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  1. 2020

  2. Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery–Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln

    Perepelina, K., Kostina, A., Klauzen, P., Khudiakov, A., Rabino, M., Crasto, S., Zlotina, A., Fomicheva, Y., Sergushichev, A., Oganesian, M., Dmitriev, A., Kostareva, A., Di Pasquale, E. & Malashicheva, A., Aug 2020, In: Stem Cell Research. 47, 5 p., 101895.

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

  3. Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.

    Klauzen, P., Perepelina, K., Khudiakov, A., Zlotina, A., Fomicheva, Y., Pervunina, T., Vershinina, T., Kostareva, A. & Malashicheva, A., Mar 2020, In: Stem Cell Research. 43, 5 p., 101719.

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

  4. Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg.

    Khudiakov, A., Perepelina, K., Klauzen, P., Zlotina, A., Gusev, K., Kaznacheyeva, E., Malashicheva, A. & Kostareva, A., Mar 2020, In: Stem Cell Research. 43, 5 p., 101720.

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

  5. Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery–Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.

    Perepelina, K., Klauzen, P., Khudiakov, A., Zlotina, A., Fomicheva, Y., Rudenko, D., Gordeev, M., Sergushichev, A., Malashicheva, A. & Kostareva, A., Mar 2020, In: Stem Cell Research. 43, 5 p., 101714.

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

  6. 2019

  7. Tissue-Specific Influence of Lamin A Mutations on Notch Signaling and Osteogenic Phenotype of Primary Human Mesenchymal Cells

    Perepelina, K., Klauzen, P., Kostareva, A. & Malashicheva, A., 21 Mar 2019, In: Cells. 8, 3, 17 p., 266.

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

  8. Lamin a mutations influence notch signaling and the osteogenic phenotype of human primary mesenchymal cells in a tissue-specific manner

    Perepelina, K., Klauzen, P., Kostareva, A. & Malashicheva, A., 1 Jan 2019, In: Biopolymers and Cell. 35, 3, 1 p.

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

ID: 13809252