Xanthine oxidase is hyper-active in Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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Xanthine oxidase is hyper-active in Duchenne muscular dystrophy

Published:2018-12 Issue: Volume:129 Page:364-371
ISSN:0891-5849
Container-title:Free Radical Biology and Medicine
language:en
Short-container-title:Free Radical Biology and Medicine

Author:

Lindsay Angus,McCourt Preston M.,Karachunski Peter,Lowe Dawn A.,Ervasti James M.

Funder

Muscular Dystrophy Association

University of Minnesota AHC Seed

Gregory Marzolf Jr. Foundation

National Institutes of Health

Publisher

Elsevier BV

Subject

Physiology (medical),Biochemistry

Reference58 articles.

1. The role of free radicals in the pathophysiology of muscular dystrophy;Tidball;J. Appl. Physiol.,2007

2. Evidence of oxidative stress in mdx mouse muscle: studies of the pre-necrotic state;Disatnik;J. Neurol. Sci.,1998

3. Oxidative damage to muscle protein in Duchenne muscular dystrophy;Haycock;Neuroreport,1996

4. Muscle cells from mdx mice have an increased susceptibility to oxidative stress;Rando;Neuromuscul. Disord.,1998

5. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

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