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Altered Purkinje cell miRNA expression and SCA1 pathogenesis.
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2
miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis.
Nat Neurosci. 2008 Oct;11(10):1137-9. doi: 10.1038/nn.2183. Epub 2008 Aug 31.
3
Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice.
Hum Mol Genet. 2004 Oct 15;13(20):2535-43. doi: 10.1093/hmg/ddh268. Epub 2004 Aug 18.
6
Progress in pathogenesis studies of spinocerebellar ataxia type 1.
Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1079-81. doi: 10.1098/rstb.1999.0462.
7
USP7, a ubiquitin-specific protease, interacts with ataxin-1, the SCA1 gene product.
Mol Cell Neurosci. 2002 Jun;20(2):298-306. doi: 10.1006/mcne.2002.1103.
8
Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice.
Neuron. 2003 May 8;38(3):375-87. doi: 10.1016/s0896-6273(03)00258-7.
10
Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice.
J Neurosci. 2004 Oct 6;24(40):8853-61. doi: 10.1523/JNEUROSCI.2978-04.2004.

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Staufen2 dysregulation in neurodegenerative disease.
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RGS2 and female common diseases: a guard of women's health.
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Combined overexpression of ATXN1L and mutant ATXN1 knockdown by AAV rescue motor phenotypes and gene signatures in SCA1 mice.
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Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis.
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Role of Nuclear Factor Kappa B (NF-κB) Signalling in Neurodegenerative Diseases: An Mechanistic Approach.
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Modified level of miR-376a is associated with Parkinson's disease.
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Brain pathology of spinocerebellar ataxias.
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Cell biology of spinocerebellar ataxia.
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The microRNA miR-34 modulates ageing and neurodegeneration in Drosophila.
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Genetics of the dominant ataxias.
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Climbing fiber activity reduces 14-3-3-θ regulated GABA(A) receptor phosphorylation in cerebellar Purkinje cells.
Neuroscience. 2012 Jan 10;201:34-45. doi: 10.1016/j.neuroscience.2011.11.021. Epub 2011 Nov 17.
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Abnormalities in the climbing fiber-Purkinje cell circuitry contribute to neuronal dysfunction in ATXN1[82Q] mice.
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Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6.
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