Search filters

List of works by Margarita Sazonova

Analysis of mitochondrial DNA heteroplasmic mutations A1555G, C3256T, T3336C, С5178А, G12315A, G13513A, G14459A, G14846А and G15059A in CHD patients with the history of myocardial infarction

scientific article published on 03 December 2015

Association of mitochondrial genetic variation with carotid atherosclerosis

scientific article published on 09 July 2013

Association of mitochondrial mutations with the age of patients having atherosclerotic lesions.

scientific article published on 14 November 2015

Association of mutations in the mitochondrial genome with the subclinical carotid atherosclerosis in women

scientific article published on 21 April 2015

Association of the level of heteroplasmy of the 15059G>A mutation in the MT-CYB mitochondrial gene with essential hypertension.

scientific article published on May 2013

Changes of mitochondria in atherosclerosis: possible determinant in the pathogenesis of the disease.

scientific article published on 25 January 2013

Creation of Cybrid Cultures Containing mtDNA Mutations m.12315G>A and m.1555G>A, Associated with Atherosclerosis

scientific article published on 18 September 2019

Cybrid Models of Pathological Cell Processes in Different Diseases.

scientific article published on 10 June 2018

Dataset of mitochondrial genome variants associated with asymptomatic atherosclerosis.

scientific article

Impact of Mitochondrial DNA Mutations on Carotid Intima-Media Thickness in the Novosibirsk Region

scientific article published on 22 August 2020

Influence of autophagy on the genesis and development of atherosclerosis and its risk factors

scientific article

Mitochondrial Genome Mutations Associated with Myocardial Infarction.

scientific article

Mitochondrial diseases caused by mtDNA mutations: a mini-review

scientific article published on 09 October 2018

Mitochondrial genome sequencing in atherosclerosis: what's next?

scientific article

Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta

scientific article

Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta.

scientific article

Mutation C3256T of mitochondrial genome in white blood cells: novel genetic marker of atherosclerosis and coronary heart disease.

scientific article

Mutations of mitochondrial DNA in atherosclerosis and atherosclerosis-related diseases

scientific article

Mutations of mitochondrial genome in carotid atherosclerosis.

scientific article

Quantitative assessment of heteroplasmy of mitochondrial genome: perspectives in diagnostics and methodological pitfalls

scientific article

Response to: Comment on "Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis"

scientific article published on 09 August 2018

Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis.

scientific article published on 25 July 2017

Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome

scientific article published on 04 September 2008

Study of mitochondrial dysfunction using cytoplasmic hybrid

scientific article published in April 2017

Study of the activated macrophage transcriptome

scientific article published on 03 October 2015

The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis

scientific article published in August 2016

[A new method of quantitative estimation of mutant allele in mitochondrial genome]

scientific article published on 01 October 2011

[Analysis of mitochondrial haplogroups in persons with subclinical atherosclerosis based on high-throughput mtDNA sequencing]

scientific article published on 01 January 2015

[Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]

scientific article published on 01 April 1995

[Association of mitochondrial genome mutations with lipofibrous plaques in human aortic intima]

scientific article published on 01 January 2015

[Association of point mutations in human nuclear and mitochondrial genome with coronary artery disease]

scientific article published on 01 April 2012

[Association of the mutations in the human mitochondrial genome with chronic non-inflammatory diseases: type 2 diabetes, hypertension and different types of cardiomyopathy]

scientific article published on 01 July 2012

[Human pathologies associated with mutations of mitochondrial genome]

scientific article published on 01 July 2012

[Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region]

scientific article published on 01 September 1997

[TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses]

scientific article published on 01 February 1997