Zmynd11 is essential for neurogenesis by coordinating H3K36me3 modification of Epha2 and PI3K signaling pathway

Abstract 10p15.3 deletion syndrome is caused by the deficiency of MYND-type zinc finger domain-containing protein 11 (ZMYND11) and featured by global developmental delay, intellectual disability, behavioral abnormalities, etc. Although the roles of Zmynd11 is intensively studied in cancer, the funct...

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Bibliographic Details
Main Authors: Xu Yang, Lan Li, Wenzheng Qu, Xuejun Cheng, Jinyu Zhang, Yan Sun, Suxiao Liu, Guoping Peng, Rui Zheng, Xuekun Li
Format: Article
Language:English
Published: BMC 2025-04-01
Series:Cell & Bioscience
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Online Access:https://doi.org/10.1186/s13578-025-01392-z
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