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Inactivation of Epigenetic Regulators due to Mutations in Solid Tumors

Biochemistry (Moscow), 2020-07, Vol.85 (7), p.735-748

2020

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Targeting of the SWI/SNF chromatin remodeling complex in cancer therapy

Uspehi molekulârnoj onkologii, 2023-04, Vol.10 (1), p.8-17

2023

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Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases

Molecular biology (New York), 2022, Vol.56 (1), p.1-28

2022

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Molecular classifications of gastric cancer and their clinical potential

Uspehi molekulârnoj onkologii, 2024-06, Vol.11 (2), p.40-49

2024

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Epigenomics paves a new way to assess potential toxicity and chemotherapeutic response of breast tumours to 5-fluorouracil

Annals of oncology, 2018-09, Vol.29, p.vi12-vi12

2018

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Structural Alterations in Human Fibroblast Growth Factor Receptors in Carcinogenesis

Biochemistry (Moscow), 2018-08, Vol.83 (8), p.930-943

2018

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Leukotriene B4 receptors as a therapeutic target for triple-negative breast cancer

Annals of oncology, 2018-09, Vol.29, p.vi26-vi26

2018

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Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development

Onkogematologii͡a, 2024-04, Vol.19 (2), p.88-100

2024

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Diagnostic and prognostic value of long non-coding RNA PROX1‑AS1 and miR-647 expression in gastric cancer

Uspehi molekulârnoj onkologii, 2022-12, Vol.9 (4), p.50-60

2022

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Tumor Clonality: Research and Clinical Aspects

Bulletin of experimental biology and medicine, 2014-12, Vol.158 (2), p.246-251

2014

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Specific Localization of Missense Mutations in the VHL Gene in Clear Cell Renal Cell Carcinoma

Bulletin of experimental biology and medicine, 2017-08, Vol.163 (4), p.465-468

2017

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The incidence of AZF deletions, CFTR mutations and long alleles of the ar CAG repeats during the primary laboratory diagnostics in a heterogeneous group of infertily men

Urologii͡a︡ (Moscow, Russia : 1999), 2019-07, Vol.3_2019, p.101-107

2019

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THE MOLECULAR PATHOGENESIS OF BLADDER CANCER

Alʹmanakh klinicheskoĭ medit͡s︡iny, 2016-02 (41), p.79-88

2016

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Polymorphisms of KITLG, SPRY4, and BAK1 genes in patients with testicular germ cell tumors and individuals with infertility associated with AZFc deletion of the Y chromosome

Molecular biology (New York), 2016-11, Vol.50 (6), p.845-851

2016

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Polymorphisms of KITLG, SPRY4, and BAK1 genes in patients with testicular germ cell tumors and individuals with infertility associated with AZFc deletion of the Y chromosome

Molekuliarnaia biologiia, 2016-11, Vol.50 (6), p.960

2016

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Molecular genetic analysis of the intratumoral clonal heterogeneity of colorectal adenocarcinomas

Molecular biology (New York), 2008-12, Vol.42 (6), p.925-931

2008

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Frequencies of the KITLG, BAK1 and SPRY4 alleles and genotypes associating with the development of testicular germ cell tumors, are increased in patients with testicular microlithiasis

Genes & Cells, 2016-12, Vol.11 (4), p.80-83

2016

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Allelic imbalance of 17p13.1 (TP53), 1p36.1 (RUNX3), and 16p22 (CDH1) loci and microsatellite instability in gastric cancer

Molecular biology (New York), 2013-09, Vol.47 (5), p.727-732

2013

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57PLeukotriene B4 receptors abnormal gene expression is associated with either shorter or longer survival in breast cancer patients depending on the intrinsic tumour molecular subtype

Annals of oncology, 2019-11, Vol.30 (Supplement_7)

2019

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20PMatrix metalloproteinases and their tissue inhibitors genes abnormal DNA methylation in breast cancer

Annals of oncology, 2019-10, Vol.30 (Supplement_5)

2019

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826PIdentification of a spectrum of germline mutations for hereditary diffuse gastric cancer in the Russian population by next-generation sequencing

Annals of oncology, 2019-10, Vol.30 (Supplement_5)

2019

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Some molecular-genetic markers defining the pathogenesis of superficial and invasive bladder cancer

Molecular biology (New York), 2011-12, Vol.45 (6), p.929-932

2011

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34PEpigenomics paves a new way to assess potential toxicity and chemotherapeutic response of breast tumours to 5-fluorouracil

Annals of oncology, 2018-09, Vol.29 (suppl_6)

2018

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78PLeukotriene B4 receptors as a therapeutic target for triple-negative breast cancer

Annals of oncology, 2018-09, Vol.29 (suppl_6)

2018

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Genomic imprinting and human hereditary disorders

Molecular biology (New York), 2000-07, Vol.34 (4), p.554-560

Nemtsova, M V

2000

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Inactivation of Epigenetic Regulators due to Mutations in Solid Tumors

Targeting of the SWI/SNF chromatin remodeling complex in cancer therapy

Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases

Molecular classifications of gastric cancer and their clinical potential

Epigenomics paves a new way to assess potential toxicity and chemotherapeutic response of breast tumours to 5-fluorouracil

Structural Alterations in Human Fibroblast Growth Factor Receptors in Carcinogenesis

Leukotriene B4 receptors as a therapeutic target for triple-negative breast cancer

Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development

Diagnostic and prognostic value of long non-coding RNA PROX1‑AS1 and miR-647 expression in gastric cancer

Tumor Clonality: Research and Clinical Aspects

Specific Localization of Missense Mutations in the VHL Gene in Clear Cell Renal Cell Carcinoma

The incidence of AZF deletions, CFTR mutations and long alleles of the ar CAG repeats during the primary laboratory diagnostics in a heterogeneous group of infertily men

THE MOLECULAR PATHOGENESIS OF BLADDER CANCER

Polymorphisms of KITLG, SPRY4, and BAK1 genes in patients with testicular germ cell tumors and individuals with infertility associated with AZFc deletion of the Y chromosome

Polymorphisms of KITLG, SPRY4, and BAK1 genes in patients with testicular germ cell tumors and individuals with infertility associated with AZFc deletion of the Y chromosome

Molecular genetic analysis of the intratumoral clonal heterogeneity of colorectal adenocarcinomas

Frequencies of the KITLG, BAK1 and SPRY4 alleles and genotypes associating with the development of testicular germ cell tumors, are increased in patients with testicular microlithiasis

Allelic imbalance of 17p13.1 (TP53), 1p36.1 (RUNX3), and 16p22 (CDH1) loci and microsatellite instability in gastric cancer

57PLeukotriene B4 receptors abnormal gene expression is associated with either shorter or longer survival in breast cancer patients depending on the intrinsic tumour molecular subtype

20PMatrix metalloproteinases and their tissue inhibitors genes abnormal DNA methylation in breast cancer

826PIdentification of a spectrum of germline mutations for hereditary diffuse gastric cancer in the Russian population by next-generation sequencing

Some molecular-genetic markers defining the pathogenesis of superficial and invasive bladder cancer

34PEpigenomics paves a new way to assess potential toxicity and chemotherapeutic response of breast tumours to 5-fluorouracil

78PLeukotriene B4 receptors as a therapeutic target for triple-negative breast cancer

Genomic imprinting and human hereditary disorders

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