Sequence features accurately predict genome-wide MeCP2 binding in vivo.
about
Misregulation of Alternative Splicing in a Mouse Model of Rett SyndromeLoss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain.MeCP2 and CTCF: enhancing the cross-talk of silencers.Microglia from offspring of dams with allergic asthma exhibit epigenomic alterations in genes dysregulated in autism.Epigenetic Etiology of Intellectual Disability.Early-Life Gene Expression in Neurons Modulates Lasting Epigenetic States.Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.5-hydroxymethylcytosine accumulation in postmitotic neurons results in functional demethylation of expressed genes.A unified computational framework for modeling genome-wide nucleosome landscape
P2860
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P2860
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@ast
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@en
type
label
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@ast
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@en
prefLabel
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@ast
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
@en
P2093
P2860
P356
P1476
Sequence features accurately predict genome-wide MeCP2 binding in vivo
@en
P2093
Dag H Yasui
H Tomas Rube
Huaiyang Chen
John F Hess
Miroslav Hejna
Qizhi Gong
P2860
P2888
P356
10.1038/NCOMMS11025
P407
P577
2016-03-24T00:00:00Z