Show items per page
Elements: 304
Page 1 on 7
 TitleAuthors / EditorsDate
add to browser selection
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
add to browser selection
A GAL4-HP1 fusion protein targeted near heterochromatin promotes gene silencing Seum, Carole; Spierer, Anne; Delattre, Marion; Pauli, Daniel; Spierer, Pierre 2000
add to browser selection
A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. Lane, Jérôme; Boehlen, Françoise 2013
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
A new genetic selection identifies essential residues in SecG, a component of the Escherichia coli protein export machinery Bost, S.; Belin, Dominique 1995
add to browser selection
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
add to browser selection
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
add to browser selection
A rabbit Ig lambda L chain C region gene encoding C21 allotopes Duvoisin, R. M.; Hayzer, D. J.; Belin, Dominique; Jaton, J. C. 1988
add to browser selection
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
add to browser selection
A short amino-terminal part of Arabidopsis phytochrome A induces constitutive photomorphogenic response Viczián, András; Ádám, Éva; Wolf, Iris; Bindics, János; ... Nagy, Ferenc 2012
add to browser selection
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
add to browser selection
A systematic survey of loss-of-function variants in human protein-coding genes MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
Altered composition and secretion of lysosome-derived compartments in Dictyostelium AP-3 mutant cells Charette, Steve J.; Cosson, Pierre 2008
add to browser selection
Aluminum hydroxide adjuvant induces macrophage differentiation towards a specialized antigen-presenting cell type Rimaniol, Anne-Cécile; Gras, Gabriel; Verdier, François; Capel, Francis; ... Dormont, Dominique 2004
add to browser selection
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
add to browser selection
An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36 Radhakrishna, U.; Blouin, Jean-Louis; Solanki, J. V.; Dhoriani, G. M.; Antonarakis, Stylianos 1996
add to browser selection
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola 2015
add to browser selection
Analysis of HIV-1- and CMV-specific memory CD4 T-cell responses during primary and chronic infection Harari, Alexandre; Rizzardi, G. P.; Ellefsen, Kim; Ciuffreda, Donatella; ... Pantaleo, Giuseppe 2002
add to browser selection
Arterial smooth muscle cell heterogeneity: implications for atherosclerosis and restenosis development Hao, Hiroyuki; Gabbiani, Giulio; Bochaton-Piallat, Marie-Luce 2003
add to browser selection
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis 2003
add to browser selection
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
add to browser selection
ATAB2 is a novel factor in the signalling pathway of light-controlled synthesis of photosystem proteins Barneche, Frédy; Winter, Veronika; Crèvecoeur, Michèle; Rochaix, Jean-David 2006
add to browser selection
ATM gene and lymphoid malignancies Gumy Pause, Fabienne; Wacker, Pierre; Sappino, Pascal 2004
add to browser selection
Autoantibodies to fibroblasts induce a proadhesive and proinflammatory fibroblast phenotype in patients with systemic sclerosis Chizzolini, Carlo; Raschi, Elena; Rezzonico, Roger Michel; Testoni, Cinzia; ... Meroni, Pier Luigi 2002
add to browser selection
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
add to browser selection
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia Bartoloni, Lucia; Blouin, Jean-Louis; Maiti, A. K.; Sainsbury, A.; ... Antonarakis, Stylianos 2001
add to browser selection
Beta Cell Hubs Dictate Pancreatic Islet Responses to Glucose Johnston, Natalie R; Mitchell, Ryan K; Haythorne, Elizabeth; Pessoa, Maria Paiva; ... Hodson, David J 2016
add to browser selection
Beta-cell-targeted expression of a dominant-negative hepatocyte nuclear factor-1 alpha induces a maturity-onset diabetes of the young (MODY)3-like phenotype in transgenic mice Hagenfeldt-Johansson, K. A.; Herrera, Pedro Luis; Wang, Haiyan; Gjinovci, A.; ... Wollheim, Claes 2001
add to browser selection
Biased allelic expression in human primary fibroblast single cells Borel, Christelle; Ferreira Marinheiro, Pedro; Santoni, Federico; Delaneau, Olivier; ... Antonarakis, Stylianos 2015
add to browser selection
Biological responses in stented arteries Chaabane, Chiraz; Otsuka, Fumiyuki; Virmani, Renu; Bochaton-Piallat, Marie-Luce 2013
add to browser selection
Both transmembrane domains of SecG contribute to signal sequence recognition by the Escherichia coli protein export machinery Bost, S.; Silva, Filo; Rudaz, C.; Belin, Dominique 2000
add to browser selection
Calmodulin expression distinguishes the smooth muscle cell population of human carotid plaque Coen, Matteo; Marchetti, Giovanna; Palagi, Patricia M; Zerbinati, Carlotta; ... Bochaton-Piallat, Marie-Luce 2013
add to browser selection
Calreticulin is essential for cardiac development Mesaeli, N.; Nakamura, K.; Zvaritch, E.; Dickie, P.; ... Michalak, Marek 1999
add to browser selection
Calreticulin reveals a critical Ca(2+) checkpoint in cardiac myofibrillogenesis Li, Jian; Puceat, Michel; Perez-Terzic, Carmen; Mery, Annabelle; ... Jaconi, Marisa 2002
add to browser selection
Cardiovascular risk in patients with rheumatoid arthritis Lauper, Kim; Gabay, Cem 2017
add to browser selection
Cellular genomics for complex traits Dermitzakis, Emmanouil 2012
add to browser selection
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
add to browser selection
Chemoattractant Signals and Adhesion Molecules Promoting Human Regulatory T Cell Recruitment to Porcine Endothelium Ehirchiou, Driss; Muller, Yannick D; Chicheportiche, Rachel; Heyrani Nobari, Ruhollah; ... Seebach, Jorg Dieter 2016
add to browser selection
Chromosome 21 and down syndrome: from genomics to pathophysiology Antonarakis, Stylianos; Lyle, Robert; Dermitzakis, Emmanouil; Reymond, Alexandre; Deutsch, Samuel 2004
add to browser selection
Chromosome 21: from sequence to applications Antonarakis, Stylianos 2001
<< previous | 1 | 2 | 3 | 4 | 5 | 6 | 7 |