Identification of p38 MAPK and JNK as new targets for correction of Wilson disease-causing ATP7B mutants
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Title
Identification of p38 MAPK and JNK as new targets for correction of Wilson disease-causing ATP7B mutants
Authors
Keywords
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Journal
HEPATOLOGY
Volume 63, Issue 6, Pages 1842-1859
Publisher
Wiley
Online
2015-12-14
DOI
10.1002/hep.28398
References
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Related references
Note: Only part of the references are listed.- The role of MAPK signalling pathways in the response to endoplasmic reticulum stress
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- (2011) Willianne I. M. Vonk et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Clusterin (Apolipoprotein J), a Molecular Chaperone That Facilitates Degradation of the Copper-ATPases ATP7A and ATP7B
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- (2011) S. C. Dodani et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- 2,2′-Bipyridyl based copper complexes down regulate expression of pro-inflammatory cytokines and suppress MAPKs in mitogen induced Peripheral blood mononuclear cells
- (2010) K.R. Rupesh et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
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- Efficacy, pharmacodynamics, and safety of VX-702, a novel p38 MAPK inhibitor, in rheumatoid arthritis: Results of two randomized, double-blind, placebo-controlled clinical studies
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- Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin
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- One step at a time: endoplasmic reticulum-associated degradation
- (2008) Shruthi S. Vembar et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
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