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Page 1
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: sato mt. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
Teaching NeuroImages: Retinopathy in spinocerebellar ataxia type 3.
Nascimento FA, Ferreira MG, Shiokawa N, Sato MT, Teive HAG. Nascimento FA, et al. Among authors: sato mt. Neurology. 2020 May 26;94(21):e2283-e2284. doi: 10.1212/WNL.0000000000009484. Epub 2020 Apr 24. Neurology. 2020. PMID: 32332129 No abstract available.
Potential of Human Neural Precursor Cells in Diabetic Retinopathy Therapeutics - Preclinical Model.
Saçaki CS, Mogharbel BF, Stricker PEF, Dziedzic DSM, Irioda AC, Perussolo MC, Somma AT, Montiani-Ferreira F, Moreno JCD, Dornbusch P, Sato M, Shiokawa N, de Noronha L, Nagashima S, Bacellar-Galdino M, Franco CRC, Abdelwahid E, Athayde Teixeira de Carvalho K. Saçaki CS, et al. Curr Eye Res. 2022 Mar;47(3):450-460. doi: 10.1080/02713683.2021.2002909. Epub 2021 Dec 6. Curr Eye Res. 2022. PMID: 34749546
27 results