| Literature DB >> 33360445 |
Dóra Reé1, Adrienn Borsy1, Ábel Fóthi1, Tamás I Orbán1, György Várady1, Zsuzsa Erdei1, Balázs Sarkadi1, János Réthelyi2, Nóra Varga1, Ágota Apáti3.
Abstract
DiGeorge Syndrome (DGS) Critical Region 8 (DGCR8) is a primary candidate gene in they DGS. The DGCR8 microprocessor complex subunit is an essential cofactor in the canonical miRNA biogenesis which is involved in diverse cellular functions such as cell fate decisions, apoptosis and different signaling pathways. However, the role of DGCR8 in these processes or development of DGS is not fully understood. Here we present a heterozygous DGCR8 mutant human embryonic stem cell line (HuES9DGCR8+/-) created by the CRISPR/Cas9 system. The generated HuES9DGCR8+/- cells maintain normal karyotype, morphology, pluripotency and differentiation capacity into all three germ layers.Entities:
Year: 2020 PMID: 33360445 DOI: 10.1016/j.scr.2020.102134
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020