Oxidative stress-mediated aldehyde adduction of GRP78 in a mouse model of alcoholic liver disease: functional independence of ATPase activity and chaperone function-Reference-Cited by-同舟云学术

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Oxidative stress-mediated aldehyde adduction of GRP78 in a mouse model of alcoholic liver disease: functional independence of ATPase activity and chaperone function

Published:2014-08 Issue: Volume:73 Page:411-420
ISSN:0891-5849
Container-title:Free Radical Biology and Medicine
language:en
Short-container-title:Free Radical Biology and Medicine

Author:

Galligan James J.,Fritz Kristofer S.,Backos Donald S.,Shearn Colin T.,Smathers Rebecca L.,Jiang Hua,MacLean Kenneth N.,Reigan Philip R.,Petersen Dennis R.

Funder

National Institutes of Health/National Institute of Alcoholism and Alcohol Abuse

Colorado Clinical Translational Science Institute

University of Colorado Cancer Center

NIH/NCATS Colorado CTSI

Publisher

Elsevier BV

Subject

Physiology (medical),Biochemistry

Reference43 articles.

1. Alcohol, oxidative stress and free radical damage;Albano;Proc. Nutr. Soc.,2006

2. Protein carbonylation in human diseases;Dalle-Donne;Trends Mol. Med.,2003

3. Endoplasmic reticulum stress and oxidative stress: a vicious cycle or a double-edged sword?;Malhotra;Antioxid. Redox Signaling,2007

4. Oxidative stress and the ER stress response in a murine model for early-stage alcoholic liver disease;Galligan;J. Toxicol,2012

5. Lipid peroxidation contributes to immune reactions associated with alcoholic liver disease;Mottaran;Free Radic. Biol. Med.,2002

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