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Neuron, ISSN 0896-6273, 2010, Volume 67, Issue 6, pp. 929 - 935
Journal Article
Cell, ISSN 0092-8674, 2003, Volume 113, Issue 4, pp. 457 - 468
Spinocerebellar ataxia type 1 (SCA1) is one of several neurological disorders caused by a CAG repeat expansion. In SCA1, this expansion produces an abnormally... 
PROTEIN | SIGNALING PATHWAY | SCA1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | GROWTH | DISEASE | ALPHA-SYNUCLEIN | SELECTIVE NEURODEGENERATION | CELL | DROSOPHILA | 14-3-3-PROTEINS | CELL BIOLOGY | Tyrosine 3-Monooxygenase - metabolism | Ataxin-1 | Phosphorylation | Protein Binding - genetics | Humans | Peptides - genetics | Nerve Degeneration - genetics | Phosphatidylinositol 3-Kinases - metabolism | Spinocerebellar Ataxias - metabolism | Amino Acid Sequence - genetics | Nerve Degeneration - metabolism | Ataxins | Cell Nucleus - metabolism | Peptides - metabolism | Cell Nucleus - pathology | Proto-Oncogene Proteins | Inclusion Bodies - metabolism | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Spinocerebellar Ataxias - genetics | Drosophila Proteins | Protein-Serine-Threonine Kinases - genetics | Serine - genetics | Nuclear Proteins - metabolism | Mutation - genetics | Nerve Tissue Proteins - genetics | Serine - metabolism | Nerve Tissue Proteins - metabolism | Phosphatidylinositol 3-Kinases - genetics | Proto-Oncogene Proteins c-akt | Tyrosine 3-Monooxygenase - genetics | Inclusion Bodies - genetics | Animals | Cell Nucleus - genetics | Models, Biological | Inclusion Bodies - pathology | Trinucleotide Repeat Expansion - genetics | 14-3-3 Proteins | Amino Acid Motifs - genetics | COS Cells | Drosophila melanogaster
Journal Article
Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 03/2013, Volume 33, Issue 13, pp. 5806 - 5820
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 2007, Volume 34, Issue 1, pp. 69 - 79
Journal Article
BBA - Proteins and Proteomics, ISSN 1570-9639, 05/2015, Volume 1854, Issue 5, pp. 356 - 364
Spinocerebellar ataxia type 1 (SCA1), an autosomal-dominant neurodegenerative disorder, is caused by expansion of the polyglutamine tract within ataxin-1... 
Protein degradation | Protein aggregation | Ataxin-1 | Ubiquitylation | Spinocerebellar ataxia type 1 (SCA1) | UbcH6 | CAG REPEAT | POLYGLUTAMINE | Spinocerebellar ataxia type I (SCA1) | SCA1 GENE-PRODUCT | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOPHYSICS | MUTANT ATAXIN-1 | INTERACTS | DISEASE | EXPANSION | TYPE-1 | REPRESSOR CAPICUA | Ubiquitin | Lysine
Journal Article
PLoS ONE, ISSN 1932-6203, 2009, Volume 4, Issue 12, pp. e8372 - e8372
Journal Article