Skeletal muscle-specific Sidt2 knockout in mice induced muscular dystrophy-like phenotype

Author:

Liu Huan,Jiang Wenjun,Chen Xueru,Chang Guoying,Zhao Lei,Li Xihua,Zhang Huiwen

Funder

NSFC

Shanghai Science and Technology Committee

Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference40 articles.

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2. Misregulation of autophagy and protein degradation systems in myopathies and muscular dystrophies;Sandri;J Cell Sci,2013

3. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease);Nishino;Nature,2000

4. Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function;Saftig;Nat Rev Mol Cell Biol,2009

5. Lysosomal membrane glycoproteins. Structure, biosynthesis, and intracellular trafficking;Fukuda;J Biol Chem,1991

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