Search Results - "ФОСФОРИЛИРОВАНИЕ"

Contributors: Исследование выполнено при поддержке гранта Российского научного фонда № 24-75-10057 «Идентификация клеточных маркеров дисфункции эндотелия», https://rscf.ru/project/24-75-10057/.

Source: Complex Issues of Cardiovascular Diseases; Том 14, № 2 (2025); 110-126 ; Комплексные проблемы сердечно-сосудистых заболеваний; Том 14, № 2 (2025); 110-126 ; 2587-9537 ; 2306-1278

Subject Terms: Фосфорилирование eNOS, Endothelial cells, Endothelial dysfunction, Hypertensive rats, Normotensive rats, Endothelial nitric oxide synthase, eNOS phosphorylation, Эндотелиальные клетки, Дисфункция эндотелия, Гипертензивные крысы, Нормотензивные крысы, Эндотелиальная NO-синтаза

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Relation: https://www.nii-kpssz.com/jour/article/view/1669/1030; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2051; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2052; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2053; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2054; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2055; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2056; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2057; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2058; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2059; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2060; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2061; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2062; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2063; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2064; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1669/2065; Kutikhin AG, Shishkova DK, Velikanova EA, Sinitsky MY, Sinitskaya AV, Markova VE. 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TNFα reduces eNOS activity in endothelial cells through serine 116 phosphorylation and Pin1 binding: Confirmation of a direct, inhibitory interaction of Pin1 with eNOS. Vascul Pharmacol. 2016;81:61-8. doi:10.1016/j.vph.2016.04.003.; Li C, Ruan L, Sood SG, Papapetropoulos A, Fulton D, Venema RC. Role of eNOS phosphorylation at Ser-116 in regulation of eNOS activity in endothelial cells. Vascul Pharmacol. 2007;47(5-6):257-64. doi:10.1016/j.vph.2007.07.001.; Shishkova D, Markova V, Markova Y, Sinitsky M, Sinitskaya A, Matveeva V, Torgunakova E, Lazebnaya A, Stepanov A, Kutikhin A. Physiological Concentrations of Calciprotein Particles Trigger Activation and Pro-Inflammatory Response in Endothelial Cells and Monocytes. Biochemistry (Mosc). 2025;90(1):132-160. doi:10.1134/S0006297924604064.; Ku KH, Dubinsky MK, Sukumar AN, Subramaniam N, Feasson MYM, Nair R, Tran E, Steer BM, Knight BJ, Marsden PA. 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https://doi.org/10.17802/2306-1278-2025-14-2-110-126

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Heart failure and mitochondrial dysfunction: research methods in experiment and clinical practice ; Сердечная недостаточность и митохондриальная дисфункция: методы исследования в эксперименте и клинической практике

Authors: A. A. Garganeeva, O. V. Tukish, E. A. Kuzheleva, E. F. Muslimova, M. O. Gulya, V. A. Zhargasova, S. V. Popov, А. А. Гарганеева, О. В. Тукиш, Е. А. Кужелева, Э. Ф. Муслимова, М. О. Гуля, В. А. Жаргасова, С. В. Попов

Contributors: Исследование выполнено при финансовой поддержке гранта Российского научного фонда (проект № 23-75- 00009).

Source: Acta Biomedica Scientifica; Том 10, № 1 (2025); 103-114 ; 2587-9596 ; 2541-9420

Subject Terms: окислительное фосфорилирование, mitochondria, mitochondrial dysfunction, mitochondrial DNA, mitochondrial respiration, oxidative phosphorylation, митохондрии, митохондриальная дисфункция, митохондриальная ДНК, дыхание митохондрий

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6

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Phosphorylation of Na+,K+-ATPase at Tyr10 of the α1-Subunit is Suppressed by AMPK and Enhanced by Ouabain in Cultured Kidney Cells

Authors: Metka Petrič, Anja Vidović, Klemen Dolinar, Katarina Miš, Alexander V. Chibalin, Sergej Pirkmajer

Source: J Membr Biol
The Journal of membrane biology. 2021. Vol. 254, № 5/6. P. 531-548

Access URL: https://link.springer.com/content/pdf/10.1007/s00232-021-00209-7.pdf
https://pubmed.ncbi.nlm.nih.gov/34748042
https://pubmed.ncbi.nlm.nih.gov/34748042/
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7

Academic Journal

Glyphosate treatment mediates the accumulation of small discrete 5′ and 3′-terminal fragments of 18S rRNA in plant cells ; Обработка глифосатом приводит к накоплению в клетках растений малых дискретных 5′и 3′-концевых фрагментов 18S рРНК

Authors: A. V. Zhigailov, A. S. Nizkorodova, K. O. Sharipov, N. S. Polimbetova, B. K. Iskakov, А. В. Жигайлов, А. С. Низкородова, К. О. Шарипов, Н. С. Полимбетова, Б. К. Искаков

Contributors: Current work was carried out in the framework of scientific grant AP14869357 and program OR11465447 funded by the Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan

Source: Vavilov Journal of Genetics and Breeding; Том 27, № 2 (2023); 93-98 ; Вавиловский журнал генетики и селекции; Том 27, № 2 (2023); 93-98 ; 2500-3259 ; 10.18699/VJGB-23-1

Subject Terms: голодание, 18S rRNA, discrete fragmentation, 40S ribosomal subunits, glyphosate, eIF2α phosphorylation, stress, starvation, 18S рРНК, дискретная фрагментация, 40S рибосомные субъединицы, глифосат, фосфорилирование eIF2α, стресс

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Relation: https://vavilov.elpub.ru/jour/article/view/3673/1687; Altschuler M., Mascarenhas J.P. Heat shock proteins and effects of heat shock in plants. Plant Mol. Biol. 1982;1(2):103115. DOI:10.1007/BF00024974.; Baird Th.D., Wek R.C. Eukaryotic initiation factor 2 phosphorylation and translational control in metabolism. Adv. Nutr. 2012;3:307321. DOI:10.3945/an.112.002113.; Ballard D.J., Peng H.Y., Das J.K., Kumar A., Wang L., Ren Y., Xiong X., Ren X., Yang J.M., Song J. Insights into the pathologic roles and regulation of eukaryotic elongation factor-2 kinase. Front. Mol. Biosci. 2021;8:839. DOI:10.3389/fmolb.2021.727863.; Browning K.S., Bailey-Serres J. Mechanism of cytoplasmic mRNA translation. Arabidopsis Book. 2015;13:e0176.; Chen Z., Sun Y., Yang X., Wu Z., Guo K., Niu X., Wang Q., Ruan J., Bu W., Gao S. Two featured series of rRNA-derived RNA fragments (rRFs) constitute a novel class of small RNAs. PLoS One. 2017;12: e0176458. DOI:10.1371/journal.pone.0176458.; EchevarriaZomeno S., Yanguez E., FernandezBautista N., Castro Sanz A.B., Ferrando A., Castellano M.M. Regulation of translation initiation under biotic and abiotic stresses. Int. J. Molec. Sci. 2013; 14:46704683. DOI:10.3390/ijms14034670.; Endo Y. Mechanism of action of ricin and related toxins on the inactivation of eukaryotic ribosomes. Cancer Res. Treat. 1988;37:7589. DOI:10.1007/978-1-4613-1083-9_5.; Gallie D.R., Le H., Caldwell C., Tanguay R., Hoang N.X., Brow ning K.S. The phosphorylation state of translation initiation factors is regulated developmentally and following heat shock in wheat. J. Biol. Chem. 1997;272:10461053. DOI:10.1074/jbc.272.2.1046.; Gallie D.R., Le H., Caldwell C., Browning K.S. Analysis of translation elongation factors from wheat during development and following heat shock. Biochem. Biophys. Res. Comm. 1998;245:295300. DOI:10.1006/bbrc.1998.8427.; Henras A.K., Plisson-Chastang C., O’Donohue M.F., Chakraborty A., Gleizes P.E. An overview of pre-ribosomal RNA processing in eukaryotes. Wiley Interdiscip. Rev. RNA. 2015;6(2):225242. DOI:10.1002/wrna.1269.; Hernandez G., Altmann M., Lasko P. Origins and evolution of the mechanisms regulating translation initiation in eukaryotes. Trends Biochem. Sci. 2010;35(2):6373. DOI:10.1016/j.tibs.2009.10.009.; Immanuel T.M., Greenwood D.R., MacDiarmid R.M. A critical review of translation initiation factor eIF2α kinases in plants – regulating protein synthesis during stress. Funct. Plant Biol. 2012;39(9):717 735. DOI:10.1071/FP12116.; Kamauchi S., Nakatani H., Nakano C., Urade R. Gene expression in response to endoplasmic reticulum stress in Arabidopsis thaliana. FEBS J. 2005;272(13):34613476. DOI:10.1111/j.17424658.2005.04770.x.; Kast A., Klassen R., Meinhardt F. rRNA fragmentation induced by a yeast killer toxin. Mol. Microbiol. 2014;91(3):606617. DOI:10.1111/mmi.12481.; Knutsen J.H., Rødland G.E., Bøe C.A., Håland T.W., Sunnerhagen P., Grallert B., Boye E. Stress-induced inhibition of translation independently of eIF2α phosphorylation. J. Cell Sci. 2015;128(23): 4420-4427. DOI:10.1242/jcs.176545.; Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227(5259):680685. DOI:10.1038/227680a0.; Lageix S., Lanet E., Pouch-Pelissier M.N., Espagnol M.C., Robaglia C., Deragon J.M., Pelissier T. Arabidopsis eIF2α kinase GCN2 is essential for growth in stress conditions and is activated by wounding. BMC Plant Biol. 2008;8:134. DOI:10.1186/147122298134.; Padgette S.R., Kolacz K.H., Delannay X., Re D.B., LaVallee B.J., Tinius C.N., Rhodes W.K., Otero Y.I., Barry G.F., Eichholtz D.A., Pesch ke V.M., Nida D.L., Taylor N.B., Kishore G.M. Development, identification and characterization of a Glyphosatetolerant soybean line. Crop Sci. 1995;35(5):14511461. DOI:10.3389/fpls.2016.01009.; Ruberti C., Kim S.J., Stefano G., Brandizzi F. Unfolded protein response in plants: one master, many questions. Curr. Opin. Plant Biol. 2015;27:5966. DOI:10.1016/j.pbi.2015.05.016.; Shaikhin S.M., Smailov S.K., Lee A.V., Kozhanov E.V., Iskakov B.K. Interaction of wheat germ translation initiation factor 2 with GDP and GTP. Biochimie. 1992;74(5):447454. DOI:10.1016/03009084(92)90085-s.; Smailov S.K., Lee A.V., Iskakov B.K. Study of phosphorylation of translation elongation factor 2 (EF-2) from wheat germ. FEBS Lett. 1993;321(23):219223. DOI:10.1016/00145793(93)801128.; Zhang Y., Wang Y., Kanyuka K., Parry M.A., Powers S.J., Halford N.G. GCN2-dependent phosphorylation of eukaryotic translation initiation factor-2alpha in Arabidopsis. J. Exp. Bot. 2008;59(11):3131 3141. DOI:10.1093/jxb/ern169.; Zhanybekova S.S., Polimbetova N.S., Nakisbekov N.O., Iskakov B.K. Detection of a new small RNA, induced by heat shock, in wheat seed ribosomes. Biochemistry (Moscow). 1996;61:862870.; Zhigailov A.V., Alexandrova A.M., Nizkorodova A.S., Stanbekova G.E., Kryldakov R.V., Karpova O.V., Polimbetova N.S., Halford N.G., Iskakov B.K. Evidence that Phosphorylation of the αsubunit of eIF2 does not essentially inhibit mRNA translation in wheat germ cell-free system. Front. Plant Sci. 2020;11:936. DOI:10.3389/fpls.2020.00936.; Zhigailov A.V., Polimbetova N.S., Borankul R.I., Iskakov B.K. Investigation of discrete fragmentation of 18S rRNA within 40S ribosomal subparticles of plant cells. Vestnik KazNU. Biological Series. 2013;2:8187. (in Russian); Zhigailov A.V., Polimbetova N.S., Doshchanov Kh.I., Iskakov B.K. Detection in plant cells of a new 75-nucleotide cytoplasmic RNA corresponding to the 5′terminal fragment of 18S RNA. Vestnik KazNU. Biological and Medical Series. 2014;1:191194. (in Russian); Yu Ch.Y., Cho Y., Sharma O., Kanehara K. What’s unique? The unfolded protein response in plants. J. Exp. Botany. 2021:erab513. DOI:10.1093/jxb/erab513.; https://vavilov.elpub.ru/jour/article/view/3673

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https://doi.org/10.18699/VJGB-23-13

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8

Academic Journal

DNA double-strand breaks in immunoinflammatory rheumatic diseases ; Двунитевые разрывы ДНК при иммуновоспалительных ревматических заболеваниях

Contributors: The investigation has been conducted within basic scientific topic № 1021051402790-6 "Study of immunopathology, diagnosis and therapy in the early stages of systemic rheumatic diseases.", Статья подготовлена в рамках фундаментальной темы № 1021051402790-6 «Изучение иммунопатологии, диагностики и терапии на ранних стадиях системных ревматических заболеваний».

Source: Modern Rheumatology Journal; Том 17, № 4 (2023); 13-18 ; Современная ревматология; Том 17, № 4 (2023); 13-18 ; 2310-158X ; 1996-7012

Subject Terms: р53-связывающий белок I, DNA double strand breaks, phosphorylation of histone H2AX, p53 binding protein I, двунитевые разрывы ДНК, фосфорилирование гистона H2AX

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Nat Rev Rheumatol. 2023 Apr;19(4): 200-211. doi:10.1038/s41584-022-00905-1. Epub 2023 Feb 7.; Passerini V, Ozeri-Galai E, de Pagter MS, et al. The presence of extra chromosomes leads to genomic instability. Nat Commun. 2016 Feb 15;7:10754. doi:10.1038/ncomms10754.; Chrzanowska K, Gregorek H, Dembowska-Baginska B, et al. Nijmegen breakage syndrome (NBS). Orphanet J Rare Dis. 2012 Feb 28;7:13. doi:10.1186/1750-1172-7-13.; Ванюшин БФ. Метилирование ДНК и эпигенетика. Генетика. 2006;42(9):985-997.; Кузьмина НС, Лаптева НШ, Русинова ГГ и др. Гиперметилирование промоторов генов в лейкоцитах крови человека в отдаленный период после перенесенного радиационного воздействия. Радиационная биология. Радиоэкология. 2017;(4):341-356.; Paull TT, Rogakou EP, Yamazaki V, et al. A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage. Curr Biol. 2000;10(15):886-95. doi:10.1016/s0960-9822(00)00610-2.; Sedelnikova OA, Pilch DR, Redon C, Bonner WM. Histone H2AX in DNA damage and repair. Cancer Biol Ther. 2003 May-Jun;2(3):233-5. doi:10.4161/cbt.2.3.373.; Pilch DR, Sedelnikova OA, Redon C, et al. Characteristics of gamma-H2AX foci at DNA double-strand breaks sites. Biochem Cell Biol. 2003 Jun;81(3):123-9. doi:10.1139/o03-042.; Turinetto V, Giachino C. Multiple facets of histone variant H2AX: a DNA double-strand-break marker with several biological functions. Nucleic Acids Res. 2015 Mar 11; 43(5):2489-98. doi:10.1093/nar/gkv061. Epub 2015 Feb 20.; Stucki M, Clapperton JA, Mohammad D, et al. MDC1 directly binds phosphorylated histone H2AX to regulate cellular responses to DNA double-strand breaks. Cell. 2005 Dec 29;123(7):1213-26. doi:10.1016/j.cell.2005.09.038.; Iwabuchi K, Basu BP, Kysela B, et al. Potential role for 53BP1 in DNA end-joining repair through direct interaction with DNA. J Biol Chem. 2003 Sep 19;278(38):36487-95. doi:10.1074/jbc.M304066200. Epub 2003 Jun 24.; Kuo LJ, Yang LX. Gamma-H2AX — a novel biomarker for DNA double-strand breaks. In Vivo. 2008 May-Jun;22(3):305-9.; Chowdury D, Keogh MC, Ishii H, et al. Y-H2AX dephosphorylation by protein phosphatase 2A facilitates DNA double-strand break repair. Mol Cell. 2005 Dec 9; 20(5):801-9. doi:10.1016/j.molcel.2005.10.003. Epub 2005 Nov 28.; Souliotis VL, Vlachogiannis NI, Pappa M, et al. DNA Damage Response and Oxidative Stress in Systemic Autoimmunity. Int J Mol Sci. 2019 Dec 20;21(1):55. doi:10.3390/ijms21010055.; Ferrucci, L, Fabbri E. Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty. Nat Rev Cardiol. 2018 Sep;15(9):505-522. doi:10.1038/s41569-018-0064-2.; Nastasi C, Mannarino L, D'Incalci M. DNA damage response and immune defense. Int J Mol Sci. 2020 Oct 12;21(20):7504. doi:10.3390/ijms21207504.; Alfano M. Aging, inflammation and DNA damage in the somatic testicular niche with idiopathic germ cell aplasia. Nat Commun. 2021 Sep 1;12(1):5205. doi:10.1038/s41467-021-25544-0.; Higo T. DNA single-strand break-induced DNA damage response causes heart failure. Nat Commun. 2017 Apr 24;8:15104. doi:10.1038/ncomms15104.; Saez GT. DNA Damage and Repair in Degenerative Diseases 2016. Int J Mol Sci. 2017 Jan 16;18(1):166. doi:10.3390/ijms18010166.; Klein B, Gunther C. Type I Interferon Induction in Cutaneous DNA Damage Syndromes. Front Immunol. 2021 Jul 23;12:715723. doi:10.3389/fimmu.2021.715723. eCollection 2021.; Burton DG. Faragher RG. Cellular senescence: from growth arrest to immunogenic conversion. Age (Dordr). 2015;37(2):27. doi:10.1007/s11357-015-9764-2. Epub 2015 Mar 20.; Souliotis VL, Sfikakis PP. Increased DNA double-strand breaks and enhanced apoptosis in patients with lupus nephritis. Lupus. 2015 Jul;24(8):804-15. doi:10.1177/0961203314565413. Epub 2014 Dec 26.; Souliotis VL, Vougas K, Gorgoulis VG, Sfikakis PP. Defective DNA repair and chromatin organization in patients with quiescent systemic lupus erythematosus. Arthritis Res Ther. 2016 Aug 4;18(1):182. doi:10.1186/s13075-016-1081-3.; Micheli C, Parma A, Tani C, et al. UCTD and SLE patients show increased levels of oxidative and DNA damage together with an altered kinetics of DSB repair. Mutagenesis. 2021 Nov 29;36(6):429-436. doi:10.1093/mutage/geab036.; Namas R, Renauer P, Ognenovski M, et al. Histone H2AX phosphorylation as a measure of DNA double-strand breaks and a marker of environmental stress and disease activity in lupus. Lupus Sci Med. 2016 Apr 29;3(1):e000148. doi:10.1136/lupus-2016-000148. eCollection 2016.; Rodier F, Coppe JP, Patil CK, et al. Persi-stent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion. Nat Cell Biol. 2009 Aug;11(8):973-9. doi:10.1038/ncb1909. Epub 2009 Jul 13.; Nakamura AJ, Redon CE, Bonner WM, Sedelnikova OA. Telomeredependent and telomere-independent origins of endogenous DNA damage in tumor cells. Aging (Albany NY). 2009 Feb 4;1(2):212-8. doi:10.18632/aging.100019.; Reddig A, Voss L, Guttek K, et al. Impact of Different JAK Inhibitors and Methotrexate on Lymphocyte Proliferation and DNA Damage. J Clin Med. 2021 Apr 1;10(7):1431. doi:10.3390/jcm10071431.

Availability: https://mrj.ima-press.net/mrj/article/view/1451
https://doi.org/10.14412/1996-7012-2023-4-13-18

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9

Academic Journal

Исследование условий фосфорилирования целлюлозы конденсированными фосфатами

Subject Terms: модифицированная целлюлоза, фосфор, огнестойкость фосфатов целлюлозы, фосфорнокислые растворы, фосфорные кислоты, фосфаты целлюлозы, обменная емкость целлюлозы, целлюлоза, конденсированные фосфаты, фосфаты, фосфорилирование целлюлозы, ортофосфорная кислота

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Access URL: https://elib.belstu.by/handle/123456789/52119

10

Conference

Фосфорилирование бетулина и его производных как путь синтеза перспективных биологически активных веществ

Subject Terms: БИОЛОГИЧЕСКИ АКТИВНЫЕ ВЕЩЕСТВА, ФОСФОРИЛИРОВАНИЕ, БЕТУЛИН, АЛОБЕТУЛИН, БЕТУЛОНОВЫЙ АЛЬДЕГИД

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Access URL: http://elar.urfu.ru/handle/10995/96930

11

Conference

Получение и молекулярный докинг производных диэтил(6-циано-5-оксо-7-арил-5H-тиазоло[3,2-a]пиримидин-3-ил)фосфонатов

Subject Terms: ТИАЗОЛО[3,2-A]ПИРИМИДИНЫ, МОЛЕКУЛЯРНЫЙ ДОКИНГ, ФОСФОРИЛИРОВАНИЕ, ДИЭТИЛХЛОРЭТИНФОСФОНАТ, АЦЕТИЛХОЛИНЭСТЕРАЗЫ

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12

Conference

Монофосфорилированные пиллар[5]арены как «умные» строительные блоки для конструирования наноразмерных структур

Subject Terms: ПИЛЛАР[5]АРЕН, ИНКАПСУЛЯЦИЯ, ФОСФОРИЛИРОВАНИЕ, КОМПЛЕКСООБРАЗОВАНИЕ, ПЭМ

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13

Academic Journal

RELATIONSHIP BETWEEN TYROSINE PHOSPHORYLATION AND CYTOKINE PRODUCTION BY NEUTROPHILS WITH DIFFERENT VARIANTS OF WOUND HEALING UNDER INSULIN RESISTANCE CONDITION

Authors: Сулаєва, O.

Source: Clinical anatomy and operative surgery; Vol. 6 No. 3 (2007); 23-26
Клиническая анатомия и оперативная хирургия; Том 6 № 3 (2007); 23-26
Клінічна анатомія та оперативна хірургія; Том 6 № 3 (2007); 23-26

Subject Terms: сахарный диабет, тирозиновое фосфорилирование, нейтрофилы, цитокины, diabetes mellitus, tyrosine phosphorylation, neutrophils, cytokines, цукровий діабет, тирозинове фосфорилування, нейтрофіли, цитокіни, 3. Good health

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Access URL: http://kaos.bsmu.edu.ua/article/view/253592

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14

Academic Journal

Effect of p38 MAPK on oxidative phosphorylation in regeneration of muscle tissue

Source: Nauchno-prakticheskii zhurnal «Patogenez». :66-70

Subject Terms: 0301 basic medicine, 0303 health sciences, 03 medical and health sciences, раневой процесс, wound process, oxidative phosphorylation, окислительное фосфорилирование, Oxphos, SB203580, myosatellite cell, миосателлиты, 3. Good health, р38 МАРК

Access URL: http://pathogenesis.pro/index.php/pathogenesis/article/download/237/205

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15

Academic Journal

Combined Preparation Based on Chelating Magnesium by Phosphorylated Casein. Characteristics of Its Syntesis

Authors: Palonko, R. (Roman), Arnauta, O. (Oleksii), Prys-Kadenko, V. (Victoriia), Smirnov, O. (Oleh), Kalachniuk, L. (Liliia)

Source: ScienceRise: Biological Science

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Relation: https://www.neliti.com/publications/527793/combined-preparation-based-on-chelating-magnesium-by-phosphorylated-casein-chara

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16

Academic Journal

Pathogenеsis of hepatorenal syndrome ; Патогенез гепаторенального синдрома ; Патогенез гепаторенального синдрому

Authors: Белявський, В., Роговий, Ю.

Source: Bukovinian Medical Herald; Vol. 14 No. 3 (55) (2010); 119-123 ; Буковинский медицинский вестник; Том 14 № 3 (55) (2010); 119-123 ; Буковинський медичний вісник; Том 14 № 3 (55) (2010); 119-123 ; 2413-0737 ; 1684-7903

Subject Terms: гепаторенальний синдром, вазодилатація, вазоконстрикція, тканинна гіпоксія, окиснення, фосфорилування, гепаторенальный синдром, вазодилатация, вазоконстрикция, тканевая гипоксия, окисление, фосфорилирование, hepatorenal syndrome, vasodilatation, vasoconstriction, tissue hypoxia, oxidation and phosphorylation

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Relation: http://e-bmv.bsmu.edu.ua/article/view/246292/243767

Availability: http://e-bmv.bsmu.edu.ua/article/view/246292

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17

Academic Journal

Pathogenеsis of hepatorenal syndrome

Source: Bukovinian Medical Herald; Vol. 14 No. 3 (55) (2010); 119-123
Буковинский медицинский вестник; Том 14 № 3 (55) (2010); 119-123
Буковинський медичний вісник; Том 14 № 3 (55) (2010); 119-123

Subject Terms: hepatorenal syndrome, vasodilatation, vasoconstriction, tissue hypoxia, oxidation and phosphorylation, гепаторенальний синдром, вазодилатація, вазоконстрикція, тканинна гіпоксія, окиснення, фосфорилування, гепаторенальный синдром, вазодилатация, вазоконстрикция, тканевая гипоксия, окисление, фосфорилирование, 3. Good health