REFERENCES
1. Sazonova MA, Budnikov YY, Khasanova ZB, Anton P, Sobenin IA, Orekhov A. Direct quantitative assessment of mutant allele in mitochondrial genome in atherosclerotic lesion of human aorta. Atheroscler Suppl 2007;8:45-6.
2. Postnov AY, Sazonova MA, Budnikov YY, Khazanova ZB, Sobenin IA, Orekhov AN. PO5-116 Association of somatic mitochondrial mutations with atherosclerosis. Atheroscler Suppl 2007;8:46.
3. Sobenin IA, Sazonova MA, Ivanova MM, Zhelankin AV, Myasoedova VA, Postnov AY, Nurbaev SD, Bobryshev YV, Orekhov AN. Mutation C3256T of mitochondrial genome in white blood cells: novel genetic marker of atherosclerosis and coronary heart disease. PLoS One 2012;7:e46573.
4. Sobenin IA, Sazonova MA, Postnov AY, Bobryshev YV, Orekhov AN. Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta. Clin Dev Immunol 2012;2012:832464.
5. Li H, Liu D, Lu J, Bai Y. Physiology and pathophysiology of mitochondrial DNA. Adv Exp Med Biol 2012;942:39-51.
6. de Laat P, Koene S, van den Heuvel LP, Rodenburg RJ, Janssen MC, Smeitink JA. Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A>G mutation. J Inherit Metab Dis 2012;35:1059-69.
7. Naue J, Hörer S, Sänger T, Strobl C, Hatzer-Grubwieser P, Parson W, Lutz-Bonengel S. Evidence for frequent and tissue-specific sequence heteroplasmy in human mitochondrial DNA. Mitochondrion 2015;20:82-94.
8. Chinnery PF, Zwijnenburg PJ, Walker M, Howell N, Taylor RW, Lightowlers RN, Bindoff L, Turnbull DM. Nonrandom tissue distribution of mutant mtDNA. Am J Med Genet 1999;85:498-501.
9. Miasoedova VA, Kirichenko TV, Orekhova VA, Sobenin IA, Mukhamedova NM, Martirosian DM, Karagodin VP, Orekhov AN. Study of intima-medial thickness (IMT) of the carotid arteries as an indicator of natural atherosclerosis progress in Moscow population. Patol Fiziol Eksp Ter 2012;(3):104-8.
10. Sazonova MA, Orekhov AN, Sobenin IA. Mitochondrial genome defects andatherosclerosis. Role of mitochondrial genome pathologies in atherosclerotic lesionsformation of an arterial wall. Palmarium Academic Publishing 2014. (in Russian)
11. Sazonova M, Budnikov E, Khasanova Z, Sobenin I, Postnov A, Orekhov A. Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome. Atherosclerosis 2009;204:184-90.
12. Sazonova MA, Sinyov VV, Barinova VA, Ryzhkova AI, Zhelankin AV, Postnov AY, Sobenin IA, Bobryshev YV, Orekhov AN. Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta. Biomed Res Int 2015;2015:825468.
13. Alderborn A, Kristofferson A, Hammerling U. Determination of single-nucleotide polymorphisms by real-time pyrophosphate DNA sequencing. Genome Res 2000;10:1249-58.
14. IBM Analytics. IBM SPSS. Available from: http://www.ibm.com/analytics/us/en/technology/spss/spss-trials.html#spss-trials%20n.d. [Last accessed on Jan 17, 2017].
15. Wallace DC, Brown MD, Lott MT. Mitochondrial DNA variation in human evolution and disease. Gene 1999;238:211-30.
16. Frederiksen AL, Andersen PH, Kyvik KO, Jeppesen TD, Vissing J, Schwartz M. Tissue specific distribution of the 3243A->G mtDNA mutation. J Med Genet 2006;43:671-7.
17. Litvinova NA, Voronkova AS, Nikolaeva EA, Sukhorukov VS. Tissue-specific features of mitochondrial DNA polymorphisms. Russian Bull Perinatol Pediatr 2015;60:76-8.
18. Pyle A, Taylor RW, Durham SE, Deschauer M, Schaefer AM, Samuels DC, Chinnery PF. Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation. J Med Genet 2007;44:69-74.
19. Spyropoulos A, Manford M, Horvath R, Alston CL, Yu-Wai-Man P, He L, Taylor RW, Chinnery PF. Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsy. JAMA Neurol 2013;70:1552-5.
20. Lee HY, Chung U, Park MJ, Yoo JE, Han GR, Shin KJ. Differential distribution of human mitochondrial DNA in somatic tissues and hairs. Ann Hum Genet 2006;70:59-65.