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Huntingtin Aggregation Kinetics and Their Pathological Role in a Drosophila Huntington’s Disease Model

Huntington’s disease is a neurodegenerative disorder resulting from expansion of a polyglutamine tract in the Huntingtin protein. Mutant Huntingtin forms intracellular aggregates within neurons, although it is unclear whether aggregates or more soluble forms of the protein represent the pathogenic s...

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Bibliografiske detaljer
Main Authors: Weiss, Kurt R., Kimura, Yoko, Lee, Wyan-Ching Mimi, Littleton, J. Troy
Format: Artigo
Sprog:Inglês
Udgivet: Genetics Society of America 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3276644/
https://ncbi.nlm.nih.gov/pubmed/22095086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.111.133710
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