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Page 1
Multiple Sclerosis Is Associated with Immunoglobulin Germline Gene Variation of Transitional B Cells.
Lomakin YA, Ovchinnikova LA, Zakharova MN, Ivanova MV, Simaniv TO, Kabilov MR, Bykova NA, Mukhina VS, Kaminskaya AN, Tupikin AE, Zakharova MY, Favorov AV, Illarioshkin SN, Belogurov AA, Gabibov AG. Lomakin YA, et al. Among authors: kaminskaya an. Acta Naturae. 2022 Oct-Dec;14(4):84-93. doi: 10.32607/actanaturae.11794. Acta Naturae. 2022. PMID: 36694905 Free PMC article.
Parent-of-origin effects on nuclear chromatin organization and behavior in a Drosophila model for Williams-Beuren Syndrome.
Medvedeva AV, Tokmatcheva EV, Kaminskaya AN, Vasileva SA, Nikitina EA, Zhuravlev SA, Zakharov GA, Zatsepina OG, Savvateeva-Popova EV. Medvedeva AV, et al. Among authors: kaminskaya an. Vavilovskii Zhurnal Genet Selektsii. 2021 Sep;25(5):472-485. doi: 10.18699/VJ21.054. Vavilovskii Zhurnal Genet Selektsii. 2021. PMID: 34595370 Free PMC article.
Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations.
Kol'tsova AS, Pendina AA, Efimova OA, Kaminskaya AN, Tikhonov AV, Osinovskaya NS, Sultanov IY, Shved NY, Kakhiani MI, Baranov VS. Kol'tsova AS, et al. Among authors: kaminskaya an. Bull Exp Biol Med. 2017 Sep;163(5):646-649. doi: 10.1007/s10517-017-3870-3. Epub 2017 Sep 25. Bull Exp Biol Med. 2017. PMID: 28944423
Drosophila Model for the Analysis of Genesis of LIM-kinase 1-Dependent Williams-Beuren Syndrome Cognitive Phenotypes: INDELs, Transposable Elements of the Tc1/Mariner Superfamily and MicroRNAs.
Savvateeva-Popova EV, Zhuravlev AV, Brázda V, Zakharov GA, Kaminskaya AN, Medvedeva AV, Nikitina EA, Tokmatcheva EV, Dolgaya JF, Kulikova DA, Zatsepina OG, Funikov SY, Ryazansky SS, Evgen'ev MB. Savvateeva-Popova EV, et al. Among authors: kaminskaya an. Front Genet. 2017 Sep 20;8:123. doi: 10.3389/fgene.2017.00123. eCollection 2017. Front Genet. 2017. PMID: 28979292 Free PMC article.