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Tissue transglutaminase overexpression does not modify the disease phenotype of the R6/2 mouse model of Huntington’s disease

Huntington’s disease (HD) is a devastating autosomal-dominant neurodegenerative disorder initiated by an abnormally expanded polyglutamine in the huntingtin protein. Determining the contribution of specific factors to the pathogenesis of HD should provide rational targets for therapeutic interventio...

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Main Authors: Kumar, Ashish, Kneynsberg, Andrew, Tucholski, Janusz, Perry, Giselle, van Groen, Thomas, Detloff, Peter J., Lesort, Mathieu
Formato: Artigo
Idioma:Inglês
Publicado: 2012
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3418489/
https://ncbi.nlm.nih.gov/pubmed/22698685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2012.05.015
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