Polyglutamine Tract Expansion Increases S-Nitrosylation of Huntingtin and Ataxin-1.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0163359
- By:
- Publication type:
- Article
Works matching DE "ATAXIN-1"
Results: 13
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SUMO-1 promotes degradation of the polyglutamine disease protein ataxin-3.
- Published in:
- Animal Cells & Systems, 2013, v. 17, n. 1, p. 7, doi. 10.1080/19768354.2012.738611
- By:
- Publication type:
- Article
3
A case of amyotrophic lateral sclerosis with intermediate ATXN- 1 CAG repeat expansion in a large family with spinocerebellar ataxia type 1.
- Published in:
- 2014
- By:
- Publication type:
- Letter
4
Nuclear bodies formed by polyQ-ataxin-1 protein are liquid RNA/protein droplets with tunable dynamics.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-57994-9
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- Publication type:
- Article
5
The design and delivery of a PKA inhibitory polypeptide to treat SCA1.
- Published in:
- Journal of Neurochemistry, 2014, v. 131, n. 1, p. 101, doi. 10.1111/jnc.12782
- By:
- Publication type:
- Article
6
Systematic Analysis of Fly Models with Multiple Drivers Reveals Different Effects of Ataxin-1 and Huntingtin in Neuron Subtype-Specific Expression.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0116567
- By:
- Publication type:
- Article
7
Identification of Human Proteins That Modify Misfolding and Proteotoxicity of Pathogenic Ataxin-1.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002897
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- Publication type:
- Article
8
Ataxin-1 oligomers induce local spread of pathology and decreasing them by passive immunization slows Spinocerebellar ataxia type 1 phenotypes.
- Published in:
- eLife, 2015, p. 1, doi. 10.7554/eLife.10891
- By:
- Publication type:
- Article
9
Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1.
- Published in:
- Cerebellum, 2017, v. 16, n. 2, p. 340, doi. 10.1007/s12311-016-0794-9
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- Publication type:
- Article
10
Knockdown of Acid-Sensing Ion Channel 1a (ASIC1a) Suppresses Disease Phenotype in SCA1 Mouse Model.
- Published in:
- Cerebellum, 2014, v. 13, n. 4, p. 479, doi. 10.1007/s12311-014-0563-6
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- Publication type:
- Article
11
Suppression of Calbindin-D28k Expression Exacerbates SCA1 Phenotype in a Disease Mouse Model.
- Published in:
- Cerebellum, 2012, v. 11, n. 3, p. 718, doi. 10.1007/s12311-011-0323-9
- By:
- Publication type:
- Article
12
Stabilization and Degradation Mechanisms of Cytoplasmic Ataxin-1: Supplementary Issue: Molecular and Cellular Mechanisms of Neurodegeneration.
- Published in:
- Journal of Experimental Neuroscience, 2015, n. 9, p. 123, doi. 10.4137/JEN.S25469
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- Publication type:
- Article
13
Mutant ataxin1 disrupts cerebellar development in spinocerebellar ataxia type 1.
- Published in:
- 2018
- By:
- Publication type:
- journal article