| Autor: |
Khomyakova, E. A., Fedorenko, A. V., Surdina, A. V., Volovikov, E. A., Belikova, L. D., Zerkalenkova, E. A., Lagarkova, M. A., Bogomazova, A. N. |
| Předmět: |
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| Zdroj: |
Russian Journal of Developmental Biology; Dec2023, Vol. 54 Issue 6, p365-373, 9p |
| Abstrakt: |
The deletions and mutations in the UBE2A gene cause X-linked mental retardation syndrome of the Nascimento type first described in 2006 (Nascimento et al., 2006). At the moment, approximately two dozen missense and nonsense mutations in the UBE2A gene associated with Nascimento-type mental retardation syndrome are known (Cordeddu et al., 2020). To study the role of the UBE2A gene in neurodevelopment, the authors generated a human iPSC line with knockout of the UBE2A gene (RCPCMi009-A-1) using genome editing CRISPR/Cas9 technology. The knockout of the UBE2A gene was confirmed by Western blotting. The pluripotent state of the RCPCMi009-A-1 iPSC line was confirmed by typical stem cell morphology, normal male karyotype (46,XY) maintenance, expression of pluripotency markers, and the ability to differentiate into the derivatives of three germ layers. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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