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Human Mutation|September 8, 2011
Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndromeAsma Chaoui, Yuli Watanabe, Renaud Touraine, et al.Developmental Biology|April 24, 2013
Sox10 and Itgb1 interaction in enteric neural crest cell migrationYuli Watanabe, Florence Broders-Bondon, Viviane Baral, et al.Journal of Molecular Medicine (Berlin, Germany)|February 5, 2010
Involvement of SOX10 in the pathogenesis of Hirschsprung disease: report of a truncating mutation in an isolated patientAvencia Sánchez-Mejías, Yuli Watanabe, Raquel M Fernández, et al.Plos One|August 1, 2012
Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2Viviane Baral, Asma Chaoui, Yuli Watanabe, et al.Scientific Reports|December 2, 2016
Endothelin-3 stimulates cell adhesion and cooperates with β1-integrins during enteric nervous system ontogenesisElodie Gazquez, Yuli Watanabe, Florence Broders-Bondon, et al.Gastroenterology|January 9, 2017
Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2Yuli Watanabe, Laure Stanchina, Laure Lecerf, et al.Human Mutation|December 21, 2013
An impairment of long distance SOX10 regulatory elements underlies isolated Hirschsprung diseaseLaure Lecerf, Anthula Kavo, Macarena Ruiz-Ferrer, et al.Human Molecular Genetics|June 11, 2015
Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutationsAsma Chaoui, Anthula Kavo, Viviane Baral, et al.American Journal of Human Genetics|May 7, 2013
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafnessVeronique Pingault, Virginie Bodereau, Viviane Baral, et al.Pageof 1