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Journal Abstract Search

275 related items for PubMed ID: 27381005

  • 1. 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
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  • 5. A combination of chlorzoxazone and folic acid improves recognition memory, anxiety and depression in SCA3-84Q mice.
    Marinina KS, Bezprozvanny IB, Egorova PA.
    Hum Mol Genet; 2024 Aug 06; 33(16):1406-1419. PubMed ID: 38727562
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  • 8. Human Olfactory Ensheathing Cell Transplantation Improves Motor Function in a Mouse Model of Type 3 Spinocerebellar Ataxia.
    Hsieh J, Liu JW, Harn HJ, Hsueh KW, Rajamani K, Deng YC, Chia CM, Shyu WC, Lin SZ, Chiou TW.
    Cell Transplant; 2017 Oct 06; 26(10):1611-1621. PubMed ID: 29251109
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  • 9. In vivo analysis of the spontaneous firing of cerebellar Purkinje cells in awake transgenic mice that model spinocerebellar ataxia type 2.
    Egorova PA, Gavrilova AV, Bezprozvanny IB.
    Cell Calcium; 2021 Jan 06; 93():102319. PubMed ID: 33248384
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  • 10. Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2.
    Dell'Orco JM, Pulst SM, Shakkottai VG.
    Hum Mol Genet; 2017 Oct 15; 26(20):3935-3945. PubMed ID: 29016852
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  • 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
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  • 12. 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 10; 596(17):4253-4267. PubMed ID: 29928778
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  • 13. Creatine-supplemented diet extends Purkinje cell survival in spinocerebellar ataxia type 1 transgenic mice but does not prevent the ataxic phenotype.
    Kaemmerer WF, Rodrigues CM, Steer CJ, Low WC.
    Neuroscience; 2001 Sep 10; 103(3):713-24. PubMed ID: 11274790
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  • 14. 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 10; 32(6):595-603. PubMed ID: 22393909
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  • 15. 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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  • 16. 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
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  • 17. The effect of 3,4-diaminopyridine on the patients with hereditary pure cerebellar ataxia.
    Tsunemi T, Ishikawa K, Tsukui K, Sumi T, Kitamura K, Mizusawa H.
    J Neurol Sci; 2010 May 15; 292(1-2):81-4. PubMed ID: 20181362
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  • 18. Activation of TrkB-Akt signaling rescues deficits in a mouse model of SCA6.
    Cook AA, Jayabal S, Sheng J, Fields E, Leung TCS, Quilez S, McNicholas E, Lau L, Huang S, Watt AJ.
    Sci Adv; 2022 Sep 16; 8(37):eabh3260. PubMed ID: 36112675
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  • 19. 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
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