标题
FSHD: copy number variations on the theme of muscular dystrophy
作者
关键词
-
出版物
JOURNAL OF CELL BIOLOGY
Volume 191, Issue 6, Pages 1049-1060
出版商
Rockefeller University Press
发表日期
2010-12-14
DOI
10.1083/jcb.201007028
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。- Worldwide Population Analysis of the 4q and 10q Subtelomeres Identifies Only Four Discrete Interchromosomal Sequence Transfers in Human Evolution
- (2010) Richard J.L.F. Lemmers et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Structural Variation in the Human Genome and its Role in Disease
- (2010) Paweł Stankiewicz et al. Annual Review of Medicine
- Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites
- (2010) Q. Liu et al. JOURNAL OF CELL SCIENCE
- Chromatin remodelling during development
- (2010) Lena Ho et al. NATURE
- A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
- (2010) R. J. L. F. Lemmers et al. SCIENCE
- Gene Positioning
- (2010) C. Ferrai et al. Cold Spring Harbor Perspectives in Biology
- The Nuclear Envelope
- (2010) M. W. Hetzer Cold Spring Harbor Perspectives in Biology
- In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy
- (2010) Maria V Neguembor et al. Epigenomics
- Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene
- (2010) Lauren Snider et al. PLoS Genetics
- Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation
- (2009) Beatrice Bodega et al. BMC BIOLOGY
- Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4
- (2009) Brian P. Chadwick CHROMOSOMA
- FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy
- (2009) R. D. Wuebbles et al. Disease Models & Mechanisms
- Identification of a perinuclear positioning element in human subtelomeres that requires A-type lamins and CTCF
- (2009) Alexandre Ottaviani et al. EMBO JOURNAL
- Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
- (2009) Rinse Klooster et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy
- (2009) Lauren Snider et al. HUMAN MOLECULAR GENETICS
- Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD
- (2009) Jessica C. de Greef et al. HUMAN MUTATION
- Loss of YY1 Impacts the Heterochromatic State and Meiotic Double-Strand Breaks during Mouse Spermatogenesis
- (2009) S. Wu et al. MOLECULAR AND CELLULAR BIOLOGY
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- Mechanisms of Polycomb gene silencing: knowns and unknowns
- (2009) Jeffrey A. Simon et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- DUX4c Is Up-Regulated in FSHD. It Induces the MYF5 Protein and Human Myoblast Proliferation
- (2009) Eugénie Ansseau et al. PLoS One
- Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers
- (2009) P. Arashiro et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD)
- (2009) Weihua Zeng et al. PLoS Genetics
- The D4Z4 Macrosatellite Repeat Acts as a CTCF and A-Type Lamins-Dependent Insulator in Facio-Scapulo-Humeral Dystrophy
- (2009) Alexandre Ottaviani et al. PLoS Genetics
- Histones: Annotating Chromatin
- (2008) Eric I. Campos et al. Annual Review of Genetics
- Analysis of the largest tandemly repeated DNA families in the human genome
- (2008) Peter E Warburton et al. BMC GENOMICS
- Muscular dystrophy candidate gene FRG1 is critical for muscle development
- (2008) Meredith L. Hanel et al. DEVELOPMENTAL DYNAMICS
- An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
- (2008) Darko Bosnakovski et al. EMBO JOURNAL
- DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
- (2008) Darko Bosnakovski et al. EXPERIMENTAL NEUROLOGY
- Epigenetic Silencing of CCAAT/Enhancer-binding Protein δ Activity by YY1/Polycomb Group/DNA Methyltransferase Complex
- (2008) Chiung-Yuan Ko et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Isolation of an active step I spliceosome and composition of its RNP core
- (2008) Sergey Bessonov et al. NATURE
- Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
- (2008) Lars Guelen et al. NATURE
- DNA methylation landscapes: provocative insights from epigenomics
- (2008) Miho M. Suzuki et al. NATURE REVIEWS GENETICS
- Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers
- (2008) Koji Tsumagari et al. NUCLEIC ACIDS RESEARCH
- A Functional Role for 4qA/B in the Structural Rearrangement of the 4q35 Region and in the Regulation of FRG1 and ANT1 in Facioscapulohumeral Dystrophy
- (2008) Iryna Pirozhkova et al. PLoS One
- Facioscapulohumeral Dystrophy
- (2007) Shree Pandya et al. PHYSICAL THERAPY
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