Section 52

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Anonymous 1946: COEXISTING tuberculosis and coccidioidomycosis. Bulletin of the U.S. Army Medical Department. United States. Army. Medical Department 6: 11
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Anonymous 1946: COFFEY-HUMBER cancer treatment. Bulletin-LosAngelesCountyMedicalAssociation 76(3): 136
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Meiland, F.J.M.; Reinersmann, A.; Bergvall-Kareborn, B.; Craig, D.; Moelaert, F.; Mulvenna, M.D.; Nugent, C.; Scully, T.; Bengtsson, J.E.; Dröes, R.M. 2007: COGKNOW development and evaluation of an ICT-device for people with mild dementia. Studies in Health Technology and Informatics 127: 166-177
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Rao, A.V.; Reddy, T.K.; Prabakar, E.R.; Baskaran, S.; Swaminathan, R.; Belinda, C.; Andal, G.; Verghese, A.; Kulhara, P.; Sharma, S.D.; Sathyavathy, K.; Prabakaran, N.; Jayaraman, J.; Luthra, U.K.; Parhee, R.; Kumar, N. 1989: Cognitive Disorder and Depression: (An Analysis of the Causal Relationship and Susceptibility to Relapses). Indian Journal of Psychiatry 31(3): 201-207
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Figarola, J.Lester.; Singhal, P.; Rahbar, S.; Gugiu, B.Gabriel.; Awasthi, S.; Singhal, S.S. 2013: COH-SR4 reduces body weight, improves glycemic control and prevents hepatic steatosis in high fat diet-induced obese mice. Plos one 8(12): E83801
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Laurito, M.; Oliveira, T.M.P.d.; Almirón, W.R.; Sallum, M.A.M. 2013: COi barcode versus morphological identification of Culex (Culex) (Diptera: Culicidae) species: a case study using samples from Argentina and Brazil. Memorias do Instituto Oswaldo Cruz 108(Suppl 1): 110-122
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Chen, J.; Li, Q.; Kong, L.-F.; Zheng, X.-D.; Yu, R.-H. 2010: COI-based DNA barcoding in Tapetinae species (Mollusca, Bivalvia, Veneridae) along the coast of CHINA. Dong Wu Xue Yan Jiu 31(4): 345-352
Adams, E.; Turner, J. 2010: COI1, a jasmonate receptor, is involved in ethylene-induced inhibition of Arabidopsis root growth in the light. Journal of Experimental Botany 61(15): 4373-4386
Pargmann, C.; Hall, T.; Duschek, F.; Grünewald, K.M.; Handke, J.ür. 2007: COIL emission of a modified negative branch confocal unstable resonator. Applied Optics 46(31): 7751-7756
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Yavaş, G.ök.; Koyutürk, M.; Ozsoyoğlu, M.; Gould, M.P.; Laframboise, T. 2010: COKGEN: a software for the identification of rare copy number variation from SNP microarrays. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2010: 371-382
Edan, R.A.; Luqmani, Y.A.; Masocha, W. 2013: COL-3, a chemically modified tetracycline, inhibits lipopolysaccharide-induced microglia activation and cytokine expression in the brain. Plos one 8(2): E57827
Lindahl, K.; Barnes, A.M.; Fratzl-Zelman, N.; Whyte, M.P.; Hefferan, T.E.; Makareeva, E.; Brusel, M.; Yaszemski, M.J.; Rubin, C.-J.; Kindmark, A.; Roschger, P.; Klaushofer, K.; McAlister, W.H.; Mumm, S.; Leikin, S.; Kessler, E.; Boskey, A.L.; Ljunggren, O.; Marini, J.C. 2011: COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta. Human Mutation 32(6): 598-609
Chapman, K.B.; Prendes, M.J.; Sternberg, H.; Kidd, J.L.; Funk, W.D.; Wagner, J.; West, M.D. 2012: COL10A1 expression is elevated in diverse solid tumor types and is associated with tumor vasculature. Future Oncology 8(8): 1031-1040
Errera, F.I.V.; Canani, Lís.H.; Yeh, E.; Kague, E.; Armelin-Corrêa, L.M.; Suzuki, O.T.; Tschiedel, Bíno.; Silva, M.Elizabeth.R.; Sertié, Aéa.L.; Passos-Bueno, M.Rita. 2008: COL18A1 is highly expressed during human adipocyte differentiation and the SNP c.1136C > T in its "frizzled" motif is associated with obesity in diabetes type 2 patients. Anais da Academia Brasileira de Ciencias 80(1): 167-177
McInerney-Leo, A.M.; Duncan, E.L.; Leo, P.J.; Gardiner, B.; Bradbury, L.A.; Harris, J.E.; Clark, G.R.; Brown, M.A.; Zankl, A. 2015: COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?. Clinical Genetics 88(1): 49-55
Marini, F.; Parri, S.; Masi, L.; Ciuffi, S.; Guazzini, A.; Fabbri, S.; Luzi, E.; Cianferotti, L.; Brandi, M.L. 2013: COL1A1 Sp1 variation and bone phenotypes in an Italian population. Clinical Cases in Mineral and Bone Metabolism: the Official Journal of the Italian Society of Osteoporosis Mineral Metabolism and Skeletal Diseases 10(2): 133-138
Rodrigues, A.M.; Girão, M.J.ão.B.C.; da Silva, I.D.C.G.; Sartori, M.G.F.; Martins, K.d.F.; Castro, R.d.A. 2008: COL1A1 Sp1-binding site polymorphism as a risk factor for genital prolapse. International Urogynecology Journal and Pelvic Floor Dysfunction 19(11): 1471-1475
Metlapally, R.; Li, Y-Ju.; Tran-Viet, K-Nhat.; Abbott, D.; Czaja, G.R.; Malecaze, F.; Calvas, P.; Mackey, D.; Rosenberg, T.; Paget, S.; Zayats, T.; Owen, M.J.; Guggenheim, J.A.; Young, T.L. 2009: COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Investigative Ophthalmology and Visual Science 50(9): 4080-4086
Kaneto, C.M.; Lima, P.íc.S.P.; Zanette, D.L.; Prata, K.L.; Pina Neto, J.ão.M.; de Paula, F.J.A.; Silva, W.A. 2014: COL1A1 and miR-29b show lower expression levels during osteoblast differentiation of bone marrow stromal cells from Osteogenesis Imperfecta patients. Bmc Medical Genetics 15: 45
Schrauwen, I.; Khalfallah, A.; Ealy, M.; Fransen, E.; Claes, C.; Huber, A.; Murillo, L.Rodriguez.; Masmoudi, S.; Smith, R.J.H.; Van Camp, G. 2012: COL1A1 association and otosclerosis: a meta-analysis. American Journal of Medical Genetics. Part a 158a(5): 1066-1070
Ranganath, P.; Laine, C.M.; Gupta, D.; Mäkitie, O.; Phadke, S.R. 2011: COL1A1 mutation in an Indian child with Caffey disease. Indian Journal of Pediatrics 78(7): 877-879
Rosensteel, S.M.; Wilson, R.P.; White, S.L.; Ehrlich, H.P. 2010: COL1A1 oligodeoxynucleotides decoy: biochemical and morphologic effects in an acute wound repair model. Experimental and Molecular Pathology 89(3): 307-313
He, M.; Wang, Z.; Zhao, J.; Chen, Y.; Wu, Y. 2014: COL1A1 polymorphism is associated with risks of osteosarcoma susceptibility and death. Tumour Biology: the Journal of the International Society for Oncodevelopmental Biology and Medicine 35(2): 1297-1305
Wang, W.-L.; Patel, K.U.; Coleman, N.M.; Smith-Zagone, M.J.; Ivan, D.; Reed, J.A.; López-Terrada, D.; Lazar, A.J.F.; Prieto, V.G. 2010: COL1A1:PDGFB chimeric transcripts are not present in indeterminate fibrohistiocytic lesions of the skin. American Journal of Dermatopathology 32(2): 149-153
Santovito, A.; Burgarello, C.; Cervella, P.; Caravatti, G.; Ouattara, M.; Salvarani, B.; Delpero, M. 2009: COL1A2 gene deletion polymorphism in an Italian and an Ivorian populations. Genetika 45(7): 977-981
Huang, H.; Ba, Y.; Cui, L.; Cheng, X.; Zhu, J.; Zhang, Y.; Yan, P.; Zhu, C.; Kilfoy, B.; Zhang, Y. 2008: COL1A2 gene polymorphisms (Pvu Ii and Rsa I), serum calciotropic hormone levels, and dental fluorosis. Community Dentistry and Oral Epidemiology 36(6): 517-522
Zuo, C.; Wen, F.; Li, M.; Zhang, X.; Chen, H.; Wu, K.; Zeng, R. 2012: COL1A2 polymorphic markers confer an increased risk of neovascular age-related macular degeneration in a Han Chinese population. Molecular Vision 18: 1787-1793
Tong, Y.; Xu, Y.; Scearce-Levie, K.; Ptácek, L.J.; Fu, Y.-H. 2010: COL25A1 triggers and promotes Alzheimer's disease-like pathology in vivo. Neurogenetics 11(1): 41-52
Matsubayashi, S.; Ikema, M.; Ninomiya, Y.; Yamaguchi, K.; Ikegawa, S.; Nishimura, G. 2013: COL2A1 Mutation in Spondylometaphyseal Dysplasia Algerian Type. Molecular Syndromology 4(3): 148-151
Dupont, C.él.; Baumann, C.; Le Du, N.; Schaefer, E.; Guimiot, F.; Boutaud, L.; Capri, Y.; Spaggiari, E.; Aboura, A.; Benzacken, B.; Tabet, A.-C. 2013: COL2A1 gene disruption by a balanced translocation t(12;15)(q13;q22.2) in familial Stickler syndrome. American Journal of Medical Genetics. Part a 161a (10): 2663-2665
Hämäläinen, S.; Solovieva, S.; Hirvonen, A.; Vehmas, T.; Takala, E.-P.; Riihimäki, H.; Leino-Arjas, P. 2009: COL2A1 gene polymorphisms and susceptibility to osteoarthritis of the hand in Finnish women. Annals of the Rheumatic Diseases 68(10): 1633-1637
Kluivers, K.B.; Dijkstra, J.R.; Hendriks, J.C.M.; Lince, S.L.; Vierhout, M.E.; van Kempen, L.éo.C.L. 2009: COL3A1 2209G>A is a predictor of pelvic organ prolapse. International Urogynecology Journal and Pelvic Floor Dysfunction 20(9): 1113-1118
Leistritz, D.F.; Pepin, M.G.; Schwarze, U.; Byers, P.H. 2011: COL3A1 haploinsufficiency results in a variety of Ehlers-Danlos syndrome type IV with delayed onset of complications and longer life expectancy. Genetics in Medicine: Official Journal of the American College of Medical Genetics 13(8): 717-722
Kuo, D.S.; Labelle-Dumais, C.; Gould, D.B. 2012: COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets. Human Molecular Genetics 21(R1): R97-110
Tarasov, K.V.; Sanna, S.; Scuteri, A.; Strait, J.B.; Orrù, M.; Parsa, A.; Lin, P-I.; Maschio, A.; Lai, S.; Piras, M.Grazia.; Masala, M.; Tanaka, T.; Post, W.; O'Connell, J.R.; Schlessinger, D.; Cao, A.; Nagaraja, R.; Mitchell, B.D.; Abecasis, Gçalo.R.; Shuldiner, A.R.; Uda, M.; Lakatta, E.G.; Najjar, S.S. 2009: COL4A1 is associated with arterial stiffness by genome-wide association scan. Circulation. Cardiovascular Genetics 2(2): 151-158
Leung, M.; Lewis, E.; Humphreys, P.; Miller, E.; Geraghty, M.; Lines, M.; Sell, E. 2012: COL4A1 mutation in a pediatric patient presenting with post-ictal hemiparesis. Canadian Journal of Neurological Sciences. le Journal Canadien des Sciences Neurologiques 39(5): 654-657
Bilguvar, K.; DiLuna, M.L.; Bizzarro, M.J.; Bayri, Y.; Schneider, K.C.; Lifton, R.P.; Gunel, M.; Ment, L.R. 2009: COL4A1 mutation in preterm intraventricular hemorrhage. Journal of Pediatrics 155(5): 743-745
De Vries, L.S.; Koopman, C.; Groenendaal, F.; Van Schooneveld, M.; Verheijen, F.W.; Verbeek, E.; Witkamp, T.D.; van der Worp, H.B.; Mancini, G. 2009: COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage. Annals of Neurology 65(1): 12-18
Corlobe, A.; Tournier-Lasserve, E.; Mine, M.; Menjot de Champfleur, N.; Carra Dalliere, C.; Ayrignac, X.; Labauge, P.; Arquizan, C. 2013: COL4A1 mutation revealed by an isolated brain hemorrhage. Cerebrovascular Diseases 35(6): 593-594
Lanfranconi, S.; Markus, H.S. 2010: COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review. Stroke 41(8): E513-E518
Livingston, J.; Doherty, D.; Orcesi, S.; Tonduti, D.; Piechiecchio, A.; La Piana, R.; Tournier-Lasserve, E.; Majumdar, A.; Tomkins, S.; Rice, G.; Kneen, R.; van der Knaap, M.; Crow, Y. 2011: COL4A1 mutations associated with a characteristic pattern of intracranial calcification. Neuropediatrics 42(6): 227-233
Labelle-Dumais, C.; Dilworth, D.J.; Harrington, E.P.; de Leau, M.; Lyons, D.; Kabaeva, Z.; Manzini, M.C.; Dobyns, W.B.; Walsh, C.A.; Michele, D.E.; Gould, D.B. 2011: COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. Plos Genetics 7(5): E1002062
Papandreou, A.; Tisdall, M.M.; Chong, W.K.; Cross, J.H.; Harkness, W.F.; Varadkar, S.M. 2014: COL4A1 mutations should not be a contraindication for epilepsy surgery. Child's Nervous System: Chns: Official Journal of the International Society for Pediatric Neurosurgery 30(8): 1467-1469
Tonduti, D.; Pichiecchio, A.; La Piana, R.; Livingston, J.H.; Doherty, D.A.; Majumdar, A.; Tomkins, S.; Mine, M.; Ceroni, M.; Ricca, I.; Balottin, U.; Orcesi, S. 2012: COL4A1-related disease: raised creatine kinase and cerebral calcification as useful pointers. Neuropediatrics 43(5): 283-288
Gunda, B.; Mine, M.; Kovács, T.; Hornyák, C.; Bereczki, D.án.; Várallyay, G.ör.; Rudas, G.áb.; Audrezet, M.-P.; Tournier-Lasserve, E. 2014: COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy. Journal of Neurology 261(3): 500-503
Jeanne, M.; Labelle-Dumais, C.; Jorgensen, J.; Kauffman, W.Berkeley.; Mancini, G.M.; Favor, J.; Valant, V.; Greenberg, S.M.; Rosand, J.; Gould, D.B. 2012: COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke. American Journal of Human Genetics 90(1): 91-101
Storey, H.; Savige, J.; Sivakumar, V.; Abbs, S.; Flinter, F.A. 2013: COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome. Journal of the American Society of Nephrology: Jasn 24(12): 1945-1954
Voskarides, K.; Pierides, A.; Deltas, C. 2008: COL4A3/COL4A4 mutations link familial hematuria and focal segmental glomerulosclerosis. glomerular epithelium destruction via basement membrane thinning?. Connective Tissue Research 49(3): 283-288
Ramzan, K.; Imtiaz, F.; Taibah, K.; Alnufiee, S.; Akhtar, M.; Al-Hazzaa, S.A.F.; Al-Owain, M. 2014: COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family. International Journal of Pediatric Otorhinolaryngology 78(3): 427-432
Strasser, K.; Hoefele, J.; Bergmann, C.; Büscher, A.K.; Büscher, R.; Hoyer, P.F.; Weber, S. 2012: COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9. Nephrology Dialysis Transplantation: Official Publication of the European Dialysis and Transplant Association - European Renal Association 27(11): 4236-4240
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Dankel, S.N.; Svärd, J.; Matthä, S.; Claussnitzer, M.; Klöting, N.; Glunk, V.; Fandalyuk, Z.; Grytten, E.; Solsvik, M.H.; Nielsen, H-Jørgen.; Busch, C.; Hauner, H.; Blüher, M.; Skurk, T.; Sagen, Jørn.V.; Mellgren, G. 2014: COL6A3 expression in adipocytes associates with insulin resistance and depends on PPARγ and adipocyte size. Obesity 22(8): 1807-1813
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Anonymous 1920: Colonial Medical Services: Report of the Departmental Committee. British Medical Journal 2(3116): 448-449
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Anonymous 1946: COLOR tests for vitamin A. Nutrition reviews 4: 107-109
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Schiötz, I. 1920: Colour Blind Females: The Inheritance of Colour Blindness in man. British Journal of Ophthalmology 4(8): 345-359
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Anonymous 1982: COMAR: Academics want salary parity with NHS. British Medical Journal 284(6332): 1889
Smith, R. 1982: No apples for the teachers. British Medical Journal 284(6333): 1965-1966
Anonymous 1981: COMAR: June 1981. British Medical Journal 282(6273): 1410
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Northrop, J.H.; Kunitz, M. 1928: Combination of Salts and Proteins : Iii. the Combination of Cucl(2), Mgcl(2), Cacl(2), Alcl(3), Lacl(3), Kcl, Agno(3)and Na(2)so(4)with Gelatin. Journal of General Physiology 11(5): 481-493
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Wilson, D.L. 1947: Dehydration. University of Toronto Medical Journal 25(1): 2-14
Anonymous 1951: COMBINED procaine-epiephrine to prolong anesthesia. What's new 153: 6-7 passim
Boyd, R.N.; Ziviani, J.; Sakzewski, L.; Miller, L.; Bowden, J.; Cunnington, R.; Ware, R.; Guzzetta, A.; Al Macdonell, R.; Jackson, G.D.; Abbott, D.F.; Rose, S. 2013: COMBIT: protocol of a randomised comparison trial of COMbined modified constraint induced movement therapy and bimanual intensive training with distributed model of standard upper limb rehabilitation in children with congenital hemiplegia. Bmc Neurology 13: 68
Müller, P.; Schmitt, E.; Jacob, A.; Hoheisel, J.ör.; Kaufmann, R.; Cremer, C.; Hausmann, M. 2010: COMBO-FISH enables high precision localization microscopy as a prerequisite for nanostructure analysis of genome loci. International Journal of Molecular Sciences 11(10): 4094-4105
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Schmitt, E.; Schwarz-Finsterle, J.; Stein, S.; Boxler, C.; Müller, P.; Mokhir, A.; Krämer, R.; Cremer, C.; Hausmann, M. 2010: COMBinatorial Oligo FISH: directed labeling of specific genome domains in differentially fixed cell material and live cells. Methods in Molecular Biology 659: 185-202
Zitha-Bovens, E.; Maas, P.; Wife, D.; Tijhuis, J.; Hu, Q.-N.; Kleinöder, T.; Gasteiger, J. 2009: COMDECOM: predicting the lifetime of screening compounds in DMSO solution. Journal of Biomolecular Screening 14(5): 557-565
Anonymous 1881: COMET (b), 1881. Science 2(59): 370
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Hall, A. 1880: COMET e, 1880. Science 1(21): 259
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Davidson, H.R. 1969: COMIC Ii in the Automotive Industry. Applied Optics 8(9): 1771
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Mao, X.; Gluck, N.; Chen, B.; Starokadomskyy, P.; Li, H.; Maine, G.N.; Burstein, E. 2011: COMMD1 (copper metabolism MURR1 domain-containing protein 1) regulates Cullin RING ligases by preventing CAND1 (Cullin-associated Nedd8-dissociated protein 1) binding. Journal of Biological Chemistry 286(37): 32355-32365
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McDonald, F.J. 2013: COMMD1 and ion transport proteins: what is the COMMection? Focus on "COMMD1 interacts with the COOH terminus of NKCC1 in Calu-3 airway epithelial cells to modulate NKCC1 ubiquitination". American Journal of Physiology. Cell Physiology 305(2): C129-C130
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Ke, Y.; Butt, A.G.; Swart, M.; Liu, Y.F.; McDonald, F.J. 2010: COMMD1 downregulates the epithelial sodium channel through Nedd4-2. American Journal of Physiology. Renal Physiology 298(6): F1445-F1456
Maine, G.N.; Mao, X.; Muller, P.A.; Komarck, C.M.; Klomp, L.W.J.; Burstein, E. 2009: COMMD1 expression is controlled by critical residues that determine XIAP binding. Biochemical Journal 417(2): 601-609
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Phillips-Krawczak, C.A.; Singla, A.; Starokadomskyy, P.; Deng, Z.; Osborne, D.G.; Li, H.; Dick, C.J.; Gomez, T.S.; Koenecke, M.; Zhang, J.-S.; Dai, H.; Sifuentes-Dominguez, L.F.; Geng, L.N.; Kaufmann, S.H.; Hein, M.Y.; Wallis, M.; McGaughran, J.; Gecz, J.; Sluis, B.v.d.; Billadeau, D.D.; Burstein, E. 2015: COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the copper transporter ATP7A. Molecular Biology of the Cell 26(1): 91-103
De Becdelièvre, A.; Rocca, J.ér.ém.; Aissat, A.; Drévillon, L.; Moutereau, S.ép.; Le Gouvello, S.; Hinzpeter, A.; Tarze, A.; Fanen, P. 2013: COMMD1 modulates noxious inflammation in cystic fibrosis. International Journal of Biochemistry and Cell Biology 45(11): 2402-2409
Favier, R.P.; Spee, B.; Schotanus, B.A.; van den Ingh, T.S.G.A.M.; Fieten, H.; Brinkhof, B.; Viebahn, C.S.; Penning, L.C.; Rothuizen, J. 2012: COMMD1-deficient dogs accumulate copper in hepatocytes and provide a good model for chronic hepatitis and fibrosis. Plos one 7(8): E42158
Drévillon, L.ïc.; Tanguy, G.ël.; Hinzpeter, A.; Arous, N.; de Becdelièvre, A.; Aissat, A.; Tarze, A.; Goossens, M.; Fanen, P. 2011: COMMD1-mediated ubiquitination regulates CFTR trafficking. Plos one 6(3): E18334
Li, P.; Zhang, S.; Fan, C. 2009: COMMD6 from amphioxus Branchiostoma belcheri (BbCOMMD6) interacts with creatine kinase and inhibits its activity. International Journal of Biochemistry and Cell Biology 41(12): 2459-2465
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Pickering, J.; Teo, T.H.; Thornton, R.B.; Kirkham, L.-A.; Zosky, G.R.; Clifford, H.D. 2018: Bacillus licheniformis in geogenic dust induces inflammation in respiratory epithelium. Environmental Research 164: 248-254
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Dominguez-Moñino, I.; Jurado, V.; Gonzalez-Pimentel, J.L.; Miller, A.Z.; Hermosin, B.; Saiz-Jimenez, C. 2018: Bacillus onubensis sp. nov., isolated from the air of two Andalusian caves. Systematic and Applied Microbiology 41(3): 167-172
Mingmongkolchai, S.; Panbangred, W. 2018: Bacillus probiotics: an alternative to antibiotics for livestock production. Journal of Applied Microbiology 124(6): 1334-1346
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Anonymous 1908: Bacillus Typhosus in Sputum. Hospital 45(1163): 246
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Anonymous 1900: Backache. Hospital 28(709): 68
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Usachev, K.S.; Golubev, A.A.; Validov, S.Z.; Klochkov, V.V.; Aganov, A.V.; Khusainov, I.S.; Yusupov, M.M. 2018: Backbone and side chain NMR assignments for the ribosome Elongation Factor P (EF-P) from Staphylococcus aureus. Biomolecular NMR Assignments 12(2): 351-355
Osborne, M.J.; Coutinho de Oliveira, L.; Volpon, L.; Borden, K.L.B. 2018: Backbone assignment of the apo-form of the human C-terminal domain of UDP-glucuronosyltransferase 1A (UGT1A). Biomolecular NMR Assignments 12(2): 315-318
Kaiser, F.; Bittrich, S.; Salentin, S.; Leberecht, C.; Haupt, V.J.; Krautwurst, S.; Schroeder, M.; Labudde, D. 2018: Backbone Brackets and Arginine Tweezers delineate Class i and Class Ii aminoacyl tRNA synthetases. Plos Computational Biology 14(4): E1006101
Yadav, U.; Sundd, M. 2018: Backbone chemical shift assignments of the glycine cleavage complex H protein of Escherichia coli. Biomolecular NMR Assignments 12(1): 163-165
Iadevaia, G.; Núñez-Villanueva, D.; Stross, A.E.; Hunter, C.A. 2018: Backbone conformation affects duplex initiation and duplex propagation in hybridisation of synthetic H-bonding oligomers. Organic and Biomolecular Chemistry 16(22): 4183-4190
Rubin, S.J.S.; Qvit, N. 2018: Backbone-Cyclized Peptides: a Critical Review. Current Topics in Medicinal Chemistry 18(7): 526-555
Krishnan, V.M.; Davis, I.; Baker, T.M.; Curran, D.J.; Arman, H.D.; Neidig, M.L.; Liu, A.; Tonzetich, Z.J. 2018: Backbone Dehydrogenation in Pyrrole-Based Pincer Ligands. Inorganic Chemistry 57(15): 9544-9553
Bai, Z.; Cai, C.; Yu, Z.; Wang, H. 2018: Backbone-Enabled Directional Peptide Macrocyclization through Late-Stage Palladium-Catalyzed δ-C(sp2 )-H Olefination. Angewandte Chemie 57(42): 13912-13916
Smith, G.P.; Fraccia, T.P.; Todisco, M.; Zanchetta, G.; Zhu, C.; Hayden, E.; Bellini, T.; Clark, N.A. 2018: Backbone-free duplex-stacked monomer nucleic acids exhibiting Watson-Crick selectivity. Proceedings of the National Academy of Sciences of the United States of America 115(33): E7658-E7664
Patel, J.R.; Xu, Y.; Capitini, C.; Chiti, F.; De Simone, A. 2018: Backbone NMR assignments of HypF-N under conditions generating toxic and non-toxic oligomers. Biomolecular NMR Assignments 12(2): 273-277
Isbell, H.M.; Kilpatrick, A.M.; Lin, Z.; Mahling, R.; Shea, M.A. 2018: Backbone resonance assignments of complexes of apo human calmodulin bound to IQ motif peptides of voltage-dependent sodium channels NaV1.1, NaV1.4 and NaV1.7. Biomolecular NMR Assignments 12(2): 283-289
Yogo, R.; Yanaka, S.; Kato, K. 2018: Backbone 1H, 13C, and 15N assignments of the extracellular region of human Fcγ receptor IIIb. Biomolecular NMR Assignments 12(1): 201-204
Köhler, C.; Carlström, G.ör.; Tångefjord, S.; Papavoine, T.; Lepistö, M.; Edman, K.; Akke, M. 2018: Backbone 1H, 13C, and 15N resonance assignments of the ligand binding domain of the human wildtype glucocorticoid receptor and the F602S mutant variant. Biomolecular NMR Assignments 12(2): 263-268
Yoshihara, Y.; Shiromoto, Y.; Tatsumi, M.; Hirano, M.; Kawano, T.; Arino, H.; Osako, M.; Nemoto, K. 2013: Backflow from a Metallosis-Induced Intrapelvic Mass into a Revision Hip Arthroplasty: A Case Report. JBJS case connector 3(3): 3e66
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Anonymous 1902: COMMERCIAL vs PROFESSIONAL. California State Journal of Medicine 1(2): 36
Anonymous 1946: Commission on Acute Respiratory Diseases. Association of Acute Pulmonary Lesions with Infections of the Throat. Annals of internal medicine 25: 473-487
Anonymous 1946: COMMISSION ON RESPIRATORY DISEASES. The transmission of primary atypical pneumonia to human volunteers; clinical features. Bulletin of the Johns Hopkins Hospital 79: 125-152
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Anonymous 1946: COMMISSION ON RESPIRATORY DISEASES. The transmission of primary atypical pneumonia to human volunteers; results of inoculation. Bulletin of the Johns Hopkins Hospital 79: 109-124
Rose, H.M.; Pearce, E.; Molloy, E. 1946: Effect of penicillin and streptomycin on bacterial contamination of chick embryos inoculated with unfiltered sputums. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine 62(2): 124-127
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Anonymous 1912: COMMITTEE ON PAPERS, C. Ph. A., ISSUES CALL. California State Journal of Medicine 10(3): 129
Anonymous 1946: COMMITTEE on Coordination of Cosmic-Ray Investigations; progress report for the period July 1945 to June 1946. Year book - Carnegie Institution of Washington 45: 91-95
Dander, A.; Mueller, L.A.; Gallasch, R.; Pabinger, S.; Emmert-Streib, F.; Graber, A.; Dehmer, M. 2013: COMMODE] a large-scale database of molecular descriptors using compounds from PubChem. Source Code for Biology and Medicine 8(1): 22
Anonymous 1947: COMMON Cold Research Unit; interim report on a transmission experiment. British medical journal 1(4505): 650-652
Shaefer, J.F. 1948: League for ex-patients; a promising experiment in mental hygiene. Hospitals 22(3): 55
Anonymous 1947: COMMON cold; a long-term experiment. Pharmaceutical journal 104(4342): 52
Anonymous 1947: COMMON diarrhea in Korea. HealthoftheArmy.UnitedStates.Surgeon-General'sOffice 2(8): 10
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Anonymous 1946: COMMUNITY hospitals as civilian rehabilitation centers. Archives of physical medicine and rehabilitation 27: 561-569
Jones, M.H. 1946: The cerebral palsy child; diagnosis and treatment. American Journal of Nursing 46: 465-468
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Zarrineh, P.; Fierro, A.C.; Sánchez-Rodríguez, A.; De Moor, B.; Engelen, K.; Marchal, K. 2011: COMODO: an adaptive coclustering strategy to identify conserved coexpression modules between organisms. Nucleic Acids Research 39(7): E41
Jung, W.-W.; Balce, G.C.; Cho, J.-W.; Jung, S.-C.; Hong, S.-J.; Song, H.-R. 2010: COMP and Col9A3 mutations and their relationship to the pseudoachondroplasia phenotype. International Journal of Molecular Medicine 26(6): 885-891
Ruthard, J.; Kamper, M.; Renno, J.ör.H.; Kühn, G.; Hillebrand, U.; Höllriegl, S.; Johannis, W.; Zaucke, F.; Klatt, A.R. 2014: COMP does not directly modify the expression of genes involved in cartilage homeostasis in contrast to several other cartilage matrix proteins. Connective Tissue Research 55(5-6): 348-356
Kim, S.; Kwon, J. 2013: COMP-Ang1 inhibits apoptosis as well as improves the attenuated osteogenic differentiation of mesenchymal stem cells induced by advanced glycation end products. Biochimica et Biophysica Acta 1830(10): 4928-4934
Hwang, J.-A.; Lee, E.H.; Kim, H.-W.; Park, J.B.; Jeon, B.H.; Cho, C.-H. 2009: COMP-Ang1 potentiates the antitumor activity of 5-fluorouracil by improving tissue perfusion in murine Lewis lung carcinoma. Molecular Cancer Research: Mcr 7(12): 1920-1927
Youn, S-Won.; Lee, S-Won.; Lee, J.; Jeong, H-Kyul.; Suh, J-Won.; Yoon, C-Hwan.; Kang, H-Jae.; Kim, H-Zoo.; Koh, G-Young.; Oh, B-Hee.; Park, Y-Bae.; Kim, H-Soo. 2011: COMP-Ang1 stimulates HIF-1α-mediated SDF-1 overexpression and recovers ischemic injury through BM-derived progenitor cell recruitment. Blood 117(16): 4376-4386
Jeong, B.-C.; Kim, H.-J.; Bae, I.-H.; Lee, K.-N.; Lee, K.-Y.; Oh, W.-M.; Kim, S.-H.; Kang, I.-C.; Lee, S.-E.; Koh, G.-Y.; Kim, K.-K.; Koh, J.-T. 2010: COMP-Ang1, a chimeric form of Angiopoietin 1, enhances BMP2-induced osteoblast differentiation and bone formation. Bone 46(2): 479-486
Lee, K.-N.; Seo, M.-C.; Bae, I.-H.; Oh, S.-H.; Jang, W.G.; Jeong, B.-C.; Oh, W.-M.; Kim, S.-H.; Lee, S.-E.; Shim, K.M.; Park, B.-K.; Koh, J.-T. 2010: COMP-Ang1, a variant of angiopoietin 1, inhibits serum-deprived apoptosis of mesenchymal cells via PI3K/Akt and mitogen-activated protein kinase pathways. Pharmacology 86(5-6): 327-335
Lee, H.J.; Bae, S.W.; Koh, G.Y.; Lee, Y.S. 2008: COMP-Ang1, angiopoietin-1 variant protects radiation-induced bone marrow damage in C57BL/6 mice. Journal of Radiation Research 49(3): 313-320
Happonen, K.E.; Saxne, T.; Jacobsson, L.; Sturfelt, G.; Rönnelid, J.; Mollnes, T.E.; Heinegård, D.; Turesson, C.; Blom, A.M. 2013: COMP-C3b complexes in rheumatoid arthritis with severe extraarticular manifestations. Journal of Rheumatology 40(12): 2001-2005
Park, B.-H.; Yoon, S.J.; Jang, K.Y.; Kim, M.-R.; Lee, H.-S.; Kim, K.-B.; Park, H.; Lee, S.Y.; Park, H.S.; Lim, S.T.; Song, K.-J.; Kim, J.R. 2010: COMP-angiopoietin-1 accelerates bone formation during distraction osteogenesis. Bone 46(5): 1442-1448
Sung, H.-K.; Sung, H.K.; Kim, Y.-W.; Choi, S.J.; Kim, J.-Y.; Jeune, K.H.; Won, K.-C.; Kim, J.K.; Koh, G.Y.; Koh, G.Y.; Park, S.-Y. 2009: COMP-angiopoietin-1 enhances skeletal muscle blood flow and insulin sensitivity in mice. American Journal of Physiology. Endocrinology and Metabolism 297(2): E402-E409
Kim, S.-O.; Lee, H.-S.; Ahn, K.; Park, K. 2013: COMP-angiopoietin-1 promotes cavernous angiogenesis in a type 2 diabetic rat model. Journal of Korean Medical Science 28(5): 725-730
Kosacka, J.; Nowicki, M.; Klöting, N.; Kern, M.; Stumvoll, M.; Bechmann, I.; Serke, H.; Blüher, M. 2012: COMP-angiopoietin-1 recovers molecular biomarkers of neuropathy and improves vascularisation in sciatic nerve of ob/ob mice. Plos one 7(3): E32881
Zhou, L.; Yoon, S.J.; Jang, K.Y.; Moon, Y.J.; Wagle, S.; Lee, K.B.; Park, B.-H.; Kim, J.R. 2014: COMP-angiopoietin1 potentiates the effects of bone morphogenic protein-2 on ischemic necrosis of the femoral head in rats. Plos one 9(10): E110593
Boylan, M.T. 1947: Rebuilding for social services. Surveillance Efficace 83(10): 278-280
Anonymous 1947: COMPARATIVE data on the causes of death among industrial policyholders. Statistical Bulletin 28(6): 11
Fagan, V.; Bonham, S.; Carty, M.P.; Saenz-Méndez, P.; Eriksson, L.A.; Aldabbagh, F. 2012: COMPARE analysis of the toxicity of an iminoquinone derivative of the imidazo[5,4-f]benzimidazoles with NAD(P)H:quinone oxidoreductase 1 (NQO1) activity and computational docking of quinones as NQO1 substrates. Bioorganic and Medicinal Chemistry 20(10): 3223-3232
Mansour, S.; Roy, D.-C.; Bouchard, V.; Nguyen, B.K.; Stevens, L.M.; Gobeil, F.; Rivard, A.; Leclerc, G.; Reeves, F.ço.; Noiseux, N. 2010: COMPARE-AMi trial: comparison of intracoronary injection of CD133+ bone marrow stem cells to placebo in patients after acute myocardial infarction and left ventricular dysfunction: study rationale and design. Journal of Cardiovascular Translational Research 3(2): 153-159
Kumar, D.; Prasad, D.N.; Bhatnagar, S.P. 2005: COMPARISION OF DIURETIC ACTIVITY OF ETHANOLIC EXTRACT OF AERVA LANATA (Linn.) Juss. ex. Schult and AERVA TOMENTOSA Forsk. Family: AMARANTHACEAE. Ancient Science of Life 25(2): 66-68
Kenneth, J.H. 1947: Gestation periods; a coincidence. Veterinary Record 59(8): 101
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Sadreyev, R.I.; Tang, M.; Kim, B.-H.; Grishin, N.V. 2009: COMPASS server for homology detection: improved statistical accuracy, speed and functionality. Nucleic Acids Research 37(Web Server Issue): W90-W94
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Maccari, G.; Gemignani, F.; Landi, S. 2010: COMPASSS (COMplex PAttern of Sequence Search Software), a simple and effective tool for mining complex motifs in whole genomes. Bioinformatics 26(14): 1777-1778
Anonymous 1907: Compensation for Industrial Diseases : Report of the Departmental Committee. British Medical Journal 1(2422): 1311
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Felton, J.S. 1948: Recognition of neurotic illness by the industrial nurse. Industrial Nursing 7(3): 10-15
Southey, M.C.; Park, D.J.; Nguyen-Dumont, T.; Campbell, I.; Thompson, E.; Trainer, A.H.; Chenevix-Trench, G.; Simard, J.; Dumont, M.; Soucy, P.; Thomassen, M.; Jønson, L.; Pedersen, I.S.; Hansen, T.V.; Nevanlinna, H.; Khan, S.; Sinilnikova, O.; Mazoyer, S.; Lesueur, F.; Damiola, F.; Schmutzler, R.; Meindl, A.; Hahnen, E.; Dufault, M.R.; Chris Chan, T.; Kwong, A.; Barkardóttir, R.; Radice, P.; Peterlongo, P.; Devilee, P.; Hilbers, F.; Benitez, J.; Kvist, A.; Törngren, T.; Easton, D.; Hunter, D.; Lindstrom, S.; Kraft, P.; Zheng, W.; Gao, Y.-T.; Long, J.; Ramus, S.; Feng, B.-J.; Weitzel, J.N.; Nathanson, K.; Offit, K.; Joseph, V.; Robson, M.; Schrader, K.; Wang, S.; Kim, Y.C.; Lynch, H.; Snyder, C.; Tavtigian, S.; Neuhausen, S.; Couch, F.J. 2013: COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration. Breast Cancer Research: Bcr 15(3): 402
Panse, K. 1948: A case of otitis media. Antiseptic 45(6): 414
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Crinigan, R.P. 1974: COMPOSITION OF PSROs. American Journal of Public Health 64(10): 1008
Anonymous 1948: COMPOUND fractures. Statistics of Navy Medicine 4(7): 11-13
Metcoff, J. 1949: Influence of protein nutrition on experimental infection; physiological aspects. American Journal of Public Health and the Nation's Health 39(7): 862-865
Kamihara, T.; Murakami, M.; Noda, Y.; Takeda, K.; Takegoshi, K. 2014: COMPOZER-based longitudinal cross-polarization via dipolar coupling under MAS. Journal of Magnetic Resonance 245: 94-97
Sundet, O. 1948: Enlightenment and propaganda from a psychological point of view. La Question de l'Alcool . Alcohol Problem . die Alkoholfrage . 1(3): 130-138
Anonymous 1946: COMPULSORY accident insurance in Switzerland from 1938 to 1942. International labour review 54(3-4): 179-196
Anonymous 1947: COMPUTATION of the seasonal cycle in the scabies incidence rate. HealthoftheArmy.UnitedStates.Surgeon-General'sOffice 2(7): 56
Stockman, A.K.; Danell, R.M.; Bond, J.E. 2008: COMPUTER PROGRAMS: d-novl: a program to simulate overlap between two niche-based distribution models. Molecular Ecology Resources 8(2): 290-294
Billiard, S. 2008: COMPUTER PROGRAMS: nessi: a program for numerical estimations in sporophytic self-incompatibility genetic systems. Molecular Ecology Resources 8(2): 295-298
Tallmon, D.A.; Koyuk, A.; Luikart, G.; Beaumont, M.A. 2008: COMPUTER PROGRAMS: onesamp: a program to estimate effective population size using approximate Bayesian computation. Molecular Ecology Resources 8(2): 299-301
Koenig, R. 2000: COMPUTER SCIENCE: Flushing out Nasty Viruses in the Balkans. Science 289(5486): 1863-1865
Shirts, M.; Pande, V.S. 2000: COMPUTING: Screen Savers of the World Unite!. Science 290(5498): 1903-1904
Hadji, P.; Jackisch, C.; Bolten, W.; Blettner, M.; Hindenburg, H.J.; Klein, P.; König, K.; Kreienberg, R.; Rief, W.; Wallwiener, D.; Zaun, S.; Harbeck, N. 2014: COMPliance and Arthralgia in Clinical Therapy: the COMPACT trial, assessing the incidence of arthralgia, and compliance within the first year of adjuvant anastrozole therapy. Annals of Oncology: Official Journal of the European Society for Medical Oncology 25(2): 372-377
Phillips, J.S.; Yung, M.W. 2014: COMQ-12 scores in adult patients without chronic middle ear disease. Clinical Otolaryngology: Official Journal of Ent-Uk ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology and Cervico-Facial Surgery 39(6): 362-367
Gagne, N.L.; Rivard, M.J. 2013: COMS eye plaque brachytherapy dosimetric sensitivity to source photon energy and seed design. Applied Radiation and Isotopes: Including Data Instrumentation and Methods for use in Agriculture Industry and Medicine 79: 62-66
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Langer, E. 1963: COMSAT: Europeans Wary of U.S. Plan for American-Dominated Commercial Satellite Enterprise. Science 142(3600): 1637-1640
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Reggars, J.W. 1993: Differential diagnosis of buttock pain: using a flow chart. Comsig Review 2(2): 32-37
Rebollo-Mesa, I.; Picchioni, M.; Shaikh, M.; Bramon, E.; Murray, R.; Toulopoulou, T. 2011: COMT (Val(158/108)Met) genotype moderates the impact of antipsychotic medication on verbal IQ in twins with schizophrenia. Psychiatric Genetics 21(2): 98-105
Tong, X.; Li, Z.; Wu, Y.; Fu, X.; Zhang, Y.; Fan, H. 2014: COMT 158G/A and CYP1B1 432C/G polymorphisms increase the risk of endometriosis and adenomyosis: a meta-analysis. European Journal of Obstetrics Gynecology and Reproductive Biology 179: 17-21
Guillot, C.R.; Fanning, J.R.; Liang, T.; Berman, M.E. 2015: COMT Associations with Disordered Gambling and Drinking Measures. Journal of Gambling Studies 31(2): 513-524
Sannino, S.; Gozzi, A.; Cerasa, A.; Piras, F.; Scheggia, D.; Managò, F.; Damiano, M.; Galbusera, A.; Erickson, L.C.; De Pietri Tonelli, D.; Bifone, A.; Tsaftaris, S.A.; Caltagirone, C.; Weinberger, D.R.; Spalletta, G.; Papaleo, F. 2015: COMT Genetic Reduction Produces Sexually Divergent Effects on Cortical Anatomy and Working Memory in Mice and Humans. Cerebral Cortex 25(9): 2529-2541
Soeiro-de-Souza, M.ár.G.; Bio, D.S.; David, D.P.; Rodrigues dos Santos, D.; Kerr, D.S.; Gattaz, W.F.; Machado-Vieira, R.; Moreno, R.A. 2012: COMT Met (158) modulates facial emotion recognition in bipolar i disorder mood episodes. Journal of Affective Disorders 136(3): 370-376
Uçok, A.; Oztürk, M.; Duman, Z.; Saruhan-Direskeneli, G. 2010: COMT Val 158 Met polymorphism is related with interpersonal problem solving in schizophrenia. European Psychiatry: the Journal of the Association of European Psychiatrists 25(6): 320-322
Williams, L.M.; Gatt, J.M.; Grieve, S.M.; Dobson-Stone, C.; Paul, R.H.; Gordon, E.; Schofield, P.R. 2010: COMT Val(108/158)Met polymorphism effects on emotional brain function and negativity bias. Neuroimage 53(3): 918-925
Boot, E.; Booij, J.; Zinkstok, J.R.; Baas, F.; Swillen, A.; Owen, M.J.; Murphy, D.G.; Murphy, K.C.; Linszen, D.H.; Van Amelsvoort, T.ér.ès.A. 2011: COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome. Synapse 65(9): 967-970
Farrell, S.M.; Tunbridge, E.M.; Braeutigam, S.; Harrison, P.J. 2012: COMT Val(158)Met genotype determines the direction of cognitive effects produced by catechol-O-methyltransferase inhibition. Biological Psychiatry 71(6): 538-544
Baeken, C.; Marinazzo, D.; Claes, S.; Wu, G.-R.; Van Schuerbeek, P.; De Mey, J.; Luypaert, R.; De Raedt, R. 2014: COMT Val(158)Met genotypes differentially influence subgenual cingulate functional connectivity in healthy females. Frontiers in Human Neuroscience 8: 481
Majic, T.; Rentzsch, J.; Gudlowski, Y.; Ehrlich, S.; Juckel, G.; Sander, T.; Lang, U.E.; Winterer, G.; Gallinat, J.ür. 2011: COMT Val108/158Met genotype modulates human sensory gating. Neuroimage 55(2): 818-824
Wishart, H.A.; Roth, R.M.; Saykin, A.J.; Rhodes, C.H.; Tsongalis, G.J.; Pattin, K.A.; Moore, J.H.; McAllister, T.W. 2011: COMT Val158Met Genotype and Individual Differences in Executive Function in Healthy Adults. Journal of the International Neuropsychological Society: Jins 17(1): 174-180
Witte, A.V.; Jansen, S.; Schirmacher, A.; Young, P.; Flöel, A. 2010: COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention. Frontiers in Aging Neuroscience 2: 146
Bousman, C.A.; Cherner, M.; Atkinson, J.H.; Heaton, R.K.; Grant, I.; Everall, I.P.; Hnrc Group, T. 2010: COMT Val158Met Polymorphism, Executive Dysfunction, and Sexual Risk Behavior in the Context of HIV Infection and Methamphetamine Dependence. Interdisciplinary Perspectives on Infectious Diseases 2010: 678648
Lee, Y.Ho.; Song, G.Gyu. 2014: COMT Val158Met and PPARγ Pro12Ala polymorphisms and susceptibility to Alzheimer's disease: a meta-analysis. Neurological sciences: official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 35(5): 643-651
Willmott, C.; Withiel, T.; Ponsford, J.; Burke, R. 2014: COMT Val158Met and cognitive and functional outcomes after traumatic brain injury. Journal of Neurotrauma 31(17): 1507-1514
Osinsky, R.; Hewig, J.; Alexander, N.; Hennig, J.ür. 2012: COMT Val158Met genotype and the common basis of error and conflict monitoring. Brain Research 1452: 108-118
Albaugh, M.D.; Harder, V.S.; Althoff, R.R.; Rettew, D.C.; Ehli, E.A.; Lengyel-Nelson, T.; Davies, G.E.; Ayer, L.; Sulman, J.; Stanger, C.; Hudziak, J.J. 2010: COMT Val158Met genotype as a risk factor for problem behaviors in youth. Journal of the American Academy of Child and Adolescent Psychiatry 49(8): 841-849
Hirvonen, M.M.; Någren, K.; Rinne, J.O.; Pesonen, U.; Vahlberg, T.; Hagelberg, N.; Hietala, J. 2010: COMT Val158Met genotype does not alter cortical or striatal dopamine D2 receptor availability in vivo. Molecular Imaging and Biology 12(2): 192-197
Gennatas, E.D.; Cholfin, J.A.; Zhou, J.; Crawford, R.K.; Sasaki, D.A.; Karydas, A.; Boxer, A.L.; Bonasera, S.J.; Rankin, K.P.; Gorno-Tempini, M.L.; Rosen, H.J.; Kramer, J.H.; Weiner, M.; Miller, B.L.; Seeley, W.W. 2012: COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures. Neurology 78(21): 1663-1669
Saville, C.W.N.; Lancaster, T.M.; Stefanou, M.E.; Salunkhe, G.; Lourmpa, I.; Nadkarni, A.; Boehm, S.G.; Bender, S.; Smyrnis, N.; Ettinger, U.; Feige, B.; Biscaldi, M.; Mantripragada, K.K.; Linden, D.E.J.; Klein, C. 2014: COMT Val158Met genotype is associated with fluctuations in working memory performance: converging evidence from behavioural and single-trial P3b measures. Neuroimage 100: 489-497
Hernaus, D.; Collip, D.; Lataster, J.; Ceccarini, J.; Kenis, G.; Booij, L.; Pruessner, J.; Van Laere, K.; van Winkel, R.; van Os, J.; Myin-Germeys, I. 2013: COMT Val158Met genotype selectively alters prefrontal [18F]fallypride displacement and subjective feelings of stress in response to a psychosocial stress challenge. Plos one 8(6): E65662
Stefanis, N.C.; Henquet, C.éc.; Avramopoulos, D.; Smyrnis, N.; Evdokimidis, I.; Myin-Germeys, I.; Stefanis, C.N.; Van Os, J. 2007: COMT Val158Met moderation of stress-induced psychosis. Psychological Medicine 37(11): 1651-1656
Ding, H.; Fu, Y.; Chen, W.; Wang, Z. 2010: COMT Val158Met polymorphism and breast cancer risk: evidence from 26 case-control studies. Breast Cancer Research and Treatment 123(1): 265-270
Tükel, R.şi.; Gürvit, H.; Öztürk, N.; Özata, B.; Ertekin, B.A.ş; Ertekin, E.; Baran, B.; Kalem, Şi.ük.A.ça.; Büyükgök, D.; Direskeneli, G.üh.S. 2013: COMT Val158Met polymorphism and executive functions in obsessive-compulsive disorder. Journal of Neuropsychiatry and Clinical Neurosciences 25(3): 214-221
Nobile, M.; Rusconi, M.; Bellina, M.; Marino, C.; Giorda, R.; Carlet, O.; Vanzin, L.; Molteni, M.; Battaglia, M. 2010: COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10-14. European Child and Adolescent Psychiatry 19(7): 549-557
Pomarol-Clotet, E.; Fatjó-Vilas, M.; McKenna, P.J.; Monté, G.C.; Sarró, S.; Ortiz-Gil, J.; Aguirre, C.; Gomar, J.J.; Guerrero, A.; Landin, R.; Capdevila, A.; Fañanás, L.; Salvador, R. 2010: COMT Val158Met polymorphism in relation to activation and de-activation in the prefrontal cortex: a study in patients with schizophrenia and healthy subjects. Neuroimage 53(3): 899-907
Bertolino, A.; Caforio, G.; Blasi, G.; Rampino, A.; Nardini, M.; Weinberger, D.R.; Dallapiccola, B.; Sinibaldi, L.; Douzgou, S. 2007: COMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophrenia. Schizophrenia Research 95(1-3): 253-255
Rosa, E.C.; Dickinson, D.; Apud, J.é; Weinberger, D.R.; Elvevåg, B. 2010: COMT Val158Met polymorphism, cognitive stability and cognitive flexibility: an experimental examination. Behavioral and Brain Functions: Bbf 6: 53
Swart, M.; Bruggeman, R.; Larøi, F.; Alizadeh, B.Z.; Kema, I.; Kortekaas, R.; Wiersma, D.; Aleman, A.é 2011: COMT Val158Met polymorphism, verbalizing of emotion and activation of affective brain systems. Neuroimage 55(1): 338-344
Yilmaz, Z.; Kaplan, A.S.; Zai, C.C.; Levitan, R.D.; Kennedy, J.L. 2011: COMT Val158Met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa. Progress in Neuro-Psychopharmacology and Biological Psychiatry 35(4): 948-952
Radua, J.; El-Hage, W.; Monté, G.C.; Gohier, B.; Tropeano, M.; Phillips, M.L.; Surguladze, S.A. 2014: COMT Val158Met × SLC6A4 5-HTTLPR interaction impacts on gray matter volume of regions supporting emotion processing. Social Cognitive and Affective Neuroscience 9(8): 1232-1238
Heinzerling, K.G.; McCracken, J.T.; Swanson, A.-N.; Ray, L.A.; Shoptaw, S.J. 2012: COMT Val158Met, BDNF Val66Met, and OPRM1 Asn40Asp and methamphetamine dependence treatment response: preliminary investigation. Journal of Clinical Psychopharmacology 32(1): 135-137
Hayashi, K.; Yoshimura, R.; Kakeda, S.; Kishi, T.; Abe, O.; Umene-Nakano, W.; Katsuki, A.; Hori, H.; Ikenouchi-Sugita, A.; Watanabe, K.; Ide, S.; Ueda, I.; Moriya, J.; Iwata, N.; Korogi, Y.; Kubicki, M.; Nakamura, J. 2014: COMT Val158Met, but not BDNF Val66Met, is associated with white matter abnormalities of the temporal lobe in patients with first-episode, treatment-naïve major depressive disorder: a diffusion tensor imaging study. Neuropsychiatric Disease and Treatment 10: 1183-1190
Collip, D.; van Winkel, R.; Peerbooms, O.; Lataster, T.; Thewissen, V.; Lardinois, M.; Drukker, M.; Rutten, B.P.F.; Van Os, J.; Myin-Germeys, I. 2011: COMT Val158Met-stress interaction in psychosis: role of background psychosis risk. Cns Neuroscience and Therapeutics 17(6): 612-619
Henquet, C.; Rosa, A.; Delespaul, P.; Papiol, S.; Fananás, L.; van Os, J.; Myin-Germeys, I. 2009: COMT ValMet moderation of cannabis-induced psychosis: a momentary assessment study of 'switching on' hallucinations in the flow of daily life. Acta Psychiatrica Scandinavica 119(2): 156-160
Hendershot, C.S.; Lindgren, K.P.; Liang, T.; Hutchison, K.E. 2012: COMT and ALDH2 polymorphisms moderate associations of implicit drinking motives with alcohol use. Addiction Biology 17(1): 192-201
Garcia-Garcia, M.; Barceló, F.; Clemente, I.C.; Escera, C. 2011: COMT and ANKK1 gene-gene interaction modulates contextual updating of mental representations. Neuroimage 56(3): 1641-1647