Show items per page
Elements: 33
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
A Ca(2+)-activated NADPH oxidase in testis, spleen, and lymph nodes Banfi, Botond; Molnar, Gergely; Maturana, Andrés; Steger, Klaus; ... Krause, Karl-Heinz 2001
add to browser selection
A specific endoplasmic reticulum export signal drives transport of stem cell factor (Kitl) to the cell surface Paulhe, Frédérique; Imhof, Beat; Wehrle-Haller, Bernhard 2004
add to browser selection
Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite 2001
add to browser selection
Binding of PTEN to specific PDZ domains contributes to PTEN protein stability and phosphorylation by microtubule-associated serine/threonine kinases Valiente, Miguel; Andres-Pons, Amparo; Gomar, Beatriz; Torres, Josema; ... Pulido, Rafael 2005
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map Reymond, Alexandre; Friedli, Marc; Henrichsen, C. N.; Chapot, F.; ... Antonarakis, Stylianos 2001
add to browser selection
Heme histidine ligands within gp91(phox) modulate proton conduction by the phagocyte NADPH oxidase Maturana, Andrés; Arnaudeau, Serge; Ryser, Stephan; Banfi, Botond; ... Demaurex, Nicolas 2001
add to browser selection
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
add to browser selection
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion Vu, Dung; De Moerloose, Philippe; Batorova, A.; Lazur, J.; ... Neerman Arbez, Marguerite 2005
add to browser selection
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
add to browser selection
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
add to browser selection
Isolation and initial characterization of the mouse Dnmt3l gene Aapola, Ulla; Lyle, Robert; Krohn, K.; Antonarakis, Stylianos; Peterson, P. 2001
add to browser selection
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism Xu, Cheng; Messina, Andrea; Somm, Emmanuel; Miraoui, Hichem; ... Pitteloud, Nelly 2017
add to browser selection
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy French Parkinson's Disease Genetics Study, International Parkinson's Disease Genomics Consortium 2016
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
Molecular chaperone TRAP1 regulates a metabolic switch between mitochondrial respiration and aerobic glycolysis Yoshida, Soichiro; Tsutsumi, Shinji; Muhlebach, Guillaume; Sourbier, Carole; ... Neckers, Leonard 2013
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
Selective inhibition of nuclear steroid receptor function by a protein from a human tumorigenic poxvirus Chen, N.; Baudino, T.; MacDonald, P. N.; Green, M.; ... Buller, R. M. 2000
add to browser selection
Soluble form of complement C3b/C4b receptor (CR1) results from a proteolytic cleavage in the C-terminal region of CR1 transmembrane domain Hamer, I.; Paccaud, Jean-Pierre; Belin, Dominique; Maeder, C.; Carpentier, J. L. 1998
add to browser selection
Stimulation of the gonadotropic axis by the neuropeptide Y receptor Y1 antagonist/Y4 agonist 1229U91 in the male rat Raposinho, PD; Broqua, Pierre; Hayward, A; Akinsanya, K; ... Aubert, Michel 2000
add to browser selection
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
add to browser selection
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
add to browser selection
The TPTE gene family: cellular expression, subcellular localization and alternative splicing Tapparel, Caroline; Reymond, Alexandre; Girardet, Christophe; Guillou, Louis; ... Antonarakis, Stylianos 2003
add to browser selection
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase Micale, Lucia; Fusco, Carmela; Augello, Bartolomeo; Napolitano, Luisa M. R.; ... Reymond, Alexandre 2008