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Journal Abstract Search

87 related items for PubMed ID: 15775662

  • 21. Altered frequency-dependent inactivation and steady-state inactivation of polyglutamine-expanded alpha1A in SCA6.
    Chen H, Piedras-Rentería ES.
    Am J Physiol Cell Physiol; 2007 Mar; 292(3):C1078-86. PubMed ID: 17020933
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  • 22. Proteolytic cleavage and cellular toxicity of the human alpha1A calcium channel in spinocerebellar ataxia type 6.
    Kubodera T, Yokota T, Ohwada K, Ishikawa K, Miura H, Matsuoka T, Mizusawa H.
    Neurosci Lett; 2003 Apr 24; 341(1):74-8. PubMed ID: 12676347
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  • 23. Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum.
    Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama S, Mori O, Eishi Y, Mizusawa H.
    Neuropathology; 2012 Dec 24; 32(6):595-603. PubMed ID: 22393909
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  • 29. DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6.
    Tsou WL, Hosking RR, Burr AA, Sutton JR, Ouyang M, Du X, Gomez CM, Todi SV.
    Hum Mol Genet; 2015 Aug 01; 24(15):4385-96. PubMed ID: 25954029
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  • 32. Polyglutamine length-dependent toxicity from α1ACT in Drosophila models of spinocerebellar ataxia type 6.
    Tsou WL, Qiblawi SH, Hosking RR, Gomez CM, Todi SV.
    Biol Open; 2016 Dec 15; 5(12):1770-1775. PubMed ID: 27979829
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  • 33. [Autosomal dominant spinocerebellar degeneration--new forms and pathomechanisms].
    Mizusawa H.
    Rinsho Shinkeigaku; 2004 Nov 15; 44(11):782-4. PubMed ID: 15651290
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  • 36. Vulnerability of Purkinje Cells Generated from Spinocerebellar Ataxia Type 6 Patient-Derived iPSCs.
    Ishida Y, Kawakami H, Kitajima H, Nishiyama A, Sasai Y, Inoue H, Muguruma K.
    Cell Rep; 2016 Nov 01; 17(6):1482-1490. PubMed ID: 27806289
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  • 37. Bovine CACNA1A gene and comparative analysis of the CAG repeats associated to human spinocerebellar ataxia type-6.
    Andrés-Mateos E, Cruces J, Renart J, Solís-Garrido LM, Serantes R, de Lucas-Cerrillo AM, Montiel C.
    Gene; 2006 Sep 15; 380(1):54-61. PubMed ID: 16876337
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  • 38. [A case of spinocerebellar ataxia type 6 with its initial symptom of episodic ataxia-like phenotype].
    Shimazaki H, Nakao K, Ishikawa K, Takiyama Y, Nakano I.
    No To Shinkei; 2006 Jan 15; 58(1):63-7. PubMed ID: 16482924
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  • 39. [Therapeutic strategies for the polyglutamine diseases].
    Nagai Y, Popiel HA, Fujikake N, Toda T.
    Brain Nerve; 2007 Apr 15; 59(4):393-404. PubMed ID: 17447526
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  • 40. 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
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