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The Genetic Basis of the First Patient with Wiedemann-Rautenstrauch Syndrome in the Russian Federation.
Genes (Basel). 2024 Jan 29;15(2):180. doi: 10.3390/genes15020180.
Genes (Basel). 2024.
PMID: 38397171
Free PMC article.
Molecular basis and genetics of hypohidrotic ectodermal dysplasias.
Kovalskaia VA, Cherevatova TB, Polyakov AV, Ryzhkova OP.
Kovalskaia VA, et al.
Vavilovskii Zhurnal Genet Selektsii. 2023 Oct;27(6):676-683. doi: 10.18699/VJGB-23-78.
Vavilovskii Zhurnal Genet Selektsii. 2023.
PMID: 38023809
Free PMC article.
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Novel assay to measure chromosome instability identifies Punica granatum extract that elevates CIN and has a potential for tumor- suppressing therapies.
Goncharov NV, Kovalskaia VA, Romanishin AO, Shved NA, Belousov AS, Tiasto VS, Gulaia VS, Neergheen VS, Rummun N, Liskovykh M, Larionov V, Kouprina N, Kumeiko VV.
Goncharov NV, et al. Among authors: kovalskaia va.
Front Bioeng Biotechnol. 2022 Dec 19;10:989932. doi: 10.3389/fbioe.2022.989932. eCollection 2022.
Front Bioeng Biotechnol. 2022.
PMID: 36601386
Free PMC article.
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Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia.
Kovalskaia VA, Zabnenkova VV, Petukhova MS, Markova ZG, Tabakov VY, Ryzhkova OP.
Kovalskaia VA, et al.
Genes (Basel). 2022 Nov 23;13(12):2186. doi: 10.3390/genes13122186.
Genes (Basel). 2022.
PMID: 36553453
Free PMC article.
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