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  1. 2017

  2. The high Ca2+-sensitivity associated with the Glu139del and Arg91Gly mutations in tropomyosin is caused by freezing of tropomyosin near the closed position

    Karpicheva, O. E., Симонян, А. О., Rysev, N. A., Sirenko, V. V., Redwood, C. S. & Borovikov, Y. S., 2017, In: Journal of Muscle Research and Cell Motility. p. 45

    Research output: Contribution to journal › Meeting Abstract › peer-review

  3. The reason for a high Ca2+-sensitivity associated with Arg91Gly substitution in TPM2 gene is the abnormal behavior and high flexibility of tropomyosin during the ATPase cycle

    Borovikov, Y. S., Симонян, А. О., Karpicheva, O. E., Avrova, S. V., Rysev, N. A., Piers, A. & Redwood, C. S., 2017, In: Biochemical and Biophysical Research Communications. 494, 3-4, p. 681-686 6 p.

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

  4. Влияние мутации Arg90Pro в γ-тропомиозине, ассоциированной с врожденной диспропорцией типов мышечных волокон, на конформационные перестройки актина в АТФазном цикл

    Карпичева, О. Е., Симонян, А. О., Рэдвуд, Ч. & Боровиков, Ю. С., 2017, In: Цитология. 59, 11, p. 764-765 2 p.

    Research output: Contribution to journal › Meeting Abstract › peer-review

  5. 2016

  6. Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle

    Karpicheva, O. E., Simonyan, A. O., Kuleva, N. V., Redwood, C. S. & Borovikov, Y. S., 2016, In: Biochimica et Biophysica Acta - Proteins and Proteomics. 1864, 3, p. 260-267

    Research output: Contribution to journal › Article

  7. 2015

  8. Aberrant movement of β-tropomyosin associated with congenital myopathy causes defective response of myosin heads and actin during the ATPase cycle

    Borovikov, Y. S., Avrova, S. V., Rysev, N. A., Sirenko, V. V., Simonyan, A. O., Chernev, A. A., Karpicheva, O. E., Piers, A. & Redwood, C. S., 2015, In: Archives of Biochemistry and Biophysics. 577–578, p. 13-23 13 p.

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

  9. Abnormal movement of mutant b-tropomyosin associated with congenital myopathy causes aberrant response of myosin heads and actin during the ATPase cycle

    Avrova, S., Rysev, N., Karpicheva, O., Simonyan, A., Chernev, A., Piers, A., Redwood, C. & Borovikov, Y., 2015

    Research output: Other contribution › Research

  10. The effects of alpha-tropomyosin Arg245Gly and Glu241Leu mutants on the structural states of actomyosin during the ATPase cycle

    Simonyan, A. O., Robaszkiewicz, K., Borys, D., Borovikov, Y. S. & Moraczewska, J., 2015, In: FEBS Journal. 282, 2 p.

    Research output: Contribution to journal › Meeting Abstract

  11. The effects of a-tropomyosin Arg245Gly and Glu241Leu mutants on the structural states of actomyosin during the ATPase cycle.

    Simonyan, A. O., Robaszkiewicz, K., Borys, D., Borovikov, Y. S. & Moraczewska, J., 2015

    Research output: Other contribution › Research

  12. The structural state of actomyosin in the presence of Gln147Pro mutant tropomyosin evaluated by polarized fluorimetry.

    Karpicheva, O., Simonyan, A., Piers, A., Borovikov, Y. & Redwood, C., 2015, 102 p.

    Research output: Other contribution › Research

  13. 2014

  14. Distal arthrogryposis-associated Arg91Gly mutation in β-tropomyosin induces the structural changes in the thin filaments during the atpase cycle

    Simonyan, A. H., Rysev, N. A., Chernev, A. A., Piers, A., Redwood, C. S. & BorovikovY.S., U., 2014

    Research output: Other contribution › Research

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