Lipolysis and lipophagy in lipid storage myopathies-Reference-Cited by-同舟云学术

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Lipolysis and lipophagy in lipid storage myopathies

Published:2016-07 Issue:7 Volume:1862 Page:1367-1373
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Angelini Corrado,Nascimbeni Anna Chiara,Cenacchi Giovanna,Tasca Elisabetta

Funder

Association Française contre le Myopathies-AFM

Comitato Telethon Fondazione Onlus

Eurobiobank network

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference21 articles.

1. Mutations and polymorphisms of the gene encoding the beta-subunit of the electron transfer flavoprotein in three patients with glutaric acidemia type II;Colombo;Hum. Mol. Genet.,1994

2. Recurrent hypoglycemia associated with glutaric aciduria type II in an adult;Dusheiko;N. Eng. J. Med.,1979

3. The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy;Fischer;Nat. Genet.,2007

4. TFEB links autophagy to lysosomal biogenesis;Settembre;Science,2011

5. ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1;Haemmerle;Nat. Med.,2011

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