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Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history Sabbagh, Audrey; Langaney, André; Darlu, Pierre; Gérard, Nathalie; ... Poloni, Estella S. 2008
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Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31 Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E 2014
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War exposure, 5-HTTLPR genotype and lifetime risk of depression Artero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen 2011
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Viral genotype-specific role of PNPLA3, PPARG, MTTP, and IL28B in hepatitis C virus-associated steatosis Cai, Tao; Dufour, Jean-François Jacques; Muellhaupt, Beat; Gerlach, Tilman Joern; ... Bochud, Pierre-Yves 2011
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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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Variable-number tandem repeat analysis and multilocus sequence typing data confirm the epidemiological changes observed with Staphylococcus aureus strains isolated from bloodstream infections van der Mee-Marquet, Nathalie; Francois, Patrice; Domelier, Anne-Sophie; Arnault, Laurence; ... Quentin, Roland 2009
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Usefulness of postmortem biochemistry in forensic pathology: illustrative case reports Palmiere, Cristian; Lesta, Maria Del Mar; Sabatasso, Sara; Mangin, Patrice; ... Sporkert, Frank 2012
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Use of an automated multiple-locus, variable-number tandem repeat-based method for rapid and high-throughput genotyping of Staphylococcus aureus isolates Francois, Patrice; Huyghe, Antoine; Charbonnier, Yvan; Bento, Manuela; ... Schrenzel, Jacques 2005
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Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference Young, Alexandra L; Marinescu, Razvan V; Oxtoby, Neil P; Bocchetta, Martina; ... Alexander, Daniel C 2018
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Tuberculosis cluster in an immigrant community: case identification issues and a transcultural perspective Tardin, A.; Dominice Dao, Mélissa; Bescher Ninet, Béatrice Alice; Janssens, Jean-Paul 2009
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Trends and projections of hepatitis C virus epidemiology in Latin America Kershenobich, David; Razavi, Homie A; Sánchez-Avila, Juan Francisco; Bessone, Fernando; ... Silva, Marcelo 2011
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Treatment of hepatitis C in HCV mono-infected and in HIV-HCV co-infected patients: an open-labelled comparison study Gonvers, Jean-Jacques; Heim, Markus H.; Cavassini, Matthias; Mullhaupt, Beat; ... Oneta, Carl 2010
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Treatment of chronic hepatitis C genotype 1 with triple therapy comprising telaprevir or boceprevir Rubbia-Brandt, Laura 2012
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Transgenerational stability of the Arabidopsis epigenome is coordinated by CG methylation Mathieu, Olivier; Reinders, Jon; Caikovski, Marian; Smathajitt, Chotika; Paszkowski, Jerzy 2007
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TNFA -308G>A in two international population-based cohorts and risk of asthma Castro-Giner, F.; Kogevinas, M.; Mächler, M.; de Cid, R.; ... Probst-Hensch, Nicole M. 2008
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The vitamin D receptor gene bAt (CCA) haplotype impairs the response to pegylated-interferon/ribavirin-based therapy in chronic hepatitis C patients Baur, Katharina; Mertens, Joachim C; Schmitt, Johannes; Iwata, Rika; ... Rubbia-Brandt, Laura 2012
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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe 2013
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The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro Guipponi, Michel; Vuagniaux, Gregoire; Wattenhofer, Marie; Shibuya, Kazunori; ... Rossier, B. C. 2002
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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos 1999
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The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
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The molecular and physiological responses of Physcomitrella patens to ultraviolet-B radiation Wolf, Luise; Rizzini, Luca; Stracke, Ralf; Ulm, Roman; Rensing, Stefan A 2010
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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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The impact of fibrosis and steatosis on early viral kinetics in HCV genotype 1-infected patients treated with Peg-IFN-alfa-2a and ribavirin Guedjo, Hervé; Guedj, J; Negro, Francesco; Lagging, M; ... Neumann, A U 2012
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The homeostasis model assessment of the insulin resistance score is not predictive of a sustained virological response in chronic hepatitis C patients Fattovich, Giovanna; Covolo, Loredana; Pasino, Michela; Perini, Eleonora; ... Donato, Francesco 2011
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The forensic use of behavioral genetics in criminal proceedings: Case of the MAOA-L genotype McSwiggan, Sally; Elger, Bernice Simone; Appelbaum, Paul S 2017
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The effects of CYP2D6 and CYP3A activities on the pharmacokinetics of immediate release oxycodone Samer, Caroline Flora; Daali, Youssef; Wagner, M.; Hopfgartner, Gerard; ... Desmeules, Jules Alexandre 2010
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The effect of apolipoprotein polymorphism on brain in mild cognitive impairment: a voxel-based morphometric study Pennanen, Corina; Testa, Cristina; Boccardi, Marina; Laakso, Mikko P; ... Soininen, Hilkka 2006
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The Ccr4-Not complex independently controls both Msn2-dependent transcriptional activation--via a newly identified Glc7/Bud14 type I protein phosphatase module--and TFIID promoter distribution Lenssen, Eve; James, Nicole; Pedruzzi, Ivo; Dubouloz, Frédérique; ... De Virgilio, Claudio 2005
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The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics Powell, Joseph E; Henders, Anjali K; McRae, Allan F; Caracella, Anthony; ... Montgomery, Grant W 2012
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The architecture of gene regulatory variation across multiple human tissues: the MuTHER study Nica, Alexandra; Parts, Leopold; Glass, Daniel; Nisbet, James; ... Spector, Timothy D 2011
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The AmpliChip CYP450 test: cytochrome P450 2D6 genotype assessment and phenotype prediction Rebsamen, M C.; Desmeules, Jules Alexandre; Daali, Youssef; Chiappe, A.; ... Rossier, M. F. 2009
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Testis determination requires insulin receptor family function in mice Nef, Serge; Verma-Kurvari, Sunita; Merenmies, Jussi; Vassalli, Jean-Dominique; ... Parada, Luis F. 2003
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Telomere length is not predictive of dementia or MCI conversion in the oldest old Zekry Berger, Dina Selma; Herrmann, François; Irminger-Finger, Irmgard; Ortolan, Laura; ... Krause, Karl-Heinz 2010
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Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique 2008
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Subgroup analyses of maraviroc in previously treated R5 HIV-1 infection Fätkenheuer, Gerd; Nelson, Mark; Lazzarin, Adriano; Konourina, Irina; ... van der Ryst, Elna 2008
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Structure of Pseudomonas aeruginosa populations analyzed by single nucleotide polymorphism and pulsed-field gel electrophoresis genotyping Morales, Gracia; Wiehlmann, Lutz; Gudowius, Peter; Van Delden, Christian; ... Rojo, Fernando 2004
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Stochasticité : la troisième variable Giacobino, Ariane 2013
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Stereoselective block of hERG channel by (S)-methadone and QT interval prolongation in CYP2B6 slow metabolizers Eap, C B.; Crettol, S.; Rougier, J-S.; Schläpfer, J.; ... Abriel, H. 2007
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Stereoselective block of hERG channel by (S)-methadone and QT interval prolongation in CYP2B6 slow metabolizer: Evidence of a safer cardiac profile of (R)-methadone Eap, Chin Bin; Crettol, Séverine; Rougier, J.S.; Schlaepfer, J.; ... Abriel, Hugues 2008
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Steatosis in chronic hepatitis C: friend or foe? Negro, Francesco 2008
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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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Soluble and cell-bound forms of steel factor activity play distinct roles in melanocyte precursor dispersal and survival on the lateral neural crest migration pathway Wehrle-Haller, Bernhard; Weston, J A 1995
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Sex-biased genetic effects on gene regulation in humans Dima, Antigoni; Nica, Alexandra; Montgomery, Stephen; Stranger, Barbara E; ... Dermitzakis, Emmanouil 2012
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Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy Lange, Christian M; Kutalik, Zoltan; Morikawa, Kenichi; Bibert, Stéphanie; ... Bochud, Pierre-Yves 2012
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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage International Stem Cell Initiative 2011
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Role of hepatitis C virus genotype 3 in liver fibrosis progression--a systematic review and meta-analysis Probst, Aline Valeska; Dang, T; Bochud, Murielle; Egger, M; ... Bochud, Pierre-Yves 2011
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Role of Gag mutations in PI resistance in the Swiss HIV cohort study: bystanders or contributors? Kletenkov, K; Hoffmann, D; Böni, J; Yerly Ferrillo, Sabine; ... Klimkait, T 2017
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Risk factors for treatment failure in orthopedic device-related methicillin-resistant Staphylococcus aureus infection Ferry, T.; Uckay, Ilker; Vaudaux, Pierre; Francois, Patrice; ... Lew, Daniel Pablo 2010
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Rhinovirus genome variation during chronic upper and lower respiratory tract infections Tapparel, Caroline; Cordey, Samuel; Junier, Thomas; Farinelli, Laurent Luca Denis; ... Kaiser, Laurent 2011
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Revisiting human IL-12Rbeta1 deficiency: a survey of 141 patients from 30 countries de Beaucoudrey, Ludovic; Samarina, Arina; Bustamante, Jacinta; Cobat, Aurelie; ... Casanova, J. L. 2010
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