Found: 18
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Novel function of the class I bHLH protein Daughterless in the negative regulation of proneural gene expression in the Drosophila eye.
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- EMBO Reports, 2008, v. 9, n. 11, p. 1128, doi. 10.1038/embor.2008.166
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- Article
Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31.
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- Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 274, doi. 10.3390/jcm9010274
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- Article
Nemo-like kinase is a novel regulator of spinal and bulbar muscular atrophy.
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- eLife, 2015, p. 1, doi. 10.7554/eLife.08493
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- Article
Control of planar cell polarity by interaction of DWnt4 and four‐jointed.
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- Genesis: The Journal of Genetics & Development, 2005, v. 42, n. 3, p. 150, doi. 10.1002/gene.20142
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- Article
Drosophila eye disc margin is a center for organizing long-range planar polarity.
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- Genesis: The Journal of Genetics & Development, 2004, v. 39, n. 1, p. 26, doi. 10.1002/gene.20022
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- Article
Bar Represses dPax2 and Decapentaplegic to Regulate Cell Fate and Morphogenetic Cell Death in <i>Drosophila</i> Eye.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088171
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- Article
Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1.
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- Nature, 2008, v. 452, n. 7188, p. 713, doi. 10.1038/nature06731
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- Article
Exploring the Role of Posttranslational Modifications in Spinal and Bulbar Muscular Atrophy.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.931301
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- Article
The extra-cerebellar effects of spinocerebellar ataxia type 1 (SCA1): looking beyond the cerebellum.
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- Cellular & Molecular Life Sciences, 2022, v. 79, n. 8, p. 1, doi. 10.1007/s00018-022-04419-7
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- Article
Pathogenic mechanisms underlying spinocerebellar ataxia type 1.
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- Cellular & Molecular Life Sciences, 2020, v. 77, n. 20, p. 4015, doi. 10.1007/s00018-020-03520-z
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- Article
Dysregulation of alternative splicing in spinocerebellar ataxia type 1.
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- Human Molecular Genetics, 2024, v. 33, n. 2, p. 138, doi. 10.1093/hmg/ddad170
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- Article
A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family.
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- Cells (2073-4409), 2022, v. 11, n. 19, p. 3090, doi. 10.3390/cells11193090
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- Article
Identifying Disease Signatures in the Spinocerebellar Ataxia Type 1 Mouse Cortex.
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- Cells (2073-4409), 2022, v. 11, n. 17, p. 2632, doi. 10.3390/cells11172632
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- Article
dAtaxin-2 Mediates Expanded Ataxin-1-Induced Neurodegeneration in a Drosophila Model of SCA1.
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- PLoS Genetics, 2007, v. 3, n. 12, p. e234, doi. 10.1371/journal.pgen.0030234
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- Article
Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 510, doi. 10.1093/hmg/ddq496
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- Article
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population.
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- Genes, 2020, v. 11, n. 10, p. 1206, doi. 10.3390/genes11101206
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- Article
Beyond the Glutamine Expansion: Influence of Posttranslational Modifications of Ataxin-1 in the Pathogenesis of Spinocerebellar Ataxia Type 1.
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- Molecular Neurobiology, 2014, v. 50, n. 3, p. 866, doi. 10.1007/s12035-014-8703-z
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- Article
Polyglutamine Disease Toxicity Is Regulated by Nemo-like Kinase in Spinocerebellar Ataxia Type 1.
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- Journal of Neuroscience, 2013, v. 33, n. 22, p. 9328, doi. 10.1523/JNEUROSCI.3465-12.2013
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- Article