Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice
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Title
Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 109, Issue 9, Pages 3528-3533
Publisher
Proceedings of the National Academy of Sciences
Online
2012-02-14
DOI
10.1073/pnas.1114502109
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Note: Only part of the references are listed.- Preferential accumulation of N-terminal mutant huntingtin in the nuclei of striatal neurons is regulated by phosphorylation
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- (2010) V. Maglione et al. JOURNAL OF NEUROSCIENCE
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- (2010) M. Metzler et al. JOURNAL OF NEUROSCIENCE
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- Molecular Mechanisms and Potential Therapeutical Targets in Huntington's Disease
- (2010) Chiara Zuccato et al. PHYSIOLOGICAL REVIEWS
- Polyglutamine Induced Misfolding of Huntingtin Exon1 is Modulated by the Flanking Sequences
- (2010) Vinal V. Lakhani et al. PLoS Computational Biology
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- Acetylation Targets Mutant Huntingtin to Autophagosomes for Degradation
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- Phosphorylation of Threonine 3
- (2009) Charity T. Aiken et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome
- (2009) Leslie Michels Thompson et al. JOURNAL OF CELL BIOLOGY
- Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism
- (2009) Ashwani K Thakur et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
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- (2008) Simon C. Warby et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Elimination of GD3 synthase improves memory and reduces amyloid-β plaque load in transgenic mice
- (2008) Alexandra Bernardo et al. NEUROBIOLOGY OF AGING
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