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The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington’s Disease

Date Posted: Thursday, December 03, 2015
By: Dong X, Tsuji J, Labadorf A, Roussos P, Chen JF, Myers RH, Akbarian S, Weng Z.

Huntington's disease (HD) is an autosomal-dominant neurodegenerative disorder resulting from expansion of CAG repeats in the Huntingtin (HTT) gene. Previous studies have shown mutant HTT can alter expression of genes associated with dysregulated epigenetic modifications. Read More

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