Protein aggregates in Huntington's disease
Top Cited Papers
- 30 November 2012
- journal article
- review article
- Published by Elsevier BV in Experimental Neurology
- Vol. 238 (1), 1-11
- https://doi.org/10.1016/j.expneurol.2011.12.013
Abstract
No abstract availableKeywords
Funding Information
- Ramón y Cajal program
- Ministry of Science and Innovation
- FP7-Marie Curie-IRG Program
- European Commission
- UTE-project/Foundation for Applied Medical Research
- National Institute of Neurological Disease and Stroke (2R01 NS039074, 2R01045091)
- National Institute on Aging (2P01 AG022074)
- Taube-Koret Center for Huntington's Disease Research
- Hellman Family Foundation for Alzheimer's Disease Research
- J. David Gladstone Institutes
This publication has 127 references indexed in Scilit:
- Conformation Sensors that Distinguish Monomeric Proteins from Oligomers in Live CellsCell Chemical Biology, 2010
- Serines 13 and 16 Are Critical Determinants of Full-Length Human Mutant Huntingtin Induced Disease Pathogenesis in HD MiceNeuron, 2009
- Mouse models of Huntington's disease and methodological considerations for therapeutic trialsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2009
- A Role for Ubiquitin in Selective AutophagyMolecular Cell, 2009
- Huntingtin as an essential integrator of intracellular vesicular traffickingTrends in Cell Biology, 2009
- Acetylation Targets Mutant Huntingtin to Autophagosomes for DegradationCell, 2009
- Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neuronsThe EMBO Journal, 2008
- The corticostriatal pathway in Huntington's diseaseProgress in Neurobiology, 2007
- Chaperonin TRiC Promotes the Assembly of polyQ Expansion Proteins into Nontoxic OligomersMolecular Cell, 2006
- Proteases Acting on Mutant Huntingtin Generate Cleaved Products that Differentially Build Up Cytoplasmic and Nuclear InclusionsMolecular Cell, 2002