| | Title | Authors / Editors | Date |
|
unige:11131 |
A Ca(2+)-activated NADPH oxidase in testis, spleen, and lymph nodes |
Banfi, Botond; Molnar, Gergely; Maturana, Andrés; Steger, Klaus; ... Krause, Karl-Heinz |
2001 |
|
unige:11507 |
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 |
|
unige:8619 |
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 |
|
unige:9062 |
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 |
|
unige:9079 |
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 |
|
unige:20663 |
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 |
|
unige:11508 |
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 |
|
unige:8989 |
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 |
|
unige:11451 |
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 |
|
unige:20665 |
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 |
|
unige:9080 |
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 |
|
unige:8595 |
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 |
|
unige:8747 |
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 |
|
unige:8594 |
Isolation and initial characterization of the mouse Dnmt3l gene |
Aapola, Ulla; Lyle, Robert; Krohn, K.; Antonarakis, Stylianos; Peterson, P. |
2001 |
|
unige:108163 |
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism |
Xu, Cheng; Messina, Andrea; Somm, Emmanuel; Miraoui, Hichem; ... Pitteloud, Nelly |
2017 |
|
unige:95968 |
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 |
|
unige:154163 |
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features |
Roessler, Erich; Du, Yang-Zhu; Mullor, Jose L; Casas, Esther; ... Muenke, Maximilian |
2003 |
|
unige:847 |
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 |
|
unige:9038 |
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 |
|
unige:30275 |
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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