Search Results (29)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| Jagannathan, Sujatha | Person |
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| Clinically Advanced p38 Inhibitors Suppress DUX4 Expression in Cellular and Animal Models of Facioscapulohumeral Muscular Dystrophy. | Academic Article |
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| Randomized phase 2 study of ACE-083, a muscle-promoting agent, in facioscapulohumeral muscular dystrophy. | Academic Article |
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| The evolution of DUX4 gene regulation and its implication for facioscapulohumeral muscular dystrophy. | Academic Article |
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| Campbell, Amy | Person |
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| Muscular Dystrophy, Facioscapulohumeral | Concept |
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| A Targeted Approach for Evaluating DUX4-Regulated Proteins as Potential Serum Biomarkers for Facioscapulohumeral Muscular Dystrophy Using Immunoassay Proteomics. | Academic Article |
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| Quantitative proteomics reveals key roles for post-transcriptional gene regulation in the molecular pathology of facioscapulohumeral muscular dystrophy. | Academic Article |
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| A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy. | Academic Article |
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| Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis. | Academic Article |
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| Compromised nonsense-mediated RNA decay results in truncated RNA-binding protein production upon DUX4 expression. | Academic Article |
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| DUX4-induced bidirectional HSATII satellite repeat transcripts form intranuclear double-stranded RNA foci in human cell models of FSHD. | Academic Article |
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| Elevated plasma complement components in facioscapulohumeral dystrophy. | Academic Article |
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| Emerging roles of macrosatellite repeats in genome organization and disease development. | Academic Article |
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| Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle. | Academic Article |
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