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1Academic Journal
Authors: Sevostianova, O. Iu., Chistyakova, G. N., Remizova, I. I., Sevostianova, N. E., Byzova, T. E., Севостьянова, О. Ю., Чистякова, Г. Н., Ремизова, И. И., Севостьянова, Н. Е., Бызова, Т. Е.
Subject Terms: UTERINE LEIOMYOMA, REPRODUCTIVE AGE, LYMPHOCYTE POPULATIONS, T-LYMPHOCYTE SUBPOPULATIONS, PROINFLAMMATORY MEDIATORS, ЛЕЙОМИОМА МАТКИ, РЕПРОДУКТИВНЫЙ ВОЗРАСТ, ПОПУЛЯЦИИ ЛИМФОЦИТОВ, СУБПОПУЛЯЦИИ Т-ЛИМФОЦИТОВ, ПРОВОСПАЛИТЕЛЬНЫЕ МЕДИАТОРЫ
File Description: application/pdf
Relation: Scopus; http://elib.usma.ru/handle/usma/7192
Availability: http://elib.usma.ru/handle/usma/7192
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2Academic Journal
Authors: E. I. Ermolenko, I. V. Kudryavtsev, O. I. Solovyova, A. B. Karaseva, A. N. Tsapieva, Yu. D. Kondratenko, M. P. Kotyleva, M. K. Serebryakova, I. A. Shumikhina, A. N. Suvorov, Е. И. Ермоленко, И. В. Кудрявцев, О. И. Соловьева, А. Б. Карасева, А. Н. Цапиева, Ю. Д. Кондратенко, М. П. Котылева, М. К. Серебрякова, И. А. Шумихина, А. Н. Суворов
Contributors: The work is supported by the grant of RPF 16-1510085
Source: Medical Immunology (Russia); Том 22, № 2 (2020); 335-346 ; Медицинская иммунология; Том 22, № 2 (2020); 335-346 ; 2313-741X ; 1563-0625
Subject Terms: проточная цитометрия субпопуляции Т-лимфоцитов, metagenomic analysis, flow cytometry of a subpopulation of T lymphocytes, метагеномный анализ
File Description: application/pdf
Relation: https://www.mimmun.ru/mimmun/article/view/1905/1245; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5518; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5519; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5520; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5521; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5522; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5523; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5524; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5525; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5526; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5527; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5528; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5529; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5530; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5531; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5532; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5533; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5534; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5535; https://www.mimmun.ru/mimmun/article/downloadSuppFile/1905/5536; Akehurst R.L., Brazier J.E., Mathers N., O’Keefe C., Kaltenthaler E., Morgan A., Platts M., Walters S.J. Health-related quality of life and cost impact of irritable bowel syndrome in a UK primary care setting. Pharmacoeconomics, 2002, Vol. 20, no. 7, pp. 455-462.; Averina O.V., Ermolenko E.I., Ratushniy A.Yu., Tarasova E.A., Borschev Yu.Yu., Leontieva G.F., Kramskaya T.A., Kotyleva M.P., Danilenko V.N., Suvorov A.N. Effect of probiotics on the production of cytokines in the systems in vitro. Medical Immunology (Russia), 2015, Vol. 17, no. 5, pp. 443-454. doi:10.15789/1563-0625-2015-5-443-454.; Belmer S.V. Immunological aspects of irritable bowel syndrome. Physician, 2016, no. 8, pp. 14-18.; Chong P.P., Chin V.K., Looi C.Y., Wong W.F., Madhavan P, Yong V.C. The Microbiome and irritable bowel syndrome - a review on the pathophysiology, current research and future therapy. Front. Microbiol., 2019, Vol. 10, 1136. doi:10.3389/fmicb.2019.01136.; Drossman D.A., Hasler W.L. Rome IV - Functional GI disorders: disorders of gut-brain interaction. Gastroenterology, 2016, Vol. 150, no. 6, pp. 1257-1261.; Eeckhaut V, Machiels K., Perrier C., Romero C., Maes S., Flahou B., Steppe M., Haesebrouck F., Sas B., Ducatelle R., Vermeire S., van Immerseel F. Butyricicoccus pullicaecorum in inflammatory bowel disease. Gut, 2013, Vol. 62, no. 12, pp. 1745-1752.; Forshammar J., Isaksson S., Strid H., Stotzer P.O., Sjbvall H., Simren M., Ohman L. A pilot study of colonic B cell pattern in irritable bowel syndrome. Scand. J. Gastroenterol., 2008, Vol. 43, no. 12, pp. 1461-1466.; Golovkin A.S., Asadullina I.A., Kudryavtsev I.V. Purinergic regulation of basic physiological and pathological processes. Meditsinskaya immunologiya = Medical Immunology (Russia), 2018, Vol. 20, no. 4, pp. 463-476. doi:10.15789/1563-0625-2018-4-463-476.; Gonsalkorale W.M., Perrey C., Pravica V, Whorwell P.J., Hutchinson I.V. Interleukin 10 genotypes in irritable bowel syndrome: evidence for an inflammatory component? 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Resolution of Advisory council “How to improve treatment results functional dyspepsia and irritable bowel syndrome”? Russian Journal of Gastroenterology, Hepatology, Coloproctology, 2016, no. 2, pp. 101-104.; Kassinen A., Krogius-Kurikka L., Makivuokko H., Rinttila T., Paulin L., Corander J., Malinen E., Apajalahti J., Palva A. The fecal microbiota of irritable bowel syndrome patients differs significantly from that of healthy subjects. Gastroenterology, 2007, Vol. 133, no. 1, pp. 24-33.; Kim H.Y., Kim T.S., Kim B.H. Degradation of organic sulfur compounds and the reduction of dibenzothiophene to biphenyl and hydrogen sulfide by Desulfovibrio desulfuricans M6. Biotechnol. Let., 1990, Vol. 12, no. 10, pp. 761-764.; Khaydukov S.V., Baydun L.A., Zurochka A.V., Totolian Areg A. Standardized technology “Research of subpopulation composition of peripheral blood lymphocytes using pro-tread cytofluorimeters-analyzers” (Project). 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Reduction of butyrate-and methane-producing microorganisms in patients with Irritable Bowel Syndrome. Sci. Rep., 2015, Vol. 5, 12693. doi:10.1038/srep12693.; Rajilic-Stojanovic M., Biagi E., Heilig H.G., Kajander K., Kekkonen R.A., Tims S., de Vos W.M. Global and deep molecular analysis of microbiota signatures in fecal samples from patients with irritable bowel syndrome. Gastroenterology, 2011, Vol. 141, no. 5, pp. 1792-1801.; Rigsbee L., Agans R., Shankar V., Kenche H., Khamis H.J., Michail S., Paliy O. Quantitative profiling of gut microbiota of children with diarrhea-predominant irritable bowel syndrome. Am. J. Gastroenterol., 2012, Vol. 107, no. 11, pp. 1740-1751.; Rissiek A., Baumann I., Cuapio A., Mautner A., Kolster M., Arck P.C., Dodge-Khatami A., Mittrucker H.W., Koch-Nolte F., Haag F., Tolosa E. The expression of CD39 on regulatory T cells is genetically driven and further upregulated at sites of inflammation. J. Autoimmun., 2015, Vol. 58, pp. 12-20.; Rodes L., Khan A., Paul A., Coussa-Charley M., Marinescu D., Tomaro-Duchesneau C., Shao W., Kahouli I., Prakash S. Effect of probiotics Lactobacillus and Bifidobacterium on gut-derived lipopolysaccharides and inflammatory cytokines: an in vitro study using a human colonic microbiota model. J. Microbiol. Biotechnol., 2013, Vol. 23, pp. 518-526.; Sakaguchi S., Miyara M., Costantino C.M., Hafler D.A. FOXP3+ regulatory T cells in the human immune system. Nat. Rev. Immunol., 2010, Vol. 10, pp. 490-500.; Schirmer M., Smeekens S.P., Vlamakis H., Jaeger M., Oosting M., Franzosa E.A., Ter Horst R., Jansen T., Jacobs L., Bonder M.J., Kurilshikov A., Fu J., Joosten L.A.B., Zhernakova A., Huttenhower C., Wijmenga C., Netea M.G., Xavier R.J. Linking the human gut microbiome to inflammatory cytokine production capacity. Cell, 2016, Vol. 167, no. 4, pp. 1125-1136.; Sitkin S.I., Tkachenko E.I., Vakhitov T.Ya. Metabolic bowel dysbiosis and its biomarkers. Experimental and Clinical Gastroenterology, 2015, no. 12, pp. 6-29.; Smith P.M., Howitt M.R., Panikov N., Michaud M., Gallini C.A., Bohlooly-Y M., Glickman J.N., Garrett W.S. The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis. Science, 2013, Vol. 341, pp. 569-573.; Solovyova O.I., Simanenkov V.I., Suvorov A.N., Ermolenko E.I., Shumihina I.A., Svirido D.A. Use of probiotics and pre-probiotics in the treatment ofirritable bowel syndrome. Experimental and Clinical Gastroenterology (Russia), 2017, no. 7, pp. 115-120.; Suzuki D., Ueki A., Amaishi A., Ueki K. Desulfovibrio portus sp. nov., a novel sulfate-reducing bacterium in the class Deltaproteobacteria isolated from an estuarine sediment. J. Gen. Appl. Microbiol., 2009, Vol. 55, no. 2, pp. 125-133.; Tana C., Umesaki Y., Imaoka A., Handa T., Kanazawa M., Fukudo S. Altered profiles of intestinal microbiota and organic acids may be the origin of symptoms in irritable bowel syndrome. Neurogastroenterol. Motil., 2010, Vol. 22, no. 5, pp. 512-519.; Tap J., Derrien M., Tbrnblom H., Brazeilles R., Cools-Portier S., Dore J., Stbrsrud S., le Neve B., Ohman L., Simren M. Identification of an intestinal microbiota signature associated with severity of irritable bowel syndrome. Gastroenterology, 2017, Vol. 152, pp. 111-123.; Taras D., Simmering R., Collins M.D., Lawson P.A., Blaut M. Reclassification of Eubacterium formicigenerans Holdeman and Moore 1974 as Dorea formicigenerans gen. nov., comb. nov., and description of Dorea longicatena sp. nov., isolated from human faeces. Int. J. Syst. Evol. Microbiol., 2002, Vol. 52, Pt 2, pp. 423-428.; https://www.mimmun.ru/mimmun/article/view/1905
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3Academic Journal
Authors: Ivan G. Baltadzhiev, Pavel I. Pavlov
Source: Folia Medica, Vol 57, Iss 2, Pp 93-103 (2015)
Subject Terms: субпопуляции Т-лимфоцитов - абсолютное количество, Male, 0301 basic medicine, 2. Zero hunger, 0303 health sciences, средиземноморская пятнистая лихорадка, Mediterranean spotted fever, Middle Aged, Boutonneuse Fever, Lymphocyte Activation, Severity of Illness Index, MSF severity forms, Immunophenotyping, 3. Good health, T-lymphocyte subsets absolute counts, 03 medical and health sciences, корреляции с тяжестью заболевания, T-Lymphocyte Subsets, Medicine, Humans, Female, Lymphocyte Count, 10. No inequality, Immunologic Memory
Access URL: https://pubmed.ncbi.nlm.nih.gov/26933778
https://doaj.org/article/d3b2a20bd8ba476ca0c690aba4a8e369
https://europepmc.org/article/MED/26933778
https://content.sciendo.com/view/journals/folmed/57/2/article-p93.xml
https://pubmed.ncbi.nlm.nih.gov/26933778/
https://www.degruyter.com/view/j/folmed.2015.57.issue-2/folmed-2015-0026/folmed-2015-0026.xml
https://core.ac.uk/display/89645850
https://www.ncbi.nlm.nih.gov/pubmed/26933778 -
4Academic Journal
Authors: Andreychyn, Yu. M., Kovalenko, I. S.
Source: Pathologia; Vol. 14 No. 1 (2017): Pathologia ; Патология; Том 14 № 1 (2017): Патологія ; Патологія; Том 14 № 1 (2017): Патологія ; 2310-1237 ; 2306-8027
Subject Terms: maxillary sinusitis, adenomatous polyp, subpopulation of T-lymphocytes, macrophages, plasma cells, верхнечелюстной синусит, аденоматозный полип, субпопуляции Т-лимфоцитов, макрофаги, плазматические клетки, верхньощелепний синусит, аденоматозний поліп, субпопуляції Т-лімфоцитів, плазматичні клітини
Relation: http://pat.zsmu.edu.ua/article/view/97793/95722; http://pat.zsmu.edu.ua/article/view/97793
Availability: http://pat.zsmu.edu.ua/article/view/97793
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5Academic Journal
Authors: Менделеева, Л., Богданов, Рашит, Гальцева, И., Кузьмина, Л., Гапонова, Т., Гемджян, Э., Обухова, Т., Рисинская, Н., Калинин, Н., Паровичникова, Е., Савченко, В.
Subject Terms: ТРАНСПЛАНТАЦИЯ АЛЛОГЕННЫХ ГЕМОПОЭТИЧЕСКИХ СТВОЛОВЫХ КЛЕТОК, ТРАНСФУЗИИ ЛИМФОЦИТОВ ДОНОРА, ИНТЕРЛЕЙКИН-2, СУБПОПУЛЯЦИИ Т-ЛИМФОЦИТОВ, ВЫЖИВАЕМОСТЬ
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6
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7Academic Journal
Authors: Аутеншлюс, А., Коненков, В., Короткова, И., Иванова, Г., Сидоров, С., Черенкова, М., Проскура, А., Шевченко, А., Седова, Ю., Шкунов, А.
Subject Terms: ИММУНОГЕНЕТИКА,ФЕТАЛЬНЫЙ ПРОТЕИН,СУБПОПУЛЯЦИИ Т-ЛИМФОЦИТОВ
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8Academic Journal
Source: Гематология и трансфузиология.
Subject Terms: 03 medical and health sciences, 0302 clinical medicine, ТРАНСПЛАНТАЦИЯ АЛЛОГЕННЫХ ГЕМОПОЭТИЧЕСКИХ СТВОЛОВЫХ КЛЕТОК, ТРАНСФУЗИИ ЛИМФОЦИТОВ ДОНОРА, ИНТЕРЛЕЙКИН-2, СУБПОПУЛЯЦИИ Т-ЛИМФОЦИТОВ, ВЫЖИВАЕМОСТЬ, 3. Good health
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9Academic Journal
Source: Сибирский научный медицинский журнал.
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10Report
Subject Terms: лица с высоким риском развития СД-1, Fas-рецептор, subpopulations of T-lymphocytes, Fas-mediated apoptosis, individuals with а high risk of T1DM developing, flow cytometry, Fas-re-ceptor, Fas-ligand, 3. Good health, autoreactive T-lymphocytes, сахарный диабет 1 типа, Fas-лиганд, Fas-опосредованный апоптоз, аутореактивные Т-лимфоциты, проточная цитометрия, type 1 diabetes mellitus, субпопуляции Т-лимфоцитов
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11
Contributors: Власов Тимур Дмитриевич, Vlasov Timur Dmitrievic, Строев Юрий Иванович, Stroev Urij Ivanovic
Subject Terms: антитироидные (антитиреоидные) аутоантитела, аутоиммунный тироидит (тиреоидит), кортизол, лейкоцитарная формула, лимфома, лимфоциты, пролактин, субпопуляции Т-лимфоцитов, тироидные (тиреоидные) гормоны, тиротропин (тиреотропин), antithyroid autoantibodies, autoimmune thyroiditis, cortisol, leukocyte formula, lymphoma, lymphocytes, prolactin, t-lymphocyte subpopulations, thyroidic (thyroid) hormones, thyrotropin
Relation: 022691; http://hdl.handle.net/11701/26264
Availability: http://hdl.handle.net/11701/26264
