Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
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Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.MeCP2 and CTCF: enhancing the cross-talk of silencers.Rett syndrome: a neurological disorder with metabolic components.A mutation-led search for novel functional domains in MeCP2.Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2
P2860
Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
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2017 nî lūn-bûn
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2017 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի մարտին հրատարակված գիտական հոդված
@hy
2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
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name
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@ast
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@en
type
label
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@ast
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@en
altLabel
Structure of the MeCP2–TBLR1 c ...... syndrome and related disorders
@en
prefLabel
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@ast
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@en
P2093
P2860
P50
P921
P356
P1476
Structure of the MeCP2-TBLR1 c ...... yndrome and related disorders.
@en
Structure of the MeCP2–TBLR1 c ...... syndrome and related disorders
@en
P2093
Adrian P. Bird
Atlanta G. Cook
Ceitidh Taylor
Matthew J. Lyst
Žygimantė Tarnauskaitė
P2860
P304
E3243-E3250
P356
10.1073/PNAS.1700731114
P407
P577
2017-03-27T00:00:00Z