Rbfox1 Downregulation and Altered Calpain 3 Splicing by FRG1 in a Mouse Model of Facioscapulohumeral Muscular Dystrophy (FSHD)
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Title
Rbfox1 Downregulation and Altered Calpain 3 Splicing by FRG1 in a Mouse Model of Facioscapulohumeral Muscular Dystrophy (FSHD)
Authors
Keywords
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Journal
PLoS Genetics
Volume 9, Issue 1, Pages e1003186
Publisher
Public Library of Science (PLoS)
Online
2013-01-04
DOI
10.1371/journal.pgen.1003186
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- DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy
- (2011) Linda N. Geng et al. DEVELOPMENTAL CELL
- Genome-wide characterization of transcriptional start sites in humans by integrative transcriptome analysis
- (2011) R. Yamashita et al. GENOME RESEARCH
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- (2010) Lindsay M. Wallace et al. ANNALS OF NEUROLOGY
- MicroRNAs coordinate an alternative splicing network during mouse postnatal heart development
- (2010) A. Kalsotra et al. GENES & DEVELOPMENT
- FSHD: copy number variations on the theme of muscular dystrophy
- (2010) Daphne Selvaggia Cabianca et al. JOURNAL OF CELL BIOLOGY
- 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
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- (2010) S. Bessonov et al. RNA
- A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
- (2010) R. J. L. F. Lemmers et al. SCIENCE
- 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
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- (2009) Hidehito Kuroyanagi CELLULAR AND MOLECULAR LIFE SCIENCES
- 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
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- (2009) J.-A. Lee et al. GENES & DEVELOPMENT
- 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
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- (2009) Z. Z. Tang et al. MOLECULAR AND CELLULAR BIOLOGY
- An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells
- (2009) Gene W Yeo et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Autoregulation of Fox protein expression to produce dominant negative splicing factors
- (2009) A. Damianov et al. RNA
- 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
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- (2008) Jacques S. Beckmann et al. NEUROMUSCULAR DISORDERS
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