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KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism Xu, Cheng; Messina, Andrea; Somm, Emmanuel; Miraoui, Hichem; ... Pitteloud, Nelly 2017
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Bioactive Natural Products Prioritization Using Massive Multi-informational Molecular Networks Olivon, Florent; Allard, Pierre-Marie; Koval, Alexey; Righi, Davide; ... Litaudon, Marc 2017
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Secretion of VEGF-165 has unique characteristics, including shedding from the plasma membrane Guzmán-Hernández, Maria Luisa; Potter, Gael; Egervari, Kristof Levente; Kiss, Jozsef Zoltan; Balla, Tamas 2014
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Inhibition of p38 mitogen-activated protein kinase impairs influenza virus-induced primary and secondary host gene responses and protects mice from lethal H5N1 infection Börgeling, Yvonne; Schmolke, Mirco; Viemann, Dorothee; Nordhoff, Carolin; ... Ludwig, Stephan 2014
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Niche anchorage and signaling through membrane-bound Kit-ligand/c-kit receptor are kinase independent and imatinib insensitive Tabone-Eglinger, Séverine; Calderin Sollet, Zuleika; Pinon, Perrine; Aebischer, Nicole; ... Wehrle-Haller, Bernhard 2014
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Molecular chaperone TRAP1 regulates a metabolic switch between mitochondrial respiration and aerobic glycolysis Yoshida, Soichiro; Tsutsumi, Shinji; Muhlebach, Guillaume; Sourbier, Carole; ... Neckers, Leonard 2013
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Membrane shape at the edge of the dynamin helix sets location and duration of the fission reaction Morlot, Sandrine; Galli, Valentina; Klein, Marius; Chiaruttini, Nicolas; ... Roux, Aurélien 2012
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Identification of site-specific adaptations conferring increased neural cell tropism during human enterovirus 71 infection Cordey, Samuel; Petty Ii, Thomas John; Schibler, Manuel; Martinez, Yannick; ... Tapparel, Caroline 2012
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Toxoplasma gondii aspartic protease 1 is not essential in tachyzoites Polonais, Valérie; Shea, Michael; Soldati-Favre, Dominique 2011
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Cyclophilin B interacts with sodium-potassium ATPase and is required for pump activity in proximal tubule cells of the kidney Sune, Guillermo; Sarro, Eduard; Puigmule, Marta; Lopez-Hellin, Joan; ... Meseguer, Anna 2010
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Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients Abdel Wahab, Magy; De Moerloose, Philippe; Fish, R. J.; Neerman Arbez, Marguerite 2010
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Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A' Vorjohann, Silja; Fish, Richard; Biron-Andreani, Christine; Nagaswami, Chandrasekaran; ... Neerman Arbez, Marguerite 2010
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Dimerization of Kit-ligand and efficient cell-surface presentation requires a conserved Ser-Gly-Gly-Tyr motif in its transmembrane domain Paulhe, Frédérique; Wehrle-Haller, Monique; Jacquier, M. C.; Imhof, Beat; ... Wehrle-Haller, Bernhard 2009
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Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase Micale, Lucia; Fusco, Carmela; Augello, Bartolomeo; Napolitano, Luisa M. R.; ... Reymond, Alexandre 2008
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Evaluation of [(18)F]gefitinib as a molecular imaging probe for the assessment of the epidermal growth factor receptor status in malignant tumors Su, Helen; Seimbille, Yann; Ferl, Gregory Z.; Bodenstein, Claudia; ... Weber, Wolfgang A. 2008
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Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants Vu, Dung; Di Sanza, Corinne; Neerman Arbez, Marguerite 2008
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Rickettsia conorii transcriptional response within inoculation eschar Renesto, Patricia; Rovery, Clarisse; Schrenzel, Jacques; Leroy, Quentin; ... Raoult, Didier 2008
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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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A family of aspartic proteases and a novel, dynamic and cell-cycle-dependent protease localization in the secretory pathway of Toxoplasma gondii Shea, Michael; Jäkle, Ursula; Liu, Qing; Berry, Colin; ... Soldati-Favre, Dominique 2007
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Melanomas require HEDGEHOG-GLI signaling regulated by interactions between GLI1 and the RAS-MEK/AKT pathways Stecca, Barbara; Mas, Christophe; Clement, Virginie; Zbinden, Marie; ... Ruiz Altaba, Ariel 2007
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Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations Neerman Arbez, Marguerite; De Moerloose, Philippe 2007
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Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène Vu, Dung; Neerman Arbez, Marguerite 2006
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Identification of paramyxovirus V protein residues essential for STAT protein degradation and promotion of virus replication Nishio, Machiko; Tsurudome, Masato; Ito, Morihiro; Garcin, Dominique; ... Ito, Yasuhiko 2005
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Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia Vu, Dung; Di Sanza, Corinne; Caille, Dorothee; De Moerloose, Philippe; ... Neerman Arbez, Marguerite 2005
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The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3 Merla, Giuseppe; Howald, Cedric; Antonarakis, Stylianos; Reymond, Alexandre 2004
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The junctional adhesion molecule (JAM) family members JAM-2 and JAM-3 associate with the cell polarity protein PAR-3: a possible role for JAMs in endothelial cell polarity Ebnet, Klaus; Aurrand-Lions, Michel; Kuhn, Annegret; Kiefer, Friedemann; ... Vestweber, Dietmar 2003
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PIKfyve controls fluid phase endocytosis but not recycling/degradation of endocytosed receptors or sorting of procathepsin D by regulating multivesicular body morphogenesis Ikonomov, Ognian C; Sbrissa, Diego; Foti, Michelangelo; Carpentier, Jean-Louis; Shisheva, Assia 2003
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Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA) Attanasio, Catia; David, Armelle; Neerman Arbez, Marguerite 2003
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Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12 Friedli, Marc; Guipponi, Michel; Bertrand, Sonia; Bertrand, Daniel; ... Reymond, Alexandre 2003
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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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Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2003
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Processing of proinsulin by furin, PC2, and PC3 in (co) transfected COS (monkey kidney) cells Vollenweider, F.; Kaufmann, J.; Irminger, J. C.; Halban, Philippe A. 1995
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Analysis of the resistance to heat and hydrogen peroxide stresses in COS cells transiently expressing wild type or deletion mutants of the Drosophila 27-kDa heat-shock protein Mehlen, Patrick; Briolay, Jérome; Smith, Leila; Diaz-latoud, Chantal; ... Arrigo, Andre-Patrick 1993