Диссертация (Связь мутаций митохондриального генома с формированием атеросклеротических поражений артериальной стенки), страница 46
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– V.2017. – 6934394.doi: 10.1155/2017/6934394. Epub 2017 Jul 25.505. Sazonova M.A., Postnov A.Yu., Sobenin I.A., Orekhov A.N. Role of thesomatic mutations in development of atherosclerotic lesion of human aorta. 2ndInternational Conference on Heart & Brain – ICHB, Paris, France, February 27 –March 1, 2014. E-Poster presentation.506. Sazonova M.A., Sinyov V.V., Ryzhkova A.I., Galitsyna E.V., Zhelankin A.V.,Mitrofanov K.Y., Bobryshev Y.V., Orekhov A.N., Sobenin I.A. Electronmicroscopicanalysisofmitochondriafromatheroscleroticplaques.//Atherosclerosis. – 2017.
– V.263. – e280.doi: http://dx.doi.org/10.1016/j.atherosclerosis.2017.06.905507. Schäfer A., Bauersachs J. Endothelial dysfunction, impaired endogenousplatelet inhibition and platelet activation in diabetes and atherosclerosis. // Curr.Vasc. Pharmacol. – 2008.
– V.6. – P.52-60.508.Scheer W.D., Boudreau DA.., Hixson J.E., McGill H.C., Newman W.P. 3rd,Tracy R.E., Zieske A.W., Strong J.P. ACE insert/delete polymorphism andatherosclerosis. // Atherosclerosis. – 2005. – V.178. – Issue 2. – P.241-247.509. Secher B, Fregel R, Larruga JM, Cabrera VM, Endicott P, Pestano JJ,González AM. The history of the North African mitochondrial DNA haplogroupU6 gene flow into the African, Eurasian and American continents.
BMC EvolBiol. – 2014. – May 19; Issue 14. – P.109. doi:10.1186/1471-2148-14-109.510. Shibata N., Glass C.K. Regulation of macrophage function in inflammation andatherosclerosis. // J. Lipid. Res. – 2009. – V.50. – Suppl. – P.S277-S281.511. Shimada K. Immune system and atherosclerotic disease. Heterogeneity ofLeukocyte Subsets Participating in the Pathogenesis of Atherosclerosis. // Circ. J.– 2009. – V.73. – P.994-1001.512.Schollen E., Vandenberk P., Cassiman J.J., Matthijs G. Development ofreverse dot-blot system for screening of mitochondrial DNA mutations associated336with Leber hereditary optic atrophy. // Clin.
Chem. – 1997. – V.43. – Issue 1. –P.18-23.513.Scholte A.J., Nucifora G., Delgado V., Djaberi R., Boogers M.J., SchuijfJ.D., Kharagjitsingh A.V., Jukema J.W., van der Wall E.E., Kroft L.J., de RoosA., Bax J.J. Subclinical left ventricular dysfunction and coronary atherosclerosisin asymptomatic patients with type 2 diabetes. // Eur. J. Echocardiogr. – 2011. –V.12. – Issue 2. – P.148-155.514.Schreiner P.J., Heiss G., Tyroler H.A., Morrisett J.D., Davis C.E., Smith R.Race and gender differences in the association of Lp(a) with carotid artery wallthickness.
The Atherosclerosis Risk in Communities (ARIC) Study. //Arterioscler. Thromb. Vasc. Biol. – 1996. – V.16. – Issue 3. – P.471-478.515.Scott L., Kerr A., Haydock D., Merrilees M. Subendothelial proteoglycansynthesis and transforming growth factor beta distribution correlate withsusceptibility to atherosclerosis. // J. Vasc. Res.
– 1997. – V.34. – Issue 5. –P.365-377.516.Seibel P., Lauber J., Klopstock T., Marsac C., Kadenbach B., Reichmann H.Chronic progressive external ophthalmoplegia is associated with a novel mutationin the mitochondrial tRNA(Asn) gene. // Biochem. Biophys. Res. Commun. –1994. – V.204. – Issue 2. – P.482-489.517. Silvestri G., Santorelli F.M., Shanske S., Whitley C.B., Schimmenti L.A.,Smith S.A., DiMauro S. A new mtDNA mutation in the tRNA leu(UUR) gene isassociated with maternally inherited cardiomyopathy. // Hum. Mut. – 1994. – V.3.– P.37-43.518. Sima A.V., Stancu C.S., Simionescu M. Vascular endothelium inatherosclerosis. // Cell Tissue Res. – 2009.
– V.335. – P.191-203.519.Shields K.J., Stolz D., Watkins S.C., Ahearn J.M. Complement proteins C3and C4 bind to collagen and elastin in the vascular wall: a potential role invascular stiffness and atherosclerosis. // Clin. Transl. Sci. – 2011. – V.4. – Issue 3.– P.146-152.337520.Shimoda Y., Satoh M., Nakamura M., Akatsu T., Hiramori K. Activatedtumour necrosis factor-alpha shedding process is associated with in-hospitalcomplication in patients with acute myocardial infarction.
// Clin. Sci. (Lond). –2005. – V.108. – Issue 4. – P.339-347.521.Shin W.S., Tanaka M., Suzuki J., Hemmi C., Toyo-oka T. A novelhomoplasmic mutation in mtDNA with a single evolutionary origin as a risk factorfor cardiomyopathy. // Am. J. Hum.
Genet. – 2000. – V.67. – Issue 6. – P.16171620.522.Singh R., Ellard S., Hattersley A., Harries L.W. Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of3243A>G mitochondrial point mutation. // J. Mol. Diagn. – 2006. – V.8. – Issue 2.–523.P.225-230.Shirts B.H., Hasstedt S.J., Hopkins P.N., Hunt S.C.
Evaluation of the gene-age interactions in HDL cholesterol, LDL cholesterol, and triglyceride levels: theimpact of the SORT1 polymorphism on LDL cholesterol levels is age dependent.// Atherosclerosis. – 2011. – V.217. – Issue 1. – P.139-141.524.Shivpuri S., Gallo L.C., Crouse J.R., Allison M.A. The association betweenchronic stress type and C-reactive protein in the multi-ethnic study ofatherosclerosis: does gender make a difference? // J. Behav. Med. – 2012. – V.35.– Issue 1. – P.74-85.525.Skoczynska A., Dobosz T., Poreba R., Turczyn B., Derkacz A.,Zoledziewska M., Jonkisz A., Lebioda A.
The dependence of serum interleukin-6level on PPAR-alpha polymorphism in men with coronary atherosclerosis. // Eur.J. Intern. Med. – 2005. – V.16. – Issue 7. – P.501-506.526.Snyder L.R., Kirkland J.J. and Glajch J.L. Practical HPLC MethodDevelopment. // New York: John Wiley & Sons. – 1997. – 747 p.527. Sobenin I.A., Chistiakov D.A., Sazonova M.A., Ivanova M.M., BobryshevY.V., Orekhov A.N., Postnov A.Y. Association of the level of heteroplasmy of the15059G>A mutation in the MT-CYB mitochondrial gene with essential338hypertension.
// World J. Cardiol. – 2013. – May 26; V.5. – Issue 5. – P.132-140.doi:10.4330/wjc.v5.i5.132.528. Sobenin I.A., Sazonova M.A., Postnov A.Y., Bobryshev Y.V., Orekhov A.N.Mitochondrial Mutations are Associated with Atherosclerotic Lesions in theHuman Aorta. // Clin. Dev. Immunol. – 2012. – V.2012. – 832464.doi: 10.1155/2012/832464529.
Sobenin I.A., Sazonova M.A., Postnov A.Y., Orekhov A.N. An association ofmutations of mitochondrial DNA with aortic atherosclerotic lesions. //Atherosclerosis Suppl. – 2011. – V.12. – Issue 1. – P.68.doi: http://dx.doi.org/10.1016/S1567-5688(11)70315-4530. Sazonova MA, Ryzhkova AI, Sinyov VV, Galitsyna EV, Orekhova VA,Melnichenko AA, Orekhov AN, Ravani AL, Sobenin IA. New markers ofatherosclerosis: a threshold level of heteroplasmy in mtDNA mutations.// VesselPlus 2017 Oct xx.
[Online First]531.Sobenin I.A., Zhelankin A.V., Mitrofanov K.Y., Sinyov V.V., SazonovaM.A., Postnov A.Y., Orekhov A.N. Mutations of Mitochondrial DNA inAtherosclerosis and Atherosclerosis-Related Diseases.// Curr Pharm Des. – 2015.– V.21(9). – P.1158-1163. Review.532.Sobenin I.A., Sazonova M.A., Ivanova M.M., Zhelankin A.V., MyasoedovaV.A., et al. Mutation C3256T of Mitochondrial Genome in White Blood Cells:Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease.
// PLoSOne. –2012. – V.7. – Issue 10. – e46573. doi:10.1371/journal.pone.0046573. Epub2012 Oct 2.533. Sobenin I.A., Sazonova M.A., Postnov A.Y., Bobryshev Y.V., Orekhov A.N.Changes of mitochondria in atherosclerosis: Possible determinant in thepathogenesis of the disease. // Atherosclerosis.
– 2013. – Apr.; V.227. – Issue 2. –P.283-288. doi: 10.1016/j.atherosclerosis.2013.01.006.534. Sobenin I.A., Sazonova M.A., Postnov A.Y., Salonen J.T., Bobryshev Y.V.,Orekhov A.N. Association of mitochondrial genetic variation with carotid339atherosclerosis. // PLoS One. – 2013. – Jul.9; V.8. – Issue 7. – e68070.doi:10.1371/journal.pone.0068070. Print 2013.535. Sobenin I.A., Mitrofanov K.Y., Zhelankin A.V., Sazonova M.A., PostnovA.Y., Revin V.V., Bobryshev Y.V., Orekhov AN. Quantitative assessment ofheteroplasmy of mitochondrial genome: perspectives in diagnostics andmethodological pitfalls.// Biomed.
