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"Pseudo-Beijing": evidence for convergent evolution in the direct repeat region of Mycobacterium tuberculosis Fenner, Lukas; Malla, Bijaya; Bescher Ninet, Béatrice Alice; Dubuis, Olivier; ... Gagneux, Sebastien 2011
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A frequent hypofunctional IRAK2 variant is associated with reduced spontaneous hepatitis C virus clearance Wang, Hui; El Maadidi, Souhayla; Fischer, Janett; Grabski, Elena; ... Weber, Alexander N R 2015
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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Krüger, Rejko; Sharma, Manu 2011
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A low-fibronectin-binding mutant of Staphylococcus aureus 879R4S has Tn918 inserted into its single fnb gene Greene, C.; Vaudaux, Pierre; Francois, Patrice; Proctor, R. A.; ... Foster, T. J. 1996
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A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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A multidisciplinary study of patients with early-onset PD with and without parkin mutations Lohmann, E.; Thobois, S.; Lesage, S.; Broussolle, E.; ... Brice, A. 2009
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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite 2011
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A novel hepatitis C virus (HCV) subtype from Somalia and its classification into HCV clade 3 Abid, Karim; Quadri Defilippis, Rafael; Veuthey, Anne-Lise; Hadengue, Antoine; Negro, Francesco 2000
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A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke del Río-Espínola, Alberto; Fernández-Cadenas, Israel; Giralt, Dolors; Quiroga, Adoracion; ... Montaner, Joan 2012
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A shared HLA-DRB1 epitope in the DR beta first domain is associated with Vogt-Koyanagi-Harada syndrome in Indian patients Tiercy, Jean-Marie; Rathinam, Sivakumar R.; Gex-Fabry, Marianne; Baglivo, Edoardo 2010
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A systematic review of hepatitis C virus epidemiology in Asia, Australia and Egypt Sievert, William; Altraif, Ibrahim; Razavi, Homie A; Abdo, Ayman; ... Negro, Francesco 2011
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A systematic review of hepatitis C virus epidemiology in Europe, Canada and Israel Cornberg, Markus; Razavi, Homie A; Alberti, Alfredo; Bernasconi, Enos; ... Zeuzem, Stefan 2011
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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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Absence of resistance mutations in antiretroviral-naive patients treated with ritonavir-boosted saquinavir Ananworanich, Jintanat; Hirschel, Bernard; Sirivichayakul, Sunee; Ubolyam, Sasiwimol; ... Ruxrungtham, Kiat 2006
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Alpha cell-specific Men1 ablation triggers the transdifferentiation of glucagon-expressing cells and insulinoma development Lu, Jieli; Herrera, Pedro Luis; Carreira, Christine; Bonnavion, Remy; ... Zhang, C. X. 2010
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Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
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An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos 2001
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An in vivo pathway for disulfide bond isomerization in Escherichia coli Rietsch, A.; Belin, Dominique; Martin, N.; Beckwith, J. 1996
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Antimicrobial activity of ceftaroline against methicillin-resistant Staphylococcus aureus (MRSA) isolates collected in 2013-2014 at the Geneva University Hospitals Andrey, D O; Francois, Patrice; Manzano, Caroline Stéphanie; Bonetti, E J; ... Renzoni, Adriana Maria 2017
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Appearance of a novel measles G3 strain in multiple European countries within a two month period, 2010 Brown, KE; Mulders, MN; Freymuth, F; Santibanez, S; ... Featherstone, D 2011
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Are obesity risk genes associated with binge eating in adolescence? Micali, Nadia; Field, Alison E; Treasure, Janet L; Evans, David M 2015
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Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter gene Vincze, Ilona; Perroud, Nader; Buresi, Catherine; Baud, Patrick; ... Malafosse, Alain 2008
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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 adenosine receptor gene polymorphisms and in vivo adenosine A1 receptor binding in the human brain Hohoff, Christa; Garibotto, Valentina; Elmenhorst, David; Baffa, Anna; ... Bauer, Andreas 2014
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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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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study International Consortium for Blood Pressure Genome-Wide Association Studies 2011
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Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals Johnson, Andrew D; Newton-Cheh, Christopher; Chasman, Daniel I; Ehret, Georg Benedikt; ... Levy, Daniel 2011
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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
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Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis Dieudé, P; Guedj, M; Truchetet, Marie-Elise; Wipff, J; ... Allanore, Y 2011
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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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Autoinducer production and quorum-sensing dependent phenotypes of Pseudomonas aeruginosa vary according to isolation site during colonization of intubated patients Favre-Bonte, Sabine; Chamot, Eric; Kohler, Thilo; Romand, Jaques-André; Van Delden, Christian 2007
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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity Fujita, Eriko; Tanabe, Yuko; Imhof, Beat; Momoi, Mariko Y; Momoi, Takashi 2012
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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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Calnexin deficiency leads to dysmyelination Kraus, Allison; Groenendyk, Jody; Bedard, Karen; Baldwin, T. A.; ... Michalak, Marek 2010
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Candidate genes for temporal lobe epilepsy: a replication study Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain 2008
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Catechol-O-methyltransferase Val158Met polymorphism moderates anterior cingulate volume in posttraumatic stress disorder Schulz-Heik, R Jay; Schaer, Marie; Eliez, Stéphan; Hallmayer, Joachim F; ... Woodward, Steven H 2011
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Characteristics of multidrug-resistant Acinetobacter baumannii strains isolated in Geneva during colonization or infection Cherkaoui, Abdessalam; Emonet, Stéphane Paul; Renzi, Gesuele; Schrenzel, Jacques 2015
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Characteristics of patients with chronic hepatitis C who develop hepatocellular carcinoma Kuske, Lorenz; Mensen, Armand; Müllhaupt, Beat; Negro, Francesco; ... Dufour, Jean-François Jacques 2012
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Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms Lespinasse, James; Gimelli, Stefania; Bena, Frédérique; Antonarakis, Stylianos; ... Giacobino, Ariane 2009
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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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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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Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II) Wright, J Timothy; Morris, Clark; Clements, Suzanne E.; D'Souza, Rena; ... Zonana, Jonathan 2009
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Clinical follow-up of women infected with human papillomavirus-16, either alone or with other human papillomavirus types: identification of different risk groups Cottier, Olivier; Sahli, Roland; Mihaescu, Anca; De Grandi, Pierre; ... Gerber, Stefan 2009
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Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping Kibar, Z.; Dube, M. P.; Powell, J.; McCuaig, C.; ... Rouleau, G. A. 2000
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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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Combined expressional analysis, bioinformatics and targeted proteomics identify new potential therapeutic targets in glioblastoma stem cells Stangeland, Biljana; Mughal, Awais A; Grieg, Zanina; Sandberg, Cecilie Jonsgar; ... Langmoen, Iver A 2015
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Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 2009
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Common regulatory variation impacts gene expression in a cell type-dependent manner Dimas, Antigone S.; Deutsch, Samuel; Stranger, Barbara E.; Montgomery, Stephen; ... Antonarakis, Stylianos 2009
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