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

126 related items for PubMed ID: 15474358

  • 1. Polyglutamine repeats of spinocerebellar ataxia 6 impair the cell-death-preventing effect of CaV2.1 Ca2+ channel--loss-of-function cellular model of SCA6.
    Matsuyama Z, Yanagisawa NK, Aoki Y, Black JL, Lennon VA, Mori Y, Imoto K, Inuzuka T.
    Neurobiol Dis; 2004 Nov; 17(2):198-204. PubMed ID: 15474358
    [Abstract] [Full Text] [Related]

  • 2. 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; 34(2):261-70. PubMed ID: 17188510
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Acetylcholine release at neuromuscular junctions of adult tottering mice is controlled by N-(cav2.2) and R-type (cav2.3) but not L-type (cav1.2) Ca2+ channels.
    Pardo NE, Hajela RK, Atchison WD.
    J Pharmacol Exp Ther; 2006 Dec 15; 319(3):1009-20. PubMed ID: 16982704
    [Abstract] [Full Text] [Related]

  • 5. Cell-type-specific alternative splicing in spinocerebellar ataxia type 6.
    Tsunemi T, Ishikawa K, Jin H, Mizusawa H.
    Neurosci Lett; 2008 Dec 05; 447(1):78-81. PubMed ID: 18835329
    [Abstract] [Full Text] [Related]

  • 6. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
    Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP.
    Brain; 2005 Oct 05; 128(Pt 10):2297-303. PubMed ID: 16000334
    [Abstract] [Full Text] [Related]

  • 7. Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6.
    Matsuyama Z, Wakamori M, Mori Y, Kawakami H, Nakamura S, Imoto K.
    J Neurosci; 1999 Jun 15; 19(12):RC14. PubMed ID: 10366652
    [Abstract] [Full Text] [Related]

  • 8. [Molecular physiopathology of the spinocerebellar ataxia type 6 (SCA6)].
    Cervantes-Kardasch VH, García-Martínez E.
    Rev Invest Clin; 2004 Jun 15; 56(3):368-74. PubMed ID: 15612520
    [Abstract] [Full Text] [Related]

  • 9. C-termini of P/Q-type Ca2+ channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.
    Kordasiewicz HB, Thompson RM, Clark HB, Gomez CM.
    Hum Mol Genet; 2006 May 15; 15(10):1587-99. PubMed ID: 16595610
    [Abstract] [Full Text] [Related]

  • 10. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
    Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC.
    Nat Genet; 1997 Jan 15; 15(1):62-9. PubMed ID: 8988170
    [Abstract] [Full Text] [Related]

  • 11. The Drosophila cacts2 mutation reduces presynaptic Ca2+ entry and defines an important element in Cav2.1 channel inactivation.
    Macleod GT, Chen L, Karunanithi S, Peloquin JB, Atwood HL, McRory JE, Zamponi GW, Charlton MP.
    Eur J Neurosci; 2006 Jun 15; 23(12):3230-44. PubMed ID: 16820014
    [Abstract] [Full Text] [Related]

  • 12. Spinocerebellar ataxia type 6.
    Solodkin A, Gomez CM.
    Handb Clin Neurol; 2012 Jun 15; 103():461-73. PubMed ID: 21827907
    [Abstract] [Full Text] [Related]

  • 13. omega-conotoxin GVIA alters gating charge movement of N-type (CaV2.2) calcium channels.
    Yarotskyy V, Elmslie KS.
    J Neurophysiol; 2009 Jan 15; 101(1):332-40. PubMed ID: 18971294
    [Abstract] [Full Text] [Related]

  • 14. The P/Q-type voltage-dependent calcium channel: a therapeutic target in spinocerebellar ataxia type 6.
    Gazulla J, Tintoré M.
    Acta Neurol Scand; 2007 May 15; 115(5):356-63. PubMed ID: 17489948
    [Abstract] [Full Text] [Related]

  • 15. Toxicity and endocytosis of spinocerebellar ataxia type 6 polyglutamine domains: role of myosin IIb.
    Marquèze-Pouey B, Martin-Moutot N, Sakkou-Norton M, Lévêque C, Ji Y, Cornet V, Hsiao WL, Seagar M.
    Traffic; 2008 Jul 15; 9(7):1088-100. PubMed ID: 18384641
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [Spinocerebellar ataxia type 6].
    Ishikawa K, Mizusawa H.
    Clin Calcium; 2001 Nov 01; 11(11):1451-5. PubMed ID: 15775662
    [Abstract] [Full Text] [Related]

  • 18. Alternative splicing generates a smaller assortment of CaV2.1 transcripts in cerebellar Purkinje cells than in the cerebellum.
    Kanumilli S, Tringham EW, Payne CE, Dupere JR, Venkateswarlu K, Usowicz MM.
    Physiol Genomics; 2006 Jan 12; 24(2):86-96. PubMed ID: 16278278
    [Abstract] [Full Text] [Related]

  • 19. Modified autonomic regulation in mice with a P/Q-type calcium channel mutation.
    Ohba T, Takahashi E, Murakami M.
    Biochem Biophys Res Commun; 2009 Mar 27; 381(1):27-32. PubMed ID: 19351589
    [Abstract] [Full Text] [Related]

  • 20. Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
    Watase K, Barrett CF, Miyazaki T, Ishiguro T, Ishikawa K, Hu Y, Unno T, Sun Y, Kasai S, Watanabe M, Gomez CM, Mizusawa H, Tsien RW, Zoghbi HY.
    Proc Natl Acad Sci U S A; 2008 Aug 19; 105(33):11987-92. PubMed ID: 18687887
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.