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An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome.
Snyder A, Ryan VH, Hawrot J, Lawton S, Ramos DM, Qi YA, Johnson K, Reed X, Johnson NL, Kollasch AW, Duffy M, VandeVrede L, Cochran JN, Miller BL, Toro C, Bielekova B, Yokoyama JS, Marks DS, Kwan JY, Cookson MR, Ward ME. Snyder A, et al. Among authors: ward me. Res Sq [Preprint]. 2023 Oct 19:rs.3.rs-3462973. doi: 10.21203/rs.3.rs-3462973/v1. Res Sq. 2023. PMID: 37886540 Free PMC article. Preprint.
FTLD targets brain regions expressing recently evolved genes.
Pasquini L, Pereira FL, Seddighi S, Zeng Y, Wei Y, Illán-Gala I, Vatsavayai SC, Friedberg A, Lee AJ, Brown JA, Spina S, Grinberg LT, Sirkis DW, Bonham LW, Yokoyama JS, Boxer AL, Kramer JH, Rosen HJ, Humphrey J, Gitler AD, Miller BL, Pollard KS, Ward ME, Seeley WW. Pasquini L, et al. Among authors: ward me. medRxiv [Preprint]. 2023 Oct 28:2023.10.27.23297687. doi: 10.1101/2023.10.27.23297687. medRxiv. 2023. PMID: 37961381 Free PMC article. Preprint.
HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases.
Calliari A, Daughrity LM, Albagli EA, Castellanos Otero P, Yue M, Jansen-West K, Islam NN, Caulfield T, Rawlinson B, DeTure M, Cook C, Graff-Radford NR, Day GS, Boeve BF, Knopman DS, Petersen RC, Josephs KA, Oskarsson B, Gitler AD, Dickson DW, Gendron TF, Prudencio M, Ward ME, Zhang YJ, Petrucelli L. Calliari A, et al. Among authors: ward me. Mol Neurodegener. 2024 Mar 27;19(1):29. doi: 10.1186/s13024-024-00718-8. Mol Neurodegener. 2024. PMID: 38539264 Free PMC article.
Potential mechanisms of progranulin-deficient FTLD.
Ward ME, Miller BL. Ward ME, et al. J Mol Neurosci. 2011 Nov;45(3):574-82. doi: 10.1007/s12031-011-9622-3. Epub 2011 Sep 3. J Mol Neurosci. 2011. PMID: 21892758 Free PMC article. Review.
328 results