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Selective ferroptosis vulnerability due to familial Alzheimer's disease presenilin mutations.
Greenough MA, Lane DJR, Balez R, Anastacio HTD, Zeng Z, Ganio K, McDevitt CA, Acevedo K, Belaidi AA, Koistinaho J, Ooi L, Ayton S, Bush AI. Greenough MA, et al. Among authors: ooi l. Cell Death Differ. 2022 Nov;29(11):2123-2136. doi: 10.1038/s41418-022-01003-1. Epub 2022 Apr 21. Cell Death Differ. 2022. PMID: 35449212 Free PMC article.
Generation and characterization of human induced pluripotent stem cell lines from a familial Alzheimer's disease PSEN1 A246E patient and a non-demented family member bearing wild-type PSEN1.
Muñoz SS, Balez R, Castro Cabral-da-Silva ME, Berg T, Engel M, Bax M, Do-Ha D, Stevens CH, Greenough M, Bush A, Ooi L. Muñoz SS, et al. Among authors: ooi l. Stem Cell Res. 2018 Aug;31:227-230. doi: 10.1016/j.scr.2018.08.006. Epub 2018 Aug 13. Stem Cell Res. 2018. PMID: 30138848 Free article.
Loss of Cln5 leads to altered Gad1 expression and deficits in interneuron development in mice.
Singh Y, Leinonen H, Fazaludeen F, Jaronen M, Guest D, Buckley N, Byts N, Oksa P, Jalkanen K, Iqbal I, Huuskonen M, Savchenko E, Keksa-Goldsteine V, Chew S, Myllyharju J, Tanila H, Ooi L, Koistinaho J, Kanninen KM, Malm T. Singh Y, et al. Among authors: ooi l. Hum Mol Genet. 2019 Oct 1;28(19):3309-3322. doi: 10.1093/hmg/ddz165. Hum Mol Genet. 2019. PMID: 31294445
Generation and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNFS621G familial amyotrophic lateral sclerosis patient using mRNA reprogramming.
Bax M, Balez R, Muñoz SS, Do-Ha D, Stevens CH, Berg T, Cabral-da-Silva MC, Engel M, Nicholson G, Yang S, Blair IP, Ooi L. Bax M, et al. Among authors: ooi l. Stem Cell Res. 2019 Oct;40:101530. doi: 10.1016/j.scr.2019.101530. Epub 2019 Aug 14. Stem Cell Res. 2019. PMID: 31445393 Free article.
503 results