Impairment of chaperone‐mediated autophagy leads to selective lysosomal degradation defects in the lysosomal storage disease cystinosis-Reference-Cited by-同舟云学术

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Impairment of chaperone‐mediated autophagy leads to selective lysosomal degradation defects in the lysosomal storage disease cystinosis

Published:2015-01-13 Issue:2 Volume:7 Page:158-174
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Napolitano Gennaro¹,Johnson Jennifer L¹,He Jing¹,Rocca Celine J²,Monfregola Jlenia¹,Pestonjamasp Kersi³,Cherqui Stephanie²,Catz Sergio D¹

Affiliation:

1. Department of Molecular and Experimental Medicine The Scripps Research Institute La Jolla CA USA

2. Department of Pediatrics University of California San Diego La Jolla CA USA

3. Cancer Center Microscopy Shared Resource University of California San Diego La Jolla CA USA

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201404223

Reference60 articles.

1. CTNS mutations in patients with cystinosis

2. The Chaperone-Mediated Autophagy Receptor Organizes in Dynamic Protein Complexes at the Lysosomal Membrane

3. Biosynthesis, glycosylation, movement through the Golgi system, and transport to lysosomes by an N‐linked carbohydrate‐independent mechanism of three lysosomal integral membrane proteins;Barriocanal JG;J Biol Chem,1986

4. Chaperone-Mediated Autophagy

5. Steady-state pharmacokinetics and pharmacodynamics of cysteamine bitartrate in paediatric nephropathic cystinosis patients

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