Malin Regulates Wnt Signaling Pathway through Degradation of Dishevelled2
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Malin Regulates Wnt Signaling Pathway through Degradation of Dishevelled2
Authors
Keywords
-
Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 9, Pages 6830-6839
Publisher
American Society for Biochemistry & Molecular Biology (ASBMB)
Online
2012-01-06
DOI
10.1074/jbc.m111.315135
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Dysfunctions in endosomal–lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora disease
- (2011) Rajat Puri et al. HUMAN MOLECULAR GENETICS
- Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis
- (2011) Jaiprakash Sharma et al. NEUROBIOLOGY OF DISEASE
- Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malin
- (2010) Sudheendra N.R. Rao et al. HUMAN MOLECULAR GENETICS
- Laforin, the most common protein mutated in Lafora disease, regulates autophagy
- (2010) Carmen Aguado et al. HUMAN MOLECULAR GENETICS
- Autophagy negatively regulates Wnt signalling by promoting Dishevelled degradation
- (2010) Chan Gao et al. NATURE CELL BIOLOGY
- K63-linked ubiquitination and neurodegeneration
- (2010) Kah-Leong Lim et al. NEUROBIOLOGY OF DISEASE
- TRAF6 and A20 Regulate Lysine 63-Linked Ubiquitination of Beclin-1 to Control TLR4-Induced Autophagy
- (2010) C. S. Shi et al. Science Signaling
- Dishevelled: The hub of Wnt signaling
- (2009) Chan Gao et al. CELLULAR SIGNALLING
- Lafora progressive myoclonus epilepsy: A meta-analysis of reported mutations in the first decade following the discovery of theEPM2AandNHLRC1genes
- (2009) Shweta Singh et al. HUMAN MUTATION
- Co-chaperone CHIP Stabilizes Aggregate-prone Malin, a Ubiquitin Ligase Mutated in Lafora Disease
- (2009) Sudheendra N. R. Rao et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Ubiquitin Ligase E6-AP Is Induced and Recruited to Aggresomes in Response to Proteasome Inhibition and May Be Involved in the Ubiquitination of Hsp70-bound Misfolded Proteins
- (2009) Amit Mishra et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Emerging roles of Wnts in the adult nervous system
- (2009) Nibaldo C. Inestrosa et al. NATURE REVIEWS NEUROSCIENCE
- Increased Endoplasmic Reticulum Stress and Decreased Proteasomal Function in Lafora Disease Models Lacking the Phosphatase Laforin
- (2009) Santiago Vernia et al. PLoS One
- A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome
- (2008) Alexander G. Bassuk et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The malin–laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin–proteasome system
- (2008) Punitee Garyali et al. HUMAN MOLECULAR GENETICS
- E6-AP Promotes Misfolded Polyglutamine Proteins for Proteasomal Degradation and Suppresses Polyglutamine Protein Aggregation and Toxicity
- (2008) Amit Mishra et al. JOURNAL OF BIOLOGICAL CHEMISTRY
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now