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Page 1
DNA and Histone Modifications Identify a Putative Controlling Element (CE) on the X Chromosome of Sciara coprophila.
Posukh OV, Shloma VV, Skrypnik PA, Maksimov DA, Antoshina PA, Kalashnikova DA, Nurislamov A, Lukyanchikova VA, Torgunakov N, Battulin NR, Fishman VS, Vyatkin YV, Smelova AA, Romanov SE, Laktionov PP, Valishayev D, Belyakin SN, Singh PB. Posukh OV, et al. Among authors: vyatkin yv. Cells. 2025 Aug 12;14(16):1243. doi: 10.3390/cells14161243. Cells. 2025. PMID: 40862722 Free PMC article.
Genetic landscape in Russian patients with familial left ventricular noncompaction.
Meshkov AN, Myasnikov RP, Kiseleva AV, Kulikova OV, Sotnikova EA, Kudryavtseva MM, Zharikova AA, Koretskiy SN, Mershina EA, Ramensky VE, Zaicenoka M, Vyatkin YV, Kharlap MS, Nikityuk TG, Sinitsyn VE, Divashuk MG, Kutsenko VA, Basargina EN, Barskiy VI, Sdvigova NA, Skirko OP, Efimova IA, Pokrovskaya MS, Drapkina OM. Meshkov AN, et al. Among authors: vyatkin yv. Front Cardiovasc Med. 2023 May 24;10:1205787. doi: 10.3389/fcvm.2023.1205787. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37342443 Free PMC article.
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.
Blokhina AV, Ershova AI, Kiseleva AV, Sotnikova EA, Zharikova AA, Zaicenoka M, Vyatkin YV, Ramensky VE, Kutsenko VA, Garbuzova EV, Divashuk MG, Litinskaya OA, Pokrovskaya MS, Shalnova SA, Meshkov AN, Drapkina OM. Blokhina AV, et al. Among authors: vyatkin yv. Int J Mol Sci. 2024 Nov 25;25(23):12651. doi: 10.3390/ijms252312651. Int J Mol Sci. 2024. PMID: 39684364 Free PMC article.
Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.
Blokhina AV, Ershova AI, Kiseleva AV, Sotnikova EA, Zharikova AA, Zaicenoka M, Vyatkin YV, Ramensky VE, Kutsenko VA, Litinskaya OA, Pokrovskaya MS, Shalnova SA, Meshkov AN, Drapkina OM. Blokhina AV, et al. Among authors: vyatkin yv. PLoS One. 2024 Dec 20;19(12):e0315693. doi: 10.1371/journal.pone.0315693. eCollection 2024. PLoS One. 2024. PMID: 39705280 Free PMC article.
Generation of induced pluripotent stem cell line, ICGi034-A, by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease associated with GBA mutation.
Grigor'eva EV, Drozdova ES, Sorogina DA, Malakhova AA, Pavlova SV, Vyatkin YV, Khabarova EA, Rzaev JA, Medvedev SP, Zakian SM. Grigor'eva EV, et al. Among authors: vyatkin yv. Stem Cell Res. 2022 Mar;59:102651. doi: 10.1016/j.scr.2021.102651. Epub 2021 Dec 31. Stem Cell Res. 2022. PMID: 35007918 Free article.
Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.
Sotnikova EA, Kiseleva AV, Kutsenko VA, Zharikova AA, Ramensky VE, Divashuk MG, Vyatkin YV, Klimushina MV, Ershova AI, Revazyan KZ, Skirko OP, Zaicenoka M, Efimova IA, Pokrovskaya MS, Kopylova OV, Glechan AM, Shalnova SA, Meshkov AN, Drapkina OM. Sotnikova EA, et al. Among authors: vyatkin yv. J Pers Med. 2022 Jul 12;12(7):1132. doi: 10.3390/jpm12071132. J Pers Med. 2022. PMID: 35887629 Free PMC article.
13 results