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SETD2 deficiency promotes renal fibrosis through the TGF-β/Smad signaling pathway in the absence of VHL

2022-09-10

Abstract excerpt

Renal fibrosis is the final development pathway and the most common pathological manifestation of chronic kidney disease. An important intrinsic cause of renal fibrosis is epigenetic alterations. SET domain–containing 2 (SETD2) is the sole histone H3K36 trimethyltransferase, catalyzing H3K36 dimethylation to trimethylation. There is evidence that SETD2-mediated epigenetic alterations are implicated in many disease...

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Literature Corpus work
8813cc86-6a56-58e8-bfa1-246c802838ec
DOI
10.1101/2022.09.10.507394
Open publication

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SETD2 deficiency promotes renal fibrosis through the TGF-β/Smad signaling pathway in the absence of VHLDOI 10.1101/2022.09.10.507394
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