Generation of an Induced Pluripotent Stem Cell Line ICGi045-A of a RASopathy Patient Carrying p.Glu329Lys Variant in SOS1
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Publisher
Pleiades Publishing Ltd
Link
https://link.springer.com/content/pdf/10.1134/S1062360424700036.pdf
Reference5 articles.
1. Dementyeva, E.V., Pavlova, S.V., Chernyavsky, A.M., and Zakian, S.M., Generation of an induced pluripotent stem cell line, ICGi029-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.N515del mutation in MYBPC3, Stem Cell Res., 2021, vol. 53, p. 102344. https://doi.org/10.1016/j.scr.2021.102344
2. Ma, N., Zhang, J.Z., Itzhaki, I., Zhang, S.L., Chen, H., Haddad, F., Kitani, T., Wilson, K.D., Tian, L., Shrestha, R., Wu, H., Lam, Ch.K., Sayed, N., and Wu, J.C., Determining the pathogenicity of a genomic variant of uncertain significance using CRISPR/Cas9 and human-induced pluripotent stem cells, Circulation, 2018, vol. 138, no. 23, pp. 2666–2681. https://doi.org/10.1161/circulationaha.117.032273
3. Malakhova, A.A., Grigor’eva, E.V., Pavlova, S.V., Malankhanova, T.B., Valetdinova, K.R., Vyatkin, Y.V., Khabarova, E.A., Rzaev, J.A., Zakian, S.M., and Medvedev, S.P., Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population, Stem Cell Res., 2020, vol. 48, p. 101952. https://doi.org/10.1016/j.scr.2020.101952
4. Melnik, O.V., Gudkova, Y.A., Vershinina, T.L., Nikitina, I.L., Kostareva, A.A., and Pervunina, T.M., Clinical polymorphism of RASopathies in terms of the children’s cardiology department, Consilium Medicum, 2017, vol. 19, no. 12, pp. 100–104. https://doi.org/10.26442/2075-1753_19.12.100-104
5. Sorogina, D.A., Grigor’eva, E.V., Malakhova, A.A., Pavlova, S.V., Medvedev, S.P., Vyatkin, Y.V., Khabarova, E.A., Rzaev, J.A., and Zakian, S.M., Creation of induced pluripotent stem cells ICGi044-B and ICGi044-C using reprogramming of peripheral blood mononuclear cells of a patient with Parkinson’s disease associated with c.1492T>G mutation in the GLUD2 gene, Russ. J. Dev. Biol., 2023, vol. 54, no. 1, pp. 104–111. https://doi.org/10.1134/S1062360423010125
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