Biochemical and pathological changes result from mutated Caveolin-3 in muscle-Reference-Cited by-同舟云学术

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Biochemical and pathological changes result from mutated Caveolin-3 in muscle

Published:2018-08-28 Issue:1 Volume:8 Page:
ISSN:2044-5040
Container-title:Skeletal Muscle
language:en
Short-container-title:Skeletal Muscle

Author:

González Coraspe José Andrés,Weis Joachim,Anderson Mary E.,Münchberg Ute,Lorenz Kristina,Buchkremer Stephan,Carr Stephanie,Zahedi René Peiman,Brauers Eva,Michels Hannah,Sunada Yoshihide,Lochmüller Hanns,Campbell Kevin P.,Freier Erik,Hathazi Denisa,Roos Andreas

Funder

Ministerium für Innovation, Wissenschaft und Forschung des Landes Nordrhein-Westfalen

Bundesministerium für Bildung und Forschung

Deutsche Gesellschaft für Muskelkranke

IZKF Aachen

Paul D. Wellstone Muscular Dystrophy Cooperative Research Center

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Orthopedics and Sports Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13395-018-0173-y.pdf

Reference51 articles.

1. Gazzerro E, Sotgia F, Bruno C, Lisanti MP, Minetti C. Caveolinopathies: from the biology of caveolin-3 to human diseases. Eur J Hum Genet. 2010;18:137–45.

2. Kassan A, Pham U, Nguyen Q, Reichelt ME, Cho E, Patel PM, Roth DM, Head BP, Patel HH. Caveolin-3 plays a critical role in autophagy after ischemia-reperfusion. Am J Physiol Cell Physiol. 2016;311:C854–65.

3. Takamori M. Synaptic homeostasis and its immunological disturbance in neuromuscular junction disorders. Int J Mol Sci. 2017;18(4).

4. Macias A, Gambin T, Szafranski P, Jhangiani SN, Kolasa A, Obersztyn E, Lupski JR, Stankiewicz P, Kaminska A. CAV3 mutation in a patient with transient hyperCKemia and myalgia. Neurol Neurochir Pol. 2016;50:468–73.

5. Vorgerd M, Ricker K, Ziemssen F, Kress W, Goebel HH, Nix WA, Kubisch C, Schoser BG, Mortier W. A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation. Neurology. 2001;57:2273–7.

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