CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment / Ping WANG in Molecular Autism, (October 2015)  

Public ISBD [article]  inMolecular Autism > (October 2015) . - p.1-18 Titre : CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment Type de document : texte imprimé Auteurs : Ping WANG, Auteur ; Mingyan LIN, Auteur ; Erika PEDROSA, Auteur ; Anastasia HRABOVSKY, Auteur ; Zheng ZHANG, Auteur ; Wenjun GUO, Auteur ; Herbert M. LACHMAN, Auteur ; Deyou ZHENG, Auteur Article en page(s) : p.1-18 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Disruptive mutation in the CHD8 gene is one of the top genetic risk factors in autism spectrum disorders (ASDs). Previous analyses of genome-wide CHD8 occupancy and reduced expression of CHD8 by shRNA knockdown in committed neural cells showed that CHD8 regulates multiple cell processes critical for neural functions, and its targets are enriched with ASD-associated genes. En ligne : http://dx.doi.org/10.1186/s13229-015-0048-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment [texte imprimé] / Ping WANG, Auteur ; Mingyan LIN, Auteur ; Erika PEDROSA, Auteur ; Anastasia HRABOVSKY, Auteur ; Zheng ZHANG, Auteur ; Wenjun GUO, Auteur ; Herbert M. LACHMAN, Auteur ; Deyou ZHENG, Auteur . - p.1-18. Langues : Anglais (eng) in Molecular Autism > (October 2015) . - p.1-18 Index. décimale : PER Périodiques Résumé : Disruptive mutation in the CHD8 gene is one of the top genetic risk factors in autism spectrum disorders (ASDs). Previous analyses of genome-wide CHD8 occupancy and reduced expression of CHD8 by shRNA knockdown in committed neural cells showed that CHD8 regulates multiple cell processes critical for neural functions, and its targets are enriched with ASD-associated genes. En ligne : http://dx.doi.org/10.1186/s13229-015-0048-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

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