Dr. Chern, Yijuang 陳儀莊 博士

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Energy dysfunction in Huntington's disease: insights from PGC-1α, AMPK, and CKB.

Cell Mol Life Sci., May 25, 2012

Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by a CAG trinucleotide expansion in the Huntingtin (Htt) gene. When the number of CAG repeats exceeds 36, the translated polyglutamine-expanded Htt protein interferes with the normal functions of many types of cellular machinery and causes cytotoxicity.

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