Themdxmouse as a model for carnitine deficiency in the pathogenesis of duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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Themdxmouse as a model for carnitine deficiency in the pathogenesis of duchenne muscular dystrophy

Published:2012-10-10 Issue:5 Volume:46 Page:767-772
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Zolkipli Zarazuela,Mai Lydia,Lamhonwah Anne-Marie,Tein Ingrid

Funder

Department of Paediatrics, The Hospital for Sick Children, Toronto

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.23368/fullpdf

Reference50 articles.

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

2. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin;Ervasti;J Cell Biol,1993

3. The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies;Rando;Muscle Nerve,2001

4. Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse;Gillis;J Muscle Res Cell Motil,1999

5. Functional regeneration in the hindlimb skeletal muscle of the mdx mouse;Anderson;J Muscle Res Cell Motil,1988

Cited by 2 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. Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis;Clinica Chimica Acta;2020-06

2. Improvement of Endurance of DMD Animal Model Using Natural Polyphenols;BioMed Research International;2015

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