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2. Regulation of miR-146a by RelA/NFkB and p53 in STHdh(Q111)/Hdh(Q111) cells, a cell model of Huntington's disease. Ghose J; Sinha M; Das E; Jana NR; Bhattacharyya NP PLoS One; 2011; 6(8):e23837. PubMed ID: 21887328 [TBL] [Abstract][Full Text] [Related]
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9. PRMT5- mediated symmetric arginine dimethylation is attenuated by mutant huntingtin and is impaired in Huntington's disease (HD). Ratovitski T; Arbez N; Stewart JC; Chighladze E; Ross CA Cell Cycle; 2015; 14(11):1716-29. PubMed ID: 25927346 [TBL] [Abstract][Full Text] [Related]
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11. Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin: a potential mechanism for loss of huntingtin function in Huntington's disease. Busch A; Engemann S; Lurz R; Okazawa H; Lehrach H; Wanker EE J Biol Chem; 2003 Oct; 278(42):41452-61. PubMed ID: 12888569 [TBL] [Abstract][Full Text] [Related]
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20. Huntington's disease protein contributes to RNA-mediated gene silencing through association with Argonaute and P bodies. Savas JN; Makusky A; Ottosen S; Baillat D; Then F; Krainc D; Shiekhattar R; Markey SP; Tanese N Proc Natl Acad Sci U S A; 2008 Aug; 105(31):10820-5. PubMed ID: 18669659 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]