Suppression of myopathic lamin mutations by muscle-specific activation ofAMPKand modulation of downstream signaling-Reference-Cited by-同舟云学术

Suppression of myopathic lamin mutations by muscle-specific activation ofAMPKand modulation of downstream signaling

Published:2018-09-18 Issue:3 Volume:28 Page:351-371
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Chandran Sahaana¹,Suggs Jennifer A¹,Wang Bingyan J¹^ORCID,Han Andrew¹,Bhide Shruti¹,Cryderman Diane E²,Moore Steven A³,Bernstein Sanford I¹^ORCID,Wallrath Lori L²,Melkani Girish C¹^ORCID

Affiliation:

1. Department of Biology, Molecular Biology and Heart Institutes, San Diego State University, San Diego, CA, USA

2. Department of Biochemistry, Carver College of Medicine, University of Iowa, Iowa City, IA, USA

3. Department of Pathology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA

Funder

National Institutes of Health

Muscular Dystrophy Association

University of Iowa Wellstone Muscular Dystrophy Cooperative Research Center

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/28/3/351/27520176/ddy332.pdf

Reference88 articles.

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2. Lamin mutations accelerate aging via defective export of mitochondrial mRNAs through nuclear envelope budding;Li;Curr. Biol.,2016

3. Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects;Decostre;Acta Myol.,2005

4. Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations;Carboni;Muscle Nerve,2013

5. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease;Arbustini;J. Am. Coll. Cardiol.,2002

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