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Regulatory functions and chromatin loading dynamics of linker histone H1 during endoreplication in Drosophila

Genes & development, 2017-03, Vol.31 (6), p.603-616

2017

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Genome-wide analysis of gene regulation mechanisms during Drosophila spermatogenesis

Epigenetics & chromatin, 2018-04, Vol.11 (1), p.14-14, Article 14

2018

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Functional dissection of Drosophila melanogaster SUUR protein influence on H3K27me3 profile

Epigenetics & chromatin, 2017-12, Vol.10 (1), p.56-56, Article 56

2017

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H3K9 and H4K20 methyltransferases are directly involved in the heterochromatinization of the paternal chromosomes in male Planococcus citri embryos

Chromosoma, 2023-11, Vol.132 (4), p.317-328

2023

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Genome-wide analysis of SU(VAR)3-9 distribution in chromosomes of Drosophila melanogaster

Chromosoma, 2018-03, Vol.127 (1), p.85-102

2018

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Drosophila SUUR protein associates with PCNA and binds chromatin in a cell cycle-dependent manner

Chromosoma, 2013-03, Vol.122 (1-2), p.55-66

2013

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The effects of SUUR protein suggest its role in repressive chromatin renewal during replication in Drosophila

Nucleus (Austin, Tex.), 2015, Vol.6 (4), p.249-253

2015

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Conservation of domain structure in a fast-evolving heterochromatic SUUR protein in drosophilids

Genetics (Austin), 2009-09, Vol.183 (1), p.119-129

2009

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Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss

International journal of molecular sciences, 2022-11, Vol.23 (21), p.13453

2022

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A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

PloS one, 2020-11, Vol.15 (11), p.e0242219-e0242219

2020

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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)

Genes, 2023-04, Vol.14 (4), p.928

2023

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The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)

Genes, 2023-04, Vol.14 (5), p.1001

2023

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Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)

PloS one, 2016-04, Vol.11 (4), p.e0153841-e0153841

2016

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Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

BMC medical genetics, 2018-08, Vol.19 (1), p.138-138, Article 138

2018

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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)

TheScientificWorld, 2019, Vol.2019, p.5198931-9

2019

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Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

Biomolecules (Basel, Switzerland), 2023-10, Vol.13 (10), p.1521

2023

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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

Genes, 2020-07, Vol.11 (7), p.833

2020

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Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.965-976

2021

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Different Rates of the SLC26A4 -Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)

Diagnostics (Basel), 2021-12, Vol.11 (12), p.2378

2021

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Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population

Biology (Basel, Switzerland), 2022-02, Vol.11 (2), p.257

2022

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A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

Human genetics, 2022-04, Vol.141 (3-4), p.697-707

2022

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A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia)

International journal of circumpolar health, 2019-12, Vol.78 (1), p.1630219

2019

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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)

Genes, 2019-06, Vol.10 (6), p.429

2019

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Insight into the Natural History of Pathogenic Variant c.919-2AG in the ISLC26A4/I Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia

Genes, 2023-04, Vol.14 (4)

2023

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Regulatory functions and chromatin loading dynamics of linker histone H1 during endoreplication in Drosophila

Genome-wide analysis of gene regulation mechanisms during Drosophila spermatogenesis

Functional dissection of Drosophila melanogaster SUUR protein influence on H3K27me3 profile

H3K9 and H4K20 methyltransferases are directly involved in the heterochromatinization of the paternal chromosomes in male Planococcus citri embryos

Genome-wide analysis of SU(VAR)3-9 distribution in chromosomes of Drosophila melanogaster

Drosophila SUUR protein associates with PCNA and binds chromatin in a cell cycle-dependent manner

The effects of SUUR protein suggest its role in repressive chromatin renewal during replication in Drosophila

Conservation of domain structure in a fast-evolving heterochromatic SUUR protein in drosophilids

Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

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)

The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)

Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)

Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

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

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

Different Rates of the SLC26A4 -Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)

Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population

A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha Republic, Russia)

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)

Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic)

Insight into the Natural History of Pathogenic Variant c.919-2AG in the ISLC26A4/I Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia

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