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HMOX1 and GST variants modify attenuation of FEF25-75% decline due to PM10 reduction Curjuric, I.; Imboden, M.; Schindler, C.; Downs, S. H.; ... Probst-Hensch, N. M. 2010
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Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies Mefford, Heather C.; Muhle, Hiltrud; Ostertag, Philipp; von Spiczak, S.; ... Eichler, E. E. 2010
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Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A' Vorjohann, Silja; Fish, Richard; Biron-Andreani, Christine; Nagaswami, Chandrasekaran; ... Neerman Arbez, Marguerite 2010
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A map of open chromatin in human pancreatic islets Gaulton, Kyle J.; Nammo, Takao; Pasquali, Lorenzo; Simon, Jeremy M.; ... Ferrer, Jorge 2010
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Type 2 diabetes susceptibility gene expression in normal or diabetic sorted human alpha and beta cells: correlations with age or BMI of islet donors Kirkpatrick, Clare; Marchetti, Piero; Purrello, Francesco; Piro, Salvatore; ... Wollheim, Claes 2010
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The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma Gimelli, Stefania; Beri, Silvana; Drabkin, Harry A.; Gambini, Claudio; ... Gimelli, Giorgio 2009
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Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A Cartoni, Romain; Martinou, Jean-Claude 2009
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CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD. Scholl, Hendrik P N; Fleckenstein, Monika; Fritsche, Lars G; Schmitz-Valckenberg, Steffen; ... Weber, Bernhard H F 2009
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Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration Michaud, Katarzyna; Fellmann, Florence; Abriel, Hugues; Beckmann, Jacques S.; ... Elger, Bernice Simone 2009
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Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior Guipponi, Michel; Deutsch, Samuel; Kohler, Karine; Perroud, Nader; ... Malafosse, Alain 2009
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Genetics. Life after GWA studies Dermitzakis, Emmanouil; Clark, A. G. 2009
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H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers Canu, Elisa; Boccardi, Marina; Ghidoni, Roberta; Benussi, Luisa; ... Frisoni, Giovanni 2009
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Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection Lagiou, Pagona; Georgila, Christina; Minaki, Ploumitsa; Ahrens, Wolfgang; ... Brennan, Paul J. 2009
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In vitro whole-genome analysis identifies a susceptibility locus for HIV-1 Loeuillet, Corinne; Deutsch, Samuel; Ciuffi, Angela; Robyr, Daniel; ... Telenti, Amalio 2008
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CNVs and genetic medicine (excitement and consequences of a rediscovery) Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos 2008
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Chronic active gastritis in X-linked lymphoproliferative disease Rougemont, Anne-Laure; Fournet, Jean-Christophe; Martin, Steven R.; de Saint-Basile, Geneviève; ... Le Deist, Françoise 2008
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Multiple ADH genes are associated with upper aerodigestive cancers Hashibe, Mia; Benhamou, Simone; Bouchardy Magnin, Christine 2008
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Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers Danoy, Patrick; Michiels, Stefan; Dessen, Philippe; Pignat, Cécile; ... Benhamou, Simone 2008
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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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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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