New Tricks for Nrf2: Therapeutic Targeting to Restore BK-β1 Expression?
Author:
Affiliation:
1. King’s British Heart Foundation Centre of Research Excellence, Cardiovascular Division, Faculty of Life Sciences & Medicine, King’s College London, London, U.K.
Funder
British Heart Foundation
Heart Research UK
Publisher
American Diabetes Association
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://journals.org/diabetes/diabetes/article-pdf/66/10/2538/534261/dbi170024.pdf
Reference25 articles.
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3. Keap1 represses nuclear activation of antioxidant responsive elements by Nrf2 through binding to the amino-terminal Neh2 domain;Itoh;Genes Dev,1999
4. Keap1 recruits Neh2 through binding to ETGE and DLG motifs: characterization of the two-site molecular recognition model;Tong;Mol Cell Biol,2006
5. Dimerization of substrate adaptors can facilitate cullin-mediated ubiquitylation of proteins by a “tethering” mechanism: a two-site interaction model for the Nrf2-Keap1 complex;McMahon;J Biol Chem,2006
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