Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C

Standard

Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. / Valetdinova, K. R.; Maretina, M. A.; Vyatkin, Y. V. и др.

в: Stem Cell Research, Том 48, 101941, 01.10.2020.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Valetdinova, KR, Maretina, MA, Vyatkin, YV, Perepelkina, MP, Egorova, AA, Baranov, VS, Kiselev, AV, Gershovich, PM & Zakian, SM 2020, 'Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C', Stem Cell Research, Том. 48, 101941. https://doi.org/10.1016/j.scr.2020.101941

APA

Valetdinova, K. R., Maretina, M. A., Vyatkin, Y. V., Perepelkina, M. P., Egorova, A. A., Baranov, V. S., Kiselev, A. V., Gershovich, P. M., & Zakian, S. M. (2020). Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. Stem Cell Research, 48, [101941]. https://doi.org/10.1016/j.scr.2020.101941

Vancouver

Valetdinova KR, Maretina MA, Vyatkin YV, Perepelkina MP, Egorova AA, Baranov VS и др. Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. Stem Cell Research. 2020 окт. 1;48:101941. Epub 2020 авг. 3. doi: 10.1016/j.scr.2020.101941

Author

Valetdinova, K. R. ; Maretina, M. A. ; Vyatkin, Y. V. и др. / Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. в: Stem Cell Research. 2020 ; Том 48.

BibTeX

@article{98096916f40f4931a4612a1be542b889,

title = "Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C",

abstract = "Duchenne muscular dystrophy (DMD) is a severe and rapidly progressive hereditary muscular disease with X-linked recessive inheritance, occurring mainly in males. A complete loss of dystrophin resulted from out-of-frame deletion mutations in the DMD gene leads to Duchenne muscular dystrophy. DMD induced pluripotent stem cells (iPSCs) are a suitable cell model to study muscle development and disease mechanisms underlying muscular dystrophy and to screen novel compounds with potential therapeutic effects. We generated iPSCs from a DMD patient using non-integrating episomal plasmid vectors. The obtained iPSC lines showed ESC-like morphology, expression pluripotency markers, displayed a normal karyotype and possessed trilineage differentiation potential.",

keywords = "BLOOD",

author = "Valetdinova, {K. R.} and Maretina, {M. A.} and Vyatkin, {Y. V.} and Perepelkina, {M. P.} and Egorova, {A. A.} and Baranov, {V. S.} and Kiselev, {A. V.} and Gershovich, {P. M.} and Zakian, {S. M.}",

year = "2020",

month = oct,

day = "1",

doi = "10.1016/j.scr.2020.101941",

language = "English",

volume = "48",

journal = "Stem Cell Research",

issn = "1873-5061",

publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C

AU - Valetdinova, K. R.

AU - Maretina, M. A.

AU - Vyatkin, Y. V.

AU - Perepelkina, M. P.

AU - Egorova, A. A.

AU - Baranov, V. S.

AU - Kiselev, A. V.

AU - Gershovich, P. M.

AU - Zakian, S. M.

PY - 2020/10/1

Y1 - 2020/10/1

N2 - Duchenne muscular dystrophy (DMD) is a severe and rapidly progressive hereditary muscular disease with X-linked recessive inheritance, occurring mainly in males. A complete loss of dystrophin resulted from out-of-frame deletion mutations in the DMD gene leads to Duchenne muscular dystrophy. DMD induced pluripotent stem cells (iPSCs) are a suitable cell model to study muscle development and disease mechanisms underlying muscular dystrophy and to screen novel compounds with potential therapeutic effects. We generated iPSCs from a DMD patient using non-integrating episomal plasmid vectors. The obtained iPSC lines showed ESC-like morphology, expression pluripotency markers, displayed a normal karyotype and possessed trilineage differentiation potential.

AB - Duchenne muscular dystrophy (DMD) is a severe and rapidly progressive hereditary muscular disease with X-linked recessive inheritance, occurring mainly in males. A complete loss of dystrophin resulted from out-of-frame deletion mutations in the DMD gene leads to Duchenne muscular dystrophy. DMD induced pluripotent stem cells (iPSCs) are a suitable cell model to study muscle development and disease mechanisms underlying muscular dystrophy and to screen novel compounds with potential therapeutic effects. We generated iPSCs from a DMD patient using non-integrating episomal plasmid vectors. The obtained iPSC lines showed ESC-like morphology, expression pluripotency markers, displayed a normal karyotype and possessed trilineage differentiation potential.

KW - BLOOD

UR - http://www.scopus.com/inward/record.url?scp=85089017102&partnerID=8YFLogxK

U2 - 10.1016/j.scr.2020.101941

DO - 10.1016/j.scr.2020.101941

M3 - Article

C2 - 32777771

AN - SCOPUS:85089017102

VL - 48

JO - Stem Cell Research

JF - Stem Cell Research

SN - 1873-5061

M1 - 101941

ER -

ID: 24950959