Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability

T. A. Shnaider, I. E. Pristyazhnyuk, A. G. Menzorov, N. M. Matveeva, T. V. Nikitina, A. A. Khabarova, N. A. Skryabin, A. A. Kashevarova, M. E. Lopatkina, L. P. Nazarenko, I. N. Lebedev, O. L. Serov

Результат исследования: Научные публикации в периодических изданияхстатья

Аннотация

The human induced pluripotent stem cell (iPSC) lines, ICGi009-A, ICGi009-B, ICGi013-A and ICGi013-B, were generated from skin fibroblasts of two siblings with intellectual disability. Both patients were carriers of CNTN6 gene microdeletion (Kashevarova et al., 2014). iPSC lines have normal karyotype, express pluripotency markers, are able to differentiate in vitro into derivatives of all three germ layers and represent a unique tool to study neurodevelopmental disorders.

Язык оригиналаанглийский
Номер статьи101591
Число страниц5
ЖурналStem Cell Research
Том41
DOI
СостояниеОпубликовано - 1 дек 2019

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    Shnaider, T. A., Pristyazhnyuk, I. E., Menzorov, A. G., Matveeva, N. M., Nikitina, T. V., Khabarova, A. A., Skryabin, N. A., Kashevarova, A. A., Lopatkina, M. E., Nazarenko, L. P., Lebedev, I. N., & Serov, O. L. (2019). Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability. Stem Cell Research, 41, [101591]. https://doi.org/10.1016/j.scr.2019.101591