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ChIP-Seq analysis C57BL/6 thymocytes

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https://www.ncbi.nlm.nih.gov/sra/SRP091748
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资源简介:
In this study, we show that in addition to regulating DP thymocytes survival, RORgT also controls genes that regulate thymocyte migration, proliferation, and T cell receptor (TCR) selection. Strikingly, pharmacological inhibition of RORg skews TCR gene rearrangement, limits T cell repertoire diversity, and inhibits development of autoimmune encephalomyelitis. Thus, targeting RORgT not only inhibits Th17 cell development and function but also fundamentally alters thymic-emigrant recognition of self and foreign antigens. Overall design: Examination of RORgT-bound genomic sites in C57BL/6 mouse thymocytes.
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2017-09-17
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