Mutant huntingtin and mitochondrial dysfunction
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference102 articles.
1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group;Cell,1993
2. Huntingtin is present in the nucleus, interacts with the transcriptional corepressor C-terminal binding protein, and represses transcription;Kegel;J. Biol. Chem.,2002
3. Huntingtin associates with acidic phospholipids at the plasma membrane;Kegel;J. Biol. Chem.,2005
4. The first 17 amino acids of Huntingtin modulate its sub-cellular localization, aggregation and effects on calcium homeostasis;Rockabrand;Hum. Mol. Genet.,2007
5. Wild-type huntingtin participates in protein trafficking between the Golgi and the extracellular space;Strehlow;Hum. Mol. Genet.,2007
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