KMT2D deficiency leads to cellular developmental disorders and enhancer dysregulation in neural-crest-containing brain organoids

Author:

Shan Ziyun,Zhao Yingying,Chen Xiuyu,Zhan Guodong,Huang Junju,Yang Xuejie,Xu Chongshen,Guo Ning,Xiong Zhi,Wu Fang,Liu Yujian,Liu He,Chen Biyuan,Chen Bingqiu,Sun Jiaoyang,He Jiangping,Guo Yiping,Cao Shangtao,Wu Kaixin,Mao Rui,Wu Guangming,Lin Lihui,Zou Xiaobing,Wang Jie,Chen Jiekai

Publisher

Elsevier BV

Reference52 articles.

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2. Enhancer priming by H3K4 methyltransferase mll4 controls cell fate transition;Wang;Proc Natl Acad Sci U S A,2016

3. Identification of h3k4me1-associated proteins at mammalian enhancers;Local;Nat Genet,2018

4. Dissecting kmt2d missense mutations in kabuki syndrome patients;Cocciadiferro;Hum Mol Genet,2018

5. The kmt2d kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology;Shpargel;Development,2020

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