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Intrinsic mutant HTT-mediated defects in oligodendroglial cells cause myelination thinning and behavioural abnormalities in Huntington disease

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NIAID Data Ecosystem2026-03-10 收录
下载链接:
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA488514
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资源简介:
ChIP-seq of EZH2 and SUZ12 in mouse oligodendrocytes - comparing WT mice with mice expressing mHtt (BAC) and those with oligodendrocyte specific excision of mHtt using a NG2+ Cre.
创建时间:
2018-08-29
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