All Stories

  1. Mutations of mtDNA in some Vascular and Metabolic Diseases
  2. Data on association of mitochondrial heteroplasmy with carotid intima-media thickness in subjects from Russian and Kazakh populations
  3. Creation of Cybrid Cultures Containing mtDNA Mutations m.12315G>A and m.1555G>A, Associated with Atherosclerosis
  4. Creation of Cultures Containing Mutations Linked with Cardiovascular Diseases using Transfection and Genome Editing
  5. Mitochondrial diseases caused by mtDNA mutations: a mini-review
  6. Response to: Comment on “Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis”
  7. Cybrid Models of Pathological Cell Processes in Different Diseases
  8. Mitochondrial Genome Mutations Associated with Myocardial Infarction
  9. New markers of atherosclerosis: a threshold level of heteroplasmy in mtDNA mutations
  10. Mito-SNP in mitochondrial cytopathies
  11. Association of mitochondrial genome mutations with chronic diseases of non-inflammatory genesis
  12. Electron microscopic analysis of mitochondria from atherosclerotic plaques
  13. Ultrastructural analysis of mitochondrial cristae in leukocytes of patients with atherosclerosis
  14. Creation of cybrid cultures containing mitochondrial genome mutation m.12315G>A, associated with atherosclerosis
  15. Potential use of buccal epithelium for genetic diagnosis of atherosclerosis using mtDNA mutations
  16. Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis
  17. The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis
  18. Dataset of mitochondrial genome variants associated with asymptomatic atherosclerosis
  19. 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
  20. Mitochondrial genome sequencing in atherosclerosis: what's next?
  21. Association of mitochondrial mutations with the age of patients having atherosclerotic lesions
  22. Study of the activated macrophage transcriptome
  23. Association of mutations in the mitochondrial genome with the subclinical carotid atherosclerosis in women
  24. 1A.06
  25. Mutations of mitochondrial genome in carotid atherosclerosis
  26. Mutations of Mitochondrial DNA in Atherosclerosis and Atherosclerosis-Related Diseases
  27. Mosaicism of Mitochondrial Genetic Variation in Atherosclerotic Lesions of the Human Aorta
  28. Quantitative Assessment of Heteroplasmy of Mitochondrial Genome: Perspectives in Diagnostics and Methodological Pitfalls
  29. Association of Mitochondrial Genetic Variation with Carotid Atherosclerosis
  30. Changes of mitochondria in atherosclerosis: Possible determinant in the pathogenesis of the disease
  31. Association of the level of heteroplasmy of the 15059G>A mutation in the MT-CYB mitochondrial gene with essential hypertension
  32. Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease
  33. Mitochondrial Mutations are Associated with Atherosclerotic Lesions in the Human Aorta
  34. Corrigendum to “Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome” [Atherosclerosis 204 (2009) 184–190]
  35. Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome