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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

319 related items for PubMed ID: 18687887

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [SCA6: From gene identification to recent progress on pathogenesis].
    Watase K, Ishikawa K, Mizusawa H.
    Rinsho Shinkeigaku; 2010 Nov; 50(11):858-60. PubMed ID: 21921472
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6.
    Tsou WL, Soong BW, Paulson HL, Rodríguez-Lebrón E.
    Neurobiol Dis; 2011 Sep; 43(3):533-42. PubMed ID: 21550405
    [Abstract] [Full Text] [Related]

  • 7. Loss of Flocculus Purkinje Cell Firing Precision Leads to Impaired Gaze Stabilization in a Mouse Model of Spinocerebellar Ataxia Type 6 (SCA6).
    Chang HHV, Cook AA, Watt AJ, Cullen KE.
    Cells; 2022 Sep 02; 11(17):. PubMed ID: 36078147
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.
    Restituito S, Thompson RM, Eliet J, Raike RS, Riedl M, Charnet P, Gomez CM.
    J Neurosci; 2000 Sep 01; 20(17):6394-403. PubMed ID: 10964945
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Spinocerebellar ataxia type 6 protein aggregates cause deficits in motor learning and cerebellar plasticity.
    Mark MD, Krause M, Boele HJ, Kruse W, Pollok S, Kuner T, Dalkara D, Koekkoek S, De Zeeuw CI, Herlitze S.
    J Neurosci; 2015 Jun 10; 35(23):8882-95. PubMed ID: 26063920
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6.
    Jayabal S, Chang HH, Cullen KE, Watt AJ.
    Sci Rep; 2016 Jul 06; 6():29489. PubMed ID: 27381005
    [Abstract] [Full Text] [Related]

  • 17. Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model.
    Aikawa T, Mogushi K, Iijima-Tsutsui K, Ishikawa K, Sakurai M, Tanaka H, Mizusawa H, Watase K.
    Hum Mol Genet; 2015 Sep 01; 24(17):4780-91. PubMed ID: 26034136
    [Abstract] [Full Text] [Related]

  • 18. Properties of human Cav2.1 channel with a spinocerebellar ataxia type 6 mutation expressed in Purkinje cells.
    Saegusa H, Wakamori M, Matsuda Y, Wang J, Mori Y, Zong S, Tanabe T.
    Mol Cell Neurosci; 2007 Feb 01; 34(2):261-70. PubMed ID: 17188510
    [Abstract] [Full Text] [Related]

  • 19. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A, D'Angelo MG, Salati R, Villa L, Germinasi C, Frattini T, Meola G, Turconi AC, Bresolin N, Bassi MT.
    J Neurol Sci; 2006 Feb 15; 241(1-2):13-7. PubMed ID: 16325861
    [Abstract] [Full Text] [Related]

  • 20. CaV2.1 channelopathies.
    Pietrobon D.
    Pflugers Arch; 2010 Jul 15; 460(2):375-93. PubMed ID: 20204399
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.