Polyglutamine-Induced Neurodegeneration: Pathogenesis is Linked to Native Protein Biochemistry Function

 


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Air date: Monday, November 19, 2007, 12:00:00 PM
Category: Neuroscience
Runtime: 75 minutes
NLM Title: Polyglutamine-induced neurodegeneration : pathogenesis is linked to native protein biochemistry function [electronic resource] / Harry Orr.
Series: Molecular basis of the polyglutamine neurogeneerative disease SCA1
Author: Orr, Harry.
National Institutes of Health (U.S.)
Publisher: [Bethesda, Md. : National Institutes of Health, 2007]
Other Title(s): Molecular basis of the polyglutamine neurogeneerative disease SCA1
Abstract: (CIT): Dr. Orr discovered that an expanded glutamine tract in the ataxin-1 gene is the cause of the inherited neurodegenerative disease, spinocerebellar ataxia type 1 (SCA1). His current research focuses on understanding how polyglutamine tracts lead to neuronal dysfunction and neurodegeneration. His development of a conditional mouse model of Sca1 has yielded a number of insights into the molecular defects caused by the mutant ataxin-1 and how this affects Purkinje cell and cerebellar function and development.
Subjects: Nerve Tissue Proteins
Nuclear Proteins
Spinocerebellar Ataxias--etiology
Publication Types: Government Publications
Lectures
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NLM Classification: WL 320
NLM ID: 101322969
CIT File ID: 14157
CIT Live ID: 6169
Permanent link: http://videocast.nih.gov/launch.asp?14157

 

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