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Journal Abstract Search

174 related items for PubMed ID: 20687492

  • 1. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.
    Tada M, Yokoseki A, Sato T, Makifuchi T, Onodera O.
    Adv Exp Med Biol; 2010; 685():21-33. PubMed ID: 20687492
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  • 2. DNA single-strand break repair is impaired in aprataxin-related ataxia.
    Hirano M, Yamamoto A, Mori T, Lan L, Iwamoto TA, Aoki M, Shimada K, Furiya Y, Kariya S, Asai H, Yasui A, Nishiwaki T, Imoto K, Kobayashi N, Kiriyama T, Nagata T, Konishi N, Itoyama Y, Ueno S.
    Ann Neurol; 2007 Feb; 61(2):162-74. PubMed ID: 17315206
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  • 3. Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.
    Takahashi T, Tada M, Igarashi S, Koyama A, Date H, Yokoseki A, Shiga A, Yoshida Y, Tsuji S, Nishizawa M, Onodera O.
    Nucleic Acids Res; 2007 Feb; 35(11):3797-809. PubMed ID: 17519253
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  • 6. Spinocerebellar ataxia with ocular motor apraxia and DNA repair.
    Onodera O.
    Neuropathology; 2006 Aug; 26(4):361-7. PubMed ID: 16961074
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  • 7. Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.
    Sano Y, Date H, Igarashi S, Onodera O, Oyake M, Takahashi T, Hayashi S, Morimatsu M, Takahashi H, Makifuchi T, Fukuhara N, Tsuji S.
    Ann Neurol; 2004 Feb; 55(2):241-9. PubMed ID: 14755728
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  • 11. [Molecular mechanism for spinocerebellar ataxias].
    Onodera O.
    Rinsho Shinkeigaku; 2009 Nov; 49(11):750-2. PubMed ID: 20030201
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  • 14. Short half-lives of ataxia-associated aprataxin proteins in neuronal cells.
    Hirano M, Asai H, Kiriyama T, Furiya Y, Iwamoto T, Nishiwaki T, Yamamoto A, Mori T, Ueno S.
    Neurosci Lett; 2007 May 29; 419(2):184-7. PubMed ID: 17485165
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  • 15. Complex Movement Disorders in Ataxia with Oculomotor Apraxia Type 1: Beyond the Cerebellar Syndrome.
    Pedroso JL, Vale TC, da Costa SCG, Santos M, Alonso I, Barsottini OGP.
    Tremor Other Hyperkinet Mov (N Y); 2020 Oct 07; 10():39. PubMed ID: 33101765
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  • 17. Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
    Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nuñez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M.
    Mol Neurobiol; 2022 Jun 07; 59(6):3845-3858. PubMed ID: 35420381
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  • 18. Structure of an aprataxin-DNA complex with insights into AOA1 neurodegenerative disease.
    Tumbale P, Appel CD, Kraehenbuehl R, Robertson PD, Williams JS, Krahn J, Ahel I, Williams RS.
    Nat Struct Mol Biol; 2011 Oct 09; 18(11):1189-95. PubMed ID: 21984210
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