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The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation.
Kovalskaia VA, Kungurtseva AL, Bostanova FM, Vasiliev PA, Tabakov VY, Orlova MD, Povolotskaya IS, Novoselova OG, Bikanov RA, Akhyamova MA, Tikhonovich YV, Popovich AV, Vitebskaya AV, Dadali EL, Ryzhkova OP. Kovalskaia VA, et al. Among authors: orlova md. Genes (Basel). 2024 Jan 29;15(2):180. doi: 10.3390/genes15020180. Genes (Basel). 2024. PMID: 38397171 Free PMC article.
Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12.
Panchuk IO, Grigorieva OV, Kondrateva EV, Kurshakova EV, Tabakov V, Bychkov IO, Zakharova E, Orlova MD, Voronina ES, Pozhitnova VO, Lavrov AV, Smirnikhina SA, Kutsev SI. Panchuk IO, et al. Among authors: orlova md. Stem Cell Res. 2023 Sep;71:103183. doi: 10.1016/j.scr.2023.103183. Epub 2023 Aug 15. Stem Cell Res. 2023. PMID: 37643494 Free article.
Accumulation of Circulating Cell-Free CpG-Enriched Ribosomal DNA Fragments on the Background of High Endonuclease Activity of Blood Plasma in Schizophrenic Patients.
Ershova ES, Jestkova EM, Martynov AV, Shmarina GV, Umriukhin PE, Bravve LV, Zakharova NV, Kostyuk GP, Saveliev DV, Orlova MD, Bogush M, Kutsev SI, Veiko NN, Kostyuk SV. Ershova ES, et al. Among authors: orlova md. Int J Genomics. 2019 Aug 5;2019:8390585. doi: 10.1155/2019/8390585. eCollection 2019. Int J Genomics. 2019. PMID: 31467866 Free PMC article.