Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene-Reference-Cited by-同舟云学术

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Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene

Published:2017-01-09 Issue: Volume: Page:ddw389
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Le Dour Caroline,Macquart Coline,Sera Fusako,Homma Shunichi,Bonne Gisele,Morrow John P.,Worman Howard J.,Muchir Antoine

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/26/2/333/10935466/ddw389.pdf

Reference48 articles.

1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

2. Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

3. Primary Prevention of Sudden Death in Patients with Lamin A/C Gene Mutations

4. Heart involvement in lamin A/C related diseases;Ben Yaou;Arch. Mal. Coeur Vaiss,2006

5. LMNA cardiomyopathy: cell biology and genetics meet clinical medicine

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2. mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice;Circulation: Heart Failure;2024-04

3. From gene to mechanics: a comprehensive insight into the mechanobiology of LMNA mutations in cardiomyopathy;Cell Communication and Signaling;2024-03-27

4. Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNA gene mutation;The Journal of Physiological Sciences;2023-11-08

5. Modulation of cytoskeleton in cardiomyopathy caused by mutations inLMNAgene;American Journal of Physiology-Cell Physiology;2023-06-01

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