Found: 24
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Clusterin ameliorates tau pathology in vivo by inhibiting fibril formation.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01079-1
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- Article
Generation and characterization of monoclonal antibodies against pathologically phosphorylated TDP-43.
- Published in:
- PLoS ONE, 2024, v. 19, n. 4, p. 1, doi. 10.1371/journal.pone.0298080
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- Publication type:
- Article
Tau exhibits unique seeding properties in globular glial tauopathy.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0691-9
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- Publication type:
- Article
Enhanced phosphorylation of T153 in soluble tau is a defining biochemical feature of the A152T tau risk variant.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0661-2
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- Publication type:
- Article
Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of <italic>C9ORF72</italic>-repeat induced toxicity.
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- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0545-x
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- Publication type:
- Article
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia.
- Published in:
- 2020
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- Publication type:
- journal article
Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72-associated amyotrophic lateral sclerosis.
- Published in:
- Science Translational Medicine, 2017, v. 9, n. 383, p. 1, doi. 10.1126/scitranslmed.aai7866
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- Publication type:
- Article
Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosis.
- Published in:
- 2017
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- Publication type:
- journal article
Correction: TDP-43 and other hnRNPs regulate cryptic exon inclusion of a key ALS/FTD risk gene, UNC13A.
- Published in:
- 2023
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- Publication type:
- Correction Notice
TDP-43 and other hnRNPs regulate cryptic exon inclusion of a key ALS/FTD risk gene, UNC13A.
- Published in:
- PLoS Biology, 2023, v. 21, n. 3, p. 1, doi. 10.1371/journal.pbio.3002028
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- Publication type:
- Article
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 17, p. 3421, doi. 10.1093/hmg/ddx233
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- Publication type:
- Article
Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72.
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- Acta Neuropathologica, 2015, v. 130, n. 6, p. 863, doi. 10.1007/s00401-015-1480-6
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- Publication type:
- Article
Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers.
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- Acta Neuropathologica, 2015, v. 130, n. 4, p. 559, doi. 10.1007/s00401-015-1474-4
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- Publication type:
- Article
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress.
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- Acta Neuropathologica, 2014, v. 128, n. 4, p. 505, doi. 10.1007/s00401-014-1336-5
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- Publication type:
- Article
Antisense transcripts of the expanded <i>C9ORF72</i> hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 6, p. 829, doi. 10.1007/s00401-013-1192-8
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- Publication type:
- Article
Reduced <i>C9orf72</i> gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood.
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- Acta Neuropathologica, 2013, v. 126, n. 6, p. 895, doi. 10.1007/s00401-013-1199-1
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- Publication type:
- Article
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementia.
- Published in:
- Science Translational Medicine, 2024, v. 16, n. 730, p. 1, doi. 10.1126/scitranslmed.adf9735
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- Publication type:
- Article
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 566, p. 1, doi. 10.1126/scitranslmed.abb7086
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- Publication type:
- Article
C9orf72 poly(GR) aggregation induces TDP-43 proteinopathy.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 559, p. 1, doi. 10.1126/scitranslmed.abb3774
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- Publication type:
- Article
Correction: HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases.
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- 2024
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- Publication type:
- Correction Notice
HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases.
- Published in:
- Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00718-8
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- Publication type:
- Article
HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases.
- Published in:
- Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00718-8
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- Publication type:
- Article
Astrocyte-derived clusterin suppresses amyloid formation in vivo.
- Published in:
- Molecular Neurodegeneration, 2020, v. 15, n. 1, p. N.PAG, doi. 10.1186/s13024-020-00416-1
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- Publication type:
- Article
Aberrant deposition of stress granule-resident proteins linked to C9orf72-associated TDP-43 proteinopathy.
- Published in:
- Molecular Neurodegeneration, 2019, v. 14, n. 1, p. N.PAG, doi. 10.1186/s13024-019-0310-z
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- Publication type:
- Article