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Why are suppressors of amber mutations so frequent among Escherichia coli K12 strains?. A plausible explanation for a long-lasting puzzle Belin, Dominique 2003
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Whole-genome sequencing of Staphylococcus aureus strain RN4220, a key laboratory strain used in virulence research, identifies mutations that affect not only virulence factors but also the fitness of the strain Nair, Dhanalakshmi; Memmi, Guido; Hernandez, David; Bard, Jonathan; ... Cheung, Ambrose L 2011
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When is a child with status epilepticus likely to have Dravet syndrome? Le Gal, François; Lebon, Sébastien; Ramelli, Gian Paolo; Datta, Alexandre; ... Korff, Christian 2014
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VPS35 mutations in Parkinson disease Vilariño-Güell, Carles; Wider, Christian; Ross, Owen A; Dachsel, Justus C; ... Farrer, Matthew J 2011
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Variable region sequences of pathogenic anti-mouse red blood cell autoantibodies from autoimmune NZB mice Reininger, Luc; Shibata, T.; Ozaki, S.; Shirai, Toshikazu; ... Izui, Shozo 1990
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UV-B signaling pathways and fluence rate dependent transcriptional regulation of ARIADNE12 Lang-Mladek, Christina; Xie, Lisi; Nigam, Neha; Chumak, Nina; ... Hauser, Marie-Theres 2012
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Two rotating cilia in the node cavity are sufficient to break left-right symmetry in the mouse embryo Shinohara, Kyosuke; Kawasumi, Aiko; Takamatsu, Atsuko; Yoshiba, Satoko; ... Hamada, Hiroshi 2012
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Two regulatory levels of transcriptional gene silencing in Arabidopsis Mittelsten Scheid, Ortrun; Probst, Aline V.; Afsar, Karin; Paszkowski, Jerzy 2002
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Two novel mutations affecting mRNA splicing of the neurofibromatosis type 1 (NF1) gene Perrin, G.; Morris, Michael Andréw; Antonarakis, Stylianos; Boltshauser, E.; Hutter, Pierre 1996
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Two means of transcriptional reactivation within heterochromatin Probst, Aline V.; Fransz, Paul F.; Paszkowski, Jerzy; Mittelsten Scheid, Ortrun 2003
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Two colons-two cancers: paradigm shift and clinical implications Gervaz, Pascal; Bucher, Pascal Alain Robert; Morel, Philippe 2004
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TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum Kern, Ilse 2011
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Treatment of congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2008
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Transmission of HIV-1 drug resistance in Switzerland: a 10-year molecular epidemiology survey Yerly Ferrillo, Sabine; von Wyl, Viktor; Ledergerber, Bruno; Boni, Jurg; ... Perrin, Luc 2007
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Transgenic mice with ocular overexpression of an adrenomedullin receptor reflect human acute angle-closure glaucoma Ittner, Lars M; Schwerdtfeger, Kerstin; Kunz, Thomas H; Muff, Roman; ... Fischer, Jan A 2008
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Transgenerational stability of the Arabidopsis epigenome is coordinated by CG methylation Mathieu, Olivier; Reinders, Jon; Caikovski, Marian; Smathajitt, Chotika; Paszkowski, Jerzy 2007
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Transcriptome analysis of the responses of Staphylococcus aureus to antimicrobial peptides and characterization of the roles of vraDE and vraSR in antimicrobial resistance Pietiäinen, Milla; Francois, Patrice; Hyyryläinen, Hanne-Leena; Tangomo, Manuela; ... Kontinen, Vesa P. 2009
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Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter Leupin, Olivier; Attanasio, Catia; Marguerat, Samuel; Tapernoux, Myriam; ... Conrad, Bernard 2005
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Transcription initiation of the yeast IMD2 gene is abolished in response to nutrient limitation through a sequence in its coding region Escobar-Henriques, Mafalda; Collart, Martine; Daignan-Fornier, Bertrand 2003
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Toxicity, efficacy, plasma drug concentrations and protease mutations in patients with advanced HIV infection treated with ritonavir plus saquinavir. Swiss HIV Cohort Study Lorenzi, P.; Yerly Ferrillo, Sabine; Abderrakim, K.; Fathi, Marc; ... Hirschel, Bernard 1997
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Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study Trinquand, Amélie; Tanguy-Schmidt, Aline; Ben Abdelali, Raouf; Lambert, Jérôme; ... Asnafi, Vahid 2013
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To aggregate or not to aggregate Neerman Arbez, Marguerite 2007
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TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness Guipponi, Michel; Antonarakis, Stylianos; Scott, Hamish Steele 2008
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Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing Fasquelle, Lydie; Scott, Hamish S; Lenoir, Marc; Wang, Jing; ... Delprat, Benjamin 2011
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TM9/Phg1 and SadA proteins control surface expression and stability of SibA adhesion molecules in Dictyostelium Froquet, Romain Bruno; Le Coadic, Marion; Perrin Simonnot, Jackie; Cherix, Nathalie; ... Cosson, Pierre 2012
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Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter Guzman, L. M.; Belin, Dominique; Carson, M. J.; Beckwith, J. 1995
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Thrombophilia in patients with retinal vein occlusion: a retrospective analysis Risse, Franziska; Frank, Rolf Dario; Weinberger, Andreas 2014
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THO/Sub2p functions to coordinate 3'-end processing with gene-nuclear pore association Rougemaille, Mathieu; Dieppois, Guennaelle; Kisseleva-Romanova, Elena; Gudipati, Rajani Kanth; ... Libri, Domenico 2008
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Thérapies ciblées du cancer pulmonaire: tests moléculaires à partir d’échantillons cytologiques Pusztaszeri, Marc; Pache, J-C; Mach, Nicolas; Gasche-Soccal, Paola Marina Alessandra; Mckee, Thomas Alexander 2011
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The zinc finger-containing transcription factor Gata-4 is expressed in the developing endocrine pancreas and activates glucagon gene expression Ritz-Laser, Beate; Mamin, Aline; Brun, Thierry; Avril, Isabelle; ... Philippe, Jacques 2005
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The Yaa mutation promoting murine lupus causes defective development of marginal zone B cells Amano, Hirofumi; Amano, Eri; Moll, Thomas; Marinkovic, Dragan; ... Izui, Shozo 2003
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The Yaa gene abrogates the major histocompatibility complex association of murine lupus in (NZB x BXSB)F1 hybrid mice Merino, Ramon; Iwamoto, Masahiro; Gershwin, M. E.; Izui, Shozo 1994
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The Y chromosome from autoimmune BXSB/MpJ mice induces a lupus-like syndrome in (NZW x C57BL/6)F1 male mice, but not in C57BL/6 male mice Izui, Shozo; Higaki, M.; Morrow, D.; Merino, Ramon 1988
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The Vam6 GEF controls TORC1 by activating the EGO complex Binda, Matteo; Péli-Gulli, Marie-Pierre; Bonfils, Grégory; Panchaud, Nicolas; ... De Virgilio, Claudio 2009
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The TPTE gene family: cellular expression, subcellular localization and alternative splicing Tapparel, Caroline; Reymond, Alexandre; Girardet, Christophe; Guillou, Louis; ... Antonarakis, Stylianos 2003
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The TATA-binding protein-associated factor yTafII19p functionally interacts with components of the global transcriptional regulator Ccr4-Not complex and physically interacts with the Not5 subunit Lemaire, Marc; Collart, Martine 2000
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The SWISS-PROT protein sequence data bank, recent developments Bairoch, Amos Marc; Boeckmann, Brigitte 1993
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The stringent response of Staphylococcus aureus and its impact on survival after phagocytosis through the induction of intracellular PSMs expression Geiger, Tobias; Francois, Patrice; Liebeke, Manuel; Fraunholz, Martin; ... Wolz, Christiane 2012
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The Sgp3 locus on mouse chromosome 13 regulates nephritogenic gp70 autoantigen expression and predisposes to autoimmunity Laporte, Catherine; Ballester, Benoit; Mary, Charles; Izui, Shozo; Reininger, Luc 2003
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The Sendai paramyxovirus accessory C proteins inhibit viral genome amplification in a promoter-specific fashion Cadd, Tamarra Leigh; Garcin, Dominique; Tapparel, Caroline; Itoh, M; ... Kolakofsky, Daniel 1996
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The S box of major histocompatibility complex class II promoters is a key determinant for recruitment of the transcriptional co-activator CIITA Muhlethaler-Mottet, Annick; Krawczyk, Michal; Masternak, Krzysztof; Spilianakis, Charalambos; ... Reith, Walter 2004
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The presenilin-1 familial Alzheimer's disease mutation P117L decreases neuronal differentiation of embryonic murine neural progenitor cells Eder-Colli, Lorenza; Abad-Estarlich, Noelia; Pannetier, Carine; Vallet, Philippe; ... Savioz, Armand 2009
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The PPH1 phosphatase is specifically involved in LHCII dephosphorylation and state transitions in Arabidopsis Shapiguzov, Alexey; Ingelsson, Björn; Samol, Iga; Andres, Charles; ... Goldschmidt-Clermont, Michel P. 2010
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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos 1999
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The p21-activated kinase 3 implicated in mental retardation regulates spine morphogenesis through a Cdc42-dependent pathway Kreis, Patricia; Thevenot, Emmanuel; Rousseau, Veronique; Boda, Bernadett; ... Barnier, J. V. 2007
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The novel chloroplast outer membrane kinase KOC1 is a required component of the plastid protein import machinery Zufferey, Mónica; Montandon, Cyrille; Douet, Véronique; Demarsy, Emilie; ... Kessler, Felix 2017
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The NOT, SPT3, and MOT1 genes functionally interact to regulate transcription at core promoters Collart, Martine 1996
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The NC2 repressor is dispensable in yeast mutated for the Sin4p component of the holoenzyme and plays roles similar to Mot1p in vivo Lemaire, Marc; Xie, Jun; Meisterernst, Michael; Collart, Martine 2000
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The NC2 alpha and beta subunits play different roles in vivo Creton, Sandrine; Svejstrup, Jesper Q; Collart, Martine 2002
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The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
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