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Nicolas B Gomez

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Citations 77
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Recent Articles
1.
Dykstra M, Weskamp K, Gomez N, Waksmacki J, Tank E, Glineburg M, et al.
Cell Rep . 2025 Jan; 44(1):115113. PMID: 39792557
The nuclear RNA-binding protein TDP43 is integrally involved in the pathogenesis of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). Previous studies uncovered N-terminal TDP43 isoforms that are predominantly...
2.
Dykstra M, Weskamp K, Gomez N, Waksmacki J, Tank E, Glineburg M, et al.
bioRxiv . 2024 Jul; PMID: 39005384
The nuclear RNA-binding protein TDP43 is integrally involved in the pathogenesis of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). Previous studies uncovered N-terminal TDP43 isoforms that are predominantly...
3.
Tseng Y, Krans A, Malik I, Deng X, Yildirim E, Ovunc S, et al.
Nucleic Acids Res . 2024 Feb; 52(10):5928-5949. PMID: 38412259
A GGGGCC (G4C2) hexanucleotide repeat expansion in C9ORF72 causes amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD), while a CGG trinucleotide repeat expansion in FMR1 leads to the neurodegenerative disorder Fragile...
4.
Tseng Y, Malik I, Deng X, Krans A, Jansen-West K, Tank E, et al.
bioRxiv . 2023 Jun; PMID: 37333274
A GGGGCC (G4C2) hexanucleotide repeat expansion in causes amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD), while a CGG trinucleotide repeat expansion in leads to the neurodegenerative disorder Fragile X-associated tremor/ataxia...
5.
Sidibe H, Khalfallah Y, Xiao S, Gomez N, Fakim H, Tank E, et al.
Brain . 2021 Jun; 144(11):3461-3476. PMID: 34115105
TDP-43 nuclear depletion and concurrent cytoplasmic accumulation in vulnerable neurons is a hallmark feature of progressive neurodegenerative proteinopathies such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Cellular stress...
6.
Weskamp K, Tank E, Miguez R, McBride J, Gomez N, White M, et al.
J Clin Invest . 2019 Nov; 130(3):1139-1155. PMID: 31714900
Cortical hyperexcitability and mislocalization of the RNA-binding protein TDP43 are highly conserved features in amyotrophic lateral sclerosis (ALS). Nevertheless, the relationship between these phenomena remains poorly defined. Here, we showed...