scholarly article | Q13442814 |
P50 | author | Yuri V Bobryshev | Q88065781 |
Igor A. Sobenin | Q38323510 | ||
Alexander Orekhov | Q51464003 | ||
Margarita Sazonova | Q57081240 | ||
Anton Postnov | Q59705092 | ||
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A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy. | Q50512793 | ||
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Autoantibody against oxidised LDL and progression of carotid atherosclerosis | Q59704366 | ||
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA | Q73031929 | ||
P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | aorta | Q101004 |
atherosclerosis | Q12252367 | ||
P304 | page(s) | 832464 | |
P577 | publication date | 2012-09-11 | |
P1433 | published in | Clinical and Developmental Immunology | Q15754140 |
P1476 | title | Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta | |
P478 | volume | 2012 |
Q86885855 | 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 |
Q36997420 | Association of mitochondrial genetic variation with carotid atherosclerosis |
Q53276957 | Association of mitochondrial mutations with the age of patients having atherosclerotic lesions. |
Q36872528 | Association of the level of heteroplasmy of the 15059G>A mutation in the MT-CYB mitochondrial gene with essential hypertension. |
Q92703463 | Changes in Mitochondrial Genome Associated with Predisposition to Atherosclerosis and Related Disease |
Q55419759 | Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations. |
Q34239967 | Emerging roles of mitochondria ROS in atherosclerotic lesions: causation or association? |
Q89994270 | Heteroplasmic Variants of Mitochondrial DNA in Atherosclerotic Lesions of Human Aortic Intima |
Q33600464 | Mitochondria, endothelial cell function, and vascular diseases |
Q90883733 | Mitochondrial 3243A > G mutation confers pro-atherogenic and pro-inflammatory properties in MELAS iPS derived endothelial cells |
Q48620870 | Mitochondrial DNA haplogroup D4b is a protective factor for ischemic stroke in Chinese Han population |
Q46755952 | Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders |
Q35193558 | Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta. |
Q41213847 | Quantitative assessment of heteroplasmy of mitochondrial genome: perspectives in diagnostics and methodological pitfalls |
Q58792826 | Response to: Comment on "Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis" |
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