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Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia).
Diagnostics (Basel). 2021 Dec 17;11(12):2378. doi: 10.3390/diagnostics11122378.
Diagnostics (Basel). 2021.
PMID: 34943614
Free PMC article.
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
Zytsar MV, Barashkov NA, Bady-Khoo MS, Shubina-Olejnik OA, Danilenko NG, Bondar AA, Morozov IV, Solovyev AV, Danilchenko VY, Maximov VN, Posukh OL.
Zytsar MV, et al. Among authors: danilchenko vy.
BMC Med Genet. 2018 Aug 7;19(1):138. doi: 10.1186/s12881-018-0650-5.
BMC Med Genet. 2018.
PMID: 30086704
Free PMC article.
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High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect.
Zytsar MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Morozov IV, Bondar AA, Posukh OL.
Zytsar MV, et al. Among authors: danilchenko vy.
Genes (Basel). 2020 Jul 21;11(7):833. doi: 10.3390/genes11070833.
Genes (Basel). 2020.
PMID: 32708339
Free PMC article.
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Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss.
Danilchenko VY, Zytsar MV, Maslova EA, Posukh OL.
Danilchenko VY, et al.
Int J Mol Sci. 2022 Nov 3;23(21):13453. doi: 10.3390/ijms232113453.
Int J Mol Sci. 2022.
PMID: 36362242
Free PMC article.
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Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia).
Danilchenko VY, Zytsar MV, Maslova EA, Orishchenko KE, Posukh OL.
Danilchenko VY, et al.
Genes (Basel). 2023 Apr 17;14(4):928. doi: 10.3390/genes14040928.
Genes (Basel). 2023.
PMID: 37107686
Free PMC article.
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Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains.
Posukh OL, Maslova EA, Danilchenko VY, Zytsar MV, Orishchenko KE.
Posukh OL, et al. Among authors: danilchenko vy.
Biomolecules. 2023 Oct 13;13(10):1521. doi: 10.3390/biom13101521.
Biomolecules. 2023.
PMID: 37892203
Free PMC article.
Review.
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Unique Mutational Spectrum of the GJB2 Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys).
Posukh OL, Zytsar MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Bondar AA, Morozov IV, Maximov VN, Voevoda MI.
Posukh OL, et al. Among authors: danilchenko vy.
Genes (Basel). 2019 Jun 5;10(6):429. doi: 10.3390/genes10060429.
Genes (Basel). 2019.
PMID: 31195736
Free PMC article.
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