Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
Published 2012 View Full Article
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Title
Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 109, Issue 40, Pages 16234-16239
Publisher
Proceedings of the National Academy of Sciences
Online
2012-09-18
DOI
10.1073/pnas.1209508109
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Note: Only part of the references are listed.- Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis
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- A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function
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- Human HMGCS2 Regulates Mitochondrial Fatty Acid Oxidation andFGF21Expression in HepG2 Cell Line
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- DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo
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- ROAST: rotation gene set tests for complex microarray experiments
- (2010) Di Wu et al. BIOINFORMATICS
- A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
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- Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene
- (2010) Lauren Snider et al. PLoS Genetics
- Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample
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- 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
- Id3 Is a Direct Transcriptional Target of Pax7 in Quiescent Satellite Cells
- (2009) Deepak Kumar et al. MOLECULAR BIOLOGY OF THE CELL
- Genetics of human gene expression: mapping DNA variants that influence gene expression
- (2009) Vivian G. Cheung et al. NATURE REVIEWS GENETICS
- 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
- An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
- (2008) Darko Bosnakovski et al. EMBO JOURNAL
- Gene Expression Profiling in Limb-Girdle Muscular Dystrophy 2A
- (2008) Amets Sáenz et al. PLoS One
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