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223 related items for PubMed ID: 36078147

  • 1. 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]

  • 2. Transient cerebellar alterations during development prior to obvious motor phenotype in a mouse model of spinocerebellar ataxia type 6.
    Jayabal S, Ljungberg L, Watt AJ.
    J Physiol; 2017 Feb 01; 595(3):949-966. PubMed ID: 27531396
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar Degeneration.
    Jayabal S, Ljungberg L, Erwes T, Cormier A, Quilez S, El Jaouhari S, Watt AJ.
    eNeuro; 2015 Jul 06; 2(6):. PubMed ID: 26730403
    [Abstract] [Full Text] [Related]

  • 5. Flocculus Purkinje cell signals in mouse Cacna1a calcium channel mutants of escalating severity: an investigation of the role of firing irregularity in ataxia.
    Stahl JS, Thumser ZC.
    J Neurophysiol; 2014 Nov 15; 112(10):2647-63. PubMed ID: 25143538
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  • 8. An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron.
    Miyazaki Y, Du X, Muramatsu S, Gomez CM.
    Sci Transl Med; 2016 Jul 13; 8(347):347ra94. PubMed ID: 27412786
    [Abstract] [Full Text] [Related]

  • 9. Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics.
    Du X, Gomez CM.
    Adv Exp Med Biol; 2018 Jul 13; 1049():147-173. PubMed ID: 29427102
    [Abstract] [Full Text] [Related]

  • 10. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
    Gomez CM, Thompson RM, Gammack JT, Perlman SL, Dobyns WB, Truwit CL, Zee DS, Clark HB, Anderson JH.
    Ann Neurol; 1997 Dec 13; 42(6):933-50. PubMed ID: 9403487
    [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. Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.
    Bavassano C, Eigentler A, Stanika R, Obermair GJ, Boesch S, Dechant G, Nat R.
    Stem Cells Dev; 2017 Nov 15; 26(22):1612-1625. PubMed ID: 28946818
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. [Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].
    Ishikawa K, Mizusawa H.
    Nihon Rinsho; 1999 Apr 19; 57(4):880-5. PubMed ID: 10222783
    [Abstract] [Full Text] [Related]

  • 16. Endosomal dysfunction contributes to cerebellar deficits in spinocerebellar ataxia type 6.
    Cook AA, Leung TCS, Rice M, Nachman M, Zadigue-Dube É, Watt AJ.
    Elife; 2023 Dec 12; 12():. PubMed ID: 38084749
    [Abstract] [Full Text] [Related]

  • 17. Altered synaptic and firing properties of cerebellar Purkinje cells in a mouse model of ARSACS.
    Ady V, Toscano-Márquez B, Nath M, Chang PK, Hui J, Cook A, Charron F, Larivière R, Brais B, McKinney RA, Watt AJ.
    J Physiol; 2018 Sep 12; 596(17):4253-4267. PubMed ID: 29928778
    [Abstract] [Full Text] [Related]

  • 18. The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.
    Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
    Acta Neuropathol; 2010 Apr 12; 119(4):447-64. PubMed ID: 20043227
    [Abstract] [Full Text] [Related]

  • 19. Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6.
    Du X, Wang J, Zhu H, Rinaldo L, Lamar KM, Palmenberg AC, Hansel C, Gomez CM.
    Cell; 2013 Jul 03; 154(1):118-33. PubMed ID: 23827678
    [Abstract] [Full Text] [Related]

  • 20. Molecular pathogenesis of spinocerebellar ataxia type 6.
    Kordasiewicz HB, Gomez CM.
    Neurotherapeutics; 2007 Apr 03; 4(2):285-94. PubMed ID: 17395139
    [Abstract] [Full Text] [Related]

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