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	Title	Authors / Editors	Date
unige:917	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
unige:9875	A GAL4-HP1 fusion protein targeted near heterochromatin promotes gene silencing	Seum, Carole; Spierer, Anne; Delattre, Marion; Pauli, Daniel; Spierer, Pierre	2000
unige:89770	A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.	Lane, Jérôme; Boehlen, Françoise	2013
unige:74113	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
unige:8706	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
unige:32236	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
unige:9881	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
unige:11165	A new genetic selection identifies essential residues in SecG, a component of the Escherichia coli protein export machinery	Bost, S.; Belin, Dominique	1995
unige:32728	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
unige:10301	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
unige:11232	A rabbit Ig lambda L chain C region gene encoding C21 allotopes	Duvoisin, R. M.; Hayzer, D. J.; Belin, Dominique; Jaton, J. C.	1988
unige:55982	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
unige:27987	A short amino-terminal part of Arabidopsis phytochrome A induces constitutive photomorphogenic response	Viczián, András; Ádám, Éva; Wolf, Iris; Bindics, János; ... Nagy, Ferenc	2012
unige:34641	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
unige:32178	A systematic survey of loss-of-function variants in human protein-coding genes	MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil	2012
unige:14331	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
unige:4581	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
unige:48161	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
unige:37175	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
unige:44745	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
unige:8818	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
unige:8866	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
unige:1884	Altered composition and secretion of lysosome-derived compartments in Dictyostelium AP-3 mutant cells	Charette, Steve J.; Cosson, Pierre	2008
unige:55484	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
unige:8981	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
unige:8978	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
unige:88214	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
unige:7287	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
unige:11288	Arterial smooth muscle cell heterogeneity: implications for atherosclerosis and restenosis development	Hao, Hiroyuki; Gabbiani, Giulio; Bochaton-Piallat, Marie-Luce	2003
unige:8725	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
unige:32737	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
unige:6796	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
unige:55542	ATM gene and lymphoid malignancies	Gumy Pause, Fabienne; Wacker, Pierre; Sappino, Pascal	2004
unige:44721	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
unige:9319	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
unige:8625	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
unige:100304	Beta Cell Hubs Dictate Pancreatic Islet Responses to Glucose	Johnston, Natalie R; Mitchell, Ryan K; Haythorne, Elizabeth; Pessoa, Maria Paiva; ... Hodson, David J	2016
unige:8778	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
unige:77355	Biased allelic expression in human primary fibroblast single cells	Borel, Christelle; Ferreira Marinheiro, Pedro; Santoni, Federico; Delaneau, Olivier; ... Antonarakis, Stylianos	2015
unige:41352	Biological responses in stented arteries	Chaabane, Chiraz; Otsuka, Fumiyuki; Virmani, Renu; Bochaton-Piallat, Marie-Luce	2013
unige:11168	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
unige:41353	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
unige:11470	Calreticulin is essential for cardiac development	Mesaeli, N.; Nakamura, K.; Zvaritch, E.; Dickie, P.; ... Michalak, Marek	1999
unige:11424	Calreticulin reveals a critical Ca(2+) checkpoint in cardiac myofibrillogenesis	Li, Jian; Puceat, Michel; Perez-Terzic, Carmen; Mery, Annabelle; ... Jaconi, Marisa	2002
unige:110680	Cardiovascular risk in patients with rheumatoid arthritis	Lauper, Kim; Gabay, Cem	2017
unige:32196	Cellular genomics for complex traits	Dermitzakis, Emmanouil	2012
unige:8855	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
unige:99470	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
unige:8611	Chromosome 21 and down syndrome: from genomics to pathophysiology	Antonarakis, Stylianos; Lyle, Robert; Dermitzakis, Emmanouil; Reymond, Alexandre; Deutsch, Samuel	2004
unige:8603	Chromosome 21: from sequence to applications	Antonarakis, Stylianos	2001

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