Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication

Skin fibroblasts from a patient with developmental delay and chromosome 2p25.3 deletion syndrome were reprogrammed into induced pluripotent stem cells (iPSCs) and the clonal stem cell line ICAGi001-A (iTAF9-11) was established. ICAGi001-A pluripotency was demonstrated in vitro by three germ layer di...

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Veröffentlicht in:Stem cell research 2019-01, Vol.34, p.101377-101377, Article 101377
Hauptverfasser: Khabarova, A.A., Pristyazhnyuk, I.E., Nikitina, T.V., Gayner, T.A., Torkhova, N.B., Skryabin, N.A., Kashevarova, A.A., Babushkina, N.P., Markova, Zh.G., Minzhenkova, M.E., Nazarenko, L.P., Shilova, N.V., Shorina, A.R., Lebedev, I.N., Serov, O.L.
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Sprache:eng
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Zusammenfassung:Skin fibroblasts from a patient with developmental delay and chromosome 2p25.3 deletion syndrome were reprogrammed into induced pluripotent stem cells (iPSCs) and the clonal stem cell line ICAGi001-A (iTAF9-11) was established. ICAGi001-A pluripotency was demonstrated in vitro by three germ layer differentiation capacity. This line is a good model for studying of the developmental delay and brain disorder.
ISSN:1873-5061
1876-7753
DOI:10.1016/j.scr.2018.101377