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Department of Pharmacology
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Muscle xenografts reproduce key molecular features of facioscapulohumeral muscular dystrophy.
Experimental neurology 10, 2019 | Pubmed ID: 31306642
Targeted epigenetic repression by CRISPR/dSaCas9 suppresses pathogenic expression in FSHD.
Molecular therapy. Methods & clinical development Mar, 2021 | Pubmed ID: 33511244
Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models.
Disease models & mechanisms 08, 2021 | Pubmed ID: 34338285
Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects.
Diagnostics (Basel, Switzerland) Aug, 2021 | Pubmed ID: 34441403
University of Nevada, Reno School of Medicine
Morium Begam1,
Neha Narayan1,
Drew Mankowski1,
Robert Camaj1,
Nicholas Murphy1,
Kevin Roseni1,
Marie E. Pepin1,
Jacob M. Blackmer1,
Takako I. Jones2,
Joseph A. Roche1
1Physical Therapy Program, Department of Health Care Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University,
2Department of Pharmacology, University of Nevada, Reno School of Medicine
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