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A conserved phenylalanine of motif IV in superfamily 2 helicases is required for cooperative, ATP-dependent binding of RNA substrates in DEAD-box proteins Banroques, Josette; Cordin, Olivier; Doere, Monique; Linder, Patrick; Tanner, Kyle 2008
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A GAL4-HP1 fusion protein targeted near heterochromatin promotes gene silencing Seum, Carole; Spierer, Anne; Delattre, Marion; Pauli, Daniel; Spierer, Pierre 2000
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A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. Lane, Jérôme; Boehlen, Françoise 2013
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A genomic perspective on a new bacterial genus and species from the Alcaligenaceae family, Basilea psittacipulmonis Whiteson, Katrine L; Hernandez, David; Lazarevic, Vladimir; Gaia, Nadia; ... Schrenzel, Jacques 2014
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A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24 de Mollerat, X. J.; Gurrieri, Fiorella; Morgan, C. T.; Sangiorgi, Eugenio; ... Schwartz, C. E. 2003
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A multi-SNP locus-association method reveals a substantial fraction of the missing heritability Ehret, Georg Benedikt; Lamparter, David; Hoggart, Clive J.; Whittaker, John C.; ... Kutalik, Zoltán 2012
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A new gene in Drosophila melanogaster, Ravus, the phantom of the modifier of position-effect variegation Su(var)3-7 Delattre, Marion; Spierer, Anne; Hulo, Nicolas; Spierer, Pierre 2002
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A new genetic selection identifies essential residues in SecG, a component of the Escherichia coli protein export machinery Bost, S.; Belin, Dominique 1995
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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 point mutant of GAP-43 induces enhanced short-term and long-term hippocampal plasticity Hulo, S.; Alberi, Stefano; Laux, T.; Muller, Dominique; Caroni, P. 2002
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A rabbit Ig lambda L chain C region gene encoding C21 allotopes Duvoisin, R. M.; Hayzer, D. J.; Belin, Dominique; Jaton, J. C. 1988
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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Ferreiro-girani, Ana; Monnier, Nicole; Romero, Norma B; Leroy, Jean-Paul; ... Guicheney, Pascale 2002
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A short amino-terminal part of Arabidopsis phytochrome A induces constitutive photomorphogenic response Viczián, András; Ádám, Éva; Wolf, Iris; Bindics, János; ... Nagy, Ferenc 2012
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A single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomas Nikolaev, Sergey Igorievich; Sotiriou, Sotirios K; Pateras, Ioannis S; Santoni, Federico; ... Halazonetis, Thanos 2012
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A systematic survey of loss-of-function variants in human protein-coding genes MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
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A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein Breguet, Georges; Bütler, R.; Bütler-Brunner, E.; Sanchez-Mazas, Alicia 1990
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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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Accuracy of two-dimensional electrophoresis for target discovery in human colorectal cancer Ott, Vincent Olivier; Guenther, K; Steinert, R; Tortola, S; ... Reymond, M A 2001
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Acquired and reversible Pelger-Huët anomaly of polymorphonuclear neutrophils in three transplant patients receiving mycophenolate mofetil therapy Asmis, Lars; Hadaya, Karine; Majno, Pietro; Toso, Christian; ... Starobinski, Michel 2003
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Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria Dubois, Bruno; Feldman, Howard H; Jacova, Claudia; Hampel, Harald; ... Cummings, Jeffrey L 2014
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