A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease
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Title
A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 23, Issue 11, Pages 2995-3007
Publisher
Oxford University Press (OUP)
Online
2014-01-17
DOI
10.1093/hmg/ddu010
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- Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease
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- Genome-Wide Histone Acetylation Is Altered in a Transgenic Mouse Model of Huntington's Disease
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- SIRT1-dependent regulation of chromatin and transcription: Linking NAD+ metabolism and signaling to the control of cellular functions
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- Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models
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- (2008) Ying Li et al. Cell Metabolism
- Inhibition of specific HDACs and sirtuins suppresses pathogenesis in a Drosophila model of Huntington’s disease
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- Huntingtin Modulates Transcription, Occupies Gene Promoters In Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manner
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- Dysregulation of Gene Expression in Primary Neuron Models of Huntington's Disease Shows That Polyglutamine-Related Effects on the Striatal Transcriptome May Not Be Dependent on Brain Circuitry
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- Nicotinamide Restores Cognition in Alzheimer's Disease Transgenic Mice via a Mechanism Involving Sirtuin Inhibition and Selective Reduction of Thr231-Phosphotau
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