1. 2022
  2. Способ профилактического лечения коронавирусной инфекции

    Никонов, С. Д., Воевода, М. И., Майоров, А. П., Пасман, Н. М. & Гельфонд, М. Л., 4 Aug 2022, IPC No. A61N5/067, A61K31/409, A61K31/5415, A61P31/14, Роспатент - Федеральная служба по интеллектуальной собственности, Patent No. 2777462, Priority date 18 Dec 2020, Priority No. 2020142122

    Research output: PatentPatent for invention

  3. Клинико-иммунологические параллели у детей, больных COVID-19

    Obukhova, O. O., Karpovich, G. S., Ryabichenko, T. I., Skosyreva, G. A., Gorbenko, O. M., Trunov, A. N., Kuimova, I. V. & Voevoda, M. I., 2022, In: Infectious Diseases: News, Opinions, Training. 11, 2, p. 25-31 7 p., 4.

    Research output: Contribution to journalArticlepeer-review

  4. 2021
  5. Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

    Barashkov, N. A., Konovalov, F. A., Borisova, T. V., Teryutin, F. M., Solovyev, A. V., Pshennikova, V. G., Sapojnikova, N. V., Vychuzhina, L. S., Romanov, G. P., Gotovtsev, N. N., Morozov, I. V., Bondar, A. A., Platonov, F. A., Burtseva, T. E., Khusnutdinova, E. K., Posukh, O. L. & Fedorova, S. A., Jun 2021, In: European journal of human genetics. 29, 6, p. 965-976 12 p.

    Research output: Contribution to journalArticlepeer-review

  6. Molecular characteristic of treatment failure clinical isolates of Leishmania major

    Eslami, G., Hatefi, S., Ramezani, V., Tohidfar, M., Churkina, T. V., Orlov, Y. L., Hosseini, S. S., Boozhmehrani, M. J. & Vakili, M., 11 Mar 2021, In: PeerJ. 9, 10969.

    Research output: Contribution to journalArticlepeer-review

  7. In situ dissecting the evolution of gene duplication with different histone modification patterns based on high-throughput data analysis in Arabidopsis thaliana

    Wang, J., Orlov, Y. L., Li, X., Zhou, Y., Liu, Y., Yuan, C. & Chen, M., 5 Jan 2021, In: PeerJ. 9, 19 p., e10426.

    Research output: Contribution to journalArticlepeer-review

  8. Functional evaluation of a rare variant c.516g>c (p.trp172cys) in the GJB2 (connexin 26) gene associated with nonsyndromic hearing loss

    Maslova, E. A., Orishchenko, K. E. & Posukh, O. L., Jan 2021, In: Biomolecules. 11, 1, p. 1-15 15 p., 61.

    Research output: Contribution to journalArticlepeer-review

  9. Hypothalamic norepinephrine concentration and heart mass in hypertensive isiah rats are associated with a genetic locus on chromosome 18

    Redina, O. E., Smolenskaya, S. E., Polityko, Y. K., Ershov, N. I., Gilinsky, M. A. & Markel, A. L., Jan 2021, In: Journal of Personalized Medicine. 11, 2, p. 1-15 15 p., 67.

    Research output: Contribution to journalArticlepeer-review

  10. Течение GCK-MODY диабета у лиц старше 18 лет: данные проспективного наблюдения

    Ovsyannikova, A. K., Shakhtshneider, E. V., Ivanoshchuk, D. E., Voevoda, M. I. & Rymar, O. D., 2021, In: Diabetes Mellitus. 24, 2, p. 133-140 8 p., 4.

    Research output: Contribution to journalReview articlepeer-review

  11. 2020
  12. Complex assessment of pathogenicity of novel variant c.516G > C (p.Trp172Cys) in the GJB2 gene associated with hearing loss in indigenous peoples of Southern Siberia (Russia)

    Maslova, E. A., Zytsar, M. V., Danilchenko, V. Y., Orishchenko, K. E. & Posukh, O. L., 1 Dec 2020, In: European journal of human genetics. 28, Suppl 1, p. 191-192 2 p., P02.27.B.

    Research output: Contribution to journalMeeting Abstractpeer-review

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