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Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. / Grigor'eva, E. V.; Malankhanova, T. B.; Surumbayeva, A. et al.

In: Stem Cell Research, Vol. 34, 101382, 01.01.2019.

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

Harvard

Grigor'eva, EV, Malankhanova, TB, Surumbayeva, A, Minina, JM, Morozov, VV, Abramycheva, NY, Illarioshkin, SN, Malakhova, AA & Zakian, SM 2019, 'Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease', Stem Cell Research, vol. 34, 101382. https://doi.org/10.1016/j.scr.2018.101382

APA

Grigor'eva, E. V., Malankhanova, T. B., Surumbayeva, A., Minina, J. M., Morozov, V. V., Abramycheva, N. Y., Illarioshkin, S. N., Malakhova, A. A., & Zakian, S. M. (2019). Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. Stem Cell Research, 34, [101382]. https://doi.org/10.1016/j.scr.2018.101382

Vancouver

Grigor'eva EV, Malankhanova TB, Surumbayeva A, Minina JM, Morozov VV, Abramycheva NY et al. Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. Stem Cell Research. 2019 Jan 1;34:101382. doi: 10.1016/j.scr.2018.101382

Author

Grigor'eva, E. V. ; Malankhanova, T. B. ; Surumbayeva, A. et al. / Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. In: Stem Cell Research. 2019 ; Vol. 34.

BibTeX

@article{6d7f02d213514deca92cd6b9ca938171,
title = "Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease",
abstract = "Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by mutation in the HTT gene encoding HTT protein. The mutant protein leads to the neuronal death through dysregulation of multiple cellular processes. HD human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the disease study. iPSC line from HD patient with 47 CAG repeats in HTT was generated from blood mononuclear cells by non-integrating episomal vectors. The iPSC line retained the mutation, expressed pluripotency markers, had a normal karyotype and displayed in vitro differentiation to the three germ layers.",
keywords = "Adult, Cell Culture Techniques/methods, Cell Line, Cellular Reprogramming, Female, Humans, Huntington Disease/blood, Induced Pluripotent Stem Cells/pathology, Leukocytes, Mononuclear/pathology",
author = "Grigor'eva, {E. V.} and Malankhanova, {T. B.} and A. Surumbayeva and Minina, {J. M.} and Morozov, {V. V.} and Abramycheva, {N. Yu} and Illarioshkin, {S. N.} and Malakhova, {A. A.} and Zakian, {S. M.}",
note = "Publisher Copyright: {\textcopyright} 2019 The Authors",
year = "2019",
month = jan,
day = "1",
doi = "10.1016/j.scr.2018.101382",
language = "English",
volume = "34",
journal = "Stem Cell Research",
issn = "1873-5061",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease

AU - Grigor'eva, E. V.

AU - Malankhanova, T. B.

AU - Surumbayeva, A.

AU - Minina, J. M.

AU - Morozov, V. V.

AU - Abramycheva, N. Yu

AU - Illarioshkin, S. N.

AU - Malakhova, A. A.

AU - Zakian, S. M.

N1 - Publisher Copyright: © 2019 The Authors

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by mutation in the HTT gene encoding HTT protein. The mutant protein leads to the neuronal death through dysregulation of multiple cellular processes. HD human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the disease study. iPSC line from HD patient with 47 CAG repeats in HTT was generated from blood mononuclear cells by non-integrating episomal vectors. The iPSC line retained the mutation, expressed pluripotency markers, had a normal karyotype and displayed in vitro differentiation to the three germ layers.

AB - Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by mutation in the HTT gene encoding HTT protein. The mutant protein leads to the neuronal death through dysregulation of multiple cellular processes. HD human induced pluripotent stem cells (iPSCs) represent a useful and valid model for the disease study. iPSC line from HD patient with 47 CAG repeats in HTT was generated from blood mononuclear cells by non-integrating episomal vectors. The iPSC line retained the mutation, expressed pluripotency markers, had a normal karyotype and displayed in vitro differentiation to the three germ layers.

KW - Adult

KW - Cell Culture Techniques/methods

KW - Cell Line

KW - Cellular Reprogramming

KW - Female

KW - Humans

KW - Huntington Disease/blood

KW - Induced Pluripotent Stem Cells/pathology

KW - Leukocytes, Mononuclear/pathology

UR - http://www.scopus.com/inward/record.url?scp=85059966398&partnerID=8YFLogxK

U2 - 10.1016/j.scr.2018.101382

DO - 10.1016/j.scr.2018.101382

M3 - Article

C2 - 30658253

AN - SCOPUS:85059966398

VL - 34

JO - Stem Cell Research

JF - Stem Cell Research

SN - 1873-5061

M1 - 101382

ER -

ID: 18142199