Skeletal muscle-specific Sidt2 knockout in mice induced muscular dystrophy-like phenotype-Reference-Cited by-同舟云学术

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

Published:2018-08 Issue: Volume:85 Page:259-270
ISSN:0026-0495
Container-title:Metabolism
language:en
Short-container-title:Metabolism

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.

1. Sarcolipin: a key thermogenic and metabolic regulator in skeletal muscle;Pant;Trends Endocrinol Metab,2016

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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3. Structural insight into the human SID1 transmembrane family member 2 reveals its lipid hydrolytic activity;Nature Communications;2023-06-15

4. SIDT2 Inhibits Phosphorothioate Antisense Oligonucleotide Activity by Regulating Cellular Localization of Lysosomes;Nucleic Acid Therapeutics;2023-04-01

5. The functions of SID1 transmembrane family, member 2 ( Sidt2 );The FEBS Journal;2022-10-14

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