Cardiomyopathy in the dystrophin/utrophin-deficient mouse model of severe muscular dystrophy is characterized by dysregulation of matrix metalloproteinases-Reference-Cited by-同舟云学术

Cardiomyopathy in the dystrophin/utrophin-deficient mouse model of severe muscular dystrophy is characterized by dysregulation of matrix metalloproteinases

Published:2012-11 Issue:11 Volume:22 Page:1006-1014
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Delfín Dawn A.,Zang Kara E.,Schill Kevin E.,Patel Nikita T.,Janssen Paul M.L.,Raman Subha V.,Rafael-Fortney Jill A.

Funder

Muscular Dystrophy Association

Publisher

Elsevier BV

Subject

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

Reference49 articles.

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3. Dystrophin: from non-ischemic cardiomyopathy to ischemic cardiomyopathy;Zheng;Med Hypotheses,2008

4. Emergent dilated cardiomyopathy caused by targeted repair of dystrophic skeletal muscle;Townsend;Mol Ther,2008

5. Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy;Duan;Hum Mol Genet,2006

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