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    Academic Journal

    Contributors: 1

    Source: Russian Journal of Infection and Immunity; Vol 12, No 4 (2022); 668-676 ; Инфекция и иммунитет; Vol 12, No 4 (2022); 668-676 ; 2313-7398 ; 2220-7619

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  3. 3
    Academic Journal

    Contributors: Исследование проводилось за счет средств государственного задания, тема НИР «Изучение патогенеза открытоугольной глаукомы на основе оценки дисбаланса цитокинов и факторов роста» (№ АААА-А18-118082290059-3), а также в рамках договоров о научно-практическом сотрудничестве между НМИЦ «МНТК "Микрохирургия глаза" им. акад. С.Н. Федорова» и НИИКЭЛ – филиал ИЦиГ СО РАН, НИИКЭЛ и Федеральным исследовательским центром фундаментальной и трансляционной медицины СО РАН.

    Source: Bulletin of Siberian Medicine; Том 20, № 4 (2021); 86-92 ; Бюллетень сибирской медицины; Том 20, № 4 (2021); 86-92 ; 1819-3684 ; 1682-0363 ; 10.20538/1682-0363-2021-20-4

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    Relation: https://bulletin.tomsk.ru/jour/article/view/4585/3106; Егоров Е.А., Алексеев В.Н. Патогенез и лечение первичной открытоугольной глаукомы. М.: ГЭОТАР-Медиа, 2017: 224.; Stevens G.A., White R.A., Flaxman S.R., Price H., Jonas J.B., Keeffe J., Leasher J., Naidoo K., Pesudovs K., Resnikoff S., Taylor H., Bourne R.R.; Vision Loss Expert Group. Global prevalence of visual impairment and blindness: magnitude and temporal trends, 1990–2010. Ophthalmology. 2013; 120 (12): 2377–2384. DOI:10.1016/j.ophtha.2013.05.025.; Tham Y.C., Li X., Wong T.Y., Quigley H.A., Aung T., Cheng C.Y. Global prevalence of glaucoma and projections of glaucoma burden through 2040: a systematic review and meta-analysis. Ophthalmology. 2014; 121: 2081–2090. DOI:10.1016/j.ophtha.2014.05.013.; Bourne R.R., Taylor H.R., Flaxman S.R., Keeffe J., Leasher J., Naidoo K., Pesudovs K., White R.A., Wong T.Y., Resnikoff S., Jonas J.B. Vision loss expert group of the global burden of disease study. Number of people blind or visually impaired by glaucoma worldwide and in world regions 1990–2010: A meta-analysis. PLoS One. 2016; 11 (10): e0162229. DOI:10.1371/journal.pone.0162229.; Sihota R., Goyal A., Kaur J., Gupta V., Nag T.C. Scanning electron microscopy of the trabecular meshwork: understanding the pathogenesis of primary angle closure glaucoma. Indian. J. Ophthalmol. 2012; 60 (3): 183–188. DOI:10.4103/0301-4738.95868.; Huang A.S., Mohindroo C., Weinreb R.N. Aqueous humor outflow structure and function imaging. At the bench and bedside: A Review. J. Clin. Exp. Ophthalmol. 2016; 7 (4): 578. DOI:10.4172/2155-9570.1000578.; Song M.M., Lei Y., Wu J.H., Sun X.H. The progress of studies on aqueous humor dynamics abnormality induced by trabecular meshwork and Schlemm canal endothelial cell senescence and its relation with glaucoma. Zhonghua Yan Ke Za Zhi. 2017; 53 (11): 868–873. DOI:10.3760/cma.j.issn.0412-4081.2017.11.014.; Wang K., Read A.T., Sulchek T., Ethier C.R. Trabecular meshwork stiffness in glaucoma. Exp. Eye. Res. 2017; 158: 3–12. DOI:10.1016/j.exer.2016.07.011.; Черных В.В., Бгатова Н.П., Орлов Н.Б., Ермакова О.В., Трунов А.Н. Местный воспалительный процесс как возможное проявление нарушений увеолимфатического оттока внутриглазной жидкости при глаукоме. Часть 2. Национальный журнал глаукома. 2018; 17 (2): 311. DOI:10.25700/NJG.2018.02.01.; Kokubun T., Tsuda S., Kunikata H., Yasuda M., Himori N., Kunimatsu-Sanuki S., Maruyama K., Nakazawa T. Characteristic profiles of inflammatory cytokines in the aqueous humor of glaucomatous eyes. Ocul. Immunol. Inflamm. 2018; 26 (8): 1177–1188. DOI:10.1080/09273948.2017.1327605.; Khalef N., Labib H., Helmy H., El Hamid M.A., Moemen L, Fahmy I. Levels of cytokines in the aqueous humor of eyes with primary open angle glaucoma, pseudoexfoliation glaucoma and cataract. Electron Physician. 2017; 9 (2): 3833–3837. DOI:10.19082/3833.; Pantalon A., Obadă O., Constantinescu D., Feraru C., Chiseliţă D. Inflammatory model in patients with primary open angle glaucoma and diabetes. Int. J. Ophthalmol. 2019; 12 (5): 795–801. DOI:10.18240/ijo.2019.05.15.; Черных В.В., Коненков В.И., Ермакова О.В., Орлов Н.Б., Обухова О.О., Еремина А.В., Трунов А.Н. Содержание цитокинов и факторов роста во внутриглазной жидкости у пациентов с первичной открытоугольной глаукомой. Бюллетень сибирской медицины. 2019; 18 (1): 257–265. DOI:10.20538/1682-0363-2019-1-257-265.; Ten Berge J.C., Fazil Z., Van Den Born I., Wolfs R.C.W., Schreurs M.W.J., Dik W.A., Rothova A. Intraocular cytokine profile and autoimmune reactions in retinitis pigmentosa, age-related macular degeneration, glaucoma and cataract. Acta Ophthalmol. 2019; 97 (2): 185–192. DOI:10.1111/aos.13899.; Cui N., Hu M., Khalil R.A. Biochemical and biological attributes of matrix metalloproteinases. Prog. Mol. Biol. Transl. Sci. 2017; 147: 173. DOI:10.1016/bs.pmbts.2017.02.005.; Chen Q., Jin M., Yang F., Zhu J., Xiao Q., Zhang L. Matrix metalloproteinases: inflammatory regulators of cell behaviors in vascular formation and remodeling. Mediators Inflamm. 2013; 2013: 928315. DOI: 0.1155/2013/928315.; Nissinen L., Kähäri V.M. Matrix metalloproteinases in inflammation. Biochim. Biophys. Acta. 2014; 1840 (8): 2571–2580. DOI:10.1016/j.bbagen.2014.03.007. 18. Arpino V., Brock M., Gill S.E. The role of TIMPs in regulation of extracellular matrix proteolysis. Matrix Biol. 2015; 44–46: 247–254. DOI:10.1016/j.matbio.2015.03.005.; Robert S., Gicquel T., Victoni T., Valença S., Barreto E., Bailly-Maître B., Boichot E., Lagente V. Involvement of matrix metalloproteinases (MMPs) and inflammasome pathway in molecular mechanisms of fibrosis. Biosci. Rep. 2016; 36 (4): e00360. DOI:10.1042/BSR20160107.; Laronha H., Caldeira J. Structure and function of human matrix metalloproteinases. Cells. 2020; 9 (5): 1076. DOI:10.3390/cells9051076.; Singh M., Tyagi S.C. Metalloproteinases as mediators of inflammation and the eyes: molecular genetic underpinnings governing ocular pathophysiology. Int. J. Ophthalmol. 2017; 10 (8): 1308–1318. DOI:10.18240/ijo.2017.08.20.; Roupakia E., Markopoulos G.S., Kolettas E. IL-12-mediated transcriptional regulation of matrix metalloproteinases. Biosci. Rep. 2018; 38 (3). DOI: BSR20171420. 10.1042/BSR20171420.; Singh S., Maniakis-Grivas G., Singh U.K., Asher R.M., Mauri F., Elkington P.T., Friedland J.S. Interleukin-17 regulates matrix metalloproteinase activity in human pulmonary tuberculosis. J. Pathol. 2018; 244 (3): 311–322. DOI:10.1002/path.5013.; Zhang J.F., Wang G.L., Zhou Z.J., Fang X.Q., Chen S., Fan S.W. Expression of matrix metalloproteinases, tissue Inhibitors of metalloproteinases, and Interleukins in vertebral cartilage endplate. Orthop. Surg. 2018; 10 (4): 306–311. DOI:10.1111/os.12409.; De Groef L., Van Hove I., Dekeyster E., Stalmans I., Moons L. MMPs in the trabecular meshwork: promising targets for future glaucoma therapies? Invest. Ophthalmol. Vis. Sci. 2013; 54 (12): 7756–7763. DOI:10.1167/iovs.13-13088.; De Groef L., Van Hove I., Dekeyster E., Stalmans I., Moons L. MMPs in the neuroretina and optic nerve: modulators of glau coma pathogenesis and repair? Invest. Ophthalmol. Vis. Sci. 2014; 55 (3): 1953–1964. DOI:10.1167/iovs.13-13630.; Nga A.D., Yap S.L., Samsudin A., Abdul-Rahman P.S. Matrix metalloproteinases and tissue inhibitors of metalloproteinases in the aqueous humour of patients with primary angle closure glaucoma – a quantitative study. BMC Ophthalmol. 2014; 14: 33. DOI:10.1186/1471-2415-14-33.; Sahay P., Rao A., Padhy D., Sarangi S., Das G., Reddy M.M., Modak R. Functional activity of matrix metalloproteinases 2 and 9 in tears of patients with glaucoma. Invest. Ophthalmol. Vis. Sci. 2017; 58 (6): 106–113. DOI:10.1167/iovs.17-21723.; Markiewicz L., Pytel D., Mucha B., Szymanek K., Szaflik J., Szaflik J.P., Majsterek I. Altered expression levels of MMP1, MMP9, MMP12, TIMP1, and IL-1β as a risk factor for the elevated IOP and optic nerve head damage in the primary open-angle glaucoma patients. Biomed. Res. Int. 2015; 2015: 812503. DOI:10.1155/2015/812503.; Zaleska-Żmijewska A., Strzemecka E., Wawrzyniak Z.M., Szaflik J.P. Extracellular MMP-9-based assessment of ocular surface inflammation in patients with primary open-angle glaucoma. J. Ophthalmol. 2019; 2019: 1240537. DOI:10.1155/2019/1240537.; Ashworth Briggs E.L., Toh T., Eri R., Hewitt A.W., Cook A.L. TIMP1, TIMP2, and TIMP4 are increased in aqueous humor from primary open angle glaucoma patients. Mol. Vis. 2015; 21: 1162–1172.; Fountoulakis N., Labiris G., Aristeidou A., Katsanos A., Tentes I., Kortsaris A., Kozobolis V.P. Tissue inhibitor of metalloproteinase 4 in aqueous humor of patients with primary open angle glaucoma, pseudoexfoliation syndrome and pseudoexfoliative glaucoma and its role in proteolysis imbalance. BMC Ophthalmol. 2013 13: 69. DOI:10.1186/1471-2415-13-69.; https://bulletin.tomsk.ru/jour/article/view/4585

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    Academic Journal

    Source: Pathologia; Vol. 18 No. 1 (2021): Pathologia; 50-57 ; Патология; Том 18 № 1 (2021): Патология; 50-57 ; Патологія; Том 18 № 1 (2021): Патологія; 50-57 ; 2310-1237 ; 2306-8027

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    Academic Journal

    Source: REPRODUCTIVE ENDOCRINOLOGY; No. 59 (2021); 40-44
    РЕПРОДУКТИВНАЯ ЭНДОКРИНОЛОГИЯ; № 59 (2021); 40-44
    РЕПРОДУКТИВНА ЕНДОКРИНОЛОГІЯ; № 59 (2021); 40-44

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    Academic Journal

    Source: Pathologia; Vol. 16 No. 3 (2019): Pathologia ; Патология; Том 16 № 3 (2019): Патологія ; Патологія; Том 16 № 3 (2019): Патологія ; 2310-1237 ; 2306-8027

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    Academic Journal

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    Relation: УДК618.1–006:577.15; https://repository.pdmu.edu.ua/handle/123456789/11523

  13. 13
    Academic Journal

    Source: Medical Genetics; Том 16, № 10 (2017); 36-40 ; Медицинская генетика; Том 16, № 10 (2017); 36-40 ; 2073-7998

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    Relation: https://www.medgen-journal.ru/jour/article/view/335/251; Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry. Circ Res. 2003 May 2; 92(8):827-839.; Shuman Moss L.A, Jensen-Taubman S.,Stetler-Stevenson W.G. Matrix Metalloproteinases. Changing Roles in Tumor Progression and Metastasis. Am J Pathol. 2012 Dec; 181(6): 1895-1899.; Стрельников В.В., Танас А.С., Руденко В.В., Кузнецова Е.Б., Залетаев Д.В. Геномный анализ метилирования ДНК с использованием секвенирования нового поколения // Медицинская генетика. 2014; 13(3): 32-37.; Танас А.С., Кузнецова Е.Б., Борисова М.Э., Руденко В.В., Залетаев Д.В., Стрельников В.В. Дизайн метода бисульфитного секвенирования ограниченных наборов геномных локусов (RRBS) для анализа метилирования CpG-островков человека в больших выборках // Молекулярная биология. 2015; 49(4): 689-699.; Tanas A.S., Borisova M.E., Kuznetsova E.B., Rudenko V.V., Karandasheva K.O., Nemtsova M.V., Izhevskaya V.L., Simonova O.A., Larin S.S., Zaletaev D.V., Strelnikov V.V. Rapid and Affordable Genome-Wide Bisulfite DNA Sequencing by XmaI-reduced Representation Bisulfite Sequencing // Epigenomics. 2017; 9(6): 833-847.; Hegedus L., Cho H., Xie X., Eliceiri G.L. Additional MDA-MB-231 breast cancer cell matrix metalloproteinases promote invasiveness. J Cell Physiol. 2008 Aug; 216(2):480-485.; Benson C.S., Babu S.D., Radhakrishna S. et al. Expression of matrix metalloproteinases in human breast cancer tissues. Dis Markers. 2013;34(6):395-405.; Luo Y.P., Zhong M., Wang L.P. et al. Inhibitory effects of RNA interference on MMP-24 expression and invasiveness of ovarian cancer SKOV(3) cells. Nan Fang Yi Ke Da Xue Xue Bao. 2009 Apr; 29(4):781-784.; Velasco G., Cal S., Merlos-Suаrez A. et al. Human MT6-matrix metalloproteinase: identification, progelatinase A activation, and expression in brain tumors. Cancer Res. 2000 Feb 15; 60(4):877-82.; Riddick A., Shukla C., Pennington C. et al. Identification of degradome components associated with prostate cancer progression by expression analysis of human prostatic tissues. Br J Cancer. 2005 Jun 20; 92(12): 2171-2180.; Sohail A., Sun Q., Zhao H., Bernardo M.M. et al. MT4-(MMP17) and MT6-MMP (MMP25), A unique set of membrane-anchored matrix metalloproteinases: properties and expression in cancer. Cancer Metastasis Rev. 2008 Jun; 27(2):289-302.

  14. 14
    Academic Journal

    Source: Scientific studies: theory, methodology and practice; № 2; 25-33 ; Научные исследования: теория, методика и практика; № 2; 25-33

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    Relation: info:eu-repo/semantics/altIdentifier/isbn/978-5-9500768-3-1; https://interactive-plus.ru/e-articles/424/Action424-463701.pdf; 1. Ганусевич И.И. Роль матриксных металлопротеиназ (ММП) при злокачественных новообразованиях // Онкология. – Т. 12. – №1. – 2010.; 2. Калабенков И.Г. Российские реформы в цифрах и фактах. – М.: РУСАКИ, 2007. – С. 288.; 3. Клиническая фармакология по Гудману и Гилману. Т. 3 / Редактор: профессор А.Г. Гилман. – М.: Практика, 2006. – С. 250.; 4. Корман Д. Б. Основы противоопухолевой терапии. – М.: Практическая медицина, 2006. – С. 503.; 5. Северин Е.С. Учебник для вузов. – М.: ГЕОТАР-Медиа, 2008. – С. 768.; 6. Именитов Е.Н. Молекулярная онкология: клинические аспекты / Е.Н. Именитов, К.П. Хансон. – СПб.: Издательский дом СПбМАПО, 2007. – С. 211.; 7. Руководство по химиотерапии опухолевых заболеваний / Под ред. Н.И. Переводчиковой. – 3-е изд., доп. и пер. – М.: Практическая медицина, 2011. – С. 512.

  15. 15
    Academic Journal

    Contributors: НИИКПССЗ

    Source: Complex Issues of Cardiovascular Diseases; Том 6, № 4 (2017); 103-111 ; Комплексные проблемы сердечно-сосудистых заболеваний; Том 6, № 4 (2017); 103-111 ; 2587-9537 ; 2306-1278 ; 10.17802/2306-1278-2017-6-4

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    Relation: https://www.nii-kpssz.com/jour/article/view/342/297; Сторожанов Г.И., Тронина О.А., Гендлин Г.Е. Приобретенные пороки сердца. Некоторые особенности клинической картины и лечения в XXI веке. Сердечная недостаточность. 2009; Т. 10, 6: 335-341 [Storozhamv G.I., Tromm O.A., Gendlin G.E. Priobretennye poroki serdca. Nekotorye osobennosti klimcheskoj kartmy i lechenija v XXI veke. Serdechrnja nedostatochnost. 2009; T. 10, 6: 335-341. (Гп Russ)]; Briasoulis A., Tousoulis D., Papageorgiou N., Kampoli A.M., Androulakis E., Antoniades C., Tsiam is E., Latsios G., S tefarnd is C. Novel therapeu tic approaches targe tm g in atrix in etallopro tem ases in cardiovascular disease. Curr Top Med Chem. 2012; 12 (10): 1214-1221.; Abu El-Asrar A.M., Ahmad A., Bittoun E., Siddiquei M.M., Mohammad G., Mousa A., De Hertogh G., Opdenakker G. Differential expression and localization of human tissue mhibitors of metalloproteinases in proliferative diabetic retmopathy. Acta Ophthalmol. 2017. doi:10.1111/aos.13451.; Masciantonio M.G., Lee C.K.S., Arpmo V., Mehta S., Gill S.E. The balaMe between metalloproteinases and TIMPs: critical regulator of microvascular endotheial cell function in health and disease. Prog Mol Biol Trarnl Sci. 2017; 147: 101-131. doi:10.1016/bs.pmbts.2017.01.001.; Lurz J.A., Luecke C., Lang D., Besler C., Rommel K.P., Klmgel K., Kandolf R., Adams V., Schбne K., Hmdricks G., Schuler G., Linke A., Thiele H., Gutberlet M., Lurz P. CMR-Derived extracellular volume fraction as a marker for myocardial fibrosis: the importance of coexistmg myocardial. JACC Cardiovasc Imaging. 2017. doi:10.1016/j.jcmg.2017.01.025.; Rao V.H., Karnal V., Stoupa S., Agrawal D.K. MMP-1 and MMP-9 regulate epidermal growth factor-dependent collagen loss in human carotid plaque smooth muscle cells. Physiol Rep. 2014; 2 (2): e00224. doi:10.1002/phy2.224. eCollection 2014 Feb 1.; Печерина Т.Б., Груздева O.B., Кашталап B.B., Барбараш О.Л. Роль матриксных металлопротеиназ в оценке прогноза у больных инфарктом миокарда с подъемом сегмента ST в период пребывания в стационаре. Кардиология. 2013; 56 (6): 18-24 [Pecherma T.B., Gruzdeva O.V., Kashtalap V.V. Barbarash., O.L. The role of matrix metalloproteimses in assessmert: of progmsis in parients with ST-Elevation myocardial infarction during hospital stay. Kardiologija. 2013; 56 (6): 18-24. (Ш Russ)]; Garr R.J., Krasuski R.A., Eckart R.E., Wang A., Pierce C., Kisslo K.B., Harrison J.K., Bashore T.M. Peripheral blood levels of matrix metalloprotemases in patients referred for percutaneous balloon mitral valve commissurotomy. J Heart Valve Dis. 2006; 15 (3): 369-374.; Deschamps A.M., Spmale F.G. Matrix modulate and heart failure: raw concepts question old beliefs. Curr Opm Cardiol. 2005; 20 (3): 211-216.; Leong S.W., Soor G.S., Butany J., Herny J., Thangaroopan M., Leask R.L. Morphological imdmgs in 192 surgically excised native mitral valves. Can J Cardiol. 2006; 22 (12): 1055-1061.; BaMrjee T., Mukherjee S., Ghosh S., Biswas M., Dutta S., Pattari S., Chatterjee S., Bandyopadhyay A. Clmical significance of markers of collagen metabolism in rheumatic mitral valve disease. PLoS One. 2014; 9 (3): e90527. doi:10.1371/joumal.pone.0090527. eCollection 2014.; Sivakumar P., Gupta S., Sarkar S., Sen S. Uregulate of lysyl oxidase and MMPs during cardiac remodeling in human dilatedcardiomyopathy. Mol Cell Biochem. 2008; 307 (1-2): 159-167. doi:10.1007/s11010-007-9595-2; Ducharme A., Frantz S., Aikawa M., Rabkin E., Lmdsey M., Rohde L.E., Schoen F.J., Kelly R.A., Werb Z., Libby P., Lee R.T. Targeted delete of matrix metalloproteimse-9 attenuates left ventricular enlargement and collagen accumulate after experimental myocardial infarction. J Clm Invest. 2000; 106: 55-62. doi:10.1172/JCI8768; Zhu H., Zhang W., Guo C.H., Zhang G., Zhang W.D., Zhong M., Yang G.R., Ge Z.M., Zhang Y. Effects of matrix metalloprotemase-9 and tissue inhibitor-1 of metalloprotemase expression on atrial structural remodelmg during chronic atrial fibrillation. Zhonghua Yi Xue Za Zhi. 2005; 85 (1): 45-48.; Walther T., Schubert A., Falk V., Binnerr C., Kanev A., Bleiziffer S., Walther C., Doll N., Autschbach R., Mohr F.W. Regression of left ventricular hypertrophy after surgical therapy for aortic steMsis is associated with changes in extracellular matrix gene expression. Circulation 2001; 104 (12 Suppl 1): I54-158.; Jia Y., Hu D.N., Sun J., Zhou J. Correlations between MMPs and TIMPs levels in aqueous humor from high myopia and cataract parients. Curr Eye Res. 2017; 42 (4): 600-603. doi:10.1080/02713683.2016.1223317.; Roten L., Nemoto S., Simsic J., Coker M.L., Rao V., Baicu S., Defreyte G., Soloway P.J., Zile M.R., Spinale F.G. Effects of geM deletion of the tissue mhibitor of the matrixmetalloprotemase-type 1 (TIMP-1) on left ventricular geometryand function in mice. J Mol Cell Cardiol. 2000; 32 (1): 109-120. doi:10.1006/jmcc.1999.1052; Jung K. Serum or plasma: what kmd of blood sample should be used to measure circulatmg matrix metalloprotemases and their mhibitors? J Neurotomunol 2005; 162: 1-2. doi:10.1016/j.jneuroim.2004.12.021; Schwartz G.G., Olsson A.G., Ezekowitz M.D., Gam P., Oliver M.F., Waters D., Zeiher A., Chaitman B.R., Leslie S., Stem T. Effects of atorvastatm on early recurred ischemic events in acute corornry syndromes: the MIRACL study: a randomized controlled trial. JAMA. 2001; 285: 1711-1718.; Koh K., Son K.W., Ata J.Y., Jin D.K., Kim H.S., Choi Y.M., Kim D.S., Jeong E.M., Park G.S., Choi I.S., Shm E.K. Comparative effects of diet and statin on NO bioactivity and matrix metalloproteinases hypercholesterolemic patiert:s with coronary artery disease. Arterioscler Thromb Vasc Biol. 2002; 22: 9-23.

  16. 16
    Academic Journal

    Source: Almanac of Clinical Medicine; Vol 45, No 4 (2017); 280-288 ; Альманах клинической медицины; Vol 45, No 4 (2017); 280-288 ; 2587-9294 ; 2072-0505 ; 10.18786/2072-0505-2017-45-4

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  17. 17
    Academic Journal

    Source: Medical Herald of the South of Russia; № 3 (2016); 91-100 ; Медицинский вестник Юга России; № 3 (2016); 91-100 ; 2618-7876 ; 2219-8075 ; 10.21886/2219-8075-2016-3

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