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簡(jiǎn)要描述：Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CTG)n repeat expansion in the 3’-untranslated region of the myotonin protein kinase gene (DMPK). CUG-BP1 and CUG-BP2 are proteins that bind specifically to (CUG)8 oligonucleotides in vitro. While CUG-BP1 has the major binding activity in normal cells, nuclear CUG-BP2 binding activity increases in DM cells. Both CUG-BP1 and CUG-BP2 are isoforms of a novel heterogeneous nuclear ribonucleoprotein (
產(chǎn)品型號(hào)：bsm-62319R廠商性質(zhì)：生產(chǎn)廠家更新時(shí)間：2025-03-03訪 問(wèn) 量： 137產(chǎn)品分類
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