Search Results - "Maretina, M.A."

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  1. 1

    Generation of a spinal muscular atrophy type III patient-specific induced pluripotent stem cell line ICGi003-A by Ovechkina, V.S., Maretina, M.A., Egorova, A.A., Baranov, V.S., Kiselev, A.V., Zakian, S.M., Valetdinova, K.R.

    Published in Stem cell research (01-10-2020)
    “…Spinal muscular atrophy (SMA) is a genetic disease, which characterized by the degeneration of motor neurons in the spinal cord and further striated muscle…”
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    Journal Article
  2. 2

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

    Published in Stem cell research (01-10-2020)
    “…Duchenne muscular dystrophy (DMD) is a severe and rapidly progressive hereditary muscular disease with X-linked recessive inheritance, occurring mainly in…”
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    Journal Article
  3. 3

    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 by 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.

    Published in Stem cell research (01-01-2019)
    “…Spinal muscular atrophy (SMA) is a neuromuscular disease caused by deletion or mutation in SMN1 gene. SMA human induced pluripotent stem cells (iPSCs)…”
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    Journal Article
  4. 4

    Identification of specific gene methylation patterns during motor neuron differentiation from spinal muscular atrophy patient-derived iPSC by Maretina, M.A., Valetdinova, K.R., Tsyganova, N.A., Egorova, A.A., Ovechkina, V.S., Schiöth, H.B., Zakian, S.M., Baranov, V.S., Kiselev, A.V.

    Published in Gene (15-02-2022)
    “…•We studied gene methylation during motor neuron differentiation from SMA patient-derived iPSCs.•PAX6, HB9, CHAT, ARHGAP22, and SMN2 genes are differently…”
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    Journal Article