Neuroprotection for Huntington’s Disease: Ready, Set, Slow
- 1 April 2008
- journal article
- review article
- Published by Elsevier in Neurotherapeutics
- Vol. 5 (2) , 226-236
Abstract
No abstract availableKeywords
This publication has 222 references indexed in Scilit:
- Drug targeting of dysregulated transcription in Huntington's diseaseProgress in Neurobiology, 2007
- Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficitsProceedings of the National Academy of Sciences, 2007
- A small-molecule therapeutic lead for Huntington's disease: Preclinical pharmacology and efficacy of C2-8 in the R6/2 transgenic mouseProceedings of the National Academy of Sciences, 2007
- Psychiatric disorders in preclinical Huntington's diseaseJournal of Neurology, Neurosurgery & Psychiatry, 2007
- Ubiquitin conjugating enzymes participate in polyglutamine protein aggregationBMC Cell Biology, 2007
- Huntingtin Interacting Proteins Are Genetic Modifiers of NeurodegenerationPLOS Genetics, 2007
- Small molecules enhance autophagy and reduce toxicity in Huntington's disease modelsNature Chemical Biology, 2007
- OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cellsNature, 2007
- Proteasome Activator Enhances Survival of Huntington's Disease Neuronal Model CellsPLOS ONE, 2007
- Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in BrainScience, 1997