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Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines. / Valetdinova, K. R.; Maretina, M. A.; Kuranova, M. L. et al.

In: Stem Cell Research, Vol. 34, 101376, 01.01.2019.

Research output: Contribution to journal › Article › peer-review

Harvard

Valetdinova, KR, Maretina, MA, Kuranova, ML, Grigor'eva, EV, Minina, YM, Kizilova, EA, Kiselev, AV, Medvedev, SP, Baranov, VS & Zakian, SM 2019, 'Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines', Stem Cell Research, vol. 34, 101376. https://doi.org/10.1016/j.scr.2018.101376

APA

Valetdinova, K. R., Maretina, M. A., Kuranova, M. L., Grigor'eva, E. V., Minina, Y. M., Kizilova, E. A., Kiselev, A. V., Medvedev, S. P., Baranov, V. S., & Zakian, S. M. (2019). Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines. Stem Cell Research, 34, [101376]. https://doi.org/10.1016/j.scr.2018.101376

Vancouver

Valetdinova KR, Maretina MA, Kuranova ML, Grigor'eva EV, Minina YM, Kizilova EA et al. Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines. Stem Cell Research. 2019 Jan 1;34:101376. doi: 10.1016/j.scr.2018.101376

Author

Valetdinova, K. R. ; Maretina, M. A. ; Kuranova, M. L. et al. / Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines. In: Stem Cell Research. 2019 ; Vol. 34.

BibTeX

@article{ad22312b5e814631af79738219d58b09,
title = "Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines",
abstract = "Spinal muscular atrophy (SMA) is a neuromuscular disease caused by deletion or mutation in SMN1 gene. SMA human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the study of the disorder, as they provide in vitro the target cells. We generated iPSCs from a SMA type I patient and SMA type II patient by using non-integrating episomal plasmid vectors. The resulting iPSCs are episomal-free, express pluripotency markers, display a normal karyotype, retain the mutation (homozygous deletion of SMN1) and are able to differentiate into the three germ layers.",
keywords = "BLOOD, Cell Line, Cell Culture Techniques/methods, Humans, Adult, Induced Pluripotent Stem Cells/pathology, Child, Muscular Atrophy, Spinal/pathology",
author = "Valetdinova, {K. R.} and Maretina, {M. A.} and Kuranova, {M. L.} and Grigor'eva, {E. V.} and Minina, {Y. M.} and Kizilova, {E. A.} and Kiselev, {A. V.} and Medvedev, {S. P.} and Baranov, {V. S.} and Zakian, {S. M.}",
note = "Publisher Copyright: {\textcopyright} 2019 The Authors",
year = "2019",
month = jan,
day = "1",
doi = "10.1016/j.scr.2018.101376",
language = "English",
volume = "34",
journal = "Stem Cell Research",
issn = "1873-5061",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines

AU - Valetdinova, K. R.

AU - Maretina, M. A.

AU - Kuranova, M. L.

AU - Grigor'eva, E. V.

AU - Minina, Y. M.

AU - Kizilova, E. A.

AU - Kiselev, A. V.

AU - Medvedev, S. P.

AU - Baranov, V. S.

AU - Zakian, S. M.

N1 - Publisher Copyright: © 2019 The Authors

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Spinal muscular atrophy (SMA) is a neuromuscular disease caused by deletion or mutation in SMN1 gene. SMA human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the study of the disorder, as they provide in vitro the target cells. We generated iPSCs from a SMA type I patient and SMA type II patient by using non-integrating episomal plasmid vectors. The resulting iPSCs are episomal-free, express pluripotency markers, display a normal karyotype, retain the mutation (homozygous deletion of SMN1) and are able to differentiate into the three germ layers.

AB - Spinal muscular atrophy (SMA) is a neuromuscular disease caused by deletion or mutation in SMN1 gene. SMA human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the study of the disorder, as they provide in vitro the target cells. We generated iPSCs from a SMA type I patient and SMA type II patient by using non-integrating episomal plasmid vectors. The resulting iPSCs are episomal-free, express pluripotency markers, display a normal karyotype, retain the mutation (homozygous deletion of SMN1) and are able to differentiate into the three germ layers.

KW - BLOOD

KW - Cell Line

KW - Cell Culture Techniques/methods

KW - Humans

KW - Adult

KW - Induced Pluripotent Stem Cells/pathology

KW - Child

KW - Muscular Atrophy, Spinal/pathology

UR - http://www.scopus.com/inward/record.url?scp=85060060248&partnerID=8YFLogxK

U2 - 10.1016/j.scr.2018.101376

DO - 10.1016/j.scr.2018.101376

M3 - Article

C2 - 30660867

AN - SCOPUS:85060060248

VL - 34

JO - Stem Cell Research

JF - Stem Cell Research

SN - 1873-5061

M1 - 101376

ER -

ID: 18170268