Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers-Reference-Cited by-同舟云学术

Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers

Published:1995-05 Issue:3 Volume:5 Page:209-220
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Matthews P.M.,Benjamin D.,Van Bakel I.,Squier M.V.,Nicholson L.V.B.,Sewry C.,Barnes P.R.J.,Hopkin J.,Brown R.,Hilton-Jones D.,Boyd Y.,Karpati G.,Brown G.K.,Craig I.W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference37 articles.

1. Characterization of dystrophin in muscle biopsy specimens from patients with Duchenne or Becker muscular dystrophy;Hoffman;N Engl J Med,1988

2. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy;Bonilla;Am J Pathol,1988

3. Mosaic expression of dystrophin in symptomatic carriers ou Duchenne's muscular dystrophy;Arahata;N Engl J Med,1989

4. Characterization of dystrophin in carriers of Duchenne muscular dystrophy;Clerk;J Neurol Sci,1991

5. Followup study of serum creatine kinase in carriers of Duchenne muscular dystrophy;Moser;Lancet,1974

Cited by 51 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. Prenatal risk assessment of Xp21.1 duplication involving theDMDgene by optical genome mapping;Life Science Alliance;2024-08-08

2. 263rd ENMC International Workshop: Focus on female carriers of dystrophinopathy: refining recommendations for prevention, diagnosis, surveillance, and treatment. Hoofddorp, The Netherlands, 13-15 May 2022;Neuromuscular Disorders;2023-03

3. Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle;Proceedings of the National Academy of Sciences;2023-01-03

4. Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies;Neuromuscular Disorders;2022-12

5. X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis;International Journal of Molecular Sciences;2021-07-17