The Chromatin-binding Protein HMGN1 Regulates the Expression of Methyl CpG-binding Protein 2 (MECP2) and Affects the Behavior of Mice
出版年份 2011 全文链接
标题
The Chromatin-binding Protein HMGN1 Regulates the Expression of Methyl CpG-binding Protein 2 (MECP2) and Affects the Behavior of Mice
作者
关键词
-
出版物
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 286, Issue 49, Pages 42051-42062
出版商
American Society for Biochemistry & Molecular Biology (ASBMB)
发表日期
2011-10-19
DOI
10.1074/jbc.m111.300541
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Autism Spectrum Disorders and Epigenetics
- (2011) Daria Grafodatskaya et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Transcriptomic analysis of autistic brain reveals convergent molecular pathology
- (2011) Irina Voineagu et al. NATURE
- Effects of HMGN variants on the cellular transcription profile
- (2011) M. Rochman et al. NUCLEIC ACIDS RESEARCH
- Protein Interactome Reveals Converging Molecular Pathways Among Autism Disorders
- (2011) Y. Sakai et al. Science Translational Medicine
- TheMECP2duplication syndrome
- (2010) Melissa B. Ramocki et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Binding and interplay of HMG proteins on chromatin: Lessons from live cell imaging
- (2010) Fred Catez et al. Biochimica et Biophysica Acta-Gene Regulatory Mechanisms
- Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies
- (2010) T.-P. Yang et al. BIOINFORMATICS
- Expression of the congenital heart disease 5/tryptophan rich basic protein homologue gene during heart development in Medaka fish, Oryzias latipes
- (2010) Kenji Murata et al. DEVELOPMENT GROWTH & DIFFERENTIATION
- Regions of homozygosity and their impact on complex diseases and traits
- (2010) Chee Seng Ku et al. HUMAN GENETICS
- A genome-wide scan for common alleles affecting risk for autism
- (2010) R. Anney et al. HUMAN MOLECULAR GENETICS
- Binding of the Rett syndrome protein, MeCP2, to methylated and unmethylated DNA and chromatin
- (2010) Jeffrey C. Hansen et al. IUBMB LIFE
- Down Syndrome: From Understanding the Neurobiology to Therapy
- (2010) K. Gardiner et al. JOURNAL OF NEUROSCIENCE
- Genomic Profiling of HMGN1 Reveals an Association with Chromatin at Regulatory Regions
- (2010) S. Cuddapah 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
- Brain function and chromatin plasticity
- (2010) Catherine Dulac NATURE
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Behavioural phenotyping assays for mouse models of autism
- (2010) Jill L. Silverman et al. NATURE REVIEWS NEUROSCIENCE
- Disruption of the epigenetic code: An emerging mechanism in mental retardation
- (2010) Hans van Bokhoven et al. NEUROBIOLOGY OF DISEASE
- The dynamics of HMG protein–chromatin interactions in living cellsThis paper is one of a selection of papers published in this Special Issue, entitled CSBMCB’s 51st Annual Meeting – Epigenetics and Chromatin Dynamics, and has undergone the Journal’s usual peer review process.
- (2009) Gabi Gerlitz et al. Biochemistry and Cell Biology
- Regulation of chromatin structure and function By HMGN proteins
- (2009) Yuri Postnikov et al. Biochimica et Biophysica Acta-Gene Regulatory Mechanisms
- Genetic Determinants of Pediatric Inflammatory Bowel Disease: Is Age of Onset Genetically Determined?
- (2009) Rebecca Scherr et al. DIGESTIVE DISEASES
- MeCP2 involvement in the regulation of neuronal -tubulin production
- (2009) L. Abuhatzira et al. HUMAN MOLECULAR GENETICS
- Genome wide association (GWA) predictors of anti-TNFα therapeutic responsiveness in pediatric inflammatory bowel disease
- (2009) Marla C. Dubinsky et al. INFLAMMATORY BOWEL DISEASES
- Isolation of active regulatory elements from eukaryotic chromatin using FAIRE (Formaldehyde Assisted Isolation of Regulatory Elements)
- (2009) Paul G. Giresi et al. METHODS
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
- (2009) Kai Wang et al. NATURE
- The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies
- (2009) J. O. Korbel et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The methyl-CpG-binding protein MeCP2 and neurological disease
- (2008) Adrian Bird BIOCHEMICAL SOCIETY TRANSACTIONS
- Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21
- (2008) Robert Lyle et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
- (2008) R. C. Samaco et al. HUMAN MOLECULAR GENETICS
- Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
- (2008) Subra Kugathasan et al. NATURE GENETICS
- MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription
- (2008) M. Chahrour et al. SCIENCE
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now