MeCP2 Suppresses Nuclear MicroRNA Processing and Dendritic Growth by Regulating the DGCR8/Drosha Complex-Reference-Cited by-同舟云学术

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MeCP2 Suppresses Nuclear MicroRNA Processing and Dendritic Growth by Regulating the DGCR8/Drosha Complex

Published:2014-03 Issue:5 Volume:28 Page:547-560
ISSN:1534-5807
Container-title:Developmental Cell
language:en
Short-container-title:Developmental Cell

Author:

Cheng Tian-Lin,Wang Zhizhi,Liao Qiuming,Zhu Ying,Zhou Wen-Hao,Xu Wenqing,Qiu Zilong

Publisher

Elsevier BV

Subject

Developmental Biology,Cell Biology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology

Reference45 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. MicroRNAs: genomics, biogenesis, mechanism, and function;Bartel;Cell,2004

3. Updating the profile of C-terminal MECP2 deletions in Rett syndrome;Bebbington;J. Med. Genet.,2010

4. A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome;Buschdorf;J. Mol. Med.,2004

5. microRNA functions;Bushati;Annu. Rev. Cell Dev. Biol.,2007

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