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Molecular and Cellular Biology|October 9, 2002
Intralysosomal cystine accumulation in mice lacking cystinosin, the protein defective in cystinosisStéphanie Cherqui, Caroline Sevin, Ghislaine Hamard, et al.Human Molecular Genetics|October 3, 2009
A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytesJulien Ratelade, Christelle Arrondel, Ghislaine Hamard, et al.Human Molecular Genetics|March 31, 2006
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout miceCaroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, et al.Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.Gastroenterology|October 19, 2010
Sumoylation by Ubc9 regulates the stem cell compartment and structure and function of the intestinal epithelium in miceMaud D Demarque, Karim Nacerddine, Hélène Neyret-Kahn, et al.Cell|October 24, 2006
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapseIsabelle Roux, Saaid Safieddine, Régis Nouvian, et al.The Journal of Clinical Investigation|July 4, 2007
Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in miceSandrine Billet, Sabine Bardin, Sonia Verp, et al.Nature Medicine|April 19, 2005
Lactadherin promotes VEGF-dependent neovascularizationJean-Sébastien Silvestre, Clotilde Théry, Ghislaine Hamard, et al.Pageof 2