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Frailty syndrome: a transitional state in a dynamic process Lang, Pierre Olivier; Michel, Jean-Pierre; Zekry Berger, Dina Selma 2009
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Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome Green, Tamar; Gothelf, Doron; Glaser, Bronwyn; Debbané, Martin; ... Eliez, Stéphan 2009
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Phytochemicals as modulators of neoplastic phenotypes Ding, Heidrun; Tauzin, Sébastien; Hoessli, Daniel 2009
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Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 2009
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Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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Cooperation and virulence of clinical Pseudomonas aeruginosa populations Kohler, Thilo; Buckling, Angus; Van Delden, Christian 2009
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Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotype Hubert, F. X.; Kinkel, S. A.; Crewther, P. E.; Cannon, P. Z.; ... Scott, Hamish Steele 2009
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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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Deletion of glutamate dehydrogenase in beta-cells abolishes part of the insulin secretory response not required for glucose homeostasis Carobbio, Stefania; Frigerio, Francesca; Rubi, Blanca; Vetterli, Laurene; ... Maechler, Pierre 2009
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Genetics. Life after GWA studies Dermitzakis, Emmanouil; Clark, A. G. 2009
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Genetic variation of regulatory systems Dimas, A. S.; Dermitzakis, Emmanouil 2009
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Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function Undas, Anetta; Zdziarska, Joanna; Iwaniec, Teresa; Stepien, Ewa; ... Neerman Arbez, Marguerite 2009
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Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation Zdziarska, Joanna; Undas, Anetta; Basa, Joanna; Iwaniec, Teresa; ... Neerman Arbez, Marguerite 2009
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Genome-wide association study of blood pressure and hypertension Ehret, Georg Benedikt 2009
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Neuropeptide Y knockout mice reveal a central role of NPY in the coordination of bone mass to body weight Baldock, Paul A.; Lee, Nicola J.; Driessler, Frank; Lin, Shu; ... Herzog, Herbert 2009
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Genomic analysis of an emerging multiresistant Staphylococcus aureus strain rapidly spreading in cystic fibrosis patients revealed the presence of an antibiotic inducible bacteriophage Rolain, Jean-Marc; Francois, Patrice; Hernandez, David; Bittar, Fadi; ... Raoult, Didier 2009
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Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Ehret, Georg Benedikt; O'Connor, Ashley A.; Weder, Alan; Cooper, Richard S.; Chakravarti, Aravinda 2009
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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Ganesh, Santhi K. 2009
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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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Endocytic accessory proteins are functionally distinguished by their differential effects on the maturation of clathrin-coated pits Mettlen, Marcel; Stoeber, Miriam Carolin; Loerke, Dinah; Antonescu, Costin N; ... Schmid, Sandra L 2009
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