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 TitleAuthors / EditorsDate
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The Yaa gene model of systemic lupus erythematosus Izui, Shozo; Iwamoto, Masahiro; Fossati-Jimack, Liliane; Merino, Ramon; ... Ibnou-Zekri, Nabila 1995
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Schizophrenia and chromosomal deletions within 22q11.2 Lindsay, E. A.; Morris, Michael Andréw; Gos, A.; Nestadt, G.; ... Pulver, A. E. 1995
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The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L. 1996
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Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation Hutter, Pierre; Couturier, A.; Scott, R. J.; Alday, P.; ... Buerstedde, J. M. 1996
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Control of multiple autoantibodies linked with a lupus nephritis susceptibility locus in New Zealand black mice Vyse, T. J.; Rozzo, S. J.; Drake, C. G.; Izui, Shozo; Kotzin, B. L. 1997
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Role of the major histocompatibility complex class II Ea gene in lupus susceptibility in mice Ibnou-Zekri, Nabila; Iwamoto, Masahiro; Fossati-Jimack, Liliane; McConahey, P. J.; Izui, Shozo 1997
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Contributions of Ea(z) and Eb(z) MHC genes to lupus susceptibility in New Zealand mice Vyse, T. J.; Rozzo, S. J.; Drake, C. G.; Appel, V. B.; ... Kotzin, B. L. 1998
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Identification of HLA-DR and -DQ alleles conferring susceptibility to pollen allergy and pollen associated food allergy Boehncke, Wolf-Henning; Loeliger, C.; Kuehnl, P.; Kalbacher, H.; ... Gall, H. 1998
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Polymorphisms in the Cd22 gene of inbred mouse strains Lajaunias, Frédéric; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Chicheportiche, Yves; ... Izui, Shozo 1999
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Analysis of MHC class II genes in the susceptibility to lupus in New Zealand mice Rozzo, S. J.; Vyse, T. J.; David, C. S.; Palmer, E.; ... Kotzin, B. L. 1999
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Genetic control of glycoprotein 70 autoantigen production and its influence on immune complex levels and nephritis in murine lupus Tucker, R. M.; Vyse, T. J.; Rozzo, S. J.; Roark, C. L.; ... Kotzin, B. L. 2000
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Genes predisposing to autoimmunity augment constitutive major histocompatibility complex class II-associated presentation of the self-antigen IgG2a in vivo Bartnes, K.; Li, X.; Iwamoto, Masahiro; Izui, Shozo; Hannestad, K. 2000
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Enhanced susceptibility to lupus contributed from the nonautoimmune C57BL/10, but not C57BL/6, genome Rozzo, S. J.; Vyse, T. J.; Menze, K.; Izui, Shozo; Kotzin, B. L. 2000
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Lessons from BXSB and related mouse models Izui, Shozo; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Iwamoto, Masahiro 2000
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Primary care physicians' knowledge and attitudes towards genetic testing for breast-ovarian cancer predisposition Escher, Monica; Sappino, Pascal 2000
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Autoantigen glycoprotein 70 expression is regulated by a single locus, which acts as a checkpoint for pathogenic anti-glycoprotein 70 autoantibody production and hence for the corresponding development of severe nephritis, in lupus-prone PXSB mice Haywood, M. E.; Vyse, T. J.; McDermott, Aileen; Thompson, E. M.; ... Morley, B. J. 2001
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Overexpression of plasminogen activator inhibitor type 2 in basal keratinocytes enhances papilloma formation in transgenic mice Zhou, Hong-Ming; Bolon, Isabelle; Nichols, Anthony; Wohlwend, Annelise Isabelle; Vassalli, Jean-Dominique 2001
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Klinik, Diagnose und Behandlung entzündlicher Herzkrankheiten im Kindesalter Jaeggi, Edgard; Suter, Susanne 2001
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In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis Michaud, Joelle; Wu, Feng; Osato, Motomi; Cottles, G. M.; ... Scott, Hamish Steele 2002
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The Sgp3 locus on mouse chromosome 13 regulates nephritogenic gp70 autoantigen expression and predisposes to autoimmunity Laporte, Catherine; Ballester, Benoit; Mary, Charles; Izui, Shozo; Reininger, Luc 2003
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Arterial smooth muscle cell heterogeneity: implications for atherosclerosis and restenosis development Hao, Hiroyuki; Gabbiani, Giulio; Bochaton-Piallat, Marie-Luce 2003
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Geographic patterns of functional categories of HLA-DRB1 alleles: a new approach to analyse associations between HLA-DRB1 and disease Gibert, M.; Sanchez-Mazas, Alicia 2003
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Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers Gold, Gabriel; Blouin, Jean-Louis; Herrmann, François; Michon, Agnès; ... Antonarakis, Stylianos 2003
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Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw 2003
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A novel locus regulates both retroviral glycoprotein 70 and anti-glycoprotein 70 antibody production in New Zealand mice when crossed with BALB/c Rigby, R. J.; Rozzo, S. J.; Gill, Herpreet; Fernandez-Hart, Timothy; ... Vyse, T. J. 2004
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Resistance to cerebral ischemic injury in UCP2 knockout mice: evidence for a role of UCP2 as a regulator of mitochondrial glutathione levels De Bilbao, Fabienne; Arsenijevic, Denis; Vallet, Philippe; Hjelle, O. P.; ... Giannakopoulos, Panteleimon 2004
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APOE and modulation of Alzheimer's and frontotemporal dementia Boccardi, Marina; Sabattoli, F; Testa, C; Beltramello, A; ... Frisoni, Giovanni 2004
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Clinical classification of pulmonary hypertension Simonneau, Gerald; Galiè, Nazzareno; Rubin, Lewis J; Langleben, David; ... Fishman, Alfred 2004
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Lymphoid enhancer factor-1 links two hereditary leukemia syndromes through core-binding factor alpha regulation of ELA2 Li, Feng-Qian; Person, Richard E; Takemaru, Ken-Ichi; Williams, Kayleen; ... Horwitz, Marshall 2004
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ATM gene and lymphoid malignancies Gumy Pause, Fabienne; Wacker, Pierre; Sappino, Pascal 2004
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No association between DUP25 and anxiety disorders Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie 2004
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Differential role of three major New Zealand Black-derived loci linked with Yaa-induced murine lupus nephritis Kikuchi, Shuichi; Fossati-Jimack, Liliane; Moll, Thomas; Amano, Hirofumi; ... Izui, Shozo 2005
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LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes Mehenni, Hamid; Lin-Marq, Nathalie; Buchet-Poyau, Karine; Reymond, Alexandre; ... Antonarakis, Stylianos 2005
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Double frameshift mutations in APC and MSH2 in the same individual Soravia, Claudio; De Lozier, Celia; Dobbie, Zuzana; Berthod, Claudine; ... Hutter, Pierre 2005
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Does chasing selected 'Fox' to the nucleus prevent diabetes? Wang, Haiyan; Wollheim, Claes 2005
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Attitudes of future lawyers and psychologists to the use of genetic testing for criminal behavior Elger, Bernice Simone 2005
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L'apport de la génétique moléculaire en cardiologie clinique : l'exemple de la cardiomyopathie hypertrophique Fokstuen, Siv; Blouin, Jean-Louis; Lyle, Robert; Lerch, René; ... Sigwart, Ulrich 2005
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LRP5 gene polymorphisms and idiopathic osteoporosis in men Ferrari, Serge Livio; Deutsch, Samuel; Baudoin, C.; Cohen-Solal, M.; ... de Vernejoul, M. C. 2005
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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Gothelf, Doron; Eliez, Stéphan; Thompson, Tracy; Hinard, Christine; ... Reiss, A. L. 2005
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Genetic susceptibility to polyI:C-induced IFNalpha/beta-dependent accelerated disease in lupus-prone mice Jorgensen, T. N.; Thurman, J.; Izui, Shozo; Falta, M. T.; ... Kotzin, B. L. 2006
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Double frameshift mutations in APC and MSH2 in the same individual Soravia, Claudio; DeLozier, Celia; Dobbie, Zuzana; Berthod, Claudine Rey; ... Hutter, Pierre 2006
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No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome Glaser, Bronwyn; Debbané, Martin; Hinard, Christine; Morris, Michael Andréw; ... Eliez, Stéphan 2006
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ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, D R; Sappino, Pascal 2006
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BXSB/long-lived is a recombinant inbred strain containing powerful disease suppressor loci Haywood, M. E.; Gabriel, Luisa; Rose, S. J.; Rogers, N. J.; ... Morley, B. J. 2007
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Estrogen receptor alpha is a major contributor to estrogen-mediated fetal testis dysgenesis and cryptorchidism Cederroth, Christopher; Schaad, Olivier; Descombes, Patrick; Chambon, Pierre; ... Nef, Serge 2007
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Transcriptional profiling of type 1 diabetes genes on chromosome 21 in a rat beta-cell line and human pancreatic islets Bergholdt, R; Karlsen, A E; Hagedorn, P H; Aalund, M; ... Pociot, F 2007
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Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction? Wong Christen, Cindy Wai Yin; Christen, Thomas; Pfenniger, Anna; James, Richard William; Kwak, Brenda 2007
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Gene duplication: a drive for phenotypic diversity and cause of human disease Conrad, Bernard; Antonarakis, Stylianos 2007
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Connexin37: a potential modifier gene of inflammatory disease Chanson, Marc; Kwak, Brenda 2007
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NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects Lu, Weining; Quintero-Rivera, Fabiola; Fan, Yanli; Alkuraya, Fowzan S; ... Maas, Richard L 2007
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