EurekaMag Full Text Articles Chapter 8,768
References:
Narod, S.A.; Madlensky, L.; Bradley, L.; Cole, D.; Tonin, P.; Rosen, B.; Risch, H.A. 1994: Hereditary and familial ovarian cancer in southern Ontario. Cancer 74(8): 2341-2346
Angioli, R.; Estape, R.; Mason, M.; Penalver, M. 1998: Hereditary and sporadic ovarian cancer: genetic testing and clinical implications (review). International Journal of Oncology 12(5): 1029-1034
Tadmouri, G.O. 1998: Hereditary anemias in Lebanon. Saudi Medical Journal 19(3): 237-243
Nielsen, E.W.; Gran, J.T.; Straume, B.; Mellbye, O.J.; Johansen, H.T.; Mollnes, T.E. 1996: Hereditary angio-oedema: New clinical observations and autoimmune screening, complement and kallikrein-kinin analyses. Journal of Internal Medicine 239(2): 119-130
Ishii, N.; Ono, H.; Kawaguchi, H.; Nakajima, H. 1996: Hereditary angioedema caused by a point mutation of exon 7 in the C1 inhibitor gene. British Journal of Dermatology 134(4): 731-733
da Costa, J.T.; da Silva, J.M.; Cunha, L.; Castel-Branco, M.G.; Azevedo, M.V. 1994: Hereditary angioedema presenting with adult respiratory distress syndrome. Chest 105(6): 1898-1899
Talavera, A.; Larraona, J.L.; Ramos, J.L.; López, T.; Maraver, A.; Arias, J.; Barrios, A. 1995: Hereditary angioedema: an infrequent cause of abdominal pain with ascites. American Journal of Gastroenterology 90(3): 471-474
Borum, M.L. 1998: Hereditary angioedema: an unusual case in an African-American woman. Journal of the National Medical Association 90(2): 115-118
Leimgruber, A.; Jaques, W.A.; Spaeth, P.J. 1993: Hereditary angioedema: uncomplicated maxillofacial surgery using short-term C1 inhibitor replacement therapy. International Archives of Allergy and Immunology 101(1): 107-112
Shoemaker, L.R.; Schurman, S.J.; Donaldson, V.H.; Davis, A.E. 1994: Hereditary angioneurotic oedema: Characterization of plasma kinin and vascular permeability-enhancing activities. Clinical and Experimental Immunology 95(1): 22-28
van Boven, H.H.; Olds, R.J.; Thein, S.L.; Reitsma, P.H.; Lane, D.A.; Briët, E.; Vandenbroucke, J.P.; Rosendaal, F.R. 1994: Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families. Blood 84(12): 4209-4213
Rai, A.; Wordsworth, P.; Coppock, J.S.; Zaphiropoulos, G.C.; Struthers, G.R. 1994: Hereditary arthro-ophthalmopathy (Stickler syndrome): a diagnosis to consider in familial premature osteoarthritis. British Journal of Rheumatology 33(12): 1175-1180
Sumoi, R.; Hakala-Ala-Pietilä, T.; Leminen, A.; Mecklin, J.P.; Lehtovirta, P. 1995: Hereditary aspects of endometrial adenocarcinoma. International Journal of Cancer 62(2): 132-137
McLellan, D.L.; Norman, R.W. 1995: Hereditary aspects of prostate cancer. Cmaj: Canadian Medical Association Journal 153(7): 895-900
Nachmanoff, D.B.; Segal, R.A.; Dawson, D.M.; Brown, R.B.; De Girolami, U. 1997: Hereditary ataxia with sensory neuronopathy: Biemond's ataxia. Neurology 48(1): 273-275
Leone, M.; Bottacchi, E.; D'Alessandro, G.; Kustermann, S. 1995: Hereditary ataxias and paraplegias in Valle d'Aosta, Italy: a study of prevalence and disability. Acta Neurologica Scandinavica 91(3): 183-187
Kostomakhin, N.M.; Krasota, V.F. 1994: Hereditary basis of immunity in calves-transplants. Doklady Rossiiskoi Akademii Sel'skokhozyaistvennykh Nauk 1994(2): 27-28
Grenz, H.; Peschen, M.; Wiek, K.; Schoepf, E.; Vanscheidt, W. 1998: Hereditary benign telangiectasia: An unusual variant of primary telangiectasis treated successfully with the flashlamp-pumped pulsed dye laser. Vasa 27(3): 192-195
Al-Fawaz, I.M.; Gader, A.M.; Bahakim, H.M.; Al-Mohareb, F.; Al-Momen, A.K.; Harakati, M.S. 1996: Hereditary bleeding disorders in Riyadh, Saudi Arabia. Annals of Saudi Medicine 16(3): 257-261
Kaczanowski, A.; Kiersnowska, M. 1996: Hereditary blocks in postconjugational oral morphogenesis in Tetrahymena thermophila. European Journal of Protistology 32(4): 506-512
Foulkes, W.D.; Narod, S.A. 1995: Hereditary breast and ovarian cancer: epidemiology, genetics, screening and predictive testing. Clinical and Investigative Medicine. Medecine Clinique et Experimentale 18(6): 473-483
Doepel, M.; Kellokumpu, I.H.; v Smitten, K.A. 1995: Hereditary breast cancer in Finnish women. European Journal of Surgery 161(11): 805-809
Marcus, J.N.; Watson, P.; Page, D.L.; Narod, S.A.; Lenoir, G.M.; Tonin, P.; Linder-Stephenson, L.; Salerno, G.; Conway, T.A.; Lynch, H.T. 1996: Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage. Cancer 77(4): 697-709
Narod, S.A. 1997: Hereditary breast carcinoma syndromes. Cancer 80(3 Suppl): 537-542
Stéphan, E.; de Meeus, A.; Bouvagnet, P. 1997: Hereditary bundle branch defect: Right bundle branch blocks of different causes have different morphologic characteristics. American Heart Journal 133(2): 249-256
Logan, J.I.; Harveyson, K.B.; Wisdom, G.B.; Hughes, A.E.; Archbold, G.P. 1994: Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus. Qjm: Monthly Journal of the Association of Physicians 87(11): 663-670
Kawanami, T.; Kato, T.; Daimon, M.; Tominaga, M.; Sasaki, H.; Maeda, K.; Arai, S.; Shikama, Y.; Katagiri, T. 1996: Hereditary caeruloplasmin deficiency: clinicopathological study of a patient. Journal of Neurology Neurosurgery and Psychiatry 61(5): 506-509
Lynch, H.T.; Fusaro, R.M.; Lynch, J. 1995: Hereditary cancer in adults. Cancer Detection and Prevention 19(3): 219-233
Andrykowski, M.A.; Lightner, R.; Studts, J.L.; Munn, R.K. 1997: Hereditary cancer risk notification and testing: how interested is the general population?. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology 15(5): 2139-2148
Knudson, A.G. 1996: Hereditary cancer: Two hits revisited. Journal of Cancer Research and Clinical Oncology 122(3): 135-140
de Gritz, B.G. 1997: Hereditary caprine phaeochromocytoma. Zentralblatt für Veterinarmedizin. Reihe a 44(5): 313-316
Murakami, T.; Mita, S.; Tokunaga, M.; Maeda, H.; Ueyama, H.; Kumamoto, T.; Uchino, M.; Ando, M. 1996: Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation. Journal of the Neurological Sciences 142(1-2): 111-113
Kuwamura, M.; Yoshida, T.; Yamate, J.; Kotani, T.; Sakuma, S. 1994: Hereditary cerebellar vermis defect in the Lewis rat. Brain Research. Developmental Brain Research 83(2): 294-298
Wattendorff, A.R.; Frangione, B.; Luyendijk, W.; Bots, G.T. 1995: Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies. Journal of Neurology Neurosurgery and Psychiatry 58(6): 699-705
Maat-Schieman, M.L.; Radder, C.M.; van Duinen, S.G.; Haan, J.; Roos, R.A. 1994: Hereditary cerebral hemorrhage with amyloidosis (Dutch): A model for congophilic plaque formation without neurofibrillary pathology. Acta Neuropathologica 88(4): 371-378
Bornebroek, M.; Haan, J.; Maat-Schieman, M.L.; Van Duinen, S.G.; Roos, R.A. 1996: Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I--A review of clinical, radiologic and genetic aspects. Brain Pathology 6(2): 111-114
Maat-Schieman, M.L.; van Duinen, S.G.; Bornebroek, M.; Haan, J.; Roos, R.A. 1996: Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II--A review of histopathological aspects. Brain Pathology 6(2): 115-120
Bornebroek, M.; Van Buchem, M.A.; Haan, J.; Brand, R.; Lanser, J.B.; de Bruïne, F.T.; Roos, R.A. 1996: Hereditary cerebral hemorrhage with amyloidosis-Dutch type: better correlation of cognitive deterioration with advancing age than with number of focal lesions or white matter hyperintensities. Alzheimer Disease and Associated Disorders 10(4): 224-231
Okamoto, N.; Wada, S.; Oga, T.; Kawabata, Y.; Baba, Y.; Habu, D.; Takeda, Z.; Wada, Y. 1996: Hereditary ceruloplasmin deficiency with hemosiderosis. Human Genetics 97(6): 755-758
Morita, H.; Ikeda, S.; Yamamoto, K.; Morita, S.; Yoshida, K.; Nomoto, S.; Kato, M.; Yanagisawa, N. 1995: Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family. Annals of Neurology 37(5): 646-656
Aagenaes, O. 1998: Hereditary cholestasis with lymphoedema (Aagenaes syndrome, cholestasis-lymphoedema syndrome). New cases and follow-up from infancy to adult age. Scandinavian Journal of Gastroenterology 33(4): 335-345
Vyse, T.J.; Späth, P.J.; Davies, K.A.; Morley, B.J.; Philippe, P.; Athanassiou, P.; Giles, C.M.; Walport, M.J. 1994: Hereditary complement factor I deficiency. Qjm: Monthly Journal of the Association of Physicians 87(7): 385-401
Lhotta, K.; Thoenes, W.; Glatzl, J.; Hintner, H.; Kronenberg, F.; Joannidis, M.; König, P. 1993: Hereditary complete deficiency of the fourth component of complement: effects on the kidney. Clinical Nephrology 39(3): 117-124
Dell'Osso, L.F.; Weissman, B.M.; Leigh, R.J.; Abel, L.A.; Sheth, N.V. 1993: Hereditary congenital nystagmus and gaze-holding failure: the role of the neural integrator. Neurology 43(9): 1741-1749
Schreiber, W.E.; Zhang, X.; Senz, J.; Jamani, A. 1997: Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene. Human Mutation 10(3): 196-200
Simoni, P.; Scorolli, L.; Scalinci, S.Z.; Lodi, L.; Scorolli, L.; Paolini, P.; Vacirca, A.; Zaccheroni, V.; Lodi, A.; Meduri, R. 1997: Hereditary corneal disorder (cornea guttata) and non autoimmune hyperthyroidism. Annali di Ottalmologia e Clinica Oculistica 123(9-10): 257-260
Asgeirsson, B.; Haebel, S.; Thorsteinsson, L.; Helgason, E.; Gudmundsson, K.O.; Gudmundsson, G.; Roepstorff, P. 1998: Hereditary cystatin C amyloid angiopathy: Monitoring the presence of the Leu-68fwdarwGln cystatin C variant in cerebrospinal fluids and monocyte cultures by MS. Biochemical Journal 329(3): 497-503
Peter, M.; Fawaz, L.; Drop, S.L.; Visser, H.K.; Sippell, W.G. 1997: Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. Journal of Clinical Endocrinology and Metabolism 82(11): 3525-3528
Nikonova, A.L.; Pogoda, T.V.; Metel'skaya, V.A.; Olfer'ev, A.M.; Usievich, V.M.; Limborskaya, S.A.; Oganov, R.G.; Perova, N.V. 1994: Hereditary defect of apolipoprotein B-100 as a cause of hypercholesterolemia in ischemic heart disease. Kardiologiya 34(1-2): 98-103
Cattaneo, M. 1998: Hereditary defect of the platelet ADP receptor(s). Platelets 9(3-4): 161-164
Pabinger, I.; Brücker, S.; Kyrle, P.A.; Schneider, B.; Korninger, H.C.; Niessner, H.; Lechner, K. 1992: Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening. Blood Coagulation and Fibrinolysis: An International Journal in Haemostasis and Thrombosis 3(5): 547-553
Cornudella, R.; Moreno, J.A.; Aguado, M.J.; Anso, V.; Revilla, J.M.; Calvo, M.T.; Gutierrez, M. 1995: Hereditary deficiency of factor XII and spontaneous vein thrombosis with urokinase treated. Sangre (Saragossa) 40(3): 219-222
Wakabayashi, H.; Tsuchiya, M.; Yoshino, K.; Kaku, K.; Shigei, H. 1996: Hereditary deficiency of lactate dehydrogenase H-subunit. Internal Medicine 35(7): 550-554
Egan, L.J.; Orren, A.; Doherty, J.; Würzner, R.; McCarthy, C.F. 1994: Hereditary deficiency of the seventh component of complement and recurrent meningococcal infection: investigations of an Irish family using a novel haemolytic screening assay for complement activity and C7 M/N allotyping. Epidemiology and Infection 113(2): 275-281
Boneh, A.; Bar-Ziv, J. 1996: Hereditary deficiency of vitamin K-dependent coagulation factors with skeletal abnormalities. American Journal of Medical Genetics 65(3): 241-243
Hayashi, Y.; Kakita, A.; Yamada, M.; Egawa, S.; Oyanagi, S.; Naito, H.; Tsuji, S.; Takahashi, H. 1998: Hereditary dentatorubral-pallidoluysian atrophy: Ubiquitinated filamentous inclusions in the cerebellar dentate nucleus neurons. Acta Neuropathologica 95(5): 479-482
Eccles, D.M.; van der Luijt, R.; Breukel, C.; Bullman, H.; Bunyan, D.; Fisher, A.; Barber, J.; du Boulay, C.; Primrose, J.; Burn, J.; Fodde, R. 1996: Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. American Journal of Human Genetics 59(6): 1193-1201
McMinn, T.R.; Ross, J. 1995: Hereditary dilated cardiomyopathy. Clinical Cardiology 18(1): 7-15
Kurisu, K.; Tabata, M.J. 1998: Hereditary diseases with tooth anomalies and their causal genes. Kaibogaku Zasshi. Journal of Anatomy 73(3): 201-208
Hamamy, H.; Alwan, A. 1994: Hereditary disorders in the Eastern Mediterranean Region. Bulletin of the World Health Organization 72(1): 145-154
De Braekeleer, M.; Dao, T.N. 1994: Hereditary disorders in the French Canadian population of Quebec. I. In search of founders. Human Biology 66(2): 205-223
De Braekeleer, M.; Dao, T.N. 1994: Hereditary disorders in the French Canadian population of Quebec. II. Contribution of perche. Human Biology 66(2): 225-249
Klett, C.C. 1997: Hereditary disorders of connective tissue: a review. Wound Repair and Regeneration: Official Publication of the Wound Healing Society and the European Tissue Repair Society 5(1): 3-11
Valik, D.; Jones, J.D. 1997: Hereditary disorders of purine and pyrimidine metabolism: identification of their biochemical phenotypes in the clinical laboratory. Mayo Clinic Proceedings 72(8): 719-725
Smeets, H.J.; Knoers, V.V.; van de Heuvel, L.P.; Lemmink, H.H.; Schröder, C.H.; Monnens, L.A. 1996: Hereditary disorders of the glomerular basement membrane. Pediatric Nephrology 10(6): 779-788
Helliwell, T.R.; Green, A.R.; Green, A.; Edwards, R.H. 1994: Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentin. Journal of the Neurological Sciences 124(2): 174-187
Lendon, C.L.; Lynch, T.; Norton, J.; McKeel, D.W.; Busfield, F.; Craddock, N.; Chakraverty, S.; Gopalakrishnan, G.; Shears, S.D.; Grimmett, W.; Wilhelmsen, K.C.; Hansen, L.; Morris, J.C.; Goate, A.M. 1998: Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22. Neurology 50(6): 1546-1555
Maréchal, J.; Wada, H.; Koffa, T.; Kanzaki, A.; Wilmotte, R.; Ikoma, K.; Yawata, A.; Inoue, T.; Takanashi, K.; Miura, A. 1994: Hereditary elliptocytosis associated with spectrin Le Puy in a Japanese family: Ultrastructural aspect of the red cell skeleton. European Journal of Haematology 52(2): 92-98
Romano, M.; Patriarca, P.; Melo, C.; Baralle, F.E.; Dri, P. 1994: Hereditary eosinophil peroxidase deficiency: immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defect. Proceedings of the National Academy of Sciences of the United States of America 91(26): 12496-12500
Mofid, M.Z.; Costarangos, C.; Gruber, S.B.; Koch, S.E. 1998: Hereditary epidermolytic palmoplantar keratoderma (Vörner type) in a family with Ehlers-Danlos syndrome. Journal of the American Academy of Dermatology 38(5 Pt 2): 825-830
Callenbach, P.M.; Brouwer, O.F. 1997: Hereditary epilepsy syndromes. Clinical Neurology and Neurosurgery 99(3): 159-171
Lakshmanan, J.; Eysselein, V. 1993: Hereditary error in epidermal growth factor prohormone metabolism in a rat model of autosomal dominant polycystic kidney disease. Biochemical and Biophysical Research Communications 197(3): 1083-1093
Brodsky, M.C. 1998: Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles. Ophthalmology 105(4): 717-725
Kugler, S.L.; Stenroos, E.S.; Mandelbaum, D.E.; Lehner, T.; McKoy, V.V.; Prossick, T.; Sasvari, J.; Swannick, K.; Katz, J.; Johnson, W.G. 1998: Hereditary febrile seizures: Phenotype and evidence for a chromosome 19p locus. American Journal of Medical Genetics 79(5): 354-361
Muenter, M.D.; Forno, L.S.; Hornykiewicz, O.; Kish, S.J.; Maraganore, D.M.; Caselli, R.J.; Okazaki, H.; Howard, F.M.; Snow, B.J.; Calne, D.B. 1998: Hereditary form of parkinsonism--dementia. Annals of Neurology 43(6): 768-781
Heutink, P.; Stevens, M.; Rizzu, P.; Bakker, E.; Kros, J.M.; Tibben, A.; Niermeijer, M.F.; van Duijn, C.M.; Oostra, B.A.; van Swieten, J.C. 1997: Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families. Annals of Neurology 41(2): 150-159
Radin, D.R. 1994: Hereditary generalized juvenile polyposis: Association with arteriovenous malformations and risk of malignancy. Abdominal Imaging 19(2): 140-142
Jarman, P.R.; Wood, N.W.; Davis, M.T.; Davis, P.V.; Bhatia, K.P.; Marsden, C.D.; Davis, M.B. 1997: Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity. American Journal of Human Genetics 61(4): 928-933
Bozzo, L.; de Almedia, O.P.; Scully, C.; Aldred, M.J. 1994: Hereditary gingival fibromatosis. Report of an extensive four-generation pedigree. Oral Surgery Oral Medicine and Oral Pathology 78(4): 452-454
Braun, J.; Donner, H.; Plock, K.; Rau, H.; Usadel, K.H.; Badenhoop, K. 1998: Hereditary haemochromatosis mutations (HFE) in patients with Type II diabetes mellitus. Diabetologia 41(8): 983-984
Nielsen, J.E.; Jensen, L.N.; Krabbe, K. 1995: Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. Journal of Neurology Neurosurgery and Psychiatry 59(3): 318-321
Piantanida, M.; Buscarini, E.; Dellavecchia, C.; Minelli, A.; Rossi, A.; Buscarini, L.; Danesino, C. 1996: Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2. Journal of Medical Genetics 33(6): 441-443
Haye, R.; Austad, J. 1992: Hereditary haemorrhagic teleangiectasia: unsuccessful treatment with the flashlamp-pulsed dye laser. Rhinology 30(2): 135-137
Hosni, A.A.; Innes, A.J. 1994: Hereditary haemorrhagic telangiectasia: Young's procedure in the management of epistaxis. Journal of Laryngology and Otology 108(9): 754-757
Belozerov, Y.M.; Leont'eva, I.V.; Shkol'nikova, M.A.; Strakhova, O.S.; Sebeleva, I.A.; Makarov, L.M.; Davydkin, V.V.; Dinov, B.A. 1998: Hereditary heart disease in children. Rossiiskii Vestnik Perinatologii i Pediatrii 43(1): 18-23
Adams, P.C. 1994: Hereditary hemochromatosis and red cell aplasia. American Journal of Hematology 45(3): 260-261
Waheed, A.; Parkkila, S.; Zhou, X.Y.; Tomatsu, S.; Tsuchihashi, Z.; Feder, J.N.; Schatzman, R.C.; Britton, R.S.; Bacon, B.R.; Sly, W.S. 1997: Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proceedings of the National Academy of Sciences of the United States of America 94(23): 12384-12389
Burke, W.; Thomson, E.; Khoury, M.J.; McDonnell, S.M.; Press, N.; Adams, P.C.; Barton, J.C.; Beutler, E.; Brittenham, G.; Buchanan, A.; Clayton, E.W.; Cogswell, M.E.; Meslin, E.M.; Motulsky, A.G.; Powell, L.W.; Sigal, E.; Wilfond, B.S.; Collins, F.S. 1998: Hereditary hemochromatosis: gene discovery and its implications for population-based screening. JAMA 280(2): 172-178
Totaro, A.; Rommens, J.M.; Grifa, A.; Lunardi, C.; Carella, M.; Huizenga, J.J.; Roetto, A.; Camaschella, C.; De Sandre, G.; Gasparini, P. 1996: Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class i region. Genomics 31(3): 319-326
Bacon, B.R.; Sadiq, S.A. 1997: Hereditary hemochromatosis: presentation and diagnosis in the 1990s. American Journal of Gastroenterology 92(5): 784-789
Camaschella, C.; Piperno, A. 1997: Hereditary hemochromatosis: recent advances in molecular genetics and clinical management. Haematologica 82(1): 77-84
Kanno, H.; Wei, D.C.; Chan, L.C.; Mizoguchi, H.; Ando, M.; Nakahata, T.; Narisawa, K.; Fujii, H.; Miwa, S. 1994: Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong. Blood 84(10): 3505-3509
Clark, M.R.; Shohet, S.B.; Gottfried, E.L. 1993: Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: One, two, or many disorders?. American Journal of Hematology 42(1): 25-30
Haitjema, T.; Westermann, C.J.; Overtoom, T.T.; Timmer, R.; Disch, F.; Mauser, H.; Lammers, J.W. 1996: Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): new insights in pathogenesis, complications, and treatment. Archives of Internal Medicine 156(7): 714-719
Kikuchi, K.; Kowada, M.; Tomura, N.; Johkura, H. 1994: Hereditary hemorrhagic telangiectasia associated with cerebral arteriovenous fistula and multiple cerebral arteriovenous malformations: case report. No Shinkei Geka. Neurological Surgery 22(1): 85-91
Schumacher, B.; Frieling, T.; Borchard, F.; Hengels, K.J. 1994: Hereditary hemorrhagic telangiectasia associated with multiple pulmonary arteriovenous malformations and juvenile polyposis. Zeitschrift für Gastroenterologie 32(2): 105-108
Rhodus, N.L.; Kuba, R. 1993: Hereditary hemorrhagic telangiectasia with florid osseous dysplasia. Report of a case with differential diagnostic considerations. Oral Surgery Oral Medicine and Oral Pathology 75(1): 48-53
Rambusch, E.G.; Chavan, A.; Harms, C.P.; Tietge, U.; Ocran, K.; Strassburg, C.; Wagner, S.; Galanski, M.; Creutzig, A.; Manns, M.P. 1996: Hereditary hemorrhagic telangiectasia with hepatic involvement comprising gastric vessels. Vasa 25(4): 352-357
Booth, D.R.; Tan, S.Y.; Booth, S.E.; Tennent, G.A.; Hutchinson, W.L.; Hsuan, J.J.; Totty, N.F.; Truong, O.; Soutar, A.K.; Hawkins, P.N.; Bruguera, M.; Caballería, J.; Solé, M.; Campistol, J.M.; Pepys, M.B. 1996: Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. Journal of Clinical Investigation 97(12): 2714-2721
Girelli, D.; Corrocher, R.; Bisceglia, L.; Olivieri, O.; Zelante, L.; Panozzo, G.; Gasparini, P. 1997: Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene. Blood 90(5): 2084-2088
Cazzola, M.; Bergamaschi, G.; Tonon, L.; Arbustini, E.; Grasso, M.; Vercesi, E.; Barosi, G.; Bianchi, P.E.; Cairo, G.; Arosio, P. 1997: Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA. Blood 90(2): 814-821
Szabó, J.; Heath, B.; Hill, V.M.; Jackson, C.E.; Zarbo, R.J.; Mallette, L.E.; Chew, S.L.; Besser, G.M.; Thakker, R.V.; Huff, V. 1995: Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. American Journal of Human Genetics 56(4): 944-950
Klimes, I.; Vrána, A.; Kunes, J.; Seböková, E.; Dobesová, Z.; Stolba, P.; Zicha, J. 1995: Hereditary hypertriglyceridemic rat: a new animal model of metabolic alterations in hypertension. Blood Pressure 4(3): 137-142
Just, M.; Ribera, M.; Fuente, M.J.; Bielsa, I.; Ferrándiz, C. 1998: Hereditary hypotrichosis simplex. Dermatology 196(3): 339-342
Rodriguez Diaz, E.; Fernandez Blasco, G.; Martin Pascual, A.; Armijo, M. 1995: Hereditary hypotrichosis simplex of the scalp. Dermatology (Basel) 191(2): 139-141
Mitrani-Rosenbaum, S.; Argov, Z.; Blumenfeld, A.; Seidman, C.E.; Seidman, J.G. 1996: Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Human Molecular Genetics 5(1): 159-163
Hoffmann, J.J.; Hennis, B.C.; Kluft, C.; Vijgen, M. 1993: Hereditary increase of plasma histidine-rich glycoprotein associated with abnormal heparin binding (HRG Eindhoven). Thrombosis and Haemostasis 70(6): 894-899
Brandt, J.; Welsh, K.A.; Breitner, J.C.; Folstein, M.F.; Helms, M.; Christian, J.C. 1993: Hereditary influences on cognitive functioning in older men. A study of 4000 twin pairs. Archives of Neurology 50(6): 599-603
Levy, N.T.; Meyers, A.M.; Margolius, L.P.; Verhaart, S.; Wadee, W.A. 1995: Hereditary interstitial nephritis without basement membrane changes. Nephron 69(4): 418-423
Tsigos, C.; Arai, K.; Hung, W.; Chrousos, G.P. 1993: Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene. Journal of Clinical Investigation 92(5): 2458-2461
Britton, J.W.; Uitti, R.J.; Ahlskog, J.E.; Robinson, R.G.; Kremer, B.; Hayden, M.R. 1995: Hereditary late-onset chorea without significant dementia: genetic evidence for substantial phenotypic variation in Huntington's disease. Neurology 45(3 Pt 1): 443-447
Lossos, A.; Cooperman, H.; Soffer, D.; Ben-Nariah, Z.; Sagi, E.; Gomori, M.; Abramsky, O.; Shoshan, S.; Argov, Z. 1995: Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen content. Neurology 45(2): 331-337
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Dyck, P.J.; Litchy, W.J.; Minnerath, S.; Bird, T.D.; Chance, P.F.; Schaid, D.J.; Aronson, A.E. 1994: Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis. Annals of Neurology 35(5): 608-615
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Hamiel, O.P.; Raas-Rothschild, A.; Upadhyaya, M.; Frydman, M.; Sarova-Pinhas, I.; Brand, N.; Passwell, J.H. 1993: Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant. Journal of Pediatrics 123(3): 431-434
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Moe, L.; Lium, B. 1997: Hereditary multifocal renal cystadenocarcinomas and nodular dermatofibrosis in 51 German shepherd dogs. Journal of Small Animal Practice 38(11): 498-505
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Chauplannaz, G.; Bady, B. 1994: Hereditary myasthenic syndromes with late onset. Value of electrophysiological tests. Revue Neurologique (Paris) 150(2): 142-148
Nauseef, W.M.; Brigham, S.; Cogley, M. 1994: Hereditary myeloperoxidase deficiency due to a missense mutation of arginine 569 to tryptophan. Journal of Biological Chemistry 269(2): 1212-1216
Lubbers, W.J.; Brunt, E.R.; Scheffer, H.; Litt, M.; Stulp, R.; Browne, D.L.; van Weerden, T.W. 1995: Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide. Journal of Neurology Neurosurgery and Psychiatry 59(4): 400-405
Malik, R.; Mepstead, K.; Yang, F.; Harper, C. 1993: Hereditary myopathy of Devon rex cats. Journal of Small Animal Practice 34(11): 539-546
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Uribarri, J.; Kaskas, M. 1993: Hereditary nephrogenic diabetes insipidus and bilateral nonobstructive hydronephrosis. Nephron 65(3): 346-349
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Leblanc, R.; Melanson, D.; Wilkinson, R.D. 1996: Hereditary neurocutaneous angiomatosis. Report of four cases. Journal of Neurosurgery 85(6): 1135-1142
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Amato, A.A.; Barohn, R.J. 1996: Hereditary neuropathy with liability to pressure palsies: assocation with central nervous system demyelination. Muscle and Nerve 19(6): 770-773
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Lenssen, P.P.; Gabreëls-Festen, A.A.; Valentijn, L.J.; Jongen, P.J.; van Beersum, S.E.; van Engelen, B.G.; van Wensen, P.J.; Bolhuis, P.A.; Gabreëls, F.J.; Mariman, E.C. 1998: Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. Brain: a Journal of Neurology 121: 1451-1458
Andreadou, E.; Yapijakis, C.; Paraskevas, G.P.; Stavropoulos, P.; Karadimas, C.; Zis, V.P.; Davaki, P.; Karandreas, N.; Rentzos, M.; Tsakanikas, C.; Vassilopoulos, D.; Papageorgiou, C. 1996: Hereditary neuropathy with liability to pressure palsies: The same molecular defect can result in diverse clinical presentation. Journal of Neurology 243(3): 225-230
Green, S.E.; Bradburn, D.M.; Varma, J.S.; Burn, J. 1998: Hereditary non-polyposis colorectal cancer. International Journal of Colorectal Disease 13(1): 3-12,.
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Nakashima, K.; Shimoda, M.; Sato, K.; Nanba, E.; Igo, M.; Sato, K.; Takahashi, K. 1995: Hereditary non-progressive torsion dystonia with intellectual disturbance. Internal Medicine 34(9): 843-846
Green, R.C.; Narod, S.A.; Morasse, J.; Young, T.L.; Cox, J.; Fitzgerald, G.W.; Tonin, P.; Ginsburg, O.; Miller, S.; Jothy, S. 1994: Hereditary nonpolyposis colon cancer: analysis of linkage to 2p15-16 places the COCA1 locus telomeric to D2S123 and reveals genetic heterogeneity in seven Canadian families. American Journal of Human Genetics 54(6): 1067-1077
Yasuro, M.; Mori, T.; Takahashi, K.; Miyaki, M. 1996: Hereditary nonpolyposis colorectal cancer (HNPCC) with multiple primary cancers of the skin and brain developed in a short period: Report of a case. Stomach and Intestine 31(7): 885-888
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Konishi, K.; Tajiri, H.; Fujii, T.; Boku, N.; Ohtu, A.; Yoshida, S.; Konishi, M.; Hasebe, T.; Mukai, K.; Makino, R. 1998: Hereditary nonpolyposis colorectal cancer associated with duodenal carcinoma: a case report. Japanese Journal of Clinical Oncology 28(4): 289-293
Wijnen, J.; Khan, P.M.; Vasen, H.; van der Klift, H.; Mulder, A.; van Leeuwen-Cornelisse, I.; Bakker, B.; Losekoot, M.; Møller, P.; Fodde, R. 1997: Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. American Journal of Human Genetics 61(2): 329-335
Nomizu, T.; Watanabe, F.; Yamaki, Y.; Miura, J.-Ichi; Motoki, R. 1996: Hereditary nonpolyposis colorectal cancer with endometrial cancer: Report of a family. Stomach and Intestine 31(7): 875-878
Wang, Y.; Friedl, W.; Lamberti, C.; Ruelfs, C.; Kruse, R.; Propping, P. 1997: Hereditary nonpolyposis colorectal cancer: Causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue. Human Genetics 100(3-4): 362-364
Bellacosa, A.; Genuardi, M.; Anti, M.; Viel, A.; Ponz de Leon, M. 1996: Hereditary nonpolyposis colorectal cancer: review of clinical, molecular genetics, and counseling aspects. American Journal of Medical Genetics 62(4): 353-364
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Denis, B.; Marescaux, L. 1994: Hereditary of a medullary cervical ataxia syndrome (Wobbler syndrome) in the mastiff. Recueil de Medecine Veterinaire de l'Ecole d'Alfort 170(4-5): 245-247
Yamamoto, T.; Yokoyama, A. 1996: Hereditary onset of multiple seborrheic keratoses: a variant of Leser Trélat sign?. Journal of Dermatology 23(3): 191-195
Imaeda, M.; Sumi, S.; Imaeda, H.; Suchi, M.; Kidouchi, K.; Togari, H.; Wada, Y. 1998: Hereditary orotic aciduria heterozygotes accompanied with neurological symptoms. Tohoku Journal of Experimental Medicine 185(1): 67-70
Reardon, D.M.; Seymour, C.A.; Cox, T.M.; Pinder, J.C.; Schofield, A.E.; Tanner, M.J. 1993: Hereditary ovalocytosis with compensated haemolysis. British Journal of Haematology 85(1): 197-199
Boyd, J.; Rubin, S.C. 1997: Hereditary ovarian cancer: molecular genetics and clinical implications. Gynecologic Oncology 64(2): 196-206
Chen, E.H.; Tartaglia, A.P.; Mitchell, B.S. 1993: Hereditary overexpression of adenosine deaminase in erythrocytes: evidence for a cis-acting mutation. American Journal of Human Genetics 53(4): 889-893
Chen, E.H.; Mitchell, B.S. 1994: Hereditary overexpression of adenosine deaminase in erythrocytes: studies in erythroid cell lines and transgenic mice. Blood 84(7): 2346-2353
Cambiaghi, S.; Morel, P. 1996: Hereditary painful callosities with associated features. Dermatology 193(1): 47-49
Fitzgerald, D.A.; Verbov, J.L. 1996: Hereditary palmoplantar keratoderma with deafness. British Journal of Dermatology 134(5): 939-942
Stanimirović, A.; Kansky, A.; Basta-Juzbasić, A.; Skerlev, M.; Beck, T. 1993: Hereditary palmoplantar keratoderma, type papulosa, in Croatia. Journal of the American Academy of Dermatology 29(3): 435-437
Yorifuji, T.; Matsumura, M.; Okuno, T.; Shimizu, K.; Sonomura, T.; Muroi, J.; Kuno, C.; Takahashi, Y.; Okuno, T. 1994: Hereditary pancreatic hypoplasia, diabetes mellitus, and congenital heart disease: a new syndrome?. Journal of Medical Genetics 31(4): 331-333
Finch, M.D.; Howes, N.; Ellis, I.; Mountford, R.; Sutton, R.; Raraty, M.; Neoptolemos, J.P. 1997: Hereditary pancreatitis and familial pancreatic cancer. Digestion 58(6): 564-569
Zbar, B.; Tory, K.; Merino, M.; Schmidt, L.; Glenn, G.; Choyke, P.; Walther, M.M.; Lerman, M.; Linehan, W.M. 1994: Hereditary papillary renal cell carcinoma. Journal of Urology 151(3): 561-566
Mitsui, T.; Kawai, H.; Sakoda, S.; Miyata, M.; Saito, S. 1994: Hereditary parkinsonism with multiple system degeneration: beneficial effect of anticholinergics, but not of levodopa. Journal of the Neurological Sciences 125(2): 153-157
Takahashi, Y.; Tanaka, T.; Minowa, H.; Ookubo, Y.; Sugimoto, M.; Nakajima, M.; Miyauchi, Y.; Yoshioka, A. 1996: Hereditary partial deficiency of plasminogen activator inhibitor-1 associated with a lifelong bleeding tendency. International Journal of Hematology 64(1): 61-68
Feng, Y.Z.; Liu; Jian; Zhou; Xing Ren 1994: Hereditary persistence of alpha-fetoprotein. Zhonghua Zhongliu Zazhi 16(1): 54-55
Fusaro, R.M.; Johnson, J.A. 1996: Hereditary polymorphic light eruption of American Indians: Occurrence in non-Indians with polymorphic light eruption. Journal of the American Academy of Dermatology 34(4): 612-617
Girodet, C.; Vidal, V.; Laplace-Marieze, V.; Bignon, Y.J. 1996: Hereditary predispositions to cancer: the genetic diagnosis in practice. Bulletin du Cancer 83(9): 764-768
Celik, A.F.; Katsinelos, P.; Read, N.W.; Khan, M.I.; Donnelly, T.C. 1995: Hereditary proctalgia fugax and constipation: report of a second family. Gut 36(4): 581-584
Wang, P.J.; Ko, Y.M.; Young, C.; Hwu, W.L.; Shen, Y.Z. 1994: Hereditary progressive dystonia with marked diurnal fluctuation (Segawa syndrome) in Taiwan. Brain and Development 16(2): 126-131
Schröder, K.; Hettmannsperger, U.; Schmuth, M.; Orfanos, C.E.; Goerdt, S. 1996: Hereditary progressive mucinous histiocytosis. Journal of the American Academy of Dermatology 35(2 Pt 2): 298-303
Bork, K. 1994: Hereditary progressive mucinous histiocytosis. Immunohistochemical and ultrastructural studies in an additional family. Archives of Dermatology 130(10): 1300-1304
Schlesinger, M.; Mashal, U.; Levy, J.; Fishelson, Z. 1993: Hereditary properdin deficiency in three families of Tunisian Jews. Acta Paediatrica 82(9): 744-747
Cussenot, O.; Valeri, A.; Berthon, P.; Fournier, G.; Mangin, P. 1998: Hereditary prostate cancer and other genetic predispositions to prostate cancer. Urologia Internationalis 60(Suppl): 30-34; Discussion 35
Doig, R.G.; Begley, C.G.; McGrath, K.M. 1994: Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene. Thrombosis and Haemostasis 72(2): 203-208
Song, K.S.; Park, Y.S.; Choi, C.R.; Kim, H.K.; Park, Q.; Kim, H.S. 1998: Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T). Journal of Korean Medical Science 13(2): 186-190
Wilkerson, D.K.; Burrell, L.; Cisar, L.A.; Graham, A.M.; Kim, H. 1993: Hereditary protein S deficiency in a large New Jersey kindred. Journal of Vascular Surgery 18(6): 932
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Ghorbani, K.; Carapetian, J. 1994: Hereditary pubertal genu valgum in Iran. Clinical Genetics 45(4): 190-193
DePalma, L.; Luban, N.L. 1993: Hereditary pyropoikilocytosis. Clinical and laboratory analysis in eight infants and young children. American Journal of Diseases of Children 147(1): 93-95
Kubo, S.; Kitamura, O.; Tsuda, R.; Hirose, W.; Matsumoto, H.; Nakasono, I. 1993: Hereditary recombined three-allele variant of the Gc system. Human Genetics 91(1): 71-72
Moerman, P.; Fryns, J.P.; Sastrowijoto, S.H.; Vandenberghe, K.; Lauweryns, J.M. 1994: Hereditary renal adysplasia: New observations and hypotheses. Pediatric Pathology 14(3): 405-410
Uemichi, T.; Liepnieks, J.J.; Benson, M.D. 1994: Hereditary renal amyloidosis with a novel variant fibrinogen. Journal of Clinical Investigation 93(2): 731-736
Everitt, J.I.; Goldsworthy, T.L.; Wolf, D.C.; Walker, C.L. 1992: Hereditary renal cell carcinoma in the Eker rat: a rodent familial cancer syndrome. Journal of Urology 148(6): 1932-1936
Etingof, R.N. 1998: Hereditary retinal degeneration in humans and supreme animals: Advances and difficulties. Sensornye Sistemy 12(2): 149-160
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Li, F.P.; Abramson, D.H.; Tarone, R.E.; Kleinerman, R.A.; Fraumeni, J.F.; Boice, J.D. 1997: Hereditary retinoblastoma, lipoma, and second primary cancers. Journal of the National Cancer Institute 89(1): 83-84
Gleich, O.; Klump, G.M.; Dooling, R.J. 1994: Hereditary sensorineural hearing loss in a bird. Die Naturwissenschaften 81(7): 320-323
Heckmann, J.M.; Carr, J.A.; Bell, N. 1995: Hereditary sensory and autonomic neuropathy with cataracts, mental retardation, and skin lesions: five cases. Neurology 45(7): 1405-1408
Wright, A.; Dyck, P.J. 1995: Hereditary sensory neuropathy with sensorineural deafness and early-onset dementia. Neurology 45(3 Pt 1): 560-562
Edgar, A.J.; Wickramasinghe, S.N. 1998: Hereditary sideroblastic anaemia due to a mutation in exon 10 of the erythroid 5-aminolaevulinate synthase gene. British Journal of Haematology 100(2): 389-392
Bruyn, G.W.; Bots, G.T.; Went, L.N.; Klinkhamer, P.J. 1992: Hereditary spastic dystonia with Leber's hereditary optic neuropathy: Neuropathological findings. Journal of the Neurological Sciences 113(1): 55-61
Ferrer, I.; Olivé, M.; Rivera, R.; Pou, A.; Narberhaus, B.; Ugarte, A. 1995: Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study. Neuropathology and Applied Neurobiology 21(3): 255-261
Farah, S.; Sabry, M.A.; al-Shubaili, A.F.; Anim, J.T.; Hussain, J.M.; Montaser, M.A.; Sharfuddin, K.M. 1997: Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: New entity?. Clinical Neurology and Neurosurgery 99(1): 66-70
Ahmed, F.E.; Qureshi, I.M.; Wooldridge, M.A.; Pejaver, R.K. 1996: Hereditary spastic paraplegia and Evans's syndrome. Acta Paediatrica 85(7): 879-881
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Dubé, M.P.; Mlodzienski, M.A.; Kibar, Z.; Farlow, M.R.; Ebers, G.; Harper, P.; Kolodny, E.H.; Rouleau, G.A.; Figlewicz, D.A. 1997: Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait. American Journal of Human Genetics 60(3): 625-629
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Iolascon, A.; Miraglia del Giudice, E.; Perrotta, S.; Pinto, L.; Fiorelli, G.; Cappellini, D.M.; Vasseur, C.; Bursaux, E.; Cutillo, S. 1992: Hereditary spherocytosis (HS) due to loss of anion exchange transporter. Haematologica 77(6): 450-456
Reinhart, W.H.; Wyss, E.J.; Arnold, D.; Ott, P. 1994: Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred. British Journal of Haematology 86(1): 147-155
Hassoun, H.; Vassiliadis, J.N.; Murray, J.; Yi, S.J.; Hanspal, M.; Johnson, C.A.; Palek, J. 1996: Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin. Blood 87(6): 2538-2545
Hayag-Barin, J.E.; Smith, R.E.; Tucker, F.C. 1998: Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: A case report and review of the literature. American Journal of Hematology 57(1): 82-84
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Orntoft, T.F.; Clausen, N. 1994: Hereditary spherocytosis: diagnostic and anaemia-associated aberrations of ghost proteins. Scandinavian Journal of Clinical and Laboratory Investigation 54(2): 95-103
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Poyhonen, M.; Leisti, E.L.; Kytölä, S.; Leisti, J. 1997: Hereditary spinal neurofibromatosis: a rare form of NF1?. Journal of Medical Genetics 34(3): 184-187
Magy, L.; Birouk, N.; Vallat, J.M.; Gouider, R.; Maisonobe, T.; Bouche, P.; Lyon-Caen, O.; Fontaine, B. 1997: Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system. Neurology 48(6): 1684-1690
Awidi, A.S.; Abu-Khalaf, M.; Herzallah, U.; Abu-Rajab, A.; Shannak, M.M.; Abu-Obeid, T.; al-Taher, I.; Anshasi, B. 1993: Hereditary thrombophilia among 217 consecutive patients with thromboembolic disease in Jordan. American Journal of Hematology 44(2): 95-100
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Hollán, S.; Fujii, H.; Hirono, A.; Hirono, K.; Karro, H.; Miwa, S.; Harsányi, V.; Gyódi, E.; Inselt-Kovács, M. 1993: Hereditary triosephosphate isomerase (TPI) deficiency: Two severely affected brothers one with and one without neurological symptoms. Human Genetics 92(5): 486-490
Louis, D.N.; von Deimling, A. 1995: Hereditary tumor syndromes of the nervous system: Overview and rare syndromes. Brain Pathology 5(2): 145-151
Schierbeek, H.; Beukeveld, G.J.; van Faassen, H.; van Spronsen, F.J.; Bijsterveld, K.; Venekamp-Hoolsema, E.E.; Wolthers, B.G.; Smit, G.P. 1993: Hereditary tyrosinaemia type I: a long-term study of the relationship between the urinary excretions of succinylacetone and delta-aminolevulinic acid. Journal of Inherited Metabolic Disease 16(6): 1034-1040
Ploos van Amstel, J.K.; Bergman, A.J.; van Beurden, E.A.; Roijers, J.F.; Peelen, T.; van den Berg, I.E.; Poll-The, B.T.; Kvittingen, E.A.; Berger, R. 1996: Hereditary tyrosinemia type 1: Novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene; variability of the genotype-phenotype relationship. Human Genetics 97(1): 51-59
van Spronsen, F.J.; Thomasse, Y.; Smit, G.P.; Leonard, J.V.; Clayton, P.T.; Fidler, V.; Berger, R.; Heymans, H.S. 1994: Hereditary tyrosinemia type I: A new clinical classification with difference in prognosis on dietary treatment. Hepatology 20(5): 1187-1191
Demers, S.I.; Phaneuf, D.; Tanguay, R.M. 1994: Hereditary tyrosinemia type I: strong association with haplotype 6 in French Canadians permits simple carrier detection and prenatal diagnosis. American Journal of Human Genetics 55(2): 327-333
Ilchovska, M.M.; Khristov, K.N.; Marinova, E.I. 1992: Hereditary variability of maize induced by exogenous DNA of teosinte. Fiziologiya i Biokhimiya Kul'turnykh Rastenii 24(3): 241-248
Heale, W.F. 1997: Hereditary vesicoureteric reflux: Phenotypic variation and family screening. Pediatric Nephrology 11(4): 504-507
Degrugillier, M.E.; Newman, S.M.Jr 1993: Hereditary viruses of Heliothis?, chromatin-associated virus-like particles in testes of six species of Heliothis and Helicoverpa, F-1, and backcross males. Journal of Invertebrate Pathology 61(2): 147-155
Malloy, P.J.; Eccleshall, T.R.; Gross, C.; Van Maldergem, L.; Bouillon, R.; Feldman, D. 1997: Hereditary vitamin D resistant rickets caused by a novel mutation in the vitamin D receptor that results in decreased affinity for hormone and cellular hyporesponsiveness. Journal of Clinical Investigation 99(2): 297-304
Vives Corrons, J.L.; Besson, I.; Aymerich, M.; Ayala, S.; Alloisio, N.; Delaunay, J.; Gonzalez, I.; Manrubia, E. 1995: Hereditary xerocytosis: A report of six unrelated Spanish families with leaky red cell syndrome and increased heat stability of the erythrocyte membrane. British Journal of Haematology 90(4): 817-822
Klein, M.L.; Mauldin, W.M.; Stoumbos, V.D. 1994: Heredity and age-related macular degeneration. Observations in monozygotic twins. Archives of Ophthalmology 112(7): 932-937
Stabenau, J.R.; Pollin, W. 1993: Heredity and environment in schizophrenia, revisited. The contribution of twin and high-risk studies. Journal of Nervous and Mental Disease 181(5): 290-297
Dixon, W.E.; Matheny, A.P.; Mohr, S.R. 1995: Heredity and environment in phoneme articulation: hereditary and environmental contributions to articulation proficiency. Acta Geneticae Medicae et Gemellologiae 44(2): 63-73
Licata, G.; Scaglione, R.; Corrao, S.; Ganguzza, A.; Mazzola, G.; Arnone, S.; Dichiara, M.A.; Licata, A.; Merlino, G.; Di Chiara, T. 1995: Heredity and obesity-associated hypertension: impact of hormonal characteristics and left ventricular mass. Journal of Hypertension 13(6): 611-618
Page, W.F.; Braun, M.M.; Partin, A.W.; Caporaso, N.; Walsh, P. 1997: Heredity and prostate cancer: A study of World War II veteran twins. Prostate 33(4): 240-245
Bergem, A.L. 1994: Heredity in dementia of the Alzheimer type. Clinical Genetics 46(1 Spec No): 144-149
Dahl, A.A. 1994: Heredity in personality disorders--an overview. Clinical Genetics 46(1 Spec No): 138-143
Bener, A.; al-Jawadi, T.Q.; Simsek, M.; al-Nassar, K.E. 1992: Heredity of asthma in Saudi population. European Journal of Epidemiology 8(5): 733-736
Suwa, M.; Nakamura, T.; Katsuta, S. 1996: Heredity of muscle fiber composition and correlated response of the synergistic muscle in rats. American Journal of Physiology 271(2 Part 2): R432-R436
Nakamura, T.; Masui, S.; Wada, M.; Katoh, H.; Mikami, H.; Katsuta, S. 1993: Heredity of muscle fibre composition estimated from a selection experiment in rats. European Journal of Applied Physiology and Occupational Physiology 66(1): 85-89
Martins, O.M.; Barata, G.N.; Figueiredo, F.; Ferreira, J.C. 1996: Heredity of some coat colours in Lusitana horse breed. Revista Portuguesa de Ciencias Veterinarias 91(517): 16-28
Kellner, U. 1997: Heredity retinal dystrophy. Ophthalmologe 94(2): 164-183
Fiddes, R.J.; Janes, P.W.; Sanderson, G.M.; Sivertsen, S.P.; Sutherland, R.L.; Daly, R.J. 1995: Heregulin (HRG)-induced mitogenic signaling and cytotoxic activity of a HRG/PE40 ligand toxin in human breast cancer cells. Cell Growth and Differentiation: the Molecular Biology Journal of the American Association for Cancer Research 6(12): 1567-1577
Chan, S.D.; Antoniucci, D.M.; Fok, K.S.; Alajoki, M.L.; Harkins, R.N.; Thompson, S.A.; Wada, H.G. 1995: Heregulin activation of extracellular acidification in mammary carcinoma cells is associated with expression of HER2 and HER3. Journal of Biological Chemistry 270(38): 22608-22613
Magnifico, A.; Tagliabue, E.; Ardini, E.; Casalini, P.; Colnaghi, M.I.; Ménard, S. 1998: Heregulin beta1 induces the down regulation and the ubiquitin-proteasome degradation pathway of p185HER2 oncoprotein. Febs Letters 422(2): 129-131
Baulida, J.; Carpenter, G. 1997: Heregulin degradation in the absence of rapid receptor-mediated internalization. Experimental Cell Research 232(1): 167-172
Jones, F.E.; Jerry, D.J.; Guarino, B.C.; Andrews, G.C.; Stern, D.F. 1996: Heregulin induces in vivo proliferation and differentiation of mammary epithelium into secretory lobuloalveoli. Cell Growth and Differentiation: the Molecular Biology Journal of the American Association for Cancer Research 7(8): 1031-1038
Cardillo, M.; Yankelevich, B.; Mazumder, A.; Lupu, R. 1996: Heregulin induces increase in sensitivity of an erbB-2-overexpressing breast cancer cell type to lysis by lymphokine-activated killer cells. Cancer Immunology Immunotherapy: Cii 43(1): 19-25
Li, W.; Park, J.W.; Nuijens, A.; Sliwkowski, M.X.; Keller, G.A. 1996: Heregulin is rapidly translocated to the nucleus and its transport is correlated with c-myc induction in breast cancer cells. Oncogene 12(11): 2473-2477
Carraway, K.L.; Soltoff, S.P.; Diamonti, A.J.; Cantley, L.C. 1995: Heregulin stimulates mitogenesis and phosphatidylinositol 3-kinase in mouse fibroblasts transfected with erbB2/neu and erbB3. Journal of Biological Chemistry 270(13): 7111-7116
Mincione, G.; Piccirelli, A.; Lazzereschi, D.; Salomon, D.S.; Colletta, G. 1998: Heregulin-dependent autocrine loop regulates growth of K-ras but not erbB-2 transformed rat thyroid epithelial cells. Journal of Cellular Physiology 176(2): 383-391
Wallasch, C.; Weiss, F.U.; Niederfellner, G.; Jallal, B.; Issing, W.; Ullrich, A. 1995: Heregulin-dependent regulation of HER2/neu oncogenic signaling by heterodimerization with HER3. EMBO Journal 14(17): 4267-4275
Altiok, N.; Altiok, S.; Changeux, J.P. 1997: Heregulin-stimulated acetylcholine receptor gene expression in muscle: requirement for MAP kinase and evidence for a parallel inhibitory pathway independent of electrical activity. EMBO Journal 16(4): 717-725
Gamett, D.C.; Greene, T.; Wagreich, A.R.; Kim, H.H.; Koland, J.G.; Cerione, R.A. 1995: Heregulin-stimulated signaling in rat pheochromocytoma cells. Evidence for ErbB3 interactions with Neu/ErbB2 and p85. Journal of Biological Chemistry 270(32): 19022-19027
Averbuch-Heller, L.; Poonyathalang, A.; von Maydell, R.D.; Remler, B.F. 1995: Hering's law for eyelids: still valid. Neurology 45(9): 1781-1783
Gagliardi, L.; Rusconi, F. 1995: Hering-Breuer reflex and respiratory rate: a biased association. Journal of Applied Physiology 78(4): 1575-1578
Rabbette, P.S.; Fletcher, M.E.; Dezateux, C.A.; Soriano-Brucher, H.; Stocks, J. 1994: Hering-Breuer reflex and respiratory system compliance in the first year of life: a longitudinal study. Journal of Applied Physiology 76(2): 650-656
Mortola, J.P.; Trippenbach, T.; Rezzonico, R.; Fisher, J.T.; Diaz, M.; Villena-Cabrera, N.; Peña, F. 1995: Hering-Breüer reflexes in high-altitude infants. Clinical Science 88(3): 345-350
Danbaro, G.; Oyama, K.; Mukai, F.; Tsuji, S.; Tateishi, T.; Mae, M. 1995: Heritabilities and Genetic Correlations from a Selection Experiment in Broiler Breeders using Restricted Maximum Likelihood. Japanese Poultry Science 32(4): 257-266
Bigham, M.L.; Morris, C.A.; Southey, B.R.; Baker, R.L. 1993: Heritabilities and genetic correlations for live weight and fibre traits in New Zealand Cashmere goats. Livestock Production Science 33(1-2): 91-104
Chen, C.F.; Lee, Y.P.; Lee, Z.H.; Huang, S.Y.; Huang, H.H. 1993: Heritabilities and genetic correlations of egg quality traits in Taiwan's local chicken. Asian-Australasian Journal of Animal Sciences 6(3): 433-440
Ahn, J.K.; Lee, W.Y.; Jo, D.G.; Son, D.S. 1994: Heritabilities of Growth and Wood Quality Characters in Open-pollinated Progenies of Abies holophylla Max. Journal of Korean Forestry Society 83(4): 480-485
Singh, N.P.; Chaudhary, M.C.; Brah, G.S.; Sandhu, J.S. 1996: Heritabilities of and correlations among part-and annual traits in pure-and cross-line White Leghorns. Indian Journal of Animal Sciences 66(8): 806-810
Williams-Blangero, S.; Butler, T.; Brasky, K.; Murthy, K.K. 1994: Heritabilities of clinical chemical traits in chimpanzees. Laboratory Animal Science 44(2): 141-143
Knoblauch, H.; Busjahn, A.; Münter, S.; Nagy, Z.; Faulhaber, H.D.; Schuster, H.; Luft, F.C. 1997: Heritability analysis of lipids and three gene loci in twins link the macrophage scavenger receptor to HDL cholesterol concentrations. Arteriosclerosis Thrombosis and Vascular Biology 17(10): 2054-2060
Apostolov, A. 1993: Heritability and coefficients of correlation and regression between the reproductive characters of Duroc breed swine. Genetika i Selektsiya 26(2): 118-122
Magaña, J.G.; Segura, J.C. 1997: Heritability and factors affecting growth traits and age at first calving of zebu beef heifers in south-eastern Mexico. Tropical Animal Health and Production 29(3): 185-192
Kim, D.C.; Yang, Y.H. 1998: Heritability and genetic correlation of 20 wks body weight and various body measurements in growing period in Korean ring-necked pheasant. Korean Journal of Animal Science 40(2): 145-150
Noh, E.R.; Lee, S.K.; Koo, Y.B.; Byun, K.O. 1994: Heritability and genetic gain of height in Populus davidiana in 4-year-old clonal test. Journal of Korean Forestry Society 83(2): 239-245
Kreiner, M.; Stur, I.; Mayrhoffer, G.; Mueller, S. 1992: Heritability and phenotypic correlations of behaviour traits of four Austrian bracken breeds. Journal of Animal Breeding and Genetics 109(6): 425-432
Boikovski, S. 1993: Heritability and repeatability of characters in sheep: III. Pleven black-headed breed. Genetika i Selektsiya 26(1): 73-78
Herridge, D.F.; Rose, I.A. 1994: Heritability and repeatability of enhanced N-2 fixation in early and late inbreeding generations of soybean. Crop Science 34(2): 360-367
Boikovski, S. 1993: Heritability and repeatability of the characters in sheep: II. Northeastern Bulgarian fine wool breed-Shoumen type. Genetika i Selektsiya 26(1): 67-72
Lakhani, G.P. 1992: Heritability and variability of weaning weight of large white Yorkshire pigs. Indian Journal of Animal Research 26(1): 6-8
Polupan, Y.P. 1992: Heritability and ways of selecting breeding bulls for reproducibility. Tsitologiya i Genetika 26(5): 59-63
Lukaszewicz, M.; Krencik, D. 1994: Heritability coefficients of longevity traits at different milk production levels in dairy cattle. Animal Science Papers and Reports 12(1): 27-32
Torekhanov, A.A. 1993: Heritability degree of biochemical parameters' content in milch cows' blood. Doklady Rossiiskoi Akademii Sel'skokhozyaistvennykh Nauk 1993(3): 63-65
Ansari, K.A.; Ansari, B.A. 1997: Heritability estimate of yield and yield components in bread wheat. Sarhad Journal of Agriculture 13(6): 601-606
Ahmad, M.; Vyas, O.P.; Jana, S.P.; Kirloskar, M.S.; Bhagwat, A.L. 1993: Heritability estimates and genetic correlations between egg number and egg weight in white leghorn. Indian Veterinary Journal 70(7): 633-635
Potti, J.; Merino, S. 1994: Heritability estimates and maternal effects on tarsus length in pied flycatchers, Ficedula hypoleuca. Oecologia (berlin). 100(3): 331-338
Rao, B.P.; Wagner, W.D. 1993: Heritability estimates of blood pressure in genetically selected White Carneau pigeons. Clinical and Experimental Hypertension 15(2): 367-378
Toro, J.E.; Paredes, L.I. 1996: Heritability estimates of larval shell length in the Chilean blue mussel Mytilus chilensis, under different food densities. Aquatic Living Resources 9(4): 347-350
Juliatti, F.C.; Maluf, W.R. 1996: Heritability estimates of tospovirus resistance in segregating tomato plant populations with different allelic frequencies. Fitopatologia Brasileira 21(2): 161-166
Gjerde, B.; Roer, J.E.; Lein, I.; Stoss, J.; Refstie, T. 1997: Heritability for body weight in farmed turbot. Aquaculture International 5(2): 175-178
Schmidt, G.S.; Costa, C.N.; Ledur, M.C.; Avila, V.S. De 1992: Heritability of 42 day weights for broiler breeder strains. Revista da Sociedade Brasileira de Zootecnia 21(5): 772-778
DiLalla, D.L.; Carey, G.; Gottesman, I.I.; Bouchard, T.J. 1996: Heritability of MMPi personality indicators of psychopathology in twins reared apart. Journal of Abnormal Psychology 105(4): 491-499
Naumova, A.K.; Plenge, R.M.; Bird, L.M.; Leppert, M.; Morgan, K.; Willard, H.F.; Sapienza, C. 1996: Heritability of X chromosome--inactivation phenotype in a large family. American Journal of Human Genetics 58(6): 1111-1119
Williams Blangero, S.; Blangero, J. 1995: Heritability of age at first birth in captive olive baboons. American Journal of Primatology 37(3): 233-239
Coccaro, E.F.; Bergeman, C.S.; Kavoussi, R.J.; Seroczynski, A.D. 1997: Heritability of aggression and irritability: A twin study of the Buss-Durkee aggression scales in adult male subjects. Biological Psychiatry 41(3): 273-284
Humphreys, D.G.; Mather, D.E. 1996: Heritability of beta-glucan, groat percentage, and crown rust resistance in two oat crosses. Euphytica 91(3): 359-364
Bo, S.; Cavallo Perin, P.; Scaglione, L.; Pagano, G. 1997: Heritability of cardiovascular risk parameters in subjects with increased susceptibility to non-insulin-dependent diabetes mellitus. Acta Diabetologica 34(4): 280-284,.
Zeng, C.; Naylor, E. 1996: Heritability of circatidal vertical migration rhythms in zoea larvae of the crab Carcinus maenas (L.). Journal of Experimental Marine Biology and Ecology 25 September; 2022: 239-257
Montagna, P.; Mochi, M.; Prologo, G.; Sangiorgi, S.; Pierangeli, G.; Cevoli, S.; Cortelli, P. 1998: Heritability of cluster headache. European Journal of Neurology 5(4): 343-345
Finkel, D.; Pedersen, N.L.; McGue, M.; McClearn, G.E. 1995: Heritability of cognitive abilities in adult twins: Comparison of Minnesota and Swedish data. Behavior Genetics 25(5): 421-431
Fagard, R.; Brguljan, J.; Staessen, J.; Thijs, L.; Derom, C.; Thomis, M.; Vlietinck, R. 1995: Heritability of conventional and ambulatory blood pressures. A study in twins. Hypertension 26(6 Pt 1): 919-924
Mengesha, B.; Abdulkadir, J. 1997: Heritability of diabetes mellitus in Ethiopian diabetics. East African Medical Journal 74(1): 37-40
Famula, T.R.; Oberbauer, A.M.; Brown, K.N. 1997: Heritability of epileptic seizures in the Belgian tervueren. Journal of Small Animal Practice 38(8): 349-352
Krebs, R.A.; Feder, M.E.; Lee, J. 1998: Heritability of expression of the 70KD heat-shock protein in Drosophila melanogaster and its relevance to the evolution of thermotolerance. Evolution 52(3): 841-847
Edwards, K.L.; Newman, B.; Mayer, E.; Selby, J.V.; Krauss, R.M.; Austin, M.A. 1997: Heritability of factors of the insulin resistance syndrome in women twins. Genetic Epidemiology 14(3): 241-253
Cates, D.S.; Houston, B.K.; Vavak, C.R.; Crawford, M.H.; Uttley, M. 1993: Heritability of hostility-related emotions, attitudes, and behaviors. Journal of Behavioral Medicine 16(3): 237-256
van Beijsterveldt, C.E.; Molenaar, P.C.; de Geus, E.J.; Boomsma, D.I. 1996: Heritability of human brain functioning as assessed by electroencephalography. American Journal of Human Genetics 58(3): 562-573
Young, D.A.; Waldo, M.; Rutledge, J.H.; Freedman, R. 1996: Heritability of inhibitory gating of the P50 auditory-evoked potential in monozygotic and dizygotic twins. Neuropsychobiology 33(3): 113-117
Coccaro, E.F.; Bergeman, C.S.; McClearn, G.E. 1993: Heritability of irritable impulsiveness: A study of twins reared together and apart. Psychiatry Research 48(3): 229-242
Cheskov, Y.V.; Korol, A.B. 1993: Heritability of kanamycin resistance character upon maize genetic transformation. Genetika 29(9): 1492-1499
Post, W.S.; Larson, M.G.; Myers, R.H.; Galderisi, M.; Levy, D. 1997: Heritability of left ventricular mass: the Framingham Heart Study. Hypertension 30(5): 1025-1028
Krencik, D. 1994: Heritability of longevity traits in the Polish Friesian cattle. Animal Science Papers and Reports 12(1): 21-25
Friedlander, Y.; Austin, M.A.; Newman, B.; Edwards, K.; Mayer-Davis, E.I.; King, M.C. 1997: Heritability of longitudinal changes in coronary-heart-disease risk factors in women twins. American Journal of Human Genetics 60(6): 1502-1512
Berthold, P.; Pulido, F. 1994: Heritability of migratory activity in a natural bird population. Proceedings of the Royal Society of London Series B Biological Sciences 257(1350): 311-315
Angi, M.R.; Clementi, M.; Sardei, C.; Piattelli, E.; Bisantis, C. 1993: Heritability of myopic refractive errors in identical and fraternal twins. Graefe's Archive for Clinical and Experimental Ophthalmology 231(10): 580-585
Smith, H.G.; Wettermark, K.J. 1995: Heritability of nestling growth in cross-fostered European Starlings Sturnus vulgaris. Genetics 141(2): 657-665
Kapron, M.; Zieba, G.; Lukaszewicz, M.; Kapron, H.; Janczarek, I. 1996: Heritability of performance traits in stallions exercise at Polish training establishments in 1973-1992. Prace i Materialy Zootechniczne 1996(49): 67-75
Jang, K.L.; Livesley, W.J.; Vernon, P.A.; Jackson, D.N. 1996: Heritability of personality disorder traits: A twin study. Acta Psychiatrica Scandinavica 94(6): 438-444
Rotimi, C.; Luke, A.; Li, Z.; Compton, J.; Bowsher, R.; Cooper, R. 1997: Heritability of plasma leptin in a population sample of African-American families. Genetic Epidemiology 14(3): 255-263
Tomblin, J.B.; Buckwalter, P.R. 1998: Heritability of poor language achievement among twins. Journal of Speech Language and Hearing Research: Jslhr 41(1): 188-199
Gilchrist, A.S.; Partridge, L. 1997: Heritability of pre-adult viability differences can explain apparent heritability of sperm displacement ability in Drosophila melanogaster. Proceedings. Biological Sciences 264(1386): 1271-1275
Senanayake, S.G.J.N. 1994: Heritability of quality characters and their correlations in palisade grass (Brachiaria brizantha Stapf). Tropical Agriculture 71(4): 327-329
Snieder, H.; Boomsma, D.I.; Van Doornen, L.J.; De Geus, E.J. 1997: Heritability of respiratory sinus arrhythmia: Dependency on task and respiration rate. Psychophysiology 34(3): 317-328
Rodas, G.; Calvo, M.; Estruch, A.; Garrido, E.; Ercilla, G.; Arcas, A.; Segura, R.; Ventura, J.L. 1998: Heritability of running economy: a study made on twin brothers. European Journal of Applied Physiology and Occupational Physiology 77(6): 511-516
Svetkey, L.P.; McKeown, S.P.; Wilson, A.F. 1996: Heritability of salt sensitivity in black Americans. Hypertension 28(5): 854-858
Quirino, C.R.; Bergman, J.A.G. 1998: Heritability of scrotal circumference adjusted and unadjusted for body weight in Nellore bulls, using univariate and bivariate animal models. Theriogenology 49(7): 1389-1396,
Lazarov, V.; Mikhajlova, L.; Iliev, M.; Dimitrov, N. 1995: Heritability of selection traits in sheep of Karnobat fine wool breed. Zhivotnov"dni Nauki 32(3-4): 87-90
Lemon, W.C. 1993: Heritability of selectively advantageous foraging behaviour in a small passerine. Evolutionary Ecology 7(4): 421-428
Schmidt, H.D.; Glavce, C.; Sponholz, G. 1996: Heritability of some body measurements of newborns. Homo 46(2): 174-183
Videv, V."o S.; Kr"stanov, Z.; Fenerova, J. 1992: Heritability of some meat-productivity traits in brown-cattle bull-calves. Zhivotnov"dni Nauki 29(5-8): 23-28
Ral'ko, V.P. 1992: Heritability of the restoration of pollen fertility in wheat hybrids on Triticum timopheevi Zhuk. cytoplasm. Tsitologiya i Genetika 26(3): 16-21
Kempthorne, O. 1997: Heritability: Uses and abuses. Genetica 99(2-3): 109-112
Kaneda, M.; Aoyama, H.; Teramoto, S. 1995: Heritable oligodactyly occurring only in male rats. Teratology 51(2): 79-84
Amundson, S.A.; Fortunato, J.E.; Liber, H.L. 1992: Heritable alterations at the adenine phosphoribosyltransferase (APRT) locus in human lymphoblastoid cell lines. Mutation Research 284(2): 287-295
Vogel, E.W.; Barbin, A.; Nivard, M.J.; Stack, H.F.; Waters, M.D.; Lohman, P.H. 1998: Heritable and cancer risks of exposures to anticancer drugs: Inter-species comparisons of covalent deoxyribonucleic acid-binding agents. Mutation Research 400(1-2): 509-540
Krall, E.A.; Dawson-Hughes, B. 1993: Heritable and life-style determinants of bone mineral density. Journal of Bone and Mineral Research: the Official Journal of the American Society for Bone and Mineral Research 8(1): 1-9
Schievink, W.I.; Wijdicks, E.F.; Michels, V.V.; Vockley, J.; Godfrey, M. 1998: Heritable connective tissue disorders in cervical artery dissections: a prospective study. Neurology 50(4): 1166-1169
Mundlos, S.; Olsen, B.R. 1997: Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis. FASEB Journal 11(4): 227-233
Williams, C.J.; Jimenez, S.A. 1995: Heritable diseases of cartilage caused by mutations in collagen genes. Journal of Rheumatology. Supplement 43: 28-33
Mundlos, S.; Olsen, B.R. 1997: Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development-transcription factors and signaling pathways. FASEB Journal 11(2): 125-132
Muramoto, T.; DeArmond, S.J.; Scott, M.; Telling, G.C.; Cohen, F.E.; Prusiner, S.B. 1997: Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix. Nature medicine 3(7): 750-755
Tucker, L.B. 1992: Heritable disorders of connective tissue and disability and chronic disease in childhood. Current Opinion in Rheumatology 4(5): 731-740
Bailey, J.M.; Pillard, R.C.; Neale, M.C.; Agyei, Y. 1993: Heritable factors influence sexual orientation in women. Archives of General Psychiatry 50(3): 217-223
O'connor, S.; Morzorati, S.; Christian, J.C.; Li, T.K. 1994: Heritable features of the auditory oddball event-related potential: Peaks, latencies, morphology and topography. Electroencephalography and Clinical Neurophysiology 92(2): 115-125
Sugiyama, F.; Sagara, M.; Matsuda, Y.; Horiguchi, H.; Kamma, H.; Ogata, T.; Hatae, T.; Yagami, K.; Murakami, K.; Fukamizu, A. 1995: Heritable formation of neuroectodermal tumor in transgenic mice carrying the combined E1 region gene of adenovirus type 12 with the deregulated human renin promoter. Journal of Cellular Biochemistry 57(4): 691-700
Zhu, T.; Mogensen, H.L.; Smith, S.E. 1992: Heritable paternal cytoplasmic organelles in alfalfa sperm cells: ultrastructural reconstruction and quantitative cytology. European Journal of Cell Biology 59(1): 211-218
Yang, L.; Weis, J.H.; Eichwald, E.; Kolbert, C.P.; Persing, D.H.; Weis, J.J. 1994: Heritable susceptibility to severe Borrelia burgdorferi-induced arthritis is dominant and is associated with persistence of large numbers of spirochetes in tissues. Infection and Immunity 62(2): 492-500
Adler, I.D.; Filser, J.G.; Gassner, P.; Kessler, W.; Schöneich, J.; Schriever-Schwemmer, G. 1995: Heritable translocations induced by inhalation exposure of male mice to 1,3-butadiene. Mutation Research 347(3-4): 121-127
Shastry, B.S. 1994: Heritable trinucleotide repeats and neurological disorders. Experientia 50(11-12): 1099-1105
Hori, T.; Yamauchi, M.; Seki, N.; Tsuji, S.; Kondo, I. 1993: Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families. Clinical Genetics 43(1): 34-38
D.M.ester, L.; Beenaerts, N. 1993: Heritable variation in carotenoid content in Daphnia magna. Limnology and Oceanography 38(6): 1193-1199
Premoli, M.C.; Sella, G.; Berra, G.P. 1996: Heritable variation of sex ratio in a polychaete worm. Journal of Evolutionary Biology 9(6): 845-854
Rubin, H.; Yao, A.; Chow, M. 1995: Heritable, population-wide damage to cells as the driving force of neoplastic transformation. Proceedings of the National Academy of Sciences of the United States of America 92(11): 4843-4847
Williams, L.R.; Northcroft, K. 1992: Heritage land: The case for Fryent Country Park. London Naturalist 1992(71): 33-42
Beisel, W.R. 1995: Herman Award Lecture, 1995: infection-induced malnutrition--from cholera to cytokines. American Journal of Clinical Nutrition 62(4): 813-819
Hirsch, J. 1994: Herman Award Lecture, 1994: establishing a biologic basis for human obesity. American Journal of Clinical Nutrition 60(4): 615-618
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Meyding-Lamadé, U.; Haas, J.; Lamadé, W.; Stingele, K.; Kehm, R.; Fäth, A.; Heinrich, K.; Storch Hagenlocher, B.; Wildemann, B. 1998: Herpes simplex virus encephalitis: Long-term comparative study of viral load and the expression of immunologic nitric oxide synthase in mouse brain tissue. Neuroscience Letters 244(1): 9-12
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Brunetti, C.R.; Dingwell, K.S.; Wale, C.; Graham, F.L.; Johnson, D.C. 1998: Herpes simplex virus gD and virions accumulate in endosomes by mannose 6-phosphate-dependent and -independent mechanisms. Journal of Virology 72(4): 3330-3339
Nichol, P.F.; Chang, J.Y.; Johnson, E.M.; Olivo, P.D. 1996: Herpes simplex virus gene expression in neurons: viral DNA synthesis is a critical regulatory event in the branch point between the lytic and latent pathways. Journal of Virology 70(8): 5476-5486
Devi-Rao, G.B.; Aguilar, J.S.; Rice, M.K.; Garza, H.H.; Bloom, D.C.; Hill, J.M.; Wagner, E.K. 1997: Herpes simplex virus genome replication and transcription during induced reactivation in the rabbit eye. Journal of Virology 71(9): 7039-7047
Huemer, H.P.; Wang, Y.; Garred, P.; Koistinen, V.; Oppermann, S. 1993: Herpes simplex virus glycoprotein C: molecular mimicry of complement regulatory proteins by a viral protein. Immunology 79(4): 639-647
Brunetti, C.R.; Burke, R.L.; Kornfeld, S.; Gregory, W.; Masiarz, F.R.; Dingwell, K.S.; Johnson, D.C. 1994: Herpes simplex virus glycoprotein D acquires mannose 6-phosphate residues and binds to mannose 6-phosphate receptors. Journal of Biological Chemistry 269(25): 17067-17074
Krummenacher, C.; Nicola, A.V.; Whitbeck, J.C.; Lou, H.; Hou, W.; Lambris, J.D.; Geraghty, R.J.; Spear, P.G.; Cohen, G.H.; Eisenberg, R.J. 1998: Herpes simplex virus glycoprotein D can bind to poliovirus receptor-related protein 1 or herpesvirus entry mediator, two structurally unrelated mediators of virus entry. Journal of Virology 72(9): 7064-7074
Hutchinson, L.; Roop-Beauchamp, C.; Johnson, D.C. 1995: Herpes simplex virus glycoprotein K is known to influence fusion of infected cells, yet is not on the cell surface. Journal of Virology 69(7): 4556-4563
Hutchinson, L.; Johnson, D.C. 1995: Herpes simplex virus glycoprotein K promotes egress of virus particles. Journal of Virology 69(9): 5401-5413
Dingwell, K.S.; Brunetti, C.R.; Hendricks, R.L.; Tang, Q.; Tang, M.; Rainbow, A.J.; Johnson, D.C. 1994: Herpes simplex virus glycoproteins E and I facilitate cell-to-cell spread in vivo and across junctions of cultured cells. Journal of Virology 68(2): 834-845
Irie, H.; Koyama, H.; Kubo, H.; Fukuda, A.; Aita, K.; Koike, T.; Yoshimura, A.; Yoshida, T.; Shiga, J.; Hill, T. 1998: Herpes simplex virus hepatitis in macrophage-depleted mice: the role of massive, apoptotic cell death in pathogenesis. Journal of General Virology 79: 1225-1231
Johnson, L.G.; Saldana, L.R. 1994: Herpes simplex virus hepatitis in pregnancy. A case report. Journal of Reproductive Medicine 39(7): 544-546
Kaufman, B.; Gandhi, S.A.; Louie, E.; Rizzi, R.; Illei, P. 1997: Herpes simplex virus hepatitis: case report and review. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America 24(3): 334-338
Rice, S.A.; Long, M.C.; Lam, V.; Schaffer, P.A.; Spencer, C.A. 1995: Herpes simplex virus immediate-early protein ICP22 is required for viral modification of host RNA polymerase II and establishment of the normal viral transcription program. Journal of Virology 69(9): 5550-5559
Cheung, P.; Panning, B.; Smiley, J.R. 1997: Herpes simplex virus immediate-early proteins ICP0 and ICP4 activate the endogenous human alpha-globin gene in nonerythroid cells. Journal of Virology 71(3): 1784-1793
Tabery, H.M. 1994: Herpes simplex virus in chronic relapsing keratoconjunctivitis. Acta Ophthalmologica 72(2): 265-266
Sanders, V.J.; Waddell, A.E.; Felisan, S.L.; Li, X.; Conrad, A.J.; Tourtellotte, W.W. 1996: Herpes simplex virus in postmortem multiple sclerosis brain tissue. Archives of Neurology 53(2): 125-133
Cockerham, G.C.; Krafft, A.E.; McLean, I.W. 1997: Herpes simplex virus in primary graft failure. Archives of Ophthalmology 115(5): 586-589
Gieroba, Z.J.; Zhu, B.S.; Blessing, W.W.; Wesselingh, S.L. 1995: Herpes simplex virus induces Fos expression in rat brainstem neurons. Brain Research 675(1-2): 329-332
Riffault, S.; Eloranta, M.L.; Carrat, C.; Sandberg, K.; Charley, B.; Alm, G. 1996: Herpes simplex virus induces appearance of interferon-alpha/beta-producing cells and partially interferon-alpha/beta-dependent accumulation of leukocytes in murine regional lymph nodes. Journal of Interferon and Cytokine Research: the Official Journal of the International Society for Interferon and Cytokine Research 16(12): 1007-1014
Kulomaa, P.; Paavonen, J.; Lehtinen, M. 1992: Herpes simplex virus induces unscheduled DNA synthesis in virus-infected cervical cancer cell lines. Research in Virology 143(5): 351-359
Gruenheid, S.; Gatzke, L.; Meadows, H.; Tufaro, F. 1993: Herpes simplex virus infection and propagation in a mouse L cell mutant lacking heparan sulfate proteoglycans. Journal of Virology 67(1): 93-100
Bourdarias, B.; Perro, G.; Cutillas, M.; Castede, J.C.; Lafon, M.E.; Sanchez, R. 1996: Herpes simplex virus infection in burned patients: Epidemiology of 11 cases. Burns: Journal of the International Society for Burn Injuries 22(4): 287-290
Henken, D.B.; Martin, J.R. 1992: Herpes simplex virus infection induces a selective increase in the proportion of galanin-positive neurons in mouse sensory ganglia. Experimental Neurology 118(2): 195-203
Tong, P.; Mutasim, D.F. 1996: Herpes simplex virus infection masquerading as condyloma acuminata in a patient with HIV disease. British Journal of Dermatology 134(4): 797-800
Malouf, D.J.; Oates, R.K. 1995: Herpes simplex virus infections in the neonate. Journal of Paediatrics and Child Health 31(4): 332-335
Cinque, P.; Vago, L.; Marenzi, R.; Giudici, B.; Weber, T.; Corradini, R.; Ceresa, D.; Lazzarin, A.; Linde, A. 1998: Herpes simplex virus infections of the central nervous system in human immunodeficiency virus-infected patients: clinical management by polymerase chain reaction assay of cerebrospinal fluid. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America 27(2): 303-309
Whitley, R.J.; Lakeman, F. 1995: Herpes simplex virus infections of the central nervous system: Therapeutic and diagnostic considerations. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America 20(2): 414-420
Whitley, R.J. 1994: Herpes simplex virus infections of women and their offspring: implications for a developed society. Proceedings of the National Academy of Sciences of the United States of America 91(7): 2441-2447
Lacaille, V.G.; Androlewicz, M.J. 1998: Herpes simplex virus inhibitor ICP47 destabilizes the transporter associated with antigen processing (TAP) heterodimer. Journal of Biological Chemistry 273(28): 17386-17390
Hardy, W.R.; Sandri-Goldin, R.M. 1994: Herpes simplex virus inhibits host cell splicing, and regulatory protein ICP27 is required for this effect. Journal of Virology 68(12): 7790-7799
Hayward, A.R.; Read, G.S.; Cosyns, M. 1993: Herpes simplex virus interferes with monocyte accessory cell function. Journal of Immunology 150(1): 190-196
Hodge, W.G.; Margolis, T.P. 1997: Herpes simplex virus keratitis among patients who are positive or negative for human immunodeficiency virus: an epidemiologic study. Ophthalmology 104(1): 120-124
Nakajima, H.; Furutama, D.; Kimura, F.; Shinoda, K.; Ohsawa, N.; Nakagawa, T.; Shimizu, A.; Shoji, H. 1998: Herpes simplex virus myelitis: clinical manifestations and diagnosis by the polymerase chain reaction method. European Neurology 39(3): 163-167
Mitchell, W.J.; De Santo, R.J.; Zhang, S.D.; Odenwald, W.F.; Arnheiter, H. 1993: Herpes simplex virus pathogenesis in transgenic mice is altered by the homeodomain protein Hox 1.3. Journal of Virology 67(8): 4484-4491
Mikloska, Z.; Kesson, A.M.; Penfold, M.E.; Cunningham, A.L. 1996: Herpes simplex virus protein targets for CD4 and CD8 lymphocyte cytotoxicity in cultured epidermal keratinocytes treated with interferon-gamma. Journal of Infectious Diseases 173(1): 7-17
Smetana, Z.; Ben-Hur, E.; Mendelson, E.; Salzberg, S.; Wagner, P.; Malik, Z. 1998: Herpes simplex virus proteins are damaged following photodynamic inactivation with phthalocyanines. Journal of Photochemistry and Photobiology. B Biology 44(1): 77-83
Singh, J.; Wagner, E.K. 1995: Herpes simplex virus recombination vectors designed to allow insertion of modified promoters into transcriptionally "neutral" segments of the viral genome. Virus Genes 10(2): 127-136
Thomas, J.; Kanangat, S.; Rouse, B.T. 1998: Herpes simplex virus replication-induced expression of chemokines and proinflammatory cytokines in the eye: implications in herpetic stromal keratitis. Journal of Interferon and Cytokine Research: the Official Journal of the International Society for Interferon and Cytokine Research 18(9): 681-690
Bataille, D.; Epstein, A. 1994: Herpes simplex virus replicative concatemers contain L components in inverted orientation. Virology 203(2): 384-388
Krone, M.R.; Tabet, S.R.; Paradise, M.; Wald, A.; Corey, L.; Celum, C.L. 1998: Herpes simplex virus shedding among human immunodeficiency virus-negative men who have sex with men: site and frequency of shedding. Journal of Infectious Diseases 178(4): 978-982
Jacobson, J.G.; Ruffner, K.L.; Kosz-Vnenchak, M.; Hwang, C.B.; Wobbe, K.K.; Knipe, D.M.; Coen, D.M. 1993: Herpes simplex virus thymidine kinase and specific stages of latency in murine trigeminal ganglia. Journal of Virology 67(11): 6903-6908
Balazarini, J. 1996: Herpes simplex virus thymidine kinase gene-transfected tumor cells: Sensitivity to antiherpetic drugs. Nucleosides and Nucleotides 15(1-3): 821-831
Loimas, S.; Wahlfors, J.; Jänne, J. 1998: Herpes simplex virus thymidine kinase-green fluorescent protein fusion gene: new tool for gene transfer studies and gene therapy. Biotechniques 24(4): 614-618
Hamel, W.; Magnelli, L.; Chiarugi, V.P.; Israel, M.A. 1996: Herpes simplex virus thymidine kinase/ganciclovir-mediated apoptotic death of bystander cells. Cancer Research 56(12): 2697-2702
Yamamoto, S.; Suzuki, S.; Hoshino, A.; Akimoto, M.; Shimada, T. 1997: Herpes simplex virus thymidine kinase/ganciclovir-mediated killing of tumor cell induces tumor-specific cytotoxic T cells in mice. Cancer Gene Therapy 4(2): 91-96
Baras, L.; Farber, C.M.; Van Vooren, J.P.; Parent, D. 1994: Herpes simplex virus tracheitis in a patient with the acquired immunodeficiency syndrome. European Respiratory Journal 7(11): 2091-2093
Brown, C.R.; Nakamura, M.S.; Mosca, J.D.; Hayward, G.S.; Straus, S.E.; Perera, L.P. 1995: Herpes simplex virus trans-regulatory protein ICP27 stabilizes and binds to 3' ends of labile mRNA. Journal of Virology 69(11): 7187-7195
Berkowitz, C.; Moyal, M.; Rösen-Wolff, A.; Darai, G.; Becker, Y. 1994: Herpes simplex virus type 1 (HSV-1) UL56 gene is involved in viral intraperitoneal pathogenicity to immunocompetent mice. Archives of Virology 134(1-2): 73-83
Vojvodová, A.; Matis, J.; Kúdelová, M.; Rajcáni, J. 1997: Herpes simplex virus type 1 (HSV-1) strain HSZP host shutoff gene: Nucleotide sequence and comparison with HSV-1 strains differing in early shutoff of host protein synthesis. Virus Genes 15(2): 155-159
Argnani, R.; Focher, F.; Zucchini, S.; Verri, A.; Wright, G.E.; Spadari, S.; Manservigi, R. 1995: Herpes simplex virus type 1 (HSV-1) uracil-DNA glycosylase: functional expression in Escherichia coli, biochemical characterization, and selective inhibition by 6-(p-n-octylanilino)uracil. Virology 211(1): 307-311
Tengelsen, L.A.; Pederson, N.E.; Shaver, P.R.; Wathen, M.W.; Homa, F.L. 1993: Herpes simplex virus type 1 DNA cleavage and encapsidation require the product of the UL28 gene: isolation and characterization of two UL28 deletion mutants. Journal of Virology 67(6): 3470-3480
Mitchell, W.J.; Gressens, P.; Martin, J.R.; DeSanto, R. 1994: Herpes simplex virus type 1 DNA persistence, progressive disease and transgenic immediate early gene promoter activity in chronic corneal infections in mice. Journal of General Virology 75: 1201-1210
Kühn, F.J.; Knopf, C.W. 1996: Herpes simplex virus type 1 DNA polymerase. Mutational analysis of the 3'-5'-exonuclease domain. Journal of Biological Chemistry 271(46): 29245-29254
Devi-Rao, G.B.; Bloom, D.C.; Stevens, J.G.; Wagner, E.K. 1994: Herpes simplex virus type 1 DNA replication and gene expression during explant-induced reactivation of latently infected murine sensory ganglia. Journal of Virology 68(3): 1271-1282
Dutch, R.E.; Bianchi, V.; Lehman, I.R. 1995: Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences. Journal of Virology 69(5): 3084-3089
Boehmer, P.E.; Lehman, I.R. 1993: Herpes simplex virus type 1 ICP8: helix-destabilizing properties. Journal of Virology 67(2): 711-715
Zhang, Y.; McKnight, J.L. 1993: Herpes simplex virus type 1 UL46 and UL47 deletion mutants lack VP11 and VP12 or VP13 and VP14, respectively, and exhibit altered viral thymidine kinase expression. Journal of Virology 67(3): 1482-1492
Desai, P.; DeLuca, N.A.; Person, S. 1998: Herpes simplex virus type 1 VP26 is not essential for replication in cell culture but influences production of infectious virus in the nervous system of infected mice. Virology 247(1): 115-124
Martinez, R.; Sarisky, R.T.; Weber, P.C.; Weller, S.K. 1996: Herpes simplex virus type 1 alkaline nuclease is required for efficient processing of viral DNA replication intermediates. Journal of Virology 70(4): 2075-2085
Drescher, K.M.; Whittum-Hudson, J.A. 1996: Herpes simplex virus type 1 alters transcript levels of tumor necrosis factor-alpha and interleukin-6 in retinal glial cells. IOVS Investigative Ophthalmology and Visual Science 37(11): 2302-2312
Lee, W.C.; Fuller, A.O. 1993: Herpes simplex virus type 1 and pseudorabies virus bind to a common saturable receptor on Vero cells that is not heparan sulfate. Journal of Virology 67(9): 5088-5097
Person, S.; Laquerre, S.; Desai, P.; Hempel, J. 1993: Herpes simplex virus type 1 capsid protein, VP21, originates within the UL26 open reading frame. Journal of General Virology 74: 2269-2273
Yu, D.; Weller, S.K. 1998: Herpes simplex virus type 1 cleavage and packaging proteins UL15 and UL28 are associated with B but not C capsids during packaging. Journal of Virology 72(9): 7428-7439
Pyles, R.B.; Sawtell, N.M.; Thompson, R.L. 1992: Herpes simplex virus type 1 dUTPase mutants are attenuated for neurovirulence, neuroinvasiveness, and reactivation from latency. Journal of Virology 66(11): 6706-6713
Chrétien, F.; Bélec, L.; Hilton, D.A.; Flament-Saillour, M.; Guillon, F.; Wingertsmann, L.; Baudrimont, M.; de Truchis, P.; Keohane, C.; Vital, C.; Love, S.; Gray, F. 1996: Herpes simplex virus type 1 encephalitis in acquired immunodeficiency syndrome. Neuropathology and Applied Neurobiology 22(5): 394-404
Rajcáni, J.; Sabó, A.; Mucha, V.; Kostál, M.; Compel, P. 1995: Herpes simplex virus type 1 envelope subunit vaccine not only protects against lethal virus challenge, but also may restrict latency and virus reactivation. Acta Virologica 39(1): 37-49
Steiner, I.; Mador, N.; Reibstein, I.; Spivack, J.G.; Fraser, N.W. 1994: Herpes simplex virus type 1 gene expression and reactivation of latent infection in the central nervous system. Neuropathology and Applied Neurobiology 20(3): 253-260
Kuo, Y.C.; Liu, W.T.; Lin, C.Y. 1993: Herpes simplex virus type 1 genes in human mononuclear cells and affecting cell-mediated immunity. Journal of Medical Virology 41(2): 138-145
Laquerre, S.; Anderson, D.B.; Argnani, R.; Glorioso, J.C. 1998: Herpes simplex virus type 1 glycoprotein B requires a cysteine residue at position 633 for folding, processing, and incorporation into mature infectious virus particles. Journal of Virology 72(6): 4940-4949
Jayachandra, S.; Baghian, A.; Kousoulas, K.G. 1997: Herpes simplex virus type 1 glycoprotein K is not essential for infectious virus production in actively replicating cells but is required for efficient envelopment and translocation of infectious virions from the cytoplasm to the extracellular space. Journal of Virology 71(7): 5012-5024
Lubinski, J.M.; Wang, L.; Soulika, A.M.; Burger, R.; Wetsel, R.A.; Colten, H.; Cohen, G.H.; Eisenberg, R.J.; Lambris, J.D.; Friedman, H.M. 1998: Herpes simplex virus type 1 glycoprotein gC mediates immune evasion in vivo. Journal of Virology 72(10): 8257-8263
Mikloska, Z.; Cunningham, A.L. 1998: Herpes simplex virus type 1 glycoproteins gB, gC and gD are major targets for CD4 T-lymphocyte cytotoxicity in HLA-DR expressing human epidermal keratinocytes. Journal of General Virology 79: 353-361
Preston, C.M.; Rinaldi, A.; Nicholl, M.J. 1998: Herpes simplex virus type 1 immediate early gene expression is stimulated by inhibition of protein synthesis. Journal of General Virology 79: 117-124
Phelan, A.; Clements, J.B. 1997: Herpes simplex virus type 1 immediate early protein IE63 shuttles between nuclear compartments and the cytoplasm. Journal of General Virology 78: 3327-3331
Meredith, M.; Orr, A.; Everett, R. 1994: Herpes simplex virus type 1 immediate-early protein Vmw110 binds strongly and specifically to a 135-kDa cellular protein. Virology 200(2): 457-469
Itzhaki, R.F.; Lin, W.R.; Shang, D.; Wilcock, G.K.; Faragher, B.; Jamieson, G.A. 1997: Herpes simplex virus type 1 in brain and risk of Alzheimer's disease. Lancet 349(9047): 241-244
Ito, M.; Watanabe, M.; Kamiya, H.; Sakurai, M. 1997: Herpes simplex virus type 1 induces apoptosis in peripheral blood T lymphocytes. Journal of Infectious Diseases 175(5): 1220-1224
Nicosia, M.; Deshmane, S.L.; Zabolotny, J.M.; Valyi-Nagy, T.; Fraser, N.W. 1993: Herpes simplex virus type 1 latency-associated transcript (LAT) promoter deletion mutants can express a 2-kilobase transcript mapping to the LAT region. Journal of Virology 67(12): 7276-7283
Mador, N.; Goldenberg, D.; Cohen, O.; Panet, A.; Steiner, I. 1998: Herpes simplex virus type 1 latency-associated transcripts suppress viral replication and reduce immediate-early gene mRNA levels in a neuronal cell line. Journal of Virology 72(6): 5067-5075
Lamontagne, L.; Jolicoeur, P. 1994: Herpes simplex virus type 1 pathogenicity in mice expressed by lytic infection in pre-B and B cells. Clinical Immunology and Immunopathology 73(1): 38-44
Lukonis, C.J.; Burkham, J.; Weller, S.K. 1997: Herpes simplex virus type 1 prereplicative sites are a heterogeneous population: only a subset are likely to be precursors to replication compartments. Journal of Virology 71(6): 4771-4781
Deckman, I.C.; Hagen, M.; McCann, P.J. 1992: Herpes simplex virus type 1 protease expressed in Escherichia coli exhibits autoprocessing and specific cleavage of the ICP35 assembly protein. Journal of Virology 66(12): 7362-7367
Phelan, A.; Dunlop, J.; Clements, J.B. 1996: Herpes simplex virus type 1 protein IE63 affects the nuclear export of virus intron-containing transcripts. Journal of Virology 70(8): 5255-5265
Jerome, K.R.; Tait, J.F.; Koelle, D.M.; Corey, L. 1998: Herpes simplex virus type 1 renders infected cells resistant to cytotoxic T-lymphocyte-induced apoptosis. Journal of Virology 72(1): 436-441
Bataille, D.; Epstein, A.L. 1995: Herpes simplex virus type 1 replication and recombination. Biochimie 77(10): 787-795
Conner, J.; Furlong, J.; Murray, J.; Meighan, M.; Cross, A.; Marsden, H.; Clements, J.B. 1993: Herpes simplex virus type 1 ribonucleotide reductase large subunit: Regions of the protein essential for subunit interaction and dimerization. Biochemistry 32(49): 13673-13680
Stroop, W.G.; Banks, M.C. 1994: Herpes simplex virus type 1 strain KOS-63 does not cause acute or recurrent ocular disease and does not reactivate ganglionic latency in vivo. Acta Neuropathologica 87(1): 14-22
Elliott, G.; O'Hare, P. 1998: Herpes simplex virus type 1 tegument protein VP22 induces the stabilization and hyperacetylation of microtubules. Journal of Virology 72(8): 6448-6455
Laycock, K.A.; Lee, S.F.; Stulting, R.D.; Croen, K.D.; Ostrove, J.M.; Straus, S.E.; Pepose, J.S. 1993: Herpes simplex virus type 1 transcription is not detectable in quiescent human stromal keratitis by in situ hybridization. IOVS Investigative Ophthalmology and Visual Science 34(2): 285-292
Focher, F.; Verri, A.; Spadari, S.; Manservigi, R.; Gambino, J.; Wright, G.E. 1993: Herpes simplex virus type 1 uracil-DNA glycosylase: isolation and selective inhibition by novel uracil derivatives. Biochemical Journal 292: 883-889
Umene, K. 1993: Herpes simplex virus type 1 variant a sequence generated by recombination and breakage of the a sequence in defined regions, including the one involved in recombination. Journal of Virology 67(9): 5685-5691
Huard, J.; Goins, W.F.; Glorioso, J.C. 1995: Herpes simplex virus type 1 vector mediated gene transfer to muscle. Gene Therapy 2(6): 385-392
Trybala, E.; Svennerholm, B.; Bergström, T.; Olofsson, S.; Jeansson, S.; Goodman, J.L. 1993: Herpes simplex virus type 1-induced hemagglutination: glycoprotein C mediates virus binding to erythrocyte surface heparan sulfate. Journal of Virology 67(3): 1278-1285
Jensen, H.L.; Norrild, B. 1998: Herpes simplex virus type 1-infected human embryonic lung cells studied by optimized immunogold cryosection electron microscopy. Journal of Histochemistry and Cytochemistry: Official Journal of the Histochemistry Society 46(4): 487-496
Kanangat, S.; Thomas, J.; Gangappa, S.; Babu, J.S.; Rouse, B.T. 1996: Herpes simplex virus type 1-mediated up-regulation of IL-12 (p40) mRNA expression. Implications in immunopathogenesis and protection. Journal of Immunology 156(3): 1110-1116
Jensenius, M.; Myrvang, B.; Størvold, G.; Bucher, A.; Hellum, K.B.; Bruu, A.L. 1998: Herpes simplex virus type 2 DNA detected in cerebrospinal fluid of 9 patients with Mollaret's meningitis. Acta Neurologica Scandinavica 98(3): 209-212
Tomazin, R.; van Schoot, N.E.; Goldsmith, K.; Jugovic, P.; Sempé, P.; Früh, K.; Johnson, D.C. 1998: Herpes simplex virus type 2 ICP47 inhibits human TAP but not mouse TAP. Journal of Virology 72(3): 2560-2563
Golais, F.; Csabayová, M.; Lesko, J.; Bystrická, M.; Sabó, A. 1992: Herpes simplex virus type 2 and pseudorabies virus associated growth factors and their role in the latency in vitro. Acta Virologica 36(6): 505-515
Cunningham, A.L.; Lee, F.K.; Ho, D.W.; Field, P.R.; Law, C.L.; Packham, D.R.; McCrossin, I.D.; Sjögren-Jansson, E.; Jeansson, S.; Nahmias, A.J. 1993: Herpes simplex virus type 2 antibody in patients attending antenatal or STD clinics. Medical Journal of Australia 158(8): 525-528
Boggess, K.A.; Watts, D.H.; Hobson, A.C.; Ashley, R.L.; Brown, Z.A.; Corey, L. 1997: Herpes simplex virus type 2 detection by culture and polymerase chain reaction and relationship to genital symptoms and cervical antibody status during the third trimester of pregnancy. American Journal of Obstetrics and Gynecology 176(2): 443-451
Miller, R.F.; Fox, J.D.; Waite, J.C.; Severn, A.; Brink, N.S. 1995: Herpes simplex virus type 2 encephalitis and concomitant cytomegalovirus infection in a patient with AIDS: detection of virus-specific DNA in CSF by nested polymerase chain reaction. Genitourinary Medicine 71(4): 262-264
Da Rosa-Santos, O.L.; Gonçalves Da Silva, A.; Pereira, A.C. 1996: Herpes simplex virus type 2 in Brazil: Seroepidemiologic survey. International Journal of Dermatology 35(11): 794-796
Zierhut, M.; Hemady, R.; Zhao, T.Z.; Merchant, A.; Foster, C.S. 1994: Herpes simplex virus type 2 induced retinal necrosis in BALB/c mice. Acta Ophthalmologica 72(2): 211-217
Gerber, S.I.; Cromie, W.J. 1996: Herpes simplex virus type 2 infection associated with urinary retention in the absence of genital lesions. Journal of Pediatrics 128(2): 250-251
Weinberg, A.; Canto, C.L.; Pannuti, C.S.; Kwang, W.N.; Garcia, S.A.; Zugaib, M. 1993: Herpes simplex virus type 2 infection in pregnancy: asymptomatic viral excretion at delivery and seroepidemiologic survey of two socioeconomically distinct populations in São Paulo, Brazil. Revista do Instituto de Medicina Tropical de Sao Paulo 35(3): 285-290
Bassett, I.; Donovan, B.; Bodsworth, N.J.; Field, P.R.; Ho, D.W.; Jeansson, S.; Cunningham, A.L. 1994: Herpes simplex virus type 2 infection of heterosexual men attending a sexual health centre. Medical Journal of Australia 160(11): 697-700
Sieg, S.; Yildirim, Z.; Smith, D.; Kayagaki, N.; Yagita, H.; Huang, Y.; Kaplan, D. 1996: Herpes simplex virus type 2 inhibition of Fas ligand expression. Journal of Virology 70(12): 8747-8751
Schlesinger, Y.; Tebas, P.; Gaudreault-Keener, M.; Buller, R.S.; Storch, G.A. 1995: Herpes simplex virus type 2 meningitis in the absence of genital lesions: improved recognition with use of the polymerase chain reaction. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America 20(4): 842-848
Baskin, H.; Ellermann-Eriksen, S.; Lovmand, J.; Mogensen, S.C. 1997: Herpes simplex virus type 2 synergizes with interferon-gamma in the induction of nitric oxide production in mouse macrophages through autocrine secretion of tumour necrosis factor-alpha. Journal of General Virology 78: 195-203
Aurelian, L. 1998: Herpes simplex virus type 2: unique biological properties include neoplastic potential mediated by the PK domain of the large subunit of ribonucleotide reductase. Frontiers in Bioscience: a Journal and Virtual Library 3: D237-D249
Key, N.S.; Bach, R.R.; Vercellotti, G.M.; Moldow, C.F. 1993: Herpes simplex virus type I does not require productive infection to induce tissue factor in human umbilical vein endothelial cells. Laboratory Investigation; A Journal of Technical Methods and Pathology 68(6): 645-651
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