LAMP2A, and other chaperone-mediated autophagy related proteins, do not decline with age in genetically heterogeneous UM-HET3 mice

Author:

Zhang Katherine K.1,Zhang Peichuan23,Kodur Anagha1,Erturk Ilkim4,Burns Calvin M.4,Kenyon Cynthia2,Miller Richard A.45,Endicott S. Joseph45

Affiliation:

1. University of Michigan, College of Literature, Science, and The Arts, Ann Arbor, MI 48109, USA

2. Calico Life Sciences, South San Francisco, CA 94080, USA

3. Current Affiliation: WuXi AppTec, Shanghai, China

4. University of Michigan, Department of Pathology, Ann Arbor, MI 48109, USA

5. University of Michigan Geriatrics Center, Ann Arbor, MI 48109, USA

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

Reference60 articles.

1. The coming of age of chaperone-mediated autophagy.;Cuervo;Nat Rev Mol Cell Biol,2018

2. Autophagy and aging.;Kroemer;Cell,2011

3. Protein homeostasis: live long, won’t prosper.;Hetzer;Nat Rev Mol Cell Biol,2013

4. Proteostasis and aging.;Cuervo;Nat Med,2015

5. Cross-species functional modules link proteostasis to human normal aging.;Robinson-Rechavi;PLoS Comput Biol,2019

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