Suppression of protein aggregation by chaperone modification of high molecular weight complexes
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Suppression of protein aggregation by chaperone modification of high molecular weight complexes
Authors
Keywords
-
Journal
BRAIN
Volume 135, Issue 4, Pages 1180-1196
Publisher
Oxford University Press (OUP)
Online
2012-03-07
DOI
10.1093/brain/aws022
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Hsp70 and Hsp40 Functionally Interact with Soluble Mutant Huntingtin Oligomers in a Classic ATP-dependent Reaction Cycle
- (2010) Gregor P. Lotz et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The mitochondrial UPR - protecting organelle protein homeostasis
- (2010) C. M. Haynes et al. JOURNAL OF CELL SCIENCE
- A DNAJB Chaperone Subfamily with HDAC-Dependent Activities Suppresses Toxic Protein Aggregation
- (2010) Jurre Hageman et al. MOLECULAR CELL
- Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease
- (2010) Marta Martinez-Vicente et al. NATURE NEUROSCIENCE
- Heat shock factors: integrators of cell stress, development and lifespan
- (2010) Malin Åkerfelt et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- The HSP70 chaperone machinery: J proteins as drivers of functional specificity
- (2010) Harm H. Kampinga et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- SIRT2 inhibition achieves neuroprotection by decreasing sterol biosynthesis
- (2010) Ruth Luthi-Carter et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Single-step detection of mutant huntingtin in animal and human tissues: A bioassay for Huntington’s disease
- (2009) Andreas Weiss et al. ANALYTICAL BIOCHEMISTRY
- Identical oligomeric and fibrillar structures captured from the brains of R6/2 and knock-in mouse models of Huntington's disease
- (2009) Kirupa Sathasivam et al. HUMAN MOLECULAR GENETICS
- The chaperonin TRiC blocks a huntingtin sequence element that promotes the conformational switch to aggregation
- (2009) Stephen Tam et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Genetic Knock-Down of HDAC7 Does Not Ameliorate Disease Pathogenesis in the R6/2 Mouse Model of Huntington's Disease
- (2009) Caroline L. Benn et al. PLoS One
- Formation of Polyglutamine Inclusions in a Wide Range of Non-CNS Tissues in the HdhQ150 Knock-In Mouse Model of Huntington's Disease
- (2009) Hilary Moffitt et al. PLoS One
- Distinct conformations of in vitro and in vivo amyloids of huntingtin-exon1 show different cytotoxicity
- (2009) Y. Nekooki-Machida et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Hsp104, Hsp70 and Hsp40 interplay regulates formation, growth and elimination of Sup35 prions
- (2008) James Shorter et al. EMBO JOURNAL
- Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease
- (2008) Caroline L Benn et al. Molecular Neurodegeneration
- Adapting Proteostasis for Disease Intervention
- (2008) William E. Balch et al. SCIENCE
- Polyglutamine neurodegeneration: protein misfolding revisited
- (2008) Aislinn J. Williams et al. TRENDS IN NEUROSCIENCES
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started