标题
MECP2, a multi-talented modulator of chromatin architecture
作者
关键词
-
出版物
Briefings in Functional Genomics
Volume -, Issue -, Pages elw023
出版商
Oxford University Press (OUP)
发表日期
2016-06-14
DOI
10.1093/bfgp/elw023
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- X inactivation and reactivation in X-linked diseases
- (2016) Marcella Vacca et al. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
- A High-Resolution Imaging Approach to Investigate Chromatin Architecture in Complex Tissues
- (2015) Michael W. Linhoff et al. CELL
- Disruption of DNA-methylation-dependent long gene repression in Rett syndrome
- (2015) Harrison W. Gabel et al. NATURE
- Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2
- (2015) Benyam Kinde et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Gene repositioning within the cell nucleus is not random and is determined by its genomic neighborhood
- (2015) K. Laurence Jost et al. Epigenetics & Chromatin
- Methyl-CpG-binding domain proteins: readers of the epigenome
- (2015) Qian Du et al. Epigenomics
- Reconfiguration of nucleosome-depleted regions at distal regulatory elements accompanies DNA methylation of enhancers and insulators in cancer
- (2014) Phillippa C. Taberlay et al. GENOME RESEARCH
- Cell-Type-Specific Repression by Methyl-CpG-Binding Protein 2 Is Biased toward Long Genes
- (2014) K. Sugino et al. JOURNAL OF NEUROSCIENCE
- Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping
- (2014) Kristin D. Kernohan et al. NUCLEIC ACIDS RESEARCH
- An AT-Hook Domain in MeCP2 Determines the Clinical Course of Rett Syndrome and Related Disorders
- (2013) Steven Andrew Baker et al. CELL
- SUMOylation of MeCP2 is essential for transcriptional repression and hippocampal synapse development
- (2013) Ju Cheng et al. JOURNAL OF NEUROCHEMISTRY
- Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain
- (2013) Junjie U Guo et al. NATURE NEUROSCIENCE
- Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
- (2013) Matthew J Lyst et al. NATURE NEUROSCIENCE
- Impaired in vivo binding of MeCP2 to chromatin in the absence of its DNA methyl-binding domain
- (2013) D. P. Stuss et al. NUCLEIC ACIDS RESEARCH
- Direct Homo- and Hetero-Interactions of MeCP2 and MBD2
- (2013) Annette Becker et al. PLoS One
- Global Epigenomic Reconfiguration During Mammalian Brain Development
- (2013) R. Lister et al. SCIENCE
- MeCP2 Binds to 5hmC Enriched within Active Genes and Accessible Chromatin in the Nervous System
- (2012) Marian Mellén et al. CELL
- Targeted manipulation of heterochromatin rescues MeCP2 Rett mutants and re-establishes higher order chromatin organization
- (2012) Corella S. Casas-Delucchi et al. NUCLEIC ACIDS RESEARCH
- MeCP2 Dependent Heterochromatin Reorganization during Neural Differentiation of a Novel Mecp2-Deficient Embryonic Stem Cell Reporter Line
- (2012) Bianca Bertulat et al. PLoS One
- ATRX in chromatin assembly and genome architecture during development and disease
- (2011) Nathalie G. Bérubé Biochemistry and Cell Biology
- Experimental models of Rett syndrome based on Mecp2 dysfunction
- (2011) Gaston Calfa et al. EXPERIMENTAL BIOLOGY AND MEDICINE
- Genome-wide profiling of DNA methylation in human cancer cells
- (2011) Katsumi Ogoshi et al. GENOMICS
- MeCP2 Rett mutations affect large scale chromatin organization
- (2011) Noopur Agarwal et al. HUMAN MOLECULAR GENETICS
- MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation
- (2011) Malaika K. Singleton et al. NEUROBIOLOGY OF DISEASE
- Heterochromatin maintenance and establishment: Lessons from the mouse pericentromere
- (2011) Geneviève Almouzni et al. Nucleus
- TheMECP2duplication syndrome
- (2010) Melissa B. Ramocki et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Rett syndrome: Revised diagnostic criteria and nomenclature
- (2010) Jeffrey L. Neul et al. ANNALS OF NEUROLOGY
- ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain
- (2010) Kristin D. Kernohan et al. DEVELOPMENTAL CELL
- MeCP2 Binds Cooperatively to Its Substrate and Competes with Histone H1 for Chromatin Binding Sites
- (2010) R. P. Ghosh et al. MOLECULAR AND CELLULAR BIOLOGY
- Neuronal MeCP2 Is Expressed at Near Histone-Octamer Levels and Globally Alters the Chromatin State
- (2010) Peter J. Skene et al. MOLECULAR CELL
- L1 retrotransposition in neurons is modulated by MeCP2
- (2010) Alysson R. Muotri et al. NATURE
- Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus
- (2009) Shay Ben-Shachar et al. HUMAN MOLECULAR GENETICS
- Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells
- (2009) Madeleine P Ball et al. NATURE BIOTECHNOLOGY
- 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
- The MBD protein family—Reading an epigenetic mark?
- (2008) Archana Dhasarathy et al. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
- DNA methylation landscapes: provocative insights from epigenomics
- (2008) Miho M. Suzuki et al. NATURE REVIEWS GENETICS
- Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
- (2008) J. L. Neul et al. NEUROLOGY
- MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription
- (2008) M. Chahrour et al. SCIENCE
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