Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy-Reference-Cited by-同舟云学术

Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy

Published:2020-09-01 Issue:5 Volume:78 Page:2157-2167
ISSN:1420-682X
Container-title:Cellular and Molecular Life Sciences
language:en
Short-container-title:Cell. Mol. Life Sci.

Author:

Boufroura Fatima-Zohra,Tomkiewicz-Raulet Céline,Poindessous Virginie,Castille Johan,Vilotte Jean-Luc,Bastin Jean,Mouillet-Richard Sophie,Djouadi Fatima^ORCID

Funder

AFM-Téléthon

INSERM

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00018-020-03624-6.pdf

Reference39 articles.

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2. Bonnefont JP, Djouadi F, Prip-Buus C, Gobin S, Munnich A, Bastin J (2004) Carnitine palmitoyltransferases 1 and 2: biochemical, molecular and medical aspects. Mol Aspects Med 25(5–6):495–520

3. Boufroura FZ, Le Bachelier C, Tomkiewicz-Raulet C, Schlemmer D, Benoist JF, Grondin P, Lamotte Y, Mirguet O, Mouillet-Richard S, Bastin J, Djouadi F (2018) A new AMPK activator, GSK773, corrects fatty acid oxidation and differentiation defect in CPT2-deficient myotubes. Hum Mol Genet 27(19):3417–3433. https://doi.org/10.1093/hmg/ddy254

4. Abmayr SM, Pavlath GK (2012) Myoblast fusion: lessons from flies and mice. Development 139(4):641–656. https://doi.org/10.1242/dev.068353

5. Graham ZA, Gallagher PM, Cardozo CP (2015) Focal adhesion kinase and its role in skeletal muscle. J Muscle Res Cell Motil 36(4–5):305–315. https://doi.org/10.1007/s10974-015-9415-3

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