F31 NS083167/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

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Comparison of spinocerebellar ataxia type 3 mouse models identifies early gain-of-function, cell-autonomous transcriptional changes in oligodendrocytes.

Ramani B, Panwar B, Moore LR, Wang B, Huang R, Guan Y, Paulson HL. Ramani B, et al. Hum Mol Genet. 2017 Sep 1;26(17):3362-3374. doi: 10.1093/hmg/ddx224. Hum Mol Genet. 2017. PMID: 28854700 Free PMC article.

A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript.

Ramani B, Harris GM, Huang R, Seki T, Murphy GG, Costa Mdo C, Fischer S, Saunders TL, Xia G, McEachin RC, Paulson HL. Ramani B, et al. Hum Mol Genet. 2015 Mar 1;24(5):1211-24. doi: 10.1093/hmg/ddu532. Epub 2014 Oct 15. Hum Mol Genet. 2015. PMID: 25320121 Free PMC article.

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