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Bcl11b\/Ctip2","volume":"15","author":"Simon","year":"2016","journal-title":"Genes Brain Behav"},{"key":"key\n\t\t\t\t20180726040015_awy173-B36","first-page":"2922","article-title":"A dual function of Bcl11b\/Ctip2 in hippocampal neurogenesis","volume":"31","author":"Simon","year":"2012","journal-title":"EMBO J"},{"key":"key\n\t\t\t\t20180726040015_awy173-B37","first-page":"928","article-title":"GeneMatcher: a matching tool for connecting investigators with an interest in the same gene","volume":"36","author":"Sobreira","year":"2015","journal-title":"Hum Mutat"},{"key":"key\n\t\t\t\t20180726040015_awy173-B38","first-page":"457","article-title":"Mutations in SPATA5 are associated with microcephaly, intellectual disability, seizures, and hearing loss","volume":"97","author":"Tanaka","year":"2015","journal-title":"Am J Hum Genet"},{"key":"key\n\t\t\t\t20180726040015_awy173-B39","first-page":"178","article-title":"Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration","volume":"14","author":"Thorvaldsdottir","year":"2013","journal-title":"Brief Bioinform"},{"key":"key\n\t\t\t\t20180726040015_awy173-B40","first-page":"483","article-title":"Type 2 innate lymphoid cells: at the cross-roads in allergic asthma","volume":"38","author":"van Rijt","year":"2016","journal-title":"Semin Immunopathol"},{"key":"key\n\t\t\t\t20180726040015_awy173-B41","article-title":"Ex utero electroporation and organotypic slice culture of mouse hippocampal tissue","author":"Venkataramanappa","year":"2015","journal-title":"J Vis Exp"},{"key":"key\n\t\t\t\t20180726040015_awy173-B42","first-page":"533","article-title":"Bcl11b is required for differentiation and survival of alphabeta T lymphocytes","volume":"4","author":"Wakabayashi","year":"2003","journal-title":"Nat Immunol"},{"key":"key\n\t\t\t\t20180726040015_awy173-B43","first-page":"875","article-title":"Bcl11b is essential for group 2 innate lymphoid cell development","volume":"212","author":"Walker","year":"2015","journal-title":"J Exp Med"},{"key":"key\n\t\t\t\t20180726040015_awy173-B44","first-page":"351","article-title":"The neuropeptide NMU amplifies ILC2-driven allergic lung inflammation","volume":"549","author":"Wallrapp","year":"2017","journal-title":"Nature"},{"key":"key\n\t\t\t\t20180726040015_awy173-B45","first-page":"e51262","article-title":"Selective ablation of Ctip2\/Bcl11b in epidermal keratinocytes triggers atopic dermatitis-like skin inflammatory responses in adult mice","volume":"7","author":"Wang","year":"2012","journal-title":"PLoS One"},{"key":"key\n\t\t\t\t20180726040015_awy173-B46","first-page":"183","article-title":"DNA recognition by Cys2His2 zinc finger proteins","volume":"29","author":"Wolfe","year":"2000","journal-title":"Annu Rev Biophys Biomol Struct"},{"key":"key\n\t\t\t\t20180726040015_awy173-B47","first-page":"102","article-title":"Single-cell RNA-seq identifies a PD-1hi ILC progenitor and defines its 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