ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies-Reference-Cited by-同舟云学术

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ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies

Published:2022-11 Issue:6 Volume:9 Page:1506-1520
ISSN:2352-3042
Container-title:Genes & Diseases
language:en
Short-container-title:Genes & Diseases

Author:

Christiansen Jon,Güttsches Anne-Katrin,Schara-Schmidt Ulrike,Vorgerd Matthias^ORCID,Heute Christoph,Preusse Corinna,Stenzel Werner,Roos Andreas^ORCID

Funder

European Regional Development Fund

French Muscular Dystrophy Association

AFM-Téléthon

Universität Duisburg-Essen

Publisher

Elsevier BV

Subject

Cell Biology,Genetics (clinical),Molecular Biology,Biochemistry

Reference45 articles.

1. Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies;Bolduc;Am J Hum Genet,2010

2. Anoctamins (TMEM16 proteins): functions and involvement in neurologic disease;Benarroch;Neurology,2017

3. Deficiency of Anoctamin 5/TMEM16E causes nuclear positioning defect and impairs Ca2+ signaling of differentiated C2C12 myotubes;Phuong;Korean J Physiol Pharmacol,2019

4. Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy;Xu;Skelet Muscle,2015

5. Anoctamin5 regulates cell migration and invasion in thyroid cancer;Chang;Int J Oncol,2017

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