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Characterization of cell-to-cell signaling-deficient Pseudomonas aeruginosa strains colonizing intubated patients Denervaud, Valerie; TuQuoc, Patrick; Blanc, Dominique; Favre-Bonte, Sabine Adelaide Eugenie; ... Van Delden, Christian 2004
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Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
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Pax2 mutant mice display increased number and size of islets of Langerhans but no change in insulin and glucagon content Zaiko, Maia; Estreicher, Anne; Ritz-Laser, Beate; Herrera, Pedro Luis; ... Philippe, Jacques 2004
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Codeine intoxication associated with ultrarapid CYP2D6 metabolism Gasche, Yvan; Daali, Youssef; Fathi, Marc; Chiappe, Alberto; ... Desmeules, Jules Alexandre 2004
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Infrequent transmission of HIV-1 drug-resistant variants Yerly Ferrillo, Sabine; Jost, Stéphanie; Telenti, Amalio; Flepp, Markus; ... Perrin, Luc 2004
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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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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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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia Lewis, C. M.; Blouin, Jean-Louis; Antonarakis, Stylianos 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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Failures of 1 week on, 1 week off antiretroviral therapies in a randomized trial Ananworanich, Jintanat; Nuesch, Reto; Le Braz, Michelle; Chetchotisakd, Ploechan; ... Yerly Ferrillo, Sabine 2003
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Liver disease in pediatric patients with cystic fibrosis is associated with glutathione S-transferase P1 polymorphism Henrion-Caude, Alexandra; Flamant, Cyril; Roussey, Michel; Housset, Chantal; ... Clement, Annick 2002
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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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Kjellin's syndrome: fundus autofluorescence, angiographic, and electrophysiologic findings Frisch, Inez B; Haag, Peter; Steffen, Heimo; Weber, Bernhard H F; Holz, Frank G 2002
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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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Primary immunodeficiency mutation databases Vihinen, M.; Arredondo-Vega, F. X.; Casanova, J. L.; Etzioni, A.; ... Smith, C. I. 2001
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A worldwide analysis of AG molecular diversity inferred from serology Sanchez-Mazas, Alicia; Bütler-Brunner, E.; Bütler, R.; Calderón, R.; ... Langaney, André 2001
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Donor- and ligand-dependent differences in C-C chemokine receptor 5 reexpression Sabbe, Rebecca; Picchio, Gastón R; Pastore, Cristina; Chaloin, Olivier; ... Mosier, Donald E 2001
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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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Fibrinogen gene mutations accounting for congenital afibrinogenemia Neerman Arbez, Marguerite 2001
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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness Masmoudi, S.; Antonarakis, Stylianos; Schwede, T.; Ghorbel, A. M.; ... Guipponi, Michel 2001
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