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Journal Abstract Search

468 related items for PubMed ID: 29661116

  • 1. CRISPR/Cas9-Targeted Deletion of Polyglutamine in Spinocerebellar Ataxia Type 3-Derived Induced Pluripotent Stem Cells.
    Ouyang S, Xie Y, Xiong Z, Yang Y, Xian Y, Ou Z, Song B, Chen Y, Xie Y, Li H, Sun X.
    Stem Cells Dev; 2018 Jun 01; 27(11):756-770. PubMed ID: 29661116
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  • 2. CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells.
    He L, Wang S, Peng L, Zhao H, Li S, Han X, Habimana JD, Chen Z, Wang C, Peng Y, Peng H, Xie Y, Lei L, Deng Q, Wan L, Wan N, Yuan H, Gong Y, Zou G, Li Z, Tang B, Jiang H.
    Transl Psychiatry; 2021 Sep 17; 11(1):479. PubMed ID: 34535635
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  • 7. Druggable genome screen identifies new regulators of the abundance and toxicity of ATXN3, the Spinocerebellar Ataxia type 3 disease protein.
    Ashraf NS, Sutton JR, Yang Y, Ranxhi B, Libohova K, Shaw ED, Barget AJ, Todi SV, Paulson HL, Costa MDC.
    Neurobiol Dis; 2020 Apr 17; 137():104697. PubMed ID: 31783119
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  • 8. Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3.
    Hansen SK, Stummann TC, Borland H, Hasholt LF, Tümer Z, Nielsen JE, Rasmussen MA, Nielsen TT, Daechsel JC, Fog K, Hyttel P.
    Stem Cell Res; 2016 Sep 17; 17(2):306-317. PubMed ID: 27596958
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  • 11. Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: removal of the CAG containing exon.
    Evers MM, Tran HD, Zalachoras I, Pepers BA, Meijer OC, den Dunnen JT, van Ommen GJ, Aartsma-Rus A, van Roon-Mom WM.
    Neurobiol Dis; 2013 Oct 17; 58():49-56. PubMed ID: 23659897
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  • 12. Deficiency in classical nonhomologous end-joining-mediated repair of transcribed genes is linked to SCA3 pathogenesis.
    Chakraborty A, Tapryal N, Venkova T, Mitra J, Vasquez V, Sarker AH, Duarte-Silva S, Huai W, Ashizawa T, Ghosh G, Maciel P, Sarkar PS, Hegde ML, Chen X, Hazra TK.
    Proc Natl Acad Sci U S A; 2020 Apr 07; 117(14):8154-8165. PubMed ID: 32205441
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  • 13. Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.
    Gao R, Liu Y, Silva-Fernandes A, Fang X, Paulucci-Holthauzen A, Chatterjee A, Zhang HL, Matsuura T, Choudhary S, Ashizawa T, Koeppen AH, Maciel P, Hazra TK, Sarkar PS.
    PLoS Genet; 2015 Jan 07; 11(1):e1004834. PubMed ID: 25590633
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  • 16. Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11.
    Hansen SK, Borland H, Hasholt LF, Tümer Z, Nielsen JE, Rasmussen MA, Nielsen TT, Stummann TC, Fog K, Hyttel P.
    Stem Cell Res; 2016 May 07; 16(3):589-92. PubMed ID: 27346191
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  • 18. ATXN3: a multifunctional protein involved in the polyglutamine disease spinocerebellar ataxia type 3.
    Hernández-Carralero E, Quinet G, Freire R.
    Expert Rev Mol Med; 2024 Sep 25; 26():e19. PubMed ID: 39320846
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