Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease-Reference-Cited by-同舟云学术

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Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease

Published:2012-10-02 Issue:10 Volume:7 Page:e46573
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Sobenin Igor A.,Sazonova Margarita A.,Ivanova Maria M.,Zhelankin Andrey V.,Myasoedova Veronika A.,Postnov Anton Y.,Nurbaev Serik D.,Bobryshev Yuri V.,Orekhov Alexander N.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence;Journal of Clinical Medicine;2023-03-08

2. Genetic Evaluation of Mitochondria Dysfunction in Coronary Artery Disease;Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology;2023

3. Accelerated Cardiac Aging in Patients With Congenital Heart Disease;Frontiers in Cardiovascular Medicine;2022-05-26

4. MITOCHONDRIAL MUTATIONS IN PROTEIN CODING GENES OF RESPIRATORY CHAIN INCLUDING COMPLEXES IV, V, AND MT-TRNA GENES ARE ASSOCIATED RISK FACTORS FOR CONGENITAL HEART DISEASE;EXCLI J;2022

5. Mutations of mtDNA in some Vascular and Metabolic Diseases;Current Pharmaceutical Design;2021-02-04

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