Found: 12
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The FUS gene is dual‐coding with both proteins contributing to FUS‐mediated toxicity.
- Published in:
- EMBO Reports, 2021, v. 22, n. 1, p. 1, doi. 10.15252/embr.202050640
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- Article
Unraveling the impact of disrupted nucleocytoplasmic transport systems in C9orf72-associated ALS.
- Published in:
- Frontiers in Cellular Neuroscience, 2023, p. 1, doi. 10.3389/fncel.2023.1247297
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- Article
Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis.
- Published in:
- 2015
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- Publication type:
- journal article
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 5, p. 715, doi. 10.1007/s00401-015-1401-8
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- Publication type:
- Article
Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 2, p. 273, doi. 10.1007/s00401-012-1043-z
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- Publication type:
- Article
DNA methylation age acceleration is associated with ALS age of onset and survival.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 5, p. 943, doi. 10.1007/s00401-020-02131-z
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- Publication type:
- Article
Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 2, p. 291, doi. 10.1093/hmg/ddv471
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- Publication type:
- Article
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 7, p. 1883, doi. 10.1093/hmg/ddu605
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- Publication type:
- Article
A Nonsense Mutation in Mouse <i>Tardbp</i> Affects TDP43 Alternative Splicing Activity and Causes Limb-Clasping and Body Tone Defects.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0085962
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- Article
Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022489
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- Publication type:
- Article
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.
- Published in:
- 2018
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- Publication type:
- journal article
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. 3171, doi. 10.1093/brain/awu292
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- Publication type:
- Article