Екатерина Александровна Маслова

1 - 10 out of 13Page size: 10

Sort by: Title

Изучение функциональной значимости варианта с.516G>C (p.Trp172Cys) гена GJB2, ассоциированного с потерей слуха у коренного населения Южной Сибири
Маслова, Е. А., Зыцарь, М. В., Danilchenko, V. Y., Орищенко, К. Е. & Посух, О. Л., 2020, In: Медицинская генетика. 19, 7, p. 51-53 3 p., 21.
Research output: Contribution to journal › Article › peer-review
Using Computer Vision and Deep Learning for Cells Recognition
Kudinov, V. Y., Mashukov, M. Y., Maslova, E. A., Orishchenko, K. E., Okunev, A. G. & Matveev, A. V., 14 Nov 2020, Proceedings - 2020 Science and Artificial Intelligence Conference, S.A.I.ence 2020. Institute of Electrical and Electronics Engineers Inc., p. 17-20 4 p. 9303201. (Proceedings - 2020 Science and Artificial Intelligence Conference, S.A.I.ence 2020).
Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › Research › peer-review
Unique mutational spectrum of the GJB2 gene and its pathogenic contribution to deafness in tuvinians (Southern siberia, russia): A high prevalence of rare variant c.516G>C (p.trp172Cys)
Posukh, O. L., Zytsar, M. V., Bady-Khoo, M. S., Danilchenko, V. Y., Maslova, E. A., Barashkov, N. A., Bondar, A. A., Morozov, I. V., Maximov, V. N. & Voevoda, M. I., 5 Jun 2019, In: Genes. 10, 6, 17 p., 429.
Research output: Contribution to journal › Article › peer-review
Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss
Danilchenko, V. Y., Zytsar, M. V., Maslova, E. A. & Posukh, O. L., Nov 2022, In: International Journal of Molecular Sciences. 23, 21, 13453.
Research output: Contribution to journal › Article › peer-review
Mutational spectrum of the SLC26A4 gene and its contribution to the etiology of hearing loss in the indigenous peoples of Southern Siberia (Russia)
Danilchenko, V. Y., Zytsar, M. V., Bady-Khoo, M. S., Maslova, E. A., Bondar, A. A., Morozov, I. V., Barashkov, N. A. & Posukh, O. L., 1 Dec 2020, In: European journal of human genetics. 28, Suppl 1, p. 810-811 2 p., P02.14.
Research output: Contribution to journal › Meeting Abstract › peer-review
Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia)
Danilchenko, V. Y., Zytsar, M. V., Maslova, E. A., Orishchenko, K. E. & Posukh, O. L., 17 Apr 2023, In: Genes. 14, 4, 928.
Research output: Contribution to journal › Article › peer-review
Insight into genetic and social aspects of modern communities of deaf people in Siberia for forecasting the prevalence of hereditary deafness
Posukh, O. L., Bady-Khoo, M. S., Romanov, G. P., Barashkov, N. A., Smirnova, A. A., Zytsar, M. V., Maslova, E. A., Danilchenko, V. Y., Posukh, O. V. & Lashin, S. A., Jul 2019, In: European journal of human genetics. 27, p. 1038-1038 1 p.
Research output: Contribution to journal › Meeting Abstract › peer-review
High rates of three common GJB2 mutations c.516g>c, c.-23+1g>a, c.235delc in deaf patients from southern siberia are due to the founder effect
Zytsar, M. V., Bady-Khoo, M. S., Danilchenko, V. Y., Maslova, E. A., Barashkov, N. A., Morozov, I. V., Bondar, A. A. & Posukh, O. L., 1 Jul 2020, In: Genes. 11, 7, p. 1-17 17 p., 833.
Research output: Contribution to journal › Article › peer-review
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 journal › Article › peer-review
Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains
Posukh, O. L., Maslova, E. A., Danilchenko, V. Y., Zytsar, M. V. & Orishchenko, K. E., 13 Oct 2023, In: Biomolecules. 13, 10, 1521.
Research output: Contribution to journal › Review article › peer-review

Previous 1 2 Next

ID: 3511150

Maslova, Ekaterina Aleksandrovna