These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
65 related articles for article (PubMed ID: 25910413)
1. Association of mutations in the mitochondrial genome with the subclinical carotid atherosclerosis in women. Sazonova MA; Chicheva MM; Zhelankin AV; Sobenin IA; Bobryshev YV; Orekhov AN Exp Mol Pathol; 2015 Aug; 99(1):25-32. PubMed ID: 25910413 [TBL] [Abstract][Full Text] [Related]
2. [Association of mitochondrial genome mutations with lipofibrous plaques in human aortic intima]. Sazonova MA Patol Fiziol Eksp Ter; 2015; 59(1):17-28. PubMed ID: 26226685 [TBL] [Abstract][Full Text] [Related]
3. 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. Mitrofanov KY; Zhelankin AV; Shiganova GM; Sazonova MA; Bobryshev YV; Postnov AY; Sobenin I А IA; Orekhov AN Exp Mol Pathol; 2016 Feb; 100(1):87-91. PubMed ID: 26654794 [TBL] [Abstract][Full Text] [Related]
4. Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta. Sazonova MA; Sinyov VV; Barinova VA; Ryzhkova AI; Zhelankin AV; Postnov AY; Sobenin IA; Bobryshev YV; Orekhov AN Biomed Res Int; 2015; 2015():825468. PubMed ID: 25834827 [TBL] [Abstract][Full Text] [Related]
5. Association of mitochondrial genetic variation with carotid atherosclerosis. Sobenin IA; Sazonova MA; Postnov AY; Salonen JT; Bobryshev YV; Orekhov AN PLoS One; 2013; 8(7):e68070. PubMed ID: 23874496 [TBL] [Abstract][Full Text] [Related]
6. Changes of mitochondria in atherosclerosis: possible determinant in the pathogenesis of the disease. Sobenin IA; Sazonova MA; Postnov AY; Bobryshev YV; Orekhov AN Atherosclerosis; 2013 Apr; 227(2):283-8. PubMed ID: 23395464 [TBL] [Abstract][Full Text] [Related]
7. Association of mitochondrial mutations with the age of patients having atherosclerotic lesions. Sazonova MA; Sinyov VV; Barinova VA; Ryzhkova AI; Bobryshev YV; Orekhov AN; Sobenin IA Exp Mol Pathol; 2015 Dec; 99(3):717-9. PubMed ID: 26586456 [TBL] [Abstract][Full Text] [Related]
8. Mutation C3256T of mitochondrial genome in white blood cells: novel genetic marker of atherosclerosis and coronary heart disease. Sobenin IA; Sazonova MA; Ivanova MM; Zhelankin AV; Myasoedova VA; Postnov AY; Nurbaev SD; Bobryshev YV; Orekhov AN PLoS One; 2012; 7(10):e46573. PubMed ID: 23056349 [TBL] [Abstract][Full Text] [Related]
9. Susceptibility of monocytes to activation correlates with atherogenic mitochondrial DNA mutations. Orekhov AN; Zhelankin AV; Kolmychkova KI; Mitrofanov KY; Kubekina MV; Ivanova EA; Sobenin IA Exp Mol Pathol; 2015 Dec; 99(3):672-6. PubMed ID: 26551079 [TBL] [Abstract][Full Text] [Related]
10. Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta. Sobenin IA; Sazonova MA; Postnov AY; Bobryshev YV; Orekhov AN Clin Dev Immunol; 2012; 2012():832464. PubMed ID: 22997526 [TBL] [Abstract][Full Text] [Related]
11. [The heteroplasmy level of some mutations in gene MT-CYB among women with asymptomatic atherosclerosis]. Sinyov VV; Chicheva MM; Barinova VA; Ryzhkova AI; Zilinyi RI; Karagodin VP; Postnov AY; Sobenin IA; Orekhov AN; Sazonova MA Genetika; 2016 Aug; 52(8):951-7. PubMed ID: 29368910 [TBL] [Abstract][Full Text] [Related]
12. [Analysis of mitochondrial haplogroups in persons with subclinical atherosclerosis based on high-throughput mtDNA sequencing]. Zhelankin AV; Sazonova MA; Khasanova ZB; Sinyov VV; Mitrofanov KY; Sobenin IA; Orekhov AN; Postnov AY Patol Fiziol Eksp Ter; 2015; 59(1):12-6. PubMed ID: 26226684 [TBL] [Abstract][Full Text] [Related]
13. Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis. Sazonova MA; Sinyov VV; Ryzhkova AI; Galitsyna EV; Khasanova ZB; Postnov AY; Yarygina EI; Orekhov AN; Sobenin IA Oxid Med Cell Longev; 2017; 2017():6934394. PubMed ID: 28951770 [TBL] [Abstract][Full Text] [Related]
14. Impact of low-density lipoprotein receptor mutational class on carotid atherosclerosis in patients with familial hypercholesterolemia. Junyent M; Gilabert R; Jarauta E; Núñez I; Cofán M; Civeira F; Pocoví M; Mallén M; Zambón D; Almagro F; Vega J; Tejedor D; Ros E Atherosclerosis; 2010 Feb; 208(2):437-41. PubMed ID: 19717150 [TBL] [Abstract][Full Text] [Related]
15. [A new method of quantitative estimation of mutant allele in mitochondrial genome]. Sazonova MA; Postnov AIu; Orekhov AN; sobenin IA Patol Fiziol Eksp Ter; 2011; (4):81-4. PubMed ID: 22359940 [TBL] [Abstract][Full Text] [Related]
16. Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome. Sazonova M; Budnikov E; Khasanova Z; Sobenin I; Postnov A; Orekhov A Atherosclerosis; 2009 May; 204(1):184-90. PubMed ID: 18849029 [TBL] [Abstract][Full Text] [Related]
17. Heteroplasmic Variants of Mitochondrial DNA in Atherosclerotic Lesions of Human Aortic Intima. Sobenin IA; Zhelankin AV; Khasanova ZB; Sinyov VV; Medvedeva LV; Sagaidak MO; Makeev VJ; Kolmychkova KI; Smirnova AS; Sukhorukov VN; Postnov AY; Grechko AV; Orekhov AN Biomolecules; 2019 Sep; 9(9):. PubMed ID: 31500189 [TBL] [Abstract][Full Text] [Related]
18. [C-reactive protein and carotid intima-media thickness in a population of middle-aged Koreans]. Suh M; Lee JY; Ahn SV; Kim HC; Suh I J Prev Med Public Health; 2009 Jan; 42(1):29-34. PubMed ID: 19229122 [TBL] [Abstract][Full Text] [Related]
19. IGF-I concentrations are positively associated with carotid artery atherosclerosis in women. Hietaniemi M; Pöykkö SM; Ukkola O; Päivänsalo M; Antero Kesäniemi Y Ann Med; 2005; 37(5):373-82. PubMed ID: 16179273 [TBL] [Abstract][Full Text] [Related]
20. Annexin A5 haplotypes in familial hypercholesterolemia: lack of association with carotid intima-media thickness and cardiovascular disease risk. Hiddink L; Dallinga-Thie GM; Hovingh GK; de Visser MC; Peer PG; Stalenhoef AF; van Heerde WL Atherosclerosis; 2015 Feb; 238(2):195-200. PubMed ID: 25525746 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]