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Page 1
Potential regulatory SNPs in the ATXN7L3B and KRT15 genes are associated with gender-specific colorectal cancer risk.
Per Med. 2020 Jan;17(1):43-54. doi: 10.2217/pme-2019-0059. Epub 2019 Dec 4.
Per Med. 2020.
PMID: 31797724
SIRT1 Allele Frequencies in Depressed Patients of European Descent in Russia.
Aftanas LI, Anisimenko MS, Berdyugina DA, Garanin AY, Maximov VN, Voevoda MI, Vyalova NM, Bokhan NA, Ivanova SA, Danilenko KV, Kovalenko SP.
Aftanas LI, et al. Among authors: maximov vn.
Front Genet. 2019 Jan 4;9:686. doi: 10.3389/fgene.2018.00686. eCollection 2018.
Front Genet. 2019.
PMID: 30662452
Free PMC article.
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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: maximov vn.
Genes (Basel). 2019 Jun 5;10(6):429. doi: 10.3390/genes10060429.
Genes (Basel). 2019.
PMID: 31195736
Free PMC article.
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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: maximov vn.
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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