| scholarly article | Q13442814 |
| P50 | author | Harry T. Orr | Q47823272 |
| P2093 | author name string | Gang Chen | |
| Timothy J Ebner | |||
| Lisa A Duvick | |||
| Wangcai Gao | |||
| Blake A Ebner | |||
| Justin A Barnes | |||
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| P433 | issue | 36 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Purkinje cell | Q1570272 |
| P304 | page(s) | 12778-12789 | |
| P577 | publication date | 2011-09-01 | |
| P1433 | published in | Journal of Neuroscience | Q1709864 |
| P1476 | title | Abnormalities in the climbing fiber-Purkinje cell circuitry contribute to neuronal dysfunction in ATXN1[82Q] mice | |
| P478 | volume | 31 |
| Q36245783 | Abnormalities in synaptic dynamics during development in a mouse model of spinocerebellar ataxia type 1. |
| Q36774172 | Altered Purkinje cell miRNA expression and SCA1 pathogenesis |
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| Q92131811 | Ataxic Symptoms in Huntington's Disease Transgenic Mouse Model Are Alleviated by Chlorzoxazone |
| Q39552099 | Ataxin-1 regulates the cerebellar bioenergetics proteome through the GSK3β-mTOR pathway which is altered in Spinocerebellar ataxia type 1 (SCA1). |
| Q61812325 | Brain Derived Neurotrophic Factor (BDNF) Delays Onset of Pathogenesis in Transgenic Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1) |
| Q26829511 | Cell biology of spinocerebellar ataxia |
| Q92000696 | Cerebellar Development and Circuit Maturation: A Common Framework for Spinocerebellar Ataxias |
| Q33825725 | Climbing fiber-Purkinje cell synaptic pathology in tremor and cerebellar degenerative diseases. |
| Q48514855 | Decreased expression of glutamate transporter GLAST in Bergmann glia is associated with the loss of Purkinje neurons in the spinocerebellar ataxia type 1. |
| Q37052993 | Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans |
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| Q89017844 | In Vivo Analysis of the Climbing Fiber-Purkinje Cell Circuit in SCA2-58Q Transgenic Mouse Model |
| Q37042016 | In vivo analysis of cerebellar Purkinje cell activity in SCA2 transgenic mouse model |
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| Q37992251 | Intercellular (mis)communication in neurodegenerative disease. |
| Q55405507 | Intravenous Anesthetic, Propofol Affects Synaptic Responses in Cerebellar Purkinje Cells. |
| Q38241162 | Long-term climbing fibre activity induces transcription of microRNAs in cerebellar Purkinje cells |
| Q59795532 | Molecular pathway analysis towards understanding tissue vulnerability in spinocerebellar ataxia type 1 |
| Q42363213 | Motor and Cerebellar Architectural Abnormalities during the Early Progression of Ataxia in a Mouse Model of SCA1 and How Early Prevention Leads to a Better Outcome Later in Life |
| Q26853025 | Mouse models of polyglutamine diseases: review and data table. Part I |
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| Q41486765 | Neuronal Atrophy Early in Degenerative Ataxia Is a Compensatory Mechanism to Regulate Membrane Excitability. |
| Q37307036 | New roles for the cerebellum in health and disease |
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| Q48767202 | Prolonged Type 1 Metabotropic Glutamate Receptor Dependent Synaptic Signaling Contributes to Spino-Cerebellar Ataxia Type 1. |
| Q55097137 | Purkinje Cell Signaling Deficits in Animal Models of Ataxia. |
| Q36786284 | Purkinje cell ataxin-1 modulates climbing fiber synaptic input in developing and adult mouse cerebellum |
| Q37093737 | Reduced activity of AMP-activated protein kinase protects against genetic models of motor neuron disease |
| Q36580728 | Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7 |
| Q54110032 | Reduction of protein kinase A-mediated phosphorylation of ATXN1-S776 in Purkinje cells delays onset of Ataxia in a SCA1 mouse model. |
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| Q36392945 | The cerebellum as a target for estrogen action |
| Q35340099 | The role for alterations in neuronal activity in the pathogenesis of polyglutamine repeat disorders |
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