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Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman Primates.
Tanenhaus A, Stowe T, Young A, McLaughlin J, Aeran R, Lin IW, Li J, Hosur R, Chen M, Leedy J, Chou T, Pillay S, Vila MC, Kearney JA, Moorhead M, Belle A, Tagliatela S. Tanenhaus A, et al. Among authors: kearney ja. Hum Gene Ther. 2022 Jun;33(11-12):579-597. doi: 10.1089/hum.2022.037. Hum Gene Ther. 2022. PMID: 35435735 Free PMC article.
SCN3A deficiency associated with increased seizure susceptibility.
Lamar T, Vanoye CG, Calhoun J, Wong JC, Dutton SBB, Jorge BS, Velinov M, Escayg A, Kearney JA. Lamar T, et al. Among authors: kearney ja. Neurobiol Dis. 2017 Jun;102:38-48. doi: 10.1016/j.nbd.2017.02.006. Epub 2017 Feb 22. Neurobiol Dis. 2017. PMID: 28235671 Free PMC article.
Gene expression profiling in a mouse model of Dravet syndrome.
Hawkins NA, Calhoun JD, Huffman AM, Kearney JA. Hawkins NA, et al. Among authors: kearney ja. Exp Neurol. 2019 Jan;311:247-256. doi: 10.1016/j.expneurol.2018.10.010. Epub 2018 Oct 19. Exp Neurol. 2019. PMID: 30347190 Free PMC article.
CACNA1H variants are not a cause of monogenic epilepsy.
Calhoun JD, Huffman AM, Bellinski I, Kinsley L, Bachman E, Gerard E, Kearney JA, Carvill GL. Calhoun JD, et al. Among authors: kearney ja. Hum Mutat. 2020 Jun;41(6):1138-1144. doi: 10.1002/humu.24017. Epub 2020 Apr 14. Hum Mutat. 2020. PMID: 32227660 Free PMC article.
121 results