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Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndrome.
Carbonell AU, Cho CH, Tindi JO, Counts PA, Bates JC, Erdjument-Bromage H, Cvejic S, Iaboni A, Kvint I, Rosensaft J, Banne E, Anagnostou E, Neubert TA, Scherer SW, Molholm S, Jordan BA. Carbonell AU, et al. Among authors: tindi jo. Nat Commun. 2019 Aug 6;10(1):3529. doi: 10.1038/s41467-019-11437-w. Nat Commun. 2019. PMID: 31388001 Free PMC article.
Patient-specific mutation of Dync1h1 in mice causes brain and behavioral deficits.
Ramos RL, De Heredia MMB, Zhang Y, Stout RF, Tindi JO, Wu L, Schwartz GJ, Botbol YM, Sidoli S, Poojari A, Rakowski-Anderson T, Shafit-Zagardo B. Ramos RL, et al. Among authors: tindi jo. Neurobiol Dis. 2024 Sep;199:106594. doi: 10.1016/j.nbd.2024.106594. Epub 2024 Jul 16. Neurobiol Dis. 2024. PMID: 39025270 Free article.
ANKS1B encoded AIDA-1 regulates social behaviors by controlling oligodendrocyte function.
Cho CH, Deyneko IV, Cordova-Martinez D, Vazquez J, Maguire AS, Diaz JR, Carbonell AU, Tindi JO, Cui MH, Fleysher R, Molholm S, Lipton ML, Branch CA, Hodgson L, Jordan BA. Cho CH, et al. Among authors: tindi jo. Nat Commun. 2023 Dec 21;14(1):8499. doi: 10.1038/s41467-023-43438-1. Nat Commun. 2023. PMID: 38129387 Free PMC article.