Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy miceSUMNER, Charlotte J; WEE, Claribel D; WARSING, Leigh C et al.Human molecular genetics (Print). 2009, Vol 18, Num 17, pp 3145-3152, issn 0964-6906, 8 p.Article

Etiology of Limb Girdle Muscular Dystrophy 1D/1E Determined by Laser Capture Microdissection ProteomicsGREENBERG, Steven A; SALAJEGHEH, Mohammad; JUDGE, Daniel P et al.Annals of neurology. 2012, Vol 71, Num 1, pp 141-145, issn 0364-5134, 5 p.Article

A Phase I/II trial of MYO-029 in Adult Subjects with Muscular DystrophyWAGNER, Kathryn R; FLECKENSTEIN, James L; EAGLE, Michelle et al.Annals of neurology. 2008, Vol 63, Num 5, pp 561-571, issn 0364-5134, 11 p.Article

A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell functionHOMMA, Sachiko; CHEN, Jennifer Cj; RAHIMOV, Fedik et al.European journal of human genetics. 2012, Vol 20, Num 4, pp 404-410, issn 1018-4813, 7 p.Article

Myostatin mutation associated with gross muscle hypertrophy in a childSCHUELKE, Markus; WAGNER, Kathryn R; STOLZ, Leslie E et al.The New England journal of medicine. 2004, Vol 350, Num 26, pp 2682-2688, issn 0028-4793, 7 p.Article

Genetic diseases of muscleWAGNER, Kathryn R.Neurologic clinics. 2002, Vol 20, Num 3, issn 0733-8619, vi, 645-678 [35 p.]Article

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesisLIDA JONES, Takako; CHEN, Jennifer C. J; WAGNER, Kathryn R et al.Human molecular genetics (Print). 2012, Vol 21, Num 20, pp 4419-4430, issn 0964-6906, 12 p.Article

Clinical Predictors of Conduction Disease Progression in Type I Myotonic Muscular DystrophyNAZARIAN, Saman; WAGNER, Kathryn R; CAFFO, Brian S et al.Pacing and clinical electrophysiology. 2011, Vol 34, Num 2, pp 171-176, issn 0147-8389, 6 p.Article

A soluble activin type IIB receptor improves function in a mouse model of amyotrophic lateral sclerosisMORRISON, Brett M; LACHEY, Jennifer L; COLANTUONI, Elizabeth et al.Experimental neurology (Print). 2009, Vol 217, Num 2, pp 258-268, issn 0014-4886, 11 p.Article

Loss of myostatin attenuates severity of muscular dystrophy in mdx miceWAGNER, Kathryn R; MCPHERRON, Alexandra C; WINIK, Nicole et al.Annals of neurology. 2002, Vol 52, Num 6, pp 832-836, issn 0364-5134, 5 p.Article

Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutationsWAGNER, Kathryn R; HAMED, Sherifa; HADLEY, Donald W et al.Annals of neurology. 2001, Vol 49, Num 6, pp 706-711, issn 0364-5134Article