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A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination Blouin, Jean-Louis; Christie, D. H.; Gos, A.; Lynn, A.; ... Antonarakis, Stylianos 1995
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A yeast-based assay reveals a functional defect of the Q488H polymorphism in human Hsp90alpha MacLean, Morag J.; Llordella, Marc Martínez; Bot, Nathalie; Picard, Didier 2005
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Ambiguous nucleotide calls from population-based sequencing of HIV-1 are a marker for viral diversity and the age of infection Kouyos, Roger D; von Wyl, Viktor; Yerly, Sabine; Böni, Jürg; ... Günthard, Huldrych F 2011
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An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36 Radhakrishna, U.; Blouin, Jean-Louis; Solanki, J. V.; Dhoriani, G. M.; Antonarakis, Stylianos 1996
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Association between interleukin-1 receptor antagonist (IL-1ra) gene polymorphism and early and late-onset psoriasis Tarlow, J. K.; Cork, M. J.; Clay, F. E.; Schmitt-Egenolf, M.; ... Duff, G. V. 1997
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Association Between Oxytocin Receptor Genotype, Maternal Care, and Eating Disorder Behaviours in a Community Sample of Women Micali, Nadia; Crous-Bou, Marta; Treasure, Janet; Lawson, Elizabeth A 2017
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Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A 2011
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Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression Ritchie, Karen; Jaussent, Isabelle; Stewart, Robert; Dupuy, Anne-Marie; ... Malafosse, Alain 2009
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ATM alterations in childhood non-Hodgkin lymphoma Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal 2006
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ATM gene alterations in childhood acute lymphoblastic leukemias Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David; Sappino, Pascal 2003
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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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Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1 Beiraghi, Soraya; Nath, S. K.; Gaines, Matthew; Mandhyan, D. D.; ... Radhakrishna, Uppala 2007
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beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY. Horikawa, Yohko; Horikawa, Yukio; Cox, Nancy J.; Iwasaki, Naoko; ... Bell, Graeme I. 2000
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Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically Blouin, Jean-Louis; Binkert, F.; Antonarakis, Stylianos 1994
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Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension Guessous, Idris; Dobrinas, Maria; Kutalik, Zoltán; Pruijm, Menno; ... Bochud, Murielle 2012
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Can the pharmacogenetics of GST gene polymorphisms predict the dose of busulfan in pediatric hematopoietic stem cell transplantation? Ansari Djaberi, Marc Georges; Krajinovic, Maja 2009
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval Ducros, A; Nagy, T; Alamowitch, S; Nibbio, A; ... Tournier-Lasserve, E 1996
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Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. 1995
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Chronic graft dysfunction in renal transplant patients: potential role of plasminogen activator inhibitor type 1 Lahlou, Anis; Peraldi, Marie-Noelle; Thervet, Eric; Flahault, Antoine; ... Rondeau, Eric 2002
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Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3 Chen, H.; Rossier, Colette; Nakamura, Y.; Lynn, A.; ... Antonarakis, Stylianos 1997
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Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3 Chen, H.; Rossier, Colette; Lalioti, M. D.; Lynn, A.; ... Antonarakis, Stylianos 1996
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Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins Scott, Hamish Steele; Heino, M.; Peterson, P.; Mittaz, L.; ... Antonarakis, Stylianos 1998
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Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains Adams, D. J.; Dermitzakis, Emmanouil; Cox, Tony; Smith, James; ... Bradley, Allan 2005
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COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits Perroud, Nader Ali; Jaussent, I.; Guillaume, Sébastien; Bellivier, F.; ... Courtet, P. 2010
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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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Connexin37 protects against atherosclerosis by regulating monocyte adhesion Wong Christen, Cindy Wai Yin; Christen, Thomas; Roth, Isabelle; Chadjichristos, Christos; ... Kwak, Brenda 2006
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Core genome conservation of Staphylococcus haemolyticus limits sequence based population structure analysis Cavanagh, Jorunn Pauline; Klingenberg, Claus; Hanssen, Anne-Merethe; Fredheim, Elizabeth Aarag; ... Sollid, Johanna Ericson 2012
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De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer Hernandez, David; Francois, Patrice; Farinelli, Laurent Luca Denis; Osteras, Magne; Schrenzel, Jacques 2008
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Detection of polymorphisms in the human urokinase-type plasminogen activator gene Conne, Béatrice; Berczy, M.; Belin, Dominique 1997
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Differential contribution of PB1-F2 to the virulence of highly pathogenic H5N1 influenza A virus in mammalian and avian species Schmolke, Mirco; Manicassamy, Balaji; Pena, Lindomar; Sutton, Troy; ... García-Sastre, Adolfo 2011
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Dinucleotide repeat polymorphism within ERCC5 gene Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos 1994
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Disentangling human tolerance and resistance against HIV. Regoes, Roland R; McLaren, Paul J; Battegay, Manuel; Bernasconi, Enos; ... Fellay, Jacques 2014
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Drosophila melanogaster acetylcholinesterase gene. Structure, evolution and mutations Fournier, D.; Karch, François; Bride, J M.; Hall, Lucinda M. C.; ... Spierer, Pierre 1989
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Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia Rogan, P. K.; Close, P.; Blouin, Jean-Louis; Seip, J. R.; ... Antonarakis, Stylianos 1995
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis Naveed, Mohammed; Al-Ali, M. T.; Murthy, S. K.; Al-Hajali, Sarah; ... Radhakrishna, Uppala 2006
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Entre sel et gènes ou pharmacogénomique des antihypertenseurs Ernandez, Thomas; Pechere, Antoinette; Dayer, Pierre; Desmeules, Jules Alexandre 2006
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Eukaryotic aldehyde dehydrogenase (ALDH) genes: human polymorphisms, and recommended nomenclature based on divergent evolution and chromosomal mapping Vasiliou, Vasilis; Bairoch, Amos Marc; Tipton, Keith F; Nebert, Daniel W 1999
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Evaluation de l'efficacité biologique du clopidogrel: génotype ou phénotype? Fontana, Pierre; Bonvini, Robert; Roffi, Marco; Boehlen, Françoise; ... Reny, Jean-Luc 2010
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Evidence of horizontal gene transfer between human and animal commensal Escherichia coli strains identified by microarray Grasselli, Elena; Francois, Patrice; Gutacker, Michaela; Gettler, Brian; ... Piffaretti, Jean-Claude 2008
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Evolutionary comparison provides evidence for pathogenicity of RMRP mutations Bonafe, Luisa; Dermitzakis, Emmanouil; Unger, Sheila; Greenberg, C. R.; ... Reymond, Alexandre 2005
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Fibrinogen gene regulation Fish, Richard; Neerman Arbez, Marguerite 2012
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Fortuitous detection of uniparental isodisomy of chromosome 6 Bittencourt, M. C.; Morris, Michael Andréw; Chabod, J.; Gos, A.; ... Tiberghien, P. 1997
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Functional genetic variation of human miRNAs and phenotypic consequences Borel, Christelle; Antonarakis, Stylianos 2008
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Gap junction protein Cx37 interacts with endothelial nitric oxide synthase in endothelial cells Pfenniger, Anna; Derouette, Jean-Paul; Verma, Vandana; Lin, Xianming; ... Delmar, Mario 2010
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Gene-environment interactions of selected pharmacogenes in arterial hypertension Bochud, Murielle; Guessous, Idris 2012
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Genetic and environmental risk factors for oral anticoagulant overdose Verstuyft, C.; Robert, A.; Morin, S.; Loriot, Marie-Anne; ... Becquemont, L. 2003
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Genetic implication of a novel thiamine transporter in human hypertension International Consortium for Blood Pressure Genome-Wide Association Studies 2014
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Genetic polymorphism of CCR5 gene and HIV disease: the heterozygous (CCR5/delta ccr5) genotype is neither essential nor sufficient for protection against disease progression. Swiss HIV Cohort Morawetz, R. A.; Rizzardi, G. P.; Glauser, Dominique; Rutschmann, Olivier Thierry; ... Pantaleo, G. 1997
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Genome-wide, high-resolution DNA methylation profiling using bisulfite-mediated cytosine conversion Reinders, Jon; Delucinge Vivier, Céline; Theiler, Gregory; Chollet, Didier; ... Paszkowski, Jerzy 2008
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Glutathione S-transferase polymorphisms, passive smoking, obesity, and heart rate variability in nonsmokers Probst-Hensch, Nicole M.; Imboden, Medea; Felber Dietrich, Denise; Barthelemy, Jean-Claude; ... Schwartz, Joel 2008
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