Immunohistochemical Characterization of FacioscapulohumeralMuscular Dystrophy Muscle Biopsies-Reference-Cited by-同舟云学术

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Immunohistochemical Characterization of FacioscapulohumeralMuscular Dystrophy Muscle Biopsies

Published:2015-09-02 Issue:3 Volume:2 Page:291-299
ISSN:2214-3599
Container-title:Journal of Neuromuscular Diseases
language:
Short-container-title:JND

Author:

Statland Jeffrey M.¹²,Odrzywolski Karen J.²,Shah Bharati²,Henderson Don²,Fricke Alex F.³,van der Maarel Silvére M.⁴,Tapscott Stephen J.⁵,Tawil Rabi²

Affiliation:

1. Department of Neurology, University of Kansas Medical Center, Kansas City, KS, USA

2. Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA

3. Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA

4. Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands

5. Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA

Publisher

IOS Press

Subject

Neurology (clinical),Neurology

Reference31 articles.

1. Genetic characterization of a large,historically significant Utah kindred with facioscapulohumeraldystrophy;Flanigan;Neuromuscul Disord.,2001

2. Facioscapulohumeral muscular dystrophy in the Dutch population;Padberg;Muscle Nerve,1995

3. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2;Lemmers;Nat Genet,2012

4. A unifying genetic model for facioscapulohumeral muscular dystrophy;Lemmers;Science,2010

5. Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes;Celegato;Proteomics,2006

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3. IL-6 and TNF are Potential Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy;Journal of Neuromuscular Diseases;2024-03-05

4. An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and increased skeletal muscle regeneration;Neuromuscular Disorders;2024-03

5. Voluntary wheel running improves molecular and functional deficits in a murine model of facioscapulohumeral muscular dystrophy;iScience;2024-01

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