Cryptic exon inclusion in TDP-43 proteinopathies: opportunities and challenges
Author:
Affiliation:
1. Department of Neurology, Ulm University, Ulm, Germany
Publisher
Medknow
Reference12 articles.
1. Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer’s disease;Agra Almeida Quadros;Acta Neuropathol,2024
2. Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells;Appocher;Nucleic Acids Res,2017
3. Mechanism of STMN2 cryptic splice-polyadenylation and its correction for TDP-43 proteinopathies;Baughn;Science,2023
4. Cryptic exon inclusion is a molecular signature of LATE-NC in aging brains;Chung;Acta Neuropathol,2024
5. iPSC motor neurons, but not other derived cell types, capture gene expression changes in postmortem sporadic ALS motor neurons;Held;Cell Rep,2023
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