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Your search keyword '"Coppens SE"' showing total 10 results

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1. Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design

2. Human miRNA miR-675 inhibits DUX4 expression and may be exploited as a potential treatment for Facioscapulohumeral muscular dystrophy.

3. Retrospective clinical trial experimentally validates glioblastoma genome-wide pattern of DNA copy-number alterations predictor of survival.

4. Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design.

5. AAV-mediated follistatin gene therapy improves functional outcomes in the TIC-DUX4 mouse model of FSHD.

6. Mouse Dux is myotoxic and shares partial functional homology with its human paralog DUX4.

7. RNAi-mediated Gene Silencing of Mutant Myotilin Improves Myopathy in LGMD1A Mice.

8. RNA interference inhibits DUX4-induced muscle toxicity in vivo: implications for a targeted FSHD therapy.

9. Construction of permanently inducible miRNA-based expression vectors using site-specific recombinases.

10. RNA interference improves myopathic phenotypes in mice over-expressing FSHD region gene 1 (FRG1).

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