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

doi:10.1016/j.scr.2019.101591

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

Кафедра цитологии и генетики ФЕН

Результат исследования: Научные публикации в периодических изданиях › статья › рецензирование

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 оригинала	английский
Номер статьи	101591
Число страниц	5
Журнал	Stem Cell Research
Том	41
DOI	https://doi.org/10.1016/j.scr.2019.101591
Состояние	Опубликовано - 1 дек 2019

Доступ к документу

10.1016/j.scr.2019.101591

Link to publication in Scopus

Fingerprint Подробные сведения о темах исследования «Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability». Вместе они формируют уникальный семантический отпечаток (fingerprint).

Цитировать

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

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. / Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability. В: Stem Cell Research. 2019 ; Том 41.

@article{beb6e561c2f74770a0fc2b68ddb43c98,

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

abstract = "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.",

keywords = "STEM-CELLS",

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

year = "2019",

month = dec,

day = "1",

doi = "10.1016/j.scr.2019.101591",

language = "English",

volume = "41",

journal = "Stem Cell Research",

issn = "1873-5061",

publisher = "Elsevier",

}

Shnaider, TA, Pristyazhnyuk, IE, Menzorov, AG, Matveeva, NM, Nikitina, TV, Khabarova, AA, Skryabin, NA, Kashevarova, AA, Lopatkina, ME, Nazarenko, LP, Lebedev, IN & Serov, OL 2019, 'Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability', Stem Cell Research, том. 41, 101591. https://doi.org/10.1016/j.scr.2019.101591

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

В: Stem Cell Research, Том 41, 101591, 01.12.2019.

Результат исследования: Научные публикации в периодических изданиях › статья › рецензирование

TY - JOUR

T1 - Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability

AU - Shnaider, T. A.

AU - Pristyazhnyuk, I. E.

AU - Menzorov, A. G.

AU - Matveeva, N. M.

AU - Nikitina, T. V.

AU - Khabarova, A. A.

AU - Skryabin, N. A.

AU - Kashevarova, A. A.

AU - Lopatkina, M. E.

AU - Nazarenko, L. P.

AU - Lebedev, I. N.

AU - Serov, O. L.

PY - 2019/12/1

Y1 - 2019/12/1

N2 - 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.

AB - 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.

KW - STEM-CELLS

UR - http://www.scopus.com/inward/record.url?scp=85074216203&partnerID=8YFLogxK

U2 - 10.1016/j.scr.2019.101591

DO - 10.1016/j.scr.2019.101591

M3 - Article

C2 - 31678775

AN - SCOPUS:85074216203

VL - 41

JO - Stem Cell Research

JF - Stem Cell Research

SN - 1873-5061

M1 - 101591

ER -