يعرض 1 - 10 نتائج من 27 نتيجة بحث عن '"Stanislava V. Avrova"', وقت الاستعلام: 0.82s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Molecular Mechanisms of Deregulation of Muscle Contractility Caused by the R168H Mutation in TPM3 and Its Attenuation by Therapeutic Agents

    المؤلفون: Olga E. Karpicheva, Stanislava V. Avrova, Andrey L. Bogdanov, Vladimir V. Sirenko, Charles S. Redwood, Yurii S. Borovikov

    المصدر: International Journal of Molecular Sciences, Vol 24, Iss 6, p 5829 (2023)

    مصطلحات موضوعية: tropomyosin mutation, congenital myopathy, muscle weakness, Ca2+-sensitivity of myofilaments, ATP hydrolysis cycle, muscle fibers, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/24/6/5829; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/677174c2a3e24f48bf86aef537c260e8

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  2. 2
    دورية أكاديمية
    Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7

    المؤلفون: Yurii S. Borovikov, Daria D. Andreeva, Stanislava V. Avrova, Vladimir V. Sirenko, Armen O. Simonyan, Charles S. Redwood, Olga E. Karpicheva

    المصدر: International Journal of Molecular Sciences, Vol 22, Iss 12, p 6318 (2021)

    مصطلحات موضوعية: tropomyosin, mutations in tropomyosin, muscle weakness, congenital myopathy, Ca2+-sensitivity of myofilament, ATPase activity of myosin, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/22/12/6318; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/46352c04188c4fb495e5adebd78a1b1e

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  3. 3
    دورية أكاديمية
    Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca2+ Sensitivity Inhibitor W7 Can Reduce the Damaging Effect of This Mutation

    المؤلفون: Yurii S. Borovikov, Armen O. Simonyan, Stanislava V. Avrova, Vladimir V. Sirenko, Charles S. Redwood, Olga E. Karpicheva

    المصدر: International Journal of Molecular Sciences, Vol 21, Iss 12, p 4421 (2020)

    مصطلحات موضوعية: tropomyosin, mutations in tropomyosin, muscle weakness, congenital myopathy, Ca2+-sensitivity of myofilament, ATPase activity of myosin, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/21/12/4421; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/bf9509d4a292488d85302c5bdf92eedf

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  4. 4
    دورية أكاديمية
    The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies

    المؤلفون: Yurii S. Borovikov, Olga E. Karpicheva, Armen O. Simonyan, Stanislava V. Avrova, Elena A. Rogozovets, Vladimir V. Sirenko, Charles S. Redwood

    المصدر: International Journal of Molecular Sciences, Vol 19, Iss 12, p 3975 (2018)

    مصطلحات موضوعية: actin–myosin interaction, congenital myopathy, regulation of muscle contraction, mutation in tropomyosin, ATPase activity of myosin, muscle fiber, Ca2+-sensitivity, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/19/12/3975; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/63308bccc81a48ecb3d809a5b2fbe966

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  5. 5
    The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2

    المؤلفون: Stanislava V. Avrova, Vladimir V. Sirenko, Olga E. Karpicheva, Yurii S. Borovikov, Charles Redwood, Armen O. Simonyan

    المصدر: Biochemical and Biophysical Research Communications. 523:258-262

    مصطلحات موضوعية: Male, 0301 basic medicine, Myofilament, Mutant, Biophysics, Tropomyosin, macromolecular substances, Myopathies, Nemaline, Biochemistry, TPM2, 03 medical and health sciences, Myosin head, 0302 clinical medicine, Myosin, medicine, Animals, Muscle, Skeletal, Molecular Biology, Actin, Muscle Weakness, Chemistry, Muscle weakness, Cell Biology, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, Mutation (genetic algorithm), Calcium, Rabbits, medicine.symptom

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a0b285e67cd493deae360e9c8e56b82
    https://doi.org/10.1016/j.bbrc.2019.12.061

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  6. 6
    Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7

    المؤلفون: Vladimir V. Sirenko, Olga E. Karpicheva, Stanislava V. Avrova, Charles Redwood, Armen O. Simonyan, Daria D. Andreeva, Yurii S. Borovikov

    المصدر: International Journal of Molecular Sciences
    Volume 22
    Issue 12
    International Journal of Molecular Sciences, Vol 22, Iss 6318, p 6318 (2021)

    مصطلحات موضوعية: 0301 basic medicine, Myofilament, Muscle Fibers, Skeletal, ATPase activity of myosin, tropomyosin, Myosin head, 0302 clinical medicine, Myofibrils, Myosin, Oximes, mutations in tropomyosin, congenital myopathy, n-(6-aminohexyl) 5-chloro-1-naphthalenesulfonamide (W7), Biology (General), Spectroscopy, Sulfonamides, biology, Chemistry, General Medicine, Ca2+-sensitivity of myofilament, musculoskeletal system, Tropomyosin, Troponin, Computer Science Applications, Cell biology, medicine.anatomical_structure, Rabbits, medicine.symptom, Muscle contraction, Muscle Contraction, QH301-705.5, 2,3-butanedione monoxime (BDM), macromolecular substances, Myosins, Catalysis, Article, Inorganic Chemistry, 03 medical and health sciences, medicine, Animals, Physical and Theoretical Chemistry, QD1-999, Molecular Biology, Actin, muscle weakness, Organic Chemistry, Skeletal muscle, Actins, 030104 developmental biology, Mutation, biology.protein, Calcium, 030217 neurology & neurosurgery

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcf31b3fc73deac77bcbc0a1af185c8a
    http://europepmc.org/articles/PMC8231546

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  7. 7
    The molecular mechanisms of a high Ca2+-sensitivity and muscle weakness associated with the Ala155Thr substitution in Tpm3.12

    المؤلفون: Armen O. Simonyan, Stanislava V. Avrova, Yurii S. Borovikov, Vladimir V. Sirenko, Olga E. Karpicheva, Charles Redwood

    المصدر: Biochemical and Biophysical Research Communications. 515:372-377

    مصطلحات موضوعية: 0301 basic medicine, Myofilament, biology, Chemistry, Mutant, Biophysics, Muscle weakness, macromolecular substances, Cell Biology, Biochemistry, Troponin, 03 medical and health sciences, Myosin head, 030104 developmental biology, 0302 clinical medicine, Troponin complex, 030220 oncology & carcinogenesis, Myosin, medicine, biology.protein, medicine.symptom, Molecular Biology, Actin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e228b715a36811e239315ab031a63c36
    https://doi.org/10.1016/j.bbrc.2019.05.146

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  8. 8
    Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca2+ Sensitivity Inhibitor W7 Can Reduce the Damaging Effect of This Mutation

    المؤلفون: Vladimir V. Sirenko, Olga E. Karpicheva, Stanislava V. Avrova, Armen O. Simonyan, Yurii S. Borovikov, Charles Redwood

    المصدر: International Journal of Molecular Sciences
    Volume 21
    Issue 12
    International Journal of Molecular Sciences, Vol 21, Iss 4421, p 4421 (2020)

    مصطلحات موضوعية: Myofilament, ATPase, ATPase activity of myosin, macromolecular substances, Catalysis, lcsh:Chemistry, Inorganic Chemistry, tropomyosin, Myosin head, Myosin, mental disorders, mutations in tropomyosin, congenital myopathy, medicine, Physical and Theoretical Chemistry, lcsh:QH301-705.5, Molecular Biology, Spectroscopy, Actin, muscle weakness, biology, Chemistry, Organic Chemistry, Muscle weakness, General Medicine, Troponin, Tropomyosin, troponin inhibitor W7, Computer Science Applications, lcsh:Biology (General), lcsh:QD1-999, Ca2+-sensitivity of myofilament, biology.protein, Biophysics, medicine.symptom, psychological phenomena and processes

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ecb8a0679e9fd3dfb0169fe846e3d81

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  9. 9
    The reason for the low Ca 2+ -sensitivity of thin filaments associated with the Glu41Lys mutation in the TPM2 gene is 'freezing' of tropomyosin near the outer domain of actin and inhibition of actin monomer switching off during the ATPase cycle

    المؤلفون: Charles Redwood, Stanislava V. Avrova, Nikita A. Rysev, Vladimir V. Sirenko, Olga E. Karpicheva, Yurii S. Borovikov, Armen O. Simonyan

    المصدر: Biochemical and Biophysical Research Communications. 502:209-214

    مصطلحات موضوعية: 0301 basic medicine, biology, Chemistry, Biophysics, macromolecular substances, Cell Biology, Biochemistry, Troponin, Tropomyosin, TPM2, 03 medical and health sciences, Myosin head, 030104 developmental biology, 0302 clinical medicine, Troponin complex, Mutation (genetic algorithm), Myosin, biology.protein, Molecular Biology, 030217 neurology & neurosurgery, Actin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2df56d00063cb0cdf1b1bdfbf5b32110
    https://doi.org/10.1016/j.bbrc.2018.05.145

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  10. 10
    Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene

    المؤلفون: Adam Piers, Nikita A. Rysev, Vladimir V. Sirenko, Yurii S. Borovikov, Olga E. Karpicheva, Stanislava V. Avrova, Charles Redwood

    المصدر: Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
    Scientific Reports

    مصطلحات موضوعية: 0301 basic medicine, Myofilament, Glutamine, Muscle Fibers, Skeletal, lcsh:Medicine, Fluorescence Polarization, Tropomyosin, macromolecular substances, Myosins, TPM2, Article, 03 medical and health sciences, Myosin head, medicine, Animals, Point Mutation, lcsh:Science, Actin, Psoas Muscles, Multidisciplinary, 030102 biochemistry & molecular biology, biology, Chemistry, Point mutation, lcsh:R, Muscle weakness, musculoskeletal system, Troponin, Actins, 030104 developmental biology, biology.protein, Biophysics, Calcium, lcsh:Q, Microscopy, Polarization, Rabbits, medicine.symptom

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f6f395b9a298ecc008ea1b6c927b68e
    http://link.springer.com/article/10.1038/s41598-017-17076-9

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