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New Regions With Molecular Alterations in a Rare Case of Insulinomatosis: Case Report With Literature Review.
Anoshkin K, Vasilyev I, Karandasheva K, Shugay M, Kudryavtseva V, Egorov A, Gurevich L, Mironova A, Serikov A, Kutsev S, Strelnikov V. Anoshkin K, et al. Among authors: strelnikov v. Front Endocrinol (Lausanne). 2021 Oct 19;12:760154. doi: 10.3389/fendo.2021.760154. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34737724 Free PMC article. Review.
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy.
Ivanova ME, Trubilin VN, Atarshchikov DS, Demchinsky AM, Strelnikov VV, Tanas AS, Orlova OM, Machalov AS, Overchenko KV, Markova TV, Golenkova DM, Anoshkin KI, Volodin IV, Zaletaev DV, Pulin AA, Nadelyaeva II, Kalinkin AI, Barh D. Ivanova ME, et al. Among authors: strelnikov vv. Ophthalmic Genet. 2018 Dec;39(6):706-713. doi: 10.1080/13816810.2018.1532527. Epub 2018 Oct 25. Ophthalmic Genet. 2018. PMID: 30358468
Genome-wide methylotyping resolves breast cancer epigenetic heterogeneity and suggests novel therapeutic perspectives.
Tanas AS, Sigin VO, Kalinkin AI, Litviakov NV, Slonimskaya EM, Ibragimova MK, Ignatova EO, Simonova OA, Kuznetsova EB, Kekeeva TV, Larin SS, Poddubskaya EV, Trotsenko ID, Rudenko VV, Karandasheva KO, Petrova KD, Tsyganov MM, Deryusheva IV, Kazantseva PV, Doroshenko AV, Tarabanovskaya NA, Chesnokova GG, Sekacheva MI, Nemtsova MV, Izhevskaya VL, Kutsev SI, Zaletaev DV, Strelnikov VV. Tanas AS, et al. Among authors: strelnikov vv. Epigenomics. 2019 May;11(6):605-617. doi: 10.2217/epi-2018-0213. Epub 2019 Feb 7. Epigenomics. 2019. PMID: 30729807 Free article.
Abnormal Hypermethylation of CpG Dinucleotides in Promoter Regions of Matrix Metalloproteinases Genes in Breast Cancer and Its Relation to Epigenomic Subtypes and HER2 Overexpression.
Simonova OA, Kuznetsova EB, Tanas AS, Rudenko VV, Poddubskaya EV, Kekeeva TV, Trotsenko ID, Larin SS, Kutsev SI, Zaletaev DV, Nemtsova MV, Strelnikov VV. Simonova OA, et al. Among authors: strelnikov vv. Biomedicines. 2020 May 10;8(5):116. doi: 10.3390/biomedicines8050116. Biomedicines. 2020. PMID: 32397602 Free PMC article.
Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets.
Anoshkin K, Zosen D, Karandasheva K, Untesco M, Volodin I, Alekseeva E, Parfenenkova A, Snegova E, Kim A, Dorofeeva M, Kutsev S, Strelnikov V. Anoshkin K, et al. Among authors: strelnikov v. Heliyon. 2022 Aug 19;8(8):e10291. doi: 10.1016/j.heliyon.2022.e10291. eCollection 2022 Aug. Heliyon. 2022. PMID: 36051260 Free PMC article.
Specific Features of Focal Cortical Dysplasia in Tuberous Sclerosis Complex.
Bychkova E, Dorofeeva M, Levov A, Kislyakov A, Karandasheva K, Strelnikov V, Anoshkin K. Bychkova E, et al. Among authors: strelnikov v. Curr Issues Mol Biol. 2023 May 3;45(5):3977-3996. doi: 10.3390/cimb45050254. Curr Issues Mol Biol. 2023. PMID: 37232723 Free PMC article. Review.
88 results