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9. Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1. Chen HK; Fernandez-Funez P; Acevedo SF; Lam YC; Kaytor MD; Fernandez MH; Aitken A; Skoulakis EM; Orr HT; Botas J; Zoghbi HY Cell; 2003 May; 113(4):457-68. PubMed ID: 12757707 [TBL] [Abstract][Full Text] [Related]
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11. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds. Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629 [TBL] [Abstract][Full Text] [Related]
12. Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro. Chai Y; Koppenhafer SL; Shoesmith SJ; Perez MK; Paulson HL Hum Mol Genet; 1999 Apr; 8(4):673-82. PubMed ID: 10072437 [TBL] [Abstract][Full Text] [Related]
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14. Co-chaperone CHIP promotes aggregation of ataxin-1. Choi JY; Ryu JH; Kim HS; Park SG; Bae KH; Kang S; Myung PK; Cho S; Park BC; Lee DH Mol Cell Neurosci; 2007 Jan; 34(1):69-79. PubMed ID: 17127076 [TBL] [Abstract][Full Text] [Related]
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16. Progress in pathogenesis studies of spinocerebellar ataxia type 1. Cummings CJ; Orr HT; Zoghbi HY Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1079-81. PubMed ID: 10434309 [TBL] [Abstract][Full Text] [Related]
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19. Live-cell imaging reveals divergent intracellular dynamics of polyglutamine disease proteins and supports a sequestration model of pathogenesis. Chai Y; Shao J; Miller VM; Williams A; Paulson HL Proc Natl Acad Sci U S A; 2002 Jul; 99(14):9310-5. PubMed ID: 12084819 [TBL] [Abstract][Full Text] [Related]
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