazza, J.P.; Guo, X.; Shi, W.; Georgiev, I.; Zhou, T.; Chen, X.; O'Dell, S.; Todd, J-Paul.; Kwong, P.D.; Rao, S.S.; Yang, Z-yong.; Koup, R.A.; Mascola, J.R.; Nabel, G.J. 2015: Activation and lysis of human CD4 cells latently infected with HIV-1. Nature Communications 6: 8447
Moore, J.D.; Deschênes, M.; Kurnikova, A.; Kleinfeld, D. 2014: Activation and measurement of free whisking in the lightly anesthetized rodent. Nature Protocols 9(8): 1792-1802
Angulo, J.; Cuevas, P.; Fernández, A.; Gabancho, S.; Allona, A.; Martín-Morales, A.; Moncada, I.; Sáenz de Tejada, Iñigo. 2003: Activation and potentiation of the NO/cGMP pathway by NG-hydroxyl-L-arginine in rabbit corpus cavernosum under normoxic and hypoxic conditions and ageing. British Journal of Pharmacology 138(1): 63-70
Kuo, Y.C.; Weng, S.C.; Chou, C.J.; Chang, T.T.; Tsai, W.J. 2003: Activation and proliferation signals in primary human T lymphocytes inhibited by ergosterol peroxide isolated from Cordyceps cicadae. British Journal of Pharmacology 140(5): 895-906
Rebelein, J.G.; Stiebritz, M.T.; Lee, C.Chung.; Hu, Y. 2017: Activation and reduction of carbon dioxide by nitrogenase iron proteins. Nature Chemical Biology 13(2): 147-149
Lee, J-H.; Paull, T.T. 2007: Activation and regulation of ATM kinase activity in response to DNA double-strand breaks. Oncogene 26(56): 7741-7748
Krutzik, S.R.; Ochoa, M.Teresa.; Sieling, P.A.; Uematsu, S.; Ng, Y.W.; Legaspi, A.; Liu, P.T.; Cole, S.T.; Godowski, P.J.; Maeda, Y.; Sarno, E.N.; Norgard, M.V.; Brennan, P.J.; Akira, S.; Rea, T.H.; Modlin, R.L. 2003: Activation and regulation of Toll-like receptors 2 and 1 in human leprosy. Nature Medicine 9(5): 525-532
de Rivero Vaccari, J.Pablo.; Dietrich, W.Dalton.; Keane, R.W. 2014: Activation and regulation of cellular inflammasomes: gaps in our knowledge for central nervous system injury. Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism 34(3): 369-375
Latz, E.; Xiao, T.Sam.; Stutz, A. 2013: Activation and regulation of the inflammasomes. Nature Reviews. Immunology 13(6): 397-411
Thibault, C. 1948: Activation and regulation of the parthenogenic oocyte of the rabbit. Comptes Rendus des Seances de la Societe de Biologie et de ses Filiales 142(7-8): 495-497
Walz, S.; Lorenzin, F.; Morton, J.; Wiese, K.E.; von Eyss, Börn.; Herold, S.; Rycak, L.; Dumay-Odelot, Hélène.; Karim, S.; Bartkuhn, M.; Roels, F.; Wüstefeld, T.; Fischer, M.; Teichmann, M.; Zender, L.; Wei, C-Lin.; Sansom, O.; Wolf, E.; Eilers, M. 2014: Activation and repression by oncogenic MYC shape tumour-specific gene expression profiles. Nature 511(7510): 483-487
Gartel, A.L.; Goufman, E.; Tevosian, S.G.; Shih, H.; Yee, A.S.; Tyner, A.L. 1998: Activation and repression of p21(WAF1/CIP1) transcription by RB binding proteins. Oncogene 17(26): 3463-3469
Coccia, E.M.; Del Russo, N.; Stellacci, E.; Orsatti, R.; Benedetti, E.; Marziali, G.; Hiscott, J.; Battistini, A. 1999: Activation and repression of the 2-5A synthetase and p21 gene promoters by IRF-1 and IRF-2. Oncogene 18(12): 2129-2137
Jaynes, J.B.; O'Farrell, P.H. 1988: Activation and repression of transcription by homoeodomain-containing proteins that bind a common site. Nature 336(6201): 744-749
Garcia-Doval, C.; Schwede, F.; Berk, C.; Rostøl, J.T.; Niewoehner, O.; Tejero, O.; Hall, J.; Marraffini, L.A.; Jinek, M. 2020: Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6. Nature Communications 11(1): 1596
Geppetti, P.; Trevisani, M. 2004: Activation and sensitisation of the vanilloid receptor: role in gastrointestinal inflammation and function. British Journal of Pharmacology 141(8): 1313-1320
Hardy, K.; Chaudhri, G. 1997: Activation and signal transduction via mitogen-activated protein (MAP) kinases in T lymphocytes. Immunology and Cell Biology 75(6): 528-545
Zarubin, T.; Han, J. 2005: Activation and signaling of the p38 MAP kinase pathway. Cell Research 15(1): 11-18
Toda, Y.; Hirayama, H.; Kuganathan, N.; Torrisi, A.; Sushko, P.V.; Hosono, H. 2013: Activation and splitting of carbon dioxide on the surface of an inorganic electride material. Nature Communications 4: 2378
Khaw, P.T.; Occleston, N.L.; Schultz, G.; Grierson, I.; Sherwood, M.B.; Larkin, G. 1994: Activation and suppression of fibroblast function. Eye 8: 188-195
Martens, S.; Fracchiolla, D. 2020: Activation and targeting of ATG8 protein lipidation. Cell Discovery 6: 23
Martens, S.; Fracchiolla, D. 2020: Activation and targeting of ATG8 protein lipidation. Cell Discovery 6(1): 23
Austin, C.R. 1951: Activation and the correlation between male and female elements in fertilization. Nature 168(4274): 558-559
Howard, G.; Eiges, R.; Gaudet, F.; Jaenisch, R.; Eden, A. 2008: Activation and transposition of endogenous retroviral elements in hypomethylation induced tumors in mice. Oncogene 27(3): 404-408
Labbe, J.C.; Lee, M.G.; Nurse, P.; Picard, A.; Doree, M. 1988: Activation at M-phase of a protein kinase encoded by a starfish homologue of the cell cycle control gene cdc2+. Nature 335(6187): 251-254
Kawashima, K.; Iwata, R.; Kogure, K.; Ohtomo, H.; Orihara, H.; Ido, T. 1987: Activation autoradiography: imaging and quantitative determination of endogenous and exogenous oxygen in the rat brain. Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism 7(3): 272-279
Ruanto, P.; Chismon, D.L.; Hothersall, J.; Godfrey, R.E.; Lee, D.J.; Busby, S.J.W.; Browning, D.F. 2020: Activation by NarL at the Escherichia coli ogt promoter. Biochemical Journal 477(15): 2807-2820
Rorsman, P.; Bokvist, K.; Ammälä, C.; Arkhammar, P.; Berggren, P.O.; Larsson, O.; Wåhlander, K. 1991: Activation by adrenaline of a low-conductance G protein-dependent K+ channel in mouse pancreatic B cells. Nature 349(6304): 77-79
Ko, F.N.; Huang, S.Y.; Teng, C.M. 1997: Activation by high potassium of a novel voltage-operated Ca2+ channel in rat spleen. British Journal of Pharmacology 120(4): 565-570
Bonfio, C.; Russell, D.A.; Green, N.J.; Mariani, A.; Sutherland, J.D. 2020: Activation chemistry drives the emergence of functionalised protocells. Chemical Science 11(39): 10688-10697
Gutiérrez, Jé.L.; Chandy, M.; Carrozza, M.J.; Workman, J.L. 2007: Activation domains drive nucleosome eviction by SWI/SNF. EMBO Journal 26(3): 730-740
Mäusle, S.M.; Abzaliyeva, A.; Greife, P.; Simon, P.S.; Perez, R.; Zilliges, Y.; Dau, H. 2020: Activation energies for two steps in the S2→ S3 transition of photosynthetic water oxidation from time-resolved single-frequency infrared spectroscopy. Journal of Chemical Physics 153(21): 215101
Johnson, E.G.; Mooney, L.; Graf Estes, K.; Nordahl, C.W.; Ghetti, S. 2021: Activation for newly learned words in left medial-temporal lobe during toddlers' sleep is associated with memory for words. Current Biology: Cb 31(24): 5429-5438.E5
Zavatone-Veth, J.A.; Pehlevan, C. 2021: Activation function dependence of the storage capacity of treelike neural networks. Physical Review. e 103(2): L020301
Schur, E.A.; Kleinhans, N.M.; Goldberg, J.; Buchwald, D.; Schwartz, M.W.; Maravilla, K. 2009: Activation in brain energy regulation and reward centers by food cues varies with choice of visual stimulus. International Journal of Obesity 33(6): 653-661
Ghosh, S.; Baltimore, D. 1990: Activation in vitro of NF-kappa B by phosphorylation of its inhibitor I kappa B. Nature 344(6267): 678-682
Larson, J.S.; Schuetz, T.J.; Kingston, R.E. 1988: Activation in vitro of sequence-specific DNA binding by a human regulatory factor. Nature 335(6188): 372-375
Rogozin, I.B.; Lada, A.G.; Goncearenco, A.; Green, M.R.; De, S.; Nudelman, G.; Panchenko, A.R.; Koonin, E.V.; Pavlov, Y.I. 2016: Activation induced deaminase mutational signature overlaps with CpG methylation sites in follicular lymphoma and other cancers. Scientific Reports 6: 38133
Weidberg, S.; González-Roz, A.; García-Fernández, G.; Secades-Villa, R. 2021: Activation level as a mediator between behavioral activation, sex, and depression among treatment-seeking smokers. Addictive Behaviors 114: 106715
Snipas, S.J.; Drag, M.; Stennicke, H.R.; Salvesen, G.S. 2008: Activation mechanism and substrate specificity of the Drosophila initiator caspase DRONC. Cell Death and Differentiation 15(5): 938-945
Shiraki, T. 2007: Activation mechanism of PPARgamma by its endogenous ligands. SEIKAGAKU. Journal of Japanese Biochemical Society 79(10): 960-964
Teixeira, R.D.; Holzschuh, F.; Schirmer, T. 2021: Activation mechanism of a small prototypic Rec-GGDEF diguanylate cyclase. Nature Communications 12(1): 2162
Shihoya, W.; Nishizawa, T.; Okuta, A.; Tani, K.; Dohmae, N.; Fujiyoshi, Y.; Nureki, O.; Doi, T. 2016: Activation mechanism of endothelin ET B receptor by endothelin-1. Nature 537(7620): 363-368
Liu, R.; Kang, Y.; Chen, L. 2021: Activation mechanism of human soluble guanylate cyclase by stimulators and activators. Nature Communications 12(1): 5492
Paulino, C.; Kalienkova, V.; Lam, A.K.M.; Neldner, Y.; Dutzler, R. 2017: Activation mechanism of the calcium-activated chloride channel TMEM16A revealed by cryo-EM. Nature 552(7685): 421-425
Krumm, B.; Roth, B.L. 2018: Activation mechanisms for a universal signalling protein. Nature 557(7705): 318-319
Jing, W.; Lo Pilato, J.; Kay, C.; Man, S.M. 2021: Activation mechanisms of inflammasomes by bacterial toxins. Cellular Microbiology 23(4): E13309
Purpura, D.P. 1966: Activation of "secondary" impulse trigger sites in hippocampal neurones. Nature 211(5055): 1317-1318
Murray, J.B.; Mikhael, C.; Han, G.; de Faria, L.Perciliano.; Rody, W.J.; Holliday, L.Shannon. 2021: Activation of (pro)renin by (pro)renin receptor in extracellular vesicles from osteoclasts. Scientific Reports 11(1): 9214
Gu, J.; Hou, Z.; Zhou, X.; Wang, Q.; Chen, Y.; Zhang, J. 2022: Activation of 5-HT1 receptor in lateral habenula impaired contextual fear memory and hippocampal LTP in rat. Neuroscience Letters 770: 136305
Solís-Guillén, R.ío.; Leopoldo, M.; Meneses, A.; Centurión, D. 2021: Activation of 5-HT1A and 5-HT7 receptors enhanced a positively reinforced long-term memory. Behavioural Brain Research 397: 112932
Kurokawa, K.; Takahashi, K.; Miyagawa, K.; Mochida-Saito, A.; Takeda, H.; Tsuji, M. 2021: Activation of 5-HT1A receptor reduces abnormal emotionality in stress-maladaptive mice by alleviating decreased myelin protein in the ventral hippocampus. Neurochemistry International 151: 105213
Flanagan, T.W.; Sebastian, M.N.; Battaglia, D.M.; Foster, T.P.; Maillet, E.L.; Nichols, C.D. 2019: Activation of 5-HT 2 Receptors Reduces Inflammation in Vascular Tissue and Cholesterol Levels in High-Fat Diet-Fed Apolipoprotein E Knockout Mice. Scientific Reports 9(1): 13444
Jeggo, R.D.; Wang, Y.; Jordan, D.; Ramage, A.G. 2007: Activation of 5-HT1B and 5-HT1D receptors in the rat nucleus tractus solitarius: opposing action on neurones that receive an excitatory vagal C-fibre afferent input. British Journal of Pharmacology 150(8): 987-995
Chetty, N.; Irving, H.R.; Coupar, I.M. 2006: Activation of 5-HT3 receptors in the rat and mouse intestinal tract: a comparative study. British Journal of Pharmacology 148(7): 1012-1021
Zhang, W.; Li, Y.; Du, S.; Chai, Z.; He, J. 2021: Activation of 8-17 DNAzyme with extra functional group at conserved residues is related to catalytic metal ion. Bioorganic and Medicinal Chemistry Letters 48: 128234
Al-Mashhadi, R.H.; Skøtt, O.; Vanhoutte, P.M.; Hansen, P.B. 2009: Activation of A(2) adenosine receptors dilates cortical efferent arterioles in mouse. Kidney International 75(8): 793-799
Mishra, H.K.; Dixon, K.J.; Pore, N.; Felices, M.; Miller, J.S.; Walcheck, B. 2021: Activation of ADAM17 by IL-15 Limits Human NK Cell Proliferation. Frontiers in Immunology 12: 711621
Pérez-Tenorio, G.; Stål, O. 2002: Activation of AKT/PKB in breast cancer predicts a worse outcome among endocrine treated patients. British Journal of Cancer 86(4): 540-545
Srinivasan, M.P.; Bhopale, K.K.; Caracheo, A.A.; Amer, S.M.; Khan, S.; Kaphalia, L.; Loganathan, G.; Balamurugan, A.N.; Kaphalia, B.S. 2020: Activation of AMP-activated protein kinase attenuates ethanol-induced ER/oxidative stress and lipid phenotype in human pancreatic acinar cells. Biochemical Pharmacology 180: 114174
Zhang, K.; Shi, Y.; Huang, C.; Huang, C.; Xu, P.; Zhou, C.; Liu, P.; Hu, R.; Zhuang, Y.; Li, G.; Hu, G.; Guo, X. 2021: Activation of AMP-activated protein kinase signaling pathway ameliorates steatosis in laying hen hepatocytes. Poultry Science 100(3): 100805
Wang, S.; Zhang, C.; Zhang, M.; Liang, B.; Zhu, H.; Lee, J.; Viollet, B.; Xia, L.; Zhang, Y.; Zou, M-Hui. 2012: Activation of AMP-activated protein kinase α2 by nicotine instigates formation of abdominal aortic aneurysms in mice in vivo. Nature Medicine 18(6): 902-910
Ye, L.; Zhang, X.; Zhou, Q.; Tan, B.; Xu, H.; Yi, Q.; Yan, L.; Xie, M.; Zhang, Y.; Tian, J.; Zhu, J. 2021: Activation of AMPK Promotes Maturation of Cardiomyocytes Derived from Human Induced Pluripotent Stem Cells. Frontiers in Cell and Developmental Biology 9: 644667
Huang, R.; Guo, F.; Li, Y.; Liang, Y.; Li, G.; Fu, P.; Ma, L. 2021: Activation of AMPK by triptolide alleviates nonalcoholic fatty liver disease by improving hepatic lipid metabolism, inflammation and fibrosis. Phytomedicine: International Journal of PhytoTherapy and Phytopharmacology 92: 153739
Pan, Y.; Liu, L.; Li, S.; Wang, K.; Ke, R.; Shi, W.; Wang, J.; Yan, X.; Zhang, Q.; Wang, Q.; Chai, L.; Xie, X.; Li, M. 2018: Activation of AMPK inhibits TGF-β1-induced airway smooth muscle cells proliferation and its potential mechanisms. Scientific Reports 8(1): 3624
Chen, B-lin.; Ma, Y-dong.; Meng, R-sen.; Xiong, Z-jun.; Wang, H-ning.; Zeng, J-yi.; Liu, C.; Dong, Y-gang. 2010: Activation of AMPK inhibits cardiomyocyte hypertrophy by modulating of the FOXO1/MuRF1 signaling pathway in vitro. Acta Pharmacologica Sinica 31(7): 798-804
Wang, X.-D.; Yu, W.-L.; Sun, Y. 2021: Activation of AMPK restored impaired autophagy and inhibited inflammation reaction by up-regulating SIRT1 in acute pancreatitis. Life Sciences 277: 119435
Gampala, S.; Zhang, G.; Chang, C.J.; Yang, J.-Y. 2021: Activation of AMPK sensitizes medulloblastoma to Vismodegib and overcomes Vismodegib-resistance. Faseb Bioadvances 3(6): 459-469
Pan, Y.; Liu, L.; Zhang, Q.; Shi, W.; Feng, W.; Wang, J.; Wang, Q.; Li, S.; Li, M. 2020: Activation of AMPK suppresses S1P-induced airway smooth muscle cells proliferation and its potential mechanisms. Molecular Immunology 128: 106-115
Katila, N.; Bhurtel, S.; Park, P.-H.; Hong, J.T.; Choi, D.-Y. 2020: Activation of AMPK/aPKCζ/CREB pathway by metformin is associated with upregulation of GDNF and dopamine. Biochemical Pharmacology 180: 114193
Arab, H.H.; Ashour, A.M.; Gad, A.M.; Mahmoud, A.M.; Kabel, A.M. 2021: Activation of AMPK/mTOR-driven autophagy and inhibition of NLRP3 inflammasome by saxagliptin ameliorate ethanol-induced gastric mucosal damage. Life Sciences 280: 119743
Xiang, S.; Zhang, Q.; Tang, Q.; Zheng, F.; Wu, J.; Yang, L.; Hann, S.Sunny. 2016: Activation of AMPKα mediates additive effects of solamargine and metformin on suppressing MUC1 expression in castration-resistant prostate cancer cells. Scientific Reports 6: 36721
Wu, Y.; Song, P.; Zhang, W.; Liu, J.; Dai, X.; Liu, Z.; Lu, Q.; Ouyang, C.; Xie, Z.; Zhao, Z.; Zhuo, X.; Viollet, B.; Foretz, M.; Wu, J.; Yuan, Z.; Zou, M-Hui. 2015: Activation of AMPKα2 in adipocytes is essential for nicotine-induced insulin resistance in vivo. Nature Medicine 21(4): 373-382
Watabe, M.; Ito, K.; Masuda, Y.; Nakajo, S.; Nakaya, K. 1998: Activation of AP-1 is required for bufalin-induced apoptosis in human leukemia U937 cells. Oncogene 16(6): 779-787
Palmero, I.; Murga, M.; Zubiaga, A.; Serrano, M. 2002: Activation of ARF by oncogenic stress in mouse fibroblasts is independent of E2F1 and E2F2. Oncogene 21(19): 2939-2947