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.

Autor:	Khabarova AA; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia. Electronic address: anya.khabarova@gmail.com., Pristyazhnyuk IE; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia., Nikitina TV; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Gayner TA; Institute of Chemical Biology and Fundamental Medicine, SB RAS, Novosibirsk, Russia; Group of companies 'Center of new medical technologies', Novosibirsk, Russia., Torkhova NB; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Skryabin NA; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Kashevarova AA; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Babushkina NP; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Markova ZG; Research Centre for Medical Genetics, Moscow, Russia., Minzhenkova ME; Research Centre for Medical Genetics, Moscow, Russia., Nazarenko LP; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Shilova NV; Research Centre for Medical Genetics, Moscow, Russia., Shorina AR; Clinical City Hospital №1, Novosibirsk, Russia., Lebedev IN; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia., Serov OL; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia.
Jazyk:	angličtina
Zdroj:	Stem cell research [Stem Cell Res] 2019 Jan; Vol. 34, pp. 101377. Date of Electronic Publication: 2018 Dec 18.
DOI:	10.1016/j.scr.2018.101377
Abstrakt:	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. (Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.)
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu