Genetic modifiers of D uchenne and facioscapulohumeral muscular dystrophies-Reference-Cited by-同舟云学术

Genetic modifiers of D uchenne and facioscapulohumeral muscular dystrophies

Published:2017-09-22 Issue:1 Volume:57 Page:6-15
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Hightower Rylie M.¹,Alexander Matthew S.²³

Affiliation:

1. University of Alabama at Birmingham Graduate School of Biomedical SciencesBirmingham Alabama USA

2. Department of PediatricsDivision of Neurology at Children's of Alabama and University of Alabama at BirminghamMCLM 464 Box 96, 1918 University Boulevard Birmingham Alabama35294 USA

3. Department of GeneticsUniversity of Alabama at BirminghamBirmingham Alabama USA

Funder

National Institutes of Health

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.25953

Reference136 articles.

1. Population frequencies of inherited neuromuscular diseases—A world survey

2. Evidence-based path to newborn screening for duchenne muscular dystrophy

3. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

4. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

5. Dystrophin: The protein product of the duchenne muscular dystrophy locus

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD);Journal of Neurology;2024-07-02

2. In dystrophicmdxhindlimb muscles where fibrosis is limited versican haploinsufficiency transiently improves contractile function without decreasing inflammation;2024-05-10

3. Evaluation of Neuromuscular Diseases and Complaints by Quantitative Muscle MRI;Journal of Clinical Medicine;2024-03-28

4. PAX7, a Key for Myogenesis Modulation in Muscular Dystrophies through Multiple Signaling Pathways: A Systematic Review;International Journal of Molecular Sciences;2023-08-22

5. CRISPR-Cas9 mediated endogenous utrophin upregulation improves Duchenne Muscular Dystrophy;2023-04-19