Found: 16
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Arginine is a disease modifier for polyQ disease models that stabilizes polyQ protein conformation.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
- Published in:
- Nature Genetics, 2000, v. 26, n. 2, p. 191, doi. 10.1038/79911
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- Publication type:
- Article
Abnormalities in synaptic dynamics during development in a mouse model of spinocerebellar ataxia type 1.
- Published in:
- Scientific Reports, 2015, p. 16102, doi. 10.1038/srep16102
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- Publication type:
- Article
Modelling brain diseases in mice: the challenges of design and analysis.
- Published in:
- Nature Reviews Genetics, 2003, v. 4, n. 4, p. 296, doi. 10.1038/nrg1045
- By:
- Publication type:
- Article
Differential Roles of Glial and Neuronal Glutamate Transporters in Purkinje Cell Synapses.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 38, p. 8788, doi. 10.1523/JNEUROSCI.1020-05.2005
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- Publication type:
- Article
Suppression of the novel ER protein Maxer by mutant ataxin-1 in Bergman glia contributes to non-cell-autonomous toxicity.
- Published in:
- EMBO Journal, 2010, v. 29, n. 14, p. 2446, doi. 10.1038/emboj.2010.116
- By:
- Publication type:
- Article
Proteome analysis of soluble nuclear proteins reveals that HMGB1/2 suppress genotoxic stress in polyglutamine diseases.
- Published in:
- Nature Cell Biology, 2007, v. 9, n. 4, p. 402, doi. 10.1038/ncb1553
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- Publication type:
- Article
Alternative splicing in the C-terminal tail of Ca<sub>v</sub>2.1 is essential for preventing a neurological disease in mice.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 16, p. 3094, doi. 10.1093/hmg/ddx193
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- Publication type:
- Article
Impaired striatal dopamine release in homozygous Vps35 D620N knock-in mice.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 20, p. 4507, doi. 10.1093/hmg/ddw279
- By:
- Publication type:
- Article
RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 20, p. 4432, doi. 10.1093/hmg/ddw272
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- Publication type:
- Article
Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 17, p. 4780, doi. 10.1093/hmg/ddv202
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- Publication type:
- Article
Motor discoordination and increased susceptibility to cerebellar injury in GLAST mutant mice.
- Published in:
- European Journal of Neuroscience, 1998, v. 10, n. 3, doi. 10.1046/j.1460-9568.1998.00108.x
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- Publication type:
- Article
Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01790-z
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- Publication type:
- Article
Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 21, p. 2789, doi. 10.1093/hmg/ddg300
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- Publication type:
- Article
Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse model.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Mice lacing bombesin receptor subtype-3 develop metabolic defects and obesity.
- Published in:
- Nature, 1997, v. 390, n. 6656, p. 165, doi. 10.1038/36568
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- Publication type:
- Article