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Year | Number of Results |
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2018 | 1 |
2019 | 1 |
2022 | 2 |
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TDP-43 represses cryptic exon inclusion in the FTD-ALS gene UNC13A.
Nature. 2022 Mar;603(7899):124-130. doi: 10.1038/s41586-022-04424-7. Epub 2022 Feb 23.
Nature. 2022.
PMID: 35197626
Free PMC article.
C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies.
Vatsavayai SC, Nana AL, Yokoyama JS, Seeley WW.
Vatsavayai SC, et al.
Acta Neuropathol. 2019 Jan;137(1):1-26. doi: 10.1007/s00401-018-1921-0. Epub 2018 Oct 27.
Acta Neuropathol. 2019.
PMID: 30368547
Free PMC article.
Review.
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Loss of TDP-43 function contributes to genomic instability in amyotrophic lateral sclerosis.
Fang M, Deibler SK, Nana AL, Vatsavayai SC, Banday S, Zhou Y, Almeida S, Weiss A, Brown RH, Seeley WW, Gao FB, Green MR.
Fang M, et al.
Front Neurosci. 2023 Oct 2;17:1251228. doi: 10.3389/fnins.2023.1251228. eCollection 2023.
Front Neurosci. 2023.
PMID: 37849894
Free PMC article.
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Rainwater Charitable Foundation criteria for the neuropathologic diagnosis of progressive supranuclear palsy.
Roemer SF, Grinberg LT, Crary JF, Seeley WW, McKee AC, Kovacs GG, Beach TG, Duyckaerts C, Ferrer IA, Gelpi E, Lee EB, Revesz T, White CL 3rd, Yoshida M, Pereira FL, Whitney K, Ghayal NB, Dickson DW.
Roemer SF, et al.
Acta Neuropathol. 2022 Oct;144(4):603-614. doi: 10.1007/s00401-022-02479-4. Epub 2022 Aug 10.
Acta Neuropathol. 2022.
PMID: 35947184
Free PMC article.
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