Maria V. Golubenko

Tomsk, TOM 634050, Russian Federation

Last Updated: 09/26/2026

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Found 21 publications

DNA Methylation Status of Regulatory Regions of Apoptosis-Associated Genes in Dystropy «Huntington's Disease-Non-Small Cell Lung Cancer».

DNA Methylation Status of Regulatory Regions of Apoptosis-Associated Genes in Dystropy «Huntington's Disease-Non-Small Cell Lung Cancer».

Journal: Epigenomes

Published: May 27, 2025

From North Asia to South America: Tracing the longest human migration through genomic sequencing.

From North Asia to South America: Tracing the longest human migration through genomic sequencing.

Journal: Science (New York, N.Y.)

Published: May 15, 2025

Rare missense substitutions in the mitochondrial DNA genes in patients with ventricular tachycardia.

Rare missense substitutions in the mitochondrial DNA genes in patients with ventricular tachycardia.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: March 11, 2025

Mitochondrial DNA Polymorphisms of Peripheral Blood Mononuclear Cells Associated with Sustained Ventricular Tachycardia in Patients with Cardioverter-Defibrillator Implantation Indications.

Mitochondrial DNA Polymorphisms of Peripheral Blood Mononuclear Cells Associated with Sustained Ventricular Tachycardia in Patients with Cardioverter-Defibrillator Implantation Indications.

Journal: Reviews in cardiovascular medicine

Published: September 26, 2024

Liberties of the genome: insertions of mitochondrial DNA fragments into nuclear genome.

Liberties of the genome: insertions of mitochondrial DNA fragments into nuclear genome.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: February 28, 2024

A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy.

A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy.

Journal: Frontiers in bioscience (Scholar edition)

Published: October 01, 2023

Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy.

Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy.

Journal: International journal of molecular sciences

Published: November 24, 2022

Methylation of Regulatory Regions of DNA Repair Genes in Carotid Atherosclerosis

Methylation of Regulatory Regions of DNA Repair Genes in Carotid Atherosclerosis

Journal: Molekuliarnaia biologiia

Published: November 16, 2022

Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.

Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.

Journal: Biomedical reports

Published: December 03, 2019

The Study of Associations of Polymorphisms of Candidate Gene of Cardiovascular Diseases With Reduction of Glomerular Filtration Rate in Patients With ST Segment Elevation Myocardial Infarction

The Study of Associations of Polymorphisms of Candidate Gene of Cardiovascular Diseases With Reduction of Glomerular Filtration Rate in Patients With ST Segment Elevation Myocardial Infarction

Journal: Kardiologiia

Published: March 16, 2017

Carriers of mitochondrial DNA macrohaplogroup R colonized Eurasia and Australasia from a southeast Asia core area.

Carriers of mitochondrial DNA macrohaplogroup R colonized Eurasia and Australasia from a southeast Asia core area.

Journal: BMC evolutionary biology

Published: January 29, 2017

Origin and spread of human mitochondrial DNA haplogroup U7.

Origin and spread of human mitochondrial DNA haplogroup U7.

Journal: Scientific reports

Published: December 01, 2016

Showing 1-12 of 21

Last Updated: 09/26/2026