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The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 20, p. 3925, doi. 10.1093/hmg/ddr311
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- Article
Polyrotaxane Nanocarriers Can Deliver CRISPR/Cas9 Plasmid to Dystrophic Muscle Cells to Successfully Edit the DMD Gene.
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- Advanced Therapeutics, 2019, v. 2, n. 7, p. N.PAG, doi. 10.1002/adtp.201900061
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- Article
The Development of Robust Antibodies to Sarcospan, a Dystrophin- and Integrin-Associated Protein, for Basic and Translational Research.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 11, p. 6121, doi. 10.3390/ijms25116121
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- Article
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue.
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- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03938-0
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- Article
High-throughput screening identifies modulators of sarcospan that stabilize muscle cells and exhibit activity in the mouse model of Duchenne muscular dystrophy.
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- Skeletal Muscle, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13395-020-00244-3
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- Article
Nanoparticles systemically biodistribute to regenerating skeletal muscle in DMD.
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- Journal of Nanobiotechnology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12951-023-01994-0
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- Article
Using a bioaerosol personal sampler in combination with real-time PCR analysis for rapid detection of airborne viruses.
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- Environmental Microbiology, 2007, v. 9, n. 4, p. 992, doi. 10.1111/j.1462-2920.2006.01226.x
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- Article
Dantrolene Enhances Antisense-Mediated Exon Skipping in Human and Mouse Models of Duchenne Muscular Dystrophy.
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- Science Translational Medicine, 2012, v. 4, n. 164, p. 1, doi. 10.1126/scitranslmed.3005054
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- Article
The E3 ubiquitin ligase TRIM32 regulates myoblast proliferation by controlling turnover of NDRG2.
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- Human Molecular Genetics, 2015, v. 24, n. 10, p. 2873, doi. 10.1093/hmg/ddv049
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- Article