Radically truncated MeCP2 rescues Rett syndrome-like neurological defects
Published 2017 View Full Article
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Title
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects
Authors
Keywords
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Journal
NATURE
Volume 550, Issue 7676, Pages 398-401
Publisher
Springer Nature
Online
2017-10-11
DOI
10.1038/nature24058
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Related references
Note: Only part of the references are listed.- Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders
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- An AT-Hook Domain in MeCP2 Determines the Clinical Course of Rett Syndrome and Related Disorders
- (2013) Steven Andrew Baker et al. CELL
- Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
- (2013) Matthew J Lyst et al. NATURE NEUROSCIENCE
- Multiplex Genome Engineering Using CRISPR/Cas Systems
- (2013) L. Cong et al. SCIENCE
- Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows
- (2012) Hélène Cheval et al. HUMAN MOLECULAR GENETICS
- Improved Survival and Reduced Phenotypic Severity Following AAV9/MECP2 Gene Transfer to Neonatal and Juvenile Male Mecp2 Knockout Mice
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- Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses
- (2011) Darren Goffin et al. NATURE NEUROSCIENCE
- Loss of activity-induced phosphorylation of MeCP2 enhances synaptogenesis, LTP and spatial memory
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- Neuronal MeCP2 Is Expressed at Near Histone-Octamer Levels and Globally Alters the Chromatin State
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- Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function
- (2009) J. Tao et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
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- MeCP2 Binding to DNA Depends upon Hydration at Methyl-CpG
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- MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription
- (2008) M. Chahrour et al. SCIENCE
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