These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 35(11):3797-809. PubMed ID: 17519253
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia.
    Kato T; Tamura Y; Matsumoto H; Kobayashi O; Ishiguro H; Ogawa M; Tsujikawa K; Hasegawa Y; Sakamoto M; Konagaya M; Houzen H; Takagi M; Imai K; Morio T; Yokoseki A; Onodera O; Nonoyama S
    Clin Immunol; 2021 Aug; 229():108776. PubMed ID: 34118401
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel nonsense mutation in the APTX gene associated with delayed DNA single-strand break removal fails to enhance sensitivity to different genotoxic agents.
    Crimella C; Cantoni O; Guidarelli A; Vantaggiato C; Martinuzzi A; Fiorani M; Azzolini C; Orso G; Bresolin N; Bassi MT
    Hum Mutat; 2011 Apr; 32(4):E2118-33. PubMed ID: 21412945
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spinocerebellar ataxia with ocular motor apraxia and DNA repair.
    Onodera O
    Neuropathology; 2006 Aug; 26(4):361-7. PubMed ID: 16961074
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Purkinje cell loss in the cerebellar flocculus in patients with ataxia with ocular motor apraxia type 1/early-onset ataxia with ocular motor apraxia and hypoalbuminemia.
    Sugawara M; Wada C; Okawa S; Kobayashi M; Sageshima M; Imota T; Toyoshima I
    Eur Neurol; 2008; 59(1-2):18-23. PubMed ID: 17917453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.
    Shimazaki H; Takiyama Y; Sakoe K; Ikeguchi K; Niijima K; Kaneko J; Namekawa M; Ogawa T; Date H; Tsuji S; Nakano I; Nishizawa M
    Neurology; 2002 Aug; 59(4):590-5. PubMed ID: 12196655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [DNA repair and neurodegeneration].
    Onodera O
    Rinsho Shinkeigaku; 2005 Nov; 45(11):979-81. PubMed ID: 16447779
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular mechanism for spinocerebellar ataxias].
    Onodera O
    Rinsho Shinkeigaku; 2009 Nov; 49(11):750-2. PubMed ID: 20030201
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Short-patch single-strand break repair in ataxia oculomotor apraxia-1.
    Reynolds JJ; El-Khamisy SF; Caldecott KW
    Biochem Soc Trans; 2009 Jun; 37(Pt 3):577-81. PubMed ID: 19442253
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) disease.
    Nouri N; Nouri N; Aryani O; Kamalidehghan B; Sedghi M; Houshmand M
    Iran Biomed J; 2012; 16(4):223-5. PubMed ID: 23183622
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 419(2):184-7. PubMed ID: 17485165
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 10():39. PubMed ID: 33101765
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The FHA domain of aprataxin interacts with the C-terminal region of XRCC1.
    Date H; Igarashi S; Sano Y; Takahashi T; Takahashi T; Takano H; Tsuji S; Nishizawa M; Onodera O
    Biochem Biophys Res Commun; 2004 Dec; 325(4):1279-85. PubMed ID: 15555565
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 59(6):3845-3858. PubMed ID: 35420381
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 18(11):1189-95. PubMed ID: 21984210
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.
    Bohlega SA; Shinwari JM; Al Sharif LJ; Khalil DS; Alkhairallah TS; Al Tassan NA
    BMC Med Genet; 2011 Feb; 12():27. PubMed ID: 21324166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a novel mutation in the
    Inlora J; Sailani MR; Khodadadi H; Teymurinezhad A; Takahashi S; Bernstein JA; Garshasbi M; Snyder MP
    Cold Spring Harb Mol Case Stud; 2017 Nov; 3(6):. PubMed ID: 28652255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.