Диссертация (1174185), страница 47
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Res. Int. – 2014. – V.2014. – 292017.doi: 65.1155/2014/292017536. Sobenin I.A., Sazonova M.A., Orekhov A.N.. Mutations of mitochondrialgenome and subclinical carotid atherosclerosis.// Atherosclerosis. – 2014. –V.235. – Issue 2. – e65.doi: http://dx.doi.org/10.1016/j.atherosclerosis.2014.05.164537. Sobenin I.A., Myasoedova V.A., Anisimova E.V., Pavlova X.N., MöhlenkampS., Schmermund A., Seibel R., Berenbein S., Lehmann N., Moebus S., Jöckel K.,Orekhov A.N., Erbel R. Blood serum atherogenicity and coronary arterycalcification.// Curr.
Pharm. Des. – 2014. – V.20(37). – P.5884-5888.538. Sobue K., Hayashi K., Nishida W. Expressional regulation of smooth musclecell-specific genes in association with phenotypic modulation. // Mol. Cell.Biochem. – 1999. – V.190. – P.105-118.539.Soemedi R., Topf A., Wilson I.J., Darlay R., Rahman T., Glen E., Hall D.,Huang N., Bentham J., Bhattacharya S., Cosgrove C., BrookJ. D., GranadosRiveron J., Setchfield K., Bu'lock F., Thornborough C., Devriendt K., Breckpot J.,Hofbeck M., Lathrop M., Rauch A., Blue G.M., Winlaw D.S., Hurles M.,Santibanez-Koref M., Cordell H.J., Goodship J.A., Keavney B.D.
Phenotypespecific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in2436 congenital heart disease patients and 6760 controls. // Hum. Mol. Genet. –2012. – V.21. – Issue 7. – P.1513-1520.540.Solano A., Roig M., Vives-Bauza C., Hernandez-Peña J., Garcia-Arumi E.,Playan A., Lopez-Perez M.J., Andreu A.L., Montoya J. Bilateral striatal necrosisassociated with a novel mutation in the mitochondrial ND6 gene. // Ann. Neurol. –2003. – V.54.
– Issue 4. – P.527-530.340541.Sosa M.X., Sivakumar I.K., Maragh S., Veeramachaneni V., Hariharan R.,Parulekar M., Fredrikson K.M., Harkins T.T., Lin J., Feldman A.B., Tata P., EhretG.B., Chakravarti A. Next-generation sequencing of human mitochondrialreference genomes uncovers high heteroplasmy frequency. // PLoS Comput. Biol.– 2012. – V.8. – Issue 10. – e1002737. doi:10.1371/journal.pcbi.1002737542.Srivastava A., Garg N., Mittal T., Khanna R., Gupta S., Seth P.K., Mittal B.Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction incoronary artery disease patients.
// PLoS One. – 2011. – V.6. – Issue 9. – e24123.543.Starr B., Hadfield S.G., Hutten B.A., Lansberg P.J., Leren T.P., DamgaardD., Neil H.A., Humphries S.E. Development of sensitive and specific age- andgender-specific low-density lipoprotein cholesterol cutoffs for diagnosis of firstdegree relatives with familial hypercholesterolaemia in cascade testing. // Clin.Chem.
Lab. Med. – 2008. – V.46. – Issue 6. – P.791-803.544.Stenqvist L., Paetau A., Valanne L., Suomalainen A., Pihko H. A juvenilecase of MELAS with T3271C mitochondrial DNA mutation. // Pediatr. Res. –2005. – V.58. – Issue 2. – P.258-262.545. Stemerman M.B. Effects of moderate hypercholesterolemia on rabbitendothelium.// Arteriosclerosis. – 1981. – V.1. – P.25-32.546.Sternberg D., Danan C., Lombès A., Laforêt P., Girodon E., Goossens M.,Amselem S. Exhaustive scanning approach to screen all the mitochondrial tRNAgenes for mutations and its application to the investigation of 35 independentpatients with mitochondrial disorders. // Hum. Mol.
Genet. – 1998. – V.7. – Issue1. – P.33-42.547.Sussmann M., Sarbia M., Meyer-Kirchrath J., Nüsing R.M., Schrör K.,Fischer J.W. Induction of hyaluronic acid synthase 2 (HAS2) in human vascularsmooth muscle cells by vasodilatory prostaglandins. // Circ. Res. – 2004. – V.94. –Issue 5. – P.592-600.548.Suzuki Y., Suzuki S., Hinokio Y., Chiba M., Atsumi Y., Hosokawa K.,Shimada A., Asahina T., Matsuoka K.
Diabetes associated with a novel 3264341mitochondrial tRNA(Leu)(UUR) mutation. // Diabetes Care. – 1997. – V.20. –Issue 7. – P.1138-1140.549. Svendsen E., Eide T.J. Distribution of atherosclerosis in human descendingthoracic aorta. A morphometric study. // Acta Pathol. Microbiol. Scand. A.
–1980. – V.88. – P.97-101.550. Tang S., Huang T. Characterization of mitochondrial DNA heteroplasmy usinga parallel sequencing system. // Biotechniques. – 2010. – Apr.;V.48, – Issue 4. –P.287-296.551. Tanimoto H., Nishio H., Matsuo M., Nibu K. A novel mitochondrial mutation,1556C --> T, in a Japanese patient with streptomycin-induced tinnitus. // ActaOtolaryngol.
– 2004. – Apr.; V.124. – Issue 3. – P.258-261.552.Tawata M., Hayashi J.I., Isobe K., Ohkubo E., Ohtaka M., Chen J., Aida K.,Onaya T. A new mitochondrial DNA mutation at 14577 T/C is probably a majorpathogenic mutation for maternally inherited type 2 diabetes. // Diabetes. – 2000.–V.49. – Issue 7. – P.1269–1272.553.Tengan C.H., Kiyomoto B.H., Rocha M.S., Tavares V.L., Gabbai A.A.,MoraesC.T.Mitochondrialencephalomyopathyandhypoparathyroidismassociated with a duplication and a deletion of mitochondrial deoxyribonucleicacid. // J. Clin. Endocrinol.
Metab. – 1998. – V.83. – Issue 1. – P.125-129.554.Teplyakov A.I. Endothelin-1 involved in systemic cytokine networkinflammatory response at atherosclerosis. // J. Cardiovasc. Pharmacol. – 2004. –V.44. – Issue 1. – P.274-275.555.Terasaki F., Tanaka M., Kawamura K., Kanzaki Y, Okabe M., Hayashi T.,Shimomura H., Ito T., Suwa M., Gong J.S., Zhang J., Kitaura Y. A case ofcardiomyopathy showing progression from the hypertrophic to the dilated form:association of Mt8348A->G mutation in the mitochondrial tRNA (Lys) gene withsevere ultrastructural alterations of mitochondria in cardiomyocytes.
// Jpn. Circ.J. – 2001. – V.65. – Issue 7. – P.691-694.556.Thajeb P., Ma Y.S., Tzen C.Y., Chuang C.K., Wu T.Y., Chen S.C., WeiY.H. Oculopharyngeal somatic myopathy in a patient with a novel large-scale3423,399 bp deletion and a homoplasmic T5814C transition of the mitochondrialDNA. // Clin. Neurol. Neurosurg. – 2006. – V.108. – Issue 4. – P.407-410.557.Tian C., Liu T., Fang S., Du X., Jia C.
Association of C47T polymorphismin SOD2 gene with coronary artery disease: a case-control study and a metaanalysis. // Mol. Biol. Rep. – 2012. – V.39. – Issue 5. – P.5269-5276.558.Timur A.A., Driscoll D.J., Wang Q. Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis. // Cell.Mol. Life Sci. – 2005. – V.62. – Issue 13. – P.1434-1447.559. Toikka J.O., Niemi P., Ahotura M., Nonikosti H., Viirari S.A., Ronnernaa Т.,Hartiala J.J., Raitakari O.T.
Large-artery elastic properties in young men.Relationships to serum lipoproteins and oxidized low density lipoproteins. //Arterioscler. Thromb. Vasс. Biol. – 1999. – V.19. – P.436-441.560.Tomari Y., Hino N., Nagaike T., Suzuki T., Ueda T. Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G orA10044G mutation. // J. Biol. Chem.
– 2003. – V.278. – Issue 19. – P.1682816833.561.Touboul P.J., Hennerici M.G., Meairs S., Adams H., Amarenco P.,Bornstein N., Csiba L., Desvarieux M., Ebrahim S., Hernandez Hernandez R., JaffM., Kownator S., Naqvi T., Prati P., Rundek T., Sitzer M., Schminke U., TardifJ.C., Taylor A., Vicaut E., Woo K.S. Mannheim carotid intima-media thicknessand plaque consensus (2004-2006-2011).
An update on behalf of the advisoryboard of the 3rd, 4th and 5th watching the risk symposia, at the 13th, 15th and20th European Stroke Conferences, Mannheim, Germany, 2004, Brussels,Belgium, 2006, and Hamburg, Germany, 2011. Cerebrovasc Dis. 2012; 34(4):290296. doi: 10.1159/000343145.562.Ryzhkova A.I., Sazonova M.A., Sinyov V.V., Galitsyna E.V., MelnichenkoA.A., Demakova N.A., Sobenin I.A. Shkurat T.P., Orekhov A.N.
Mito-SNP inmitochondrial cytopathies.// Atherosclerosis. – 2017. – V.263. – e280.doi: http://dx.doi.org/10.1016/j.atherosclerosis.2017.06.904343563.Torrente I., Arturi F., D’Aloiso L., Colosimo A., De Luca A., Ferretti E.,Russo D., Chiefari E., Scarpelli D., Bisceglia M., Dallapiccola B., Filetti S.Evaluation of a DHPLC-based assay for rapid detection of RET germlinemutations in Italian patients with medullary thyroid carcinoma.
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