Protein aggregates in Huntington's disease-Reference-Cited by-同舟云学术

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Protein aggregates in Huntington's disease

Published:2012-11 Issue:1 Volume:238 Page:1-11
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Arrasate Montserrat,Finkbeiner Steven

Funder

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

National Institute on Aging

Taube-Koret Center for Huntington's Disease Research

Hellman Family Foundation for Alzheimer's Disease Research

J. David Gladstone Institutes

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference136 articles.

1. Phosphorylation of threonine 3: implications for Huntingtin aggregation and neurotoxicity;Aiken;J. Biol. Chem.,2009

2. Automated microscope system for determining factors that predict neuronal fate;Arrasate;Proc. Natl. Acad. Sci. U. S. A.,2005

3. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death;Arrasate;Nature,2004

4. Kinase inhibitors modulate huntingtin cell localization and toxicity;Atwal;Nat. Chem. Biol.,2011

5. Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length;Becher;Neurobiol. Dis.,1998

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