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1Academic Journal
Source: Школа-конференция молодых ученых, аспирантов и студентов «Генетические технологии в микробиологии и микробное разнообразие».
Subject Terms: трансдукция, рассеянный склероз, иммуноцитохимия, трансфекция, плазмиды, фактор роста нервов, лентивирус, нейродегенеративные заболевания
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2Academic Journal
Authors: T. A. Milyutina, Zh. V. Udalova, Т. А. Малютина, Ж. В. Удалова
Source: Russian Journal of Parasitology; Том 17, № 4 (2023); 501-509 ; Российский паразитологический журнал; Том 17, № 4 (2023); 501-509 ; 2541-7843 ; 1998-8435 ; 10.31016/1998-8435-2023-17-4
Subject Terms: РНК-интерференция, flp genes, nematode locomotion, root-knot nematodes, nervous system, immunocytochemistry, RNA-interference, flp гены, локомоции нематод, галловые нематоды, нервная система, иммуноцитохимия
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Relation: https://vniigis.elpub.ru/jour/article/view/1094/788; Малютина Т. А., Воронин М. В. FMRFамидподобные нейропептиды – модуляторы локомоторных реакций у растительных цистообразующих паразитических нематод // Российский паразитологический журнал. 2022; Т. 16. № 1. С. 50-62. https://doi.org/10.31016/1998-8435-2022-16-1-50-62; Зиновьева С. В. Общая характеристика фитопаразитических нематод / В кн. «Фитопаразитические нематоды растений»; под ред. Зиновьевой С. В., Чижова В. Н. Москва: Товарищество научных изданий KMK, 2012. С. 10–45.; Abad P., Gouzy J. M. et al. Genome sequence of the metazoan plant-parasitic nematode Meloidogyne incognita. Nature Biotechnology. 2008; 26: 909-915. https://doi.org/10.1038/nbt.1482.; Atkinson L. E., Stevenson M., Mckoy C. J., Marks N. J., Fleming C., Zamanian M., Day T. A., Kimber M. J., Maule A. G., Mousley A. Flp-32 Ligand/receptor silencing phenocopy faster plant pathogenic nematodes. PLoS Pathogens. 2013; 9 (2): 1003169. https://doi.org/10.1371/joumal.ppat.1003169.; Holden-Dye L., Walrer R. J. Neurobiology of plant parasitic nematodes. Invertebrate Neurosciences. 2011; 11. 9-11. https://doi.org/10.1007/s10158-011-0117-2.; Johnston M. J. G., Veigh P. M., Masler S., Fleming C. C., Maule A. G. FMRFamide-like peptides in rootknot nematodes and their potential role in nematode physiology. Journal of Helminthology. 2010; 84 (3): 253-265. https://doi.org/10.1017/S0022149X09990630.; Kimber M. J., Fleming C. C. Neuromuscular function in plant parasitic nematodes: a target for novel control stratеgies? Parasitology. 2005; 131 (l): 129-142. https://doi.org/10.1017/S0031182005009157.; Kimber M. J., Fleming C. C., Bjourson A. J., Halton D. W., Maule A. G. FMRFavmide-related peptides in potato cyst nematodes. Molecular and Biochemical Parasitology. 2001; 116 (2): 199-208. https://doi.org/10.1016/s0166-6851(01)00323-1; Kumari C., Dutta T. K., Banakar P., Rao U. Сomparing the defense related gene expression changes upon root-knot attack in susceptible versus resistant kultivars of rice. Scientific Reports. 2016; 6: 22846. https://doi.org/10.1038/srep22846; Kumari С., Tushar K. Dutta, Sonam Chaudhary, Prakash Banakar, Pradeep K. Papolu, Uma Rao. Molecular characterization of FMRFamide-like peptides in Meloidogyne graminicola and analysis of their knockdown effect on nematode infectivity. Gene. 2017; 619: 50-60. https://doi.org/10.1016/j.gene.2017.03.042; Martin R. J., Robertson A. P. Control of nematode parasites with agents acting on neuro-musculature systems: lessons for neuropeptide ligand discovery. Advances in Experimental Medicine and Biology. 2010; 692: 138-154. https://doi.org/10.1007/978-1-4419-6902-6_7.; Masler E. P. Behaviour of Heterodera glycines and Meloidogyne incognita infective juveniles exposed to nematode FMRFamide-lice peptides in vitro. Nematology. 2012; 14 (5): 605-612. https://doi.org/10.1163/156854111X617879; Maule A. G., Mousley A., Marks N. J., Day T. A., Thompson D. P., Geary T. G., Halton D. W. Neuropeptide signaling systems – potential drug targets for parasite and pest control. Current Topics in Medicinal Chemistry. 2002; 2: 733–758. https://doi.org/10.2174/1568026023393697; McCoy C. J. , Atkinson L. E. , Mostafa Zamanian, Paul McVeigh, Tim A Day, Michael J. Kimber, Nikki J. Marks, Aaron G. Maule, Angela Mousley. New insights into the FLPergic complements of parasitic nematodes: Informing diaphanization approaches. EuPA Open Proteomics. 2014; 3: 262-272. https://doi.org/10.1016/j.euprot.2014.04.002; Mertens Inge, Anick Vandingenen, Tom Meeusen, Tom Janssen, Walter Luyten, Ronald J. Nachman, Arnold De Loof, Liliane Schoofs. Functional characterization of the putative orphan neuropeptide G-protein coupled receptor C26F1.6 in Caenorhabditis elegans. FEBS Letters. 2004; 573 (1-3): 55-60.; Papolu P. K., Gantasala N. P., Kamaraju D., Banakar P., Sreevathsa R., Rao. Utility of host delivered RNAI of two FMRFamide like peptides, flp-14 and flp-18, for the management of root-knot nematode, Meloidogyne incognita. PloS ONE 2013; 8 (11): e80603. https://doi.org/10.1371/journal.pone.0080603.; Peymen K., Watteyne J., Frooninckx L., Schoofs L., Beets I. The FMRFamide-like peptide family in nematodes. Frontiers in endocrinology. 2014; 90 (5): 1-21. https://doi.org/10.3389/fendo.2014.00090; Sasser J. N. Root-knot nematodes: a global menace to crop production. Plant Disease. 1980; 64: 36-41.; Singh S., Singh B., Singh A. P. Nematodes: A threat to sustainability of agriculture. Procedia Environmental Sciences. 2015; 29: 215–216. https://doi.org/10.1016/j.proenv.2015.07.270.; White J. D., Southgate E., Thompson J. N., Brenner S. The structure of the nervous system of Caenorhabditis elegans. Philosoph. Transactions of the Royal Society of London. 1985; Series B 314, 1-340.; https://vniigis.elpub.ru/jour/article/view/1094
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3Academic Journal
Authors: A.Yu. Tsygankov, S.V. Saakyan, M.G. Zhiltsova, V.V. Valskiy
Source: Российский офтальмологический журнал, Vol 11, Iss 1, Pp 17-23 (2018)
Subject Terms: 0301 basic medicine, иммуноцитохимия, рецепторы прогестерона, estrogen receptors, RE1-994, увеальная меланома, 3. Good health, Ophthalmology, 03 medical and health sciences, immunocytochemistry, 0302 clinical medicine, рецепторы эстрогена, progesterone receptors, cytology, uveal melanoma, цитология
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4Academic Journal
Authors: Kebalo, D. I., Miroshnykova, N. P., Shershniova, O. P., Pashchenko, S. M., Zvantseva, E. D.
Source: Zaporozhye Medical Journal; Vol. 22 No. 3 (2020) ; Запорожский медицинский журнал; Том 22 № 3 (2020) ; Запорізький медичний журнал; Том 22 № 3 (2020) ; 2310-1210 ; 2306-4145
Subject Terms: молочна залоза, маркери, імуноцитохімія, mammary gland, biochemical tumor markers, immunocytochemistry, молочная железа, онкомаркеры, иммуноцитохимия
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Relation: http://zmj.zsmu.edu.ua/article/view/204917/205982; http://zmj.zsmu.edu.ua/article/view/204917
Availability: http://zmj.zsmu.edu.ua/article/view/204917
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5Academic Journal
Authors: I. O. Bogolyubova, Z. K. Sailau, D. S. Bogolyubov, И. О. Боголюбова, Ж. К. Сайлау, Д. С. Боголюбов
Source: Vavilov Journal of Genetics and Breeding; Том 23, № 2 (2019); 129-134 ; Вавиловский журнал генетики и селекции; Том 23, № 2 (2019); 129-134 ; 2500-3259
Subject Terms: иммуноцитохимия, pre-implantation mouse embryos, immunocytochemistry, доимплантационные эмбрионы мыши
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Relation: https://vavilov.elpub.ru/jour/article/view/1923/1189; Banani S.F., Lee H.O., Hyman A.A., Rosen M.K. Biomolecular condensates: organizers of cel-lular biochemistry. Nat. Rev. Mol. Cell Biol. 2017;18(5):285-298. DOI 10.1038/nrm.2017.7. Bogolyubova I.O. Transcriptional activity of nuclei in 2-cell blocked mouse embryos. Tissue Cell. 2011;43(4):262-265. DOI 10.1016/j.tice.2011.03.005.; Bogolyubova I.O. Comparative analysis of the fluorescent labeling pattern of nuclei of early mouse embryos by using antibodies to various actin molecule domains. Cell Tiss. Biol. 2013;7(1):37-42. DOI 10.1134/S1990519X13010033.; Bogolyubova I.O., Bogolyubov D.S. An immunocytochemical study of interchromatin granule clusters in early mouse embryos. Biomed. Res. Int. 2013;2013:931564. DOI 10.1155/2013/ 931564.; Bogolyubova I.O., Bogolyubov D.S. Nuclear distribution of RNA polymerase II and mRNA processing machinery in early mammalian embryos. Biomed. Res. Int. 2014;2014:681596. DOI 10.1155/2014/681596.; Bogolyubova I.O., Bogolyubov D.S. Combined detection of newly synthesized RNA and nuclear proteins at the ultrastructural level: a modification of the protocol for immunoelectron micros¬copy. Cell Tiss. Biol. 2018;12(6):517-522. DOI 10.1134/S1990519X18060020.; Bogolyubova N.A., Bogolyubova I.O. Actin localization in nuclei of two-cell mouse embryos. Cell Tiss. Biol. 2009;3(5):417-422. DOI 10.1134/S1990519X09050034.; Burton A., Torres-Padilla M.E. Epigenetic reprogramming and development: a unique hetero-chromatin organization in the preimplantation mouse embryo. Brief. Funct. Genomics. 2010; 9(5-6):444-454. DOI 10.1093/bfgp/elq027.; Cho E.J., Kim J.S. Crowding effects on the formation and maintenance of nuclear bodies: in-sights from molecular-dynamics simulations of simple spherical model particles. Biophys. J. 2012;103(3):424-433. DOI 10.1016/j.bpj.2012.07.007.; Courchaine E.M., Lu A., Neugebauer K.M. Droplet organelles? EMBO J. 2016;35(15):1603- 1612. DOI 10.15252/embj.201593517.; Fadloun A., Le Gras S., Jost B., Ziegler-Birling C., Takahashi H., Gorab E., Carninci P., Torres- Padilla M.E. Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNA. Nat. Struct. Mol. Biol. 2013;20(3):332-338. DOI 10.1038/ nsmb.2495.; Ferreira J., Carmo-Fonseca M. The biogenesis of the coiled body during early mouse develop-ment. Development. 1995;121(2):601-612.; Geuskens M., Alexandre H. Ultrastructural and autoradiographic studies of nucleolar develop-ment and rDNA transcription in preimplantation mouse embryos. Cell Differ. 1984;14(2): 125-134.; Gomes E., Shorter J. The molecular language of membraneless organel¬les. J. Biol. Chem. 2018. DOI 10.1074/jbc.TM118.001192.; Hamdane N., Tremblay M.G., Dillinger S., Stefanovsky V.Y., Ne¬meth A., Moss T. Disruption of the UBF gene induces aberrant so¬matic nucleolar bodies and disrupts embryo nucleolar precursor bo¬dies. Gene. 2017;612:5-11. DOI 10.1016/j.gene.2016.09.013.; Kopecny V, Flechon J.-E., Camous S., Fulka J.Jr. Nucleologenesis and the onset of transcription in the eight-cell bovine embryo: fine struc¬tural autoradiographic study. Mol. Reprod. Dev. 1989;1(2):79-90. DOI 10.1002/mrd.1080010202.; Lanctot C., Cheutin T., Cremer M., Cavalli G., Cremer T. Dynamic ge-nome architecture in the nuclear space: regulation of gene expres-sion in three dimensions. Nat. Rev. Genet. 2007;8(2):104-115. DOI 10.1038/nrg2041.; Li E. Chromatin modification and epigenetic reprogramming in mam-malian development. Nat. Rev. Genet. 2002;3(9):662-673. DOI 10.1038/nrg887.; Martin C., Beaujean N., Brochard V., Audouard C., Zink D., Debey P. Genome restructuring in mouse embryos during reprogramming and early development. Dev. Biol. 2006;292(2):317-332. DOI 10.1016/j. ydbio.2006.01.009.; Mason K., Liu Z., Aguirre-Lavin T., Beaujean N. Chromatin and epi-genetic modifications during early mammalian development. Anim. Reprod. Sci. 2012;134(1-2):45-55. DOI 10.1016/j.anireprosci.2012. 08.010.; Meglicki M., Teperek-Tkacz M., Borsuk E. Appearance and hetero-chromatin localization of HP1a in early mouse embryos depends on cytoplasmic clock and H3S10 phosphorylation. Cell Cycle. 2012; 11(11):2189-2205. DOI 10.4161/cc.20705.; Probst A.V., Santos F., Reik W., Almouzni G., Dean W. Structural dif¬ferences in centromeric heterochromatin are spatially reconciled on fertilization in the mouse zygote. Chromosoma. 2007;116(4):403- 415. DOI 10.1007/s00412-007-0106-8.; Rajendra T.K., Praveen K., Matera A.G. Genetic analysis of nuclear bodies: from nondeterministic chaos to deterministic order. Cold Spring Harb. Symp. Quant. Biol. 2010;75:365-374. DOI 10.1101/ sqb.2010.75.043.; Richter K., Nessling M., Lichter P. Macromolecular crowding and its potential impact on nuclear function. Biochim. Biophys. Acta. 2008; 1783(11):2100-2107. DOI 10.1016/j.bbamcr.2008.07.017.; Romanova L., Korobova F., Noniashvilli E., Dyban A., Zatsepina O. High resolution mapping of ribosomal DNA in early mouse embryos by fluorescence in situ hybridization. Biol. Reprod. 2006;74(5):807- 815. DOI 10.1095/biolreprod.105.047340.; Sailau Z.K., Bogolyubov D.S., Bogolyubova I.O. Nuclear distribution of the chromatin-remodeling protein ATRX in mouse early embryo- genesis. Acta Histochem. 2017;119(1):18-25. DOI 10.1016/j.acthis. 2016.11.001.; Santenard A., Ziegler-Birling C., Koch M., Tora L., Bannister A.J., Tor- res-Padilla M.E. Heterochromatin formation in the mouse embryo requires critical residues of the histone variant H3.3. Nat. Cell Biol. 2010;12(9):853-862. DOI 10.1038/ncb2089.; Sawyer I.A., Bartek J., Dundr M. Phase separated microenvironments inside the cell nucleus are linked to disease and regulate epigenetic state, transcription and RNA processing. Semin. Cell Dev. Biol. 2018a. DOI 10.1016/j.semcdb.2018.07.001.; Sawyer I.A., Sturgill D., Dundr M. Membraneless nuclear organelles and the search for phases within phases. Wiley Interdiscip. Rev. RNA. 2018b;e1514. DOI 10.1002/wrna.1514.; Stanek D., Fox A.H. Nuclear bodies: new insights into structure and function. Curr. Opin. Cell Biol. 2017;46:94-101. DOI 10.1016/j.ceb. 2017.05.001.; Tesank J., Kopecny V, Plachot M., Mandelbaum J. Activation of nuc-leolar and extranucleolar RNA synthesis and changes in the ribo- somal content of human embryos developing in vitro. J. Reprod. Fertil. 1986а;78(2):463-470.; Tesank J., Kopecny V., Plachot M., Mandelbaum J., Dalage C., Flechon J.-E. Nucleologenesis in the human embryo developing in vitro: ultrastructural and autoradiographic analysis. Dev. Biol. 1986b;115(1):193-203.; Wang C., Liu X., Gao Y., Yang L., Li C., Liu W., Chen C., Kou X., Zhao Y., Chen J., Wang Y., Le R., Wang H., Duan T., Zhang Y., Gao S. Reprogramming of H3K9me3-dependent heterochromatin during mammalian embryo development. Nat. Cell Biol. 2018;20(5):620- 631. DOI 10.1038/s41556-018-0093-4.; Zatsepina O., Baly C., Chebrou M., Debey P. The step-wise assem¬bly of a functional nucleolus in preimplantation mouse embryos in-volves the Cajal (coiled) body. Dev. Biol. 2003;253(1):66-83.; Zhu L., Brangwynne C.P. Nuclear bodies: the emerging biophysics of nucleoplasmic phases. Curr. Opin. Cell Biol. 2015;34:23-30. DOI 10.1016/j.ceb.2015.04.003; https://vavilov.elpub.ru/jour/article/view/1923
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6Academic Journal
Authors: A. B. Villert, L. A. Kolomiets, N. V. Yunusova, A. A. Ivanova, А. Б. Виллерт, Л. А. Коломиец, Н. В. Юнусова, А. А. Иванова
Source: Siberian journal of oncology; Том 18, № 1 (2019); 116-123 ; Сибирский онкологический журнал; Том 18, № 1 (2019); 116-123 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2019-18-1
Subject Terms: иммуноцитохимия, ovarian cancer, visualization, ascite components, prognosis, pathogenesis, mesothelial cells, peritoneal carcinogenesis, ultrasound, immunocytochemistry, рак яичников, визуализация, компоненты асцита, прогноз, патогенез, мезотелиальные клетки, перитонеальный канцерогенез, ультразвуковое исследование
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Nat Rev Cancer. 2013 Apr; 13 (4): 273–82. doi:10.1038/nrc3432.; Starling E.H. On the absorption of fluids from the connective tissue spaces. J Physiol. 1896 May 5; 19 (4): 312–26.; Senger D.R., Galli S.J., Dvorak A.M., Perruzzi C.A., Harvey V.S., Dvorak H.F. Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid. Science. 1983 Feb 25; 219 (4587): 983–5.; Степанов И.В., Падеров Ю.М., Афанасьев С.Г. Перитонеальный канцероматоз. Сибирский онкологический журнал. 2014; 5: 45–53. [Stepanov I.V., Paderov Yu.M., Afanasyev S.G. Peritoneal carcinomatosis. Siberian Journal of Oncology. 2014; 5: 45–53. (in Russian)].; European Association for the Study of the Liver. EASL clinical practice guidelines on the management of ascites, spontaneous bacterial peritonitis, and hepatorenal syndrome in cirrhosis. J Hepatol. 2010 Sep; 53 (3): 397–417. doi:10.1016/j.jhep.2010.05.004.; Ивашкин В.Т. Гастроэнтерология: национальное руководство. М., 2008. 704. [Ivashkin V.T. Gastroenterology: National Guideline. Mos‐ cow, 2008. 704. (in Russian)].; Ардатская М.Д. Асцит и перитонит в практике терапевта и гастроэнтеролога. Consilium Medicum. 2009; 11 (8): 51–60. [Ardatskaya M.D. Ascites and peritonitis in the practice of therapist and gastro‐ enterologist. Consilium Medicum. 2009; 11 (8): 51–60. (in Russian)].; Inadomi J., Cello J.P., Koch J. Ultrasonographic determination of ascitic volume. Hepatology. 1996 Sep; 24 (3): 549–51. doi:10.1002/ hep.510240314.; Болдогоева И.М., Берзин С.А. Современные возможности диагностики рака яичников в онкологическом диспансере. Екатеринбург, 2007: 34–52. [Boldogoyeva I.M., Berzin S.A. Modern possibilities of diagnosis of ovarian cancer in the oncologic dispensary. Yekaterinburg, 2007. 34–52. (in Russian)].; Синицина М.Е., Чекалова М.А., Брюзгин В.В., Махова Е.Е. Место эхографии в уточнении подходов к лечению рака яичников. Опухоли женской репродуктивной системы. 2008; 4: 72–76. [Sinitsina M.Ye., Chekalova M.A., Bryuzgin V.V., Makhova Ye.Ye. Place of echography in specifying approaches to treating ovarian cancer. Tumors of female reproductive system. 2008; 4: 72–76. (in Russian)].; Степанов С.О., Митина Л.А., Гуц О.В., Беспалов П.Д. Визуализация перитонеальной диссеминации при ультразвуковом исследовании. Лучевая диагностика и терапия. 2013; 3 (4): 66–70. [Stepanov S.O., Mitina L.A., Guts O.V., Bespalov P.D. Ultrasound imaging of peritoneal dissemination. Diagnostic radiology and radiotherapy. 2013; 3 (4): 66–70. (in Russian)].; Вяткина Н.В., Фролова И.Г., Коломиец Л.А., Молчанов С.В., Виллерт А.Б. Возможности комплексного ультразвукового исследо‐ вания в дооперационном стадировании диссеминированного рака яичников. Сибирский онкологический журнал. 2016; 15 (4): 26–32. [Vyatkina N.V., Frolova I.G., Kolomiets L.A., Molchanov S.V., Villert А.B. Diagnostic value of ultrasound examination in preoperative staging of disseminated ovarian cancer. 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Impact of ascites volume on clinical outcomes in ovarian cancer: A cohort study. Gynecol Oncol. 2017 Sep; 146 (3): 491–497. doi:10.1016/j. ygyno.2017.06.008.; Tan D.S., Agarwal R., Kaye S.B. Mechanisms of transcoelomic metastasis in ovarian cancer. Lancet Oncol (2006) 7 (11): 939–1. doi:10.1016/S1470‐2045(06)70939‐1.; Lazarov N., Lazarov L., Lazarov S. Role of ascites and peritoneal cytology as prognostic factor for a patients with early epithelial ovarian cancer. Trakia Journal of Sciences. 2013; 11 (4): 359–361.; Chan J.K., Tian C., Monk B.J., Herzog T., Kapp D.S., Bell J., Young R.C.; Gynecologic Oncology Group. Prognostic factors for high‐ risk early‐stage epithelial ovarian cancer. Cancer. 2008 May 15; 112 (10): 2202–10. doi:10.1002/cncr.23390.; Kolomainen D.F., A’Hern R., Coxon F.Y., Fisher C., King D.M., Blake P.R., Barton D.P., Shepherd J.H., Kaye S.B., Gore M.E. Can patients with relapsed, previously untreated, stage I epithelial ovarian cancer be successfully treated with salvage therapy? J Clin Oncol. 2003; 21 (16): 3113–8. doi:10.1200/JCO.2003.06.119.; Puls L.E., Duniho T., Hunter J.E., Kryscio R., Blackhurst D., Gallion H. The Prognostic Implication of Ascites in Advanced‐Stage Ovarian Cancer. Gynecol Oncol. 1996 Apr; 61 (1): 109–12.; Feigenberg T., Clarke B., Virtanen C., Plotkin A., Letarte M., Rosen B., Bernardini M.Q., Kollara A., Brown T.J., Murphy K.J. Molecu‐ lar profiling and clinical outcome of high‐Grade serous ovarian cancer presenting with low‐versus high‐volume ascites. Biomed Res Int. 2014; 2014: 367103. doi:10.1155/2014/367103.; Kim S., Kim B., S. Song Y. Ascites modulates cancer cell behavior, contributing to tumor heterogeneity in ovarian cancer. Cancer Sci. 2016 Sep; 107 (9): 1173–8. doi:10.1111/cas.12987.; Latifi A., Luwor R.B., Bilandzic M., Nazaretian S., Stenvers K., Pyman J., Zhu H., Thompson E.W., Quinn M.A., Findlay J.K., Ahmed N. Isolation and characterization of tumor cells from the ascites of ovarian cancer patients: molecular phenotype of chemoresistant ovarian tumors. PLoS One. 2012; 7 (10): e46858. doi:10.1371/journal.pone.0046858.; Shield K., Ackland M.L., Ahmed N., Rice G.E. Multicellular spher‐ oids in ovarian cancer metastases: Biology and pathology. Gynecol Oncol. 2009 Apr; 113 (1): 143–8. doi:10.1016/j.ygyno.2008.11.032.; Naora H., Montell D.J. Ovarian cancer metastasis: integrating insights from disparate model organisms. Nat Rev Cancer. 2005 May; 5 (5): 355–66. doi:10.1038/nrc1611.; Ahmed N., Thompson E.W., Quinn M.A. Epithelial‐mesenchymal interconversions in normal ovarian surface epithelium and ovarian carci‐ nomas: an exception to the norm. J Cell Physiol. 2007; 213 (3): 581–8. doi:10.1002/jcp.21240.; Stanojevic Z., Rancic G., Radic S., Potic-Zecevic N., Dorðevic B., Markovic M., Todorovska I. Pathogenesis of malignant ascites in ovarian cancer patients. Arch Oncol 2004; 12 (2): 115–8.; Ho C.M., Chang S.F., Hsiao C.C., Chien T.Y., Shih D.T. Isolation and characterization of stromal progenitor cells from ascites of patients with epithelial ovarian adenocarcinoma. J Biomed Sci. 2012 Feb 14; 19: 23. doi:10.1186/1423‐0127‐19‐23.; Ahmed N., Stenvers K.L. Getting to know ovarian cancer ascites: opportunities for targeted therapy‐based translational research. Front Oncol. 2013 Sep 25; 3: 256. doi:10.3389/fonc.2013.00256.; Wintzell M., Hijerpe E., Avall Lundqvist E., Shoshan M. Protein markers of cancer‐associated fibroblasts and tumor‐initiating cells reveal subpopulations in freshly isolated ovarian cancer ascites. BMC Cancer. 2012 Aug 18; 12: 359. doi:10.1186/1471‐2407‐12‐359.; Guo L., Guo N. Exosomes: potent regulators of tumor malignancy and potential bio‐tools in clinical application. Crit Rev Oncol Hematol. 2015 Sep; 95 (3): 346–58. doi:10.1016/j.critrevonc.2015.04.002.; Halkia E., Chrelias G., Chrelias C., Esquivel J. Update on Ovarian Cancer Peritoneal Carcinomatosis Multimodal‐Treatment Con‐ siderations. Gastroenterol Res Pract. 2018 Apr 5; 2018: 5284814. doi:10.1155/2018/5284814.; Janagam C., Atla B. Study of ascitic fluid cytology in ovarian tumors. Int J Res Med Sci. 2017 Dec; 5 (12): 5227–31. doi:10.18203/2320‐ 6012.ijrms20175382.; Юнусова Н.В., Тамкович С.Н., Кондакова И.В. Экзосомы в раз‐ личных биологических жидкостях: состав и функции. Молекулярная медицина. 2017; 15 (4): 14–22. [Yunusova N.V., Tamkovich S.N., Kondakova I.V. Exosomes from various biological fluids: pattern and function. Molecular medicine. 2017; 15 (4): 14–22. (in Russian)].; Yunusova N.V., Tamkovich S.N., Stakheeva M.N., Grigor’eva A.A., Somov A.K., Tugutova E.A., Kolomiets L.A., Molchanov S.V., Afanas’ev S.G., Kakurina G.V., Choinzonov E.L., Kondakova I.V. The characterization of exosomes from biological fluids of patients with different types of cancer. AIP Conference Proceedings 1882; 2017: 020080. doi:10.1063/1.5001659.; https://www.siboncoj.ru/jour/article/view/969
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7Academic Journal
Authors: D. K. Matveeva, E. R. Andreeva, L. B. Buravkova, Д. К. Матвеева, Е. Р. Андреева, Л. Б. Буравкова
Source: Vestnik Moskovskogo universiteta. Seriya 16. Biologiya; Том 74, № 4 (2019); 294–300 ; Вестник Московского университета. Серия 16. Биология; Том 74, № 4 (2019); 294–300 ; 0137-0952
Subject Terms: сканирующая электронная микроскопия, extracellular matrix, decellularization, regenerative medicine, immunocytochemistry, scanning electron microscopy, внеклеточный матрикс, децеллюляризация, регенеративная медицина, иммуноцитохимия
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Relation: https://vestnik-bio-msu.elpub.ru/jour/article/view/798/492; Parekkadan B., Milwid J.M. Mesenchymal stem cells as therapeutics // Annu. Rev. Biomed. Eng. 2010. Vol. 12. P. 87-117.; Schraufstatter I.U., Discipio R.G., Khaldoyanidi S. Mesenchymal stem cells and their microenvironment // Front. Biosd. 2011. Vol. 16. P. 2271-2288.; Gattazzo F, Urduolo A., Bonaldo P. Extracellular matrix: a dynamic microenvironment for stem cell niche // Bioсhim. Biophys. Aсta. 2014. Vol. 1840. N 8. P. 2506-2519.; Lu H, Hoshiba T, Kawazoe N, Chen G. Autologous extracellular matrix scaffolds for tissue engineering // Biomaterials. 2011. Vol. 32. N 10. P. 2489-2499.; Hynes R.O. The extracellular matrix: not just pretty fibrils // Sсienсe. 2010. Vol. 326. N 5957. P. 1216-1219.; Joddar B, Hoshiba T, Chen G., Ito Y. Stem cell culture using cell-derived substrates // Biomater. Sd. 2014. Vol. 2. N 11. P. 1595-1603.; Hoshiba T, Lu H, Kawazoe N, Chen G. Decellularized matrices for tissue engineering // Expert Opin. Biol. Ther. 2010. Vol. 10. N 12. P. 1717-1728.; Noth U, Rackwitz L, Steinert A.F., Tuan R.S. Cell delivery therapeutics for musculoskeletal regeneration // Adv. Drug. Deliv. Rev. 2010. Vol. 62. N 7-8. P. 765-783.; Bornstein P, Duksin D, Balian G., Davidson J.M., Сгouoh E. Organization of extracellular proteins on the connective tissue cell surface: relevance to cell-matrix interactions in vitro and in vivo // Ann. N.Y. Aсad. Sсi. 1978. Vol. 312. P. 93-105.; Crapo P.M., Gilbert T.W., Badylak S.F. An overview of tissue and whole organ decellularization processes // Biomaterials. 2011. Vol. 32. N 12. P. 3233-3243.; Harvey A., Yen T, Aizman I., Tate С, Case С. Proteomic analysis of the extracellular matrix produced by mesenchymal stromal cells: implications for cell therapy mechanism // PLoS One. 2013. Vol. 8. N 11: e79283.; Lin H, Yang G, Tan J, Tuan R.S. Influence of decellularized matrix derived from human mesenchymal stem cells on their proliferation, migration and multi-lineage differentiation potential // Biomaterials. 2012. Vol. 33. N 18. P. 4480-4489.; Akasov R, Gileva A., Zaytseva-Zotova D, Burov S, Chevalot I., Guedon E, Markvicheva, E. 3D in vitro co-culture models based on normal cells and tumor spheroids formed by cyclic RGD-peptide induced cell self-assembly // Bioteсhnol. Lett. 2016. Vol. 39. N 1. P. 45-53.; Myllyharju J., Kivirikko K.I. Collagens, modifying enzymes and their mutations in humans, flies and worms // Trends. Genet. 2004. Vol. 20. N 1. P. 33-43.; Myllyharju J. Prolyl-4-hydroxylases, the key enzymes of сollagen biosynthesis // Matrix Biol. 2003. Vol. 22. N 1. P. 15-24.; Harris G.M., Raitman I., Schwarzbauer J.E. Cell-derived decellularized extracellular matrices // Methods Сell Biol. 2018. Vol. 2. N 143. P. 97-114.; He F., Chen X., Pei M. Reconstruction of an in vitro tissue-specific microenvironment to rejuvenate synovium-derived stem cells for cartilage tissue engineering // Tissue Eng. Part A. 2009. Vol. 15. N 12. P. 3809-3821.; Sun Y., Li W., Lu Z, Chen R., Ling J., Ran Q., Jilka R.L., Chen X.D. Resting repletion and osteogenesis of aged mesenсhymal stem сells by exposure to a young extraсellular matrix // FASEB J. 2011. Vol. 25. N 5. P. 1474-1485.; Prewitz M.C., Seib F.P., von Bonin M., Friedrichs J., Stifeel A., Niehage C., Werner C. Tightly anchored tissue-mimetic matrices as instructive stem cell microenvironments // Nat. Methods. 2013. Vol. 10. N 8. P. 788-794.; uoslahti E. RGD and other reсognition sequenсes for integrins // Annu. Rev. Сell Dev. Biol. 1996. Vol. 12. P. 697-715.; Zhang L., Hum M., Wang M., Li Y., Chen H., Chu C., Jiang H. Evaluation of modifying сollagenmatrix with RGD peptide through periodate oxidation // J. Biomed. Mater. Res. A. 2005. Vol. 73. N 4. P. 468-475.; Lam J., Segura T. The modulation of MSС integrin expression by RGD presentation // Biomaterials. 2013. Vol. 34. N 16. P. 3938-3947.
Availability: https://vestnik-bio-msu.elpub.ru/jour/article/view/798
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8Academic Journal
Authors: Савостикова М.В.
Subject Terms: рак молочной железы, иммуноцитохимия, рецепторы эстрогенов, рецепторы прогестерона, онкопротеин HER2/ neu, пролиферативная активность Ki67
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9Academic Journal
Subject Terms: хромогранин А, гистология, неонатальный период, иммуноцитохимия, надпочечники поросят, экстрамедуллярные хромаффинные клетки, надпочечники
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Access URL: http://cryo.net.ua/xmlui/handle/123456789/737
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10Academic Journal
Authors: A. V. Sakharova, L. V. Didenko, T. I. Muravina, R. P. Chaikovskaya, E. A. Kost, M. F. Mir-Kasimov, А. В. Сахарова, Л. В. Диденко, Т. И. Муравина, Р. П. Чайковская, Е. А. Кост, М. Ф. Мир-Касимов
Source: Neuromuscular Diseases; № 1 (2013); 35-45 ; Нервно-мышечные болезни; № 1 (2013); 35-45 ; 2413-0443 ; 2222-8721 ; 10.17650/2222-8721-2013-0-1
Subject Terms: электронная иммуноцитохимия, Borrelia burgdorferi, muscle biopsy specimens, microscopy of semithin sections, electron microscopy, electron immunocytochemistry, мышечные биопсии, микроскопия полутонких срезов, электронная микроскопия
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Relation: https://nmb.abvpress.ru/jour/article/view/39/35; Лобзин Ю.В., Усков А.Н. Нейроборрелиоз: эпидемиология, клиника, диагностика и лечение. В кн.: Нейроинфекции (Аннотированные доклады I национальной конференции с международным участием 28–29 мая 2007 г.). С. 80–83.; Хронические нейроинфекции. Под ред. И.А. Завалишина, Н.Н. Спирина, А.Н. Бойко, С.С. Никитина. М.: ГЭОТАР–Медиа, 2011. С. 224–260.; Баранова Н.С., Спирин Н.Н., Шипова Е.Г., Степанов И.О. Поражение нервной системы на отдельных стадиях Лайм-боррелиоза. Ж неврол и психиатр 2010;110;2;90–6.; Вельгин С.О., Протас И.И., Понаморев В.В. и др. Клинический полиморфизм нейроборрелиоза в поздней стадии заболевания. Ж неврол и психиатр 2006;106:8–51.; MacDonald A.B. Concurrent neocortical borreliosis and Alzheimer's disease: Demonstration of a spirochete L-cyst form. Annals NY Academy of Sciences1988; 539:468–70.; Margulis L., Maniotis A., MacAllister J. et al. Spirochet round bodies. Syphilis, Lyme disease, & AIDS: Resurgense of “the great imitator”. Symbiosis 2009;47:51–8.; Pachner A.R. Borrelia burgdorferi in nervous system: the new “great imitator”. Annals of NY Academy of Sciences 1988; 539:56–64.; Dubowitz V., Sewry C. A. (ed. by). Muscle Biopsy. A practice approach. 2007. Saunders, Elsevier London. Third edition.; Engel W.K. The essentiality of hisoto- and cytochemical studies of skeletal muscle in the investigation of neuromuscular disease. Neurology 1962;12:778–94.; de Koning P., Hoogkamp-Korstanje J.A. Diagnosis of Lyme disease by demonstration of spirochetes in tissue biopsies. Zentralbl Bakteriol Mikrobiol Hyg 1986;263:179–88.; de Koning J., Bosma R.B., Hoogkamp-Korstanje J.A. Demonstration of spirochetes in patients with Lyme disease with a modified silver stain. J Med Microbiol 1987;23:261–7.; Bettica A., Johnson A.B. Ultrastructural immunogold labeling of glial filaments in osmicated and Epoxy-embedded tissue. J Histochem Cytochem1990;38:103–9.; Comstock L.E., Thomas D.D. Penetration of endothelial cell monolayers by Borrelia burgdorferi. Infect Immun 1989;57:1626–8.; Duray P., Yin Sh.-R., Ito Y. et al. Invasion of human tissue ex vivo by Borrelia burgdorferi. J Infect Dis 2005;191:1747–54.; Hulinska D., Jirous J., Valesova M., Hercogova J. Ultrastructure of Borrelia burgdorfery in tissue of patients with Lyme disease. J Basic Microbiol 1989;29:73–83.; Hulinska D., Basta J., Murgia R., Cinco M. Intracellular morphological events observed by electron microscopy on neutrophil phagocytosis of Borrelia garinii. J Spirochetal Tick-Borne Dis 1995;2(4):82–6.; Hayes S.F, Burgdorfer W. Ultrastructure of Borrelia burgdorferi. In: K. Weber, W. Burgdorfer, eds. Aspects of Lyme borreliosis. Heidelberg: Springer-Verlag, 1993.; Aberer E., Kersten A., Klade H. et al. Heterogeneity of Borrelia burgdorfery in the skin. Am J Dermatopathol 1996; 18(6):571–9.; Brorson Ø., Brorson S.H. Transformation of cystic forms of Borrelia burgdorferi to normal, mobile spirochetes. Infection 1997;25:240–6.; Brorson Ø., Brorson S.H., Scethes J. et al. Destruction of spirochete Borrelia burgdorferi round-body propagules (RBs) by the antibiotic Tigecycline. Proc Natl Acad Sci USA 2009;106:18656–61.; Morphological Transformation in Borrelia burgdorferi and Other Spirochetes: Observations of Round Forms & Blebs, 1905–2010. 262 Studies (63 on Lyme disease; 199 on other spirochetes) Lust Updated: 26 November 2010.; Dorward D.W., Fischer E.R., Brooks D.M. Invasion and cytopatic killing of human lymphocytes by spirochetes causing Lyme disease. Clin Infect Dis 1997;25:52–8.; Елисеева И.В., Бабич Е.М., Волянский Ю.Л. и др. О роли латентных, трудно культивируемых и некультивируемых персистентных бактерий в патологии человека. Анали Мечниковського Iнституту 2006;(1):12–45.; Miklossy J., Kasas S., Zurn A.D. et al. Persisting atypical and cystic forms of Borrelia burgdorferi and local inflammation in Lyme neuroborreliosis. J Neuroinflammation 2008;5:40.; Mac Donald A.B. A life cycle for Borrelia spirochetes? Medical Hypotheses 2006;67:810–8.; Grab D.J., Perides G., Dumler J.S. et al. Borrelia burgdorferi, host-derived proteases, and the blood brain barrier. Infect Immun 2005;73(2):1014–22.; Grubhoffer L., Golovchenko M., Vancová M. et al. Lyme borreliosis: insights into tick-host-borrelia relations. Folia parasitilogica 2005;52:279–94.; Barbour A.G., Hayes S. Biology of Borrelia Species. Microbiol Rev 1986: 381–400.; Chary-Valckenaere I., Jaulhac B., Champigneulle J. et al. Ultrastructural demonstration of intracellular localization of Borrelia burgdorferi in Lyme arthritis. Brit J Rheumatol 1998;37:468–9.; Al-Robaiy S., Dihazi H., Kacza J. et al. Metamorphosis of Borrelia burgdorferi organisms – RNA, lipid and protein composition in context with the spirochetes' shape. J Basic Microbiology, Suppl: Med Microbiol 2010;50, Issue Suppl 1:5–17.; Hofhuis A., van der Giessen J.W.B., Borgsteede F. et al. Lyme borreliosis in the Netherlands: strong increase in GP consultations and hospital admissions in last past 10 years. Euro Surveill 2006;11:22/06/2006.; Lindgren E., Jeanson T.G.T. Lyme borreliosis in Europe: Influences of climate and climate change, epidemiology, ecology and adaptation measures. In: Climate Change and Adaptation Strategies for Human Health [B. Menne and K. Ebi (eds.)]. Darmstadt: Steinkopff, 2006; s.157–188.; Руководство по инфекционным болезням. Под ред. Ю.В. Лобзина. СПб.: Фолиант, 2000. 932 с.; https://nmb.abvpress.ru/jour/article/view/39
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11Academic Journal
Authors: Маринов, Димитр, Мехеда, Л., Полоцкий, Б., Лактионов, К.
Subject Terms: ЦИТОЛОГИЯ, ДИАГНОСТИКА, ВНУТРИГРУДНАЯ ЛОКАЛИЗАЦИЯ, ИММУНОЦИТОХИМИЯ, ЖИДКОСТНАЯ ЦИТОЛОГИЯ, РАК, РАК МЕТАСТАТИЧЕСКИЙ
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12Academic Journal
Authors: МУРСАЛОВ С.У., ХАММАД Е.В., СЕДОВА Е.В.
Subject Terms: ПОЛИМОРБИДНОСТЬ,МОЛЕКУЛЯРНАЯ ИММУНОЦИТОХИМИЯ,ПОЖИЛОЙ ВОЗРАСТ,POLIMORBIDITY,MOLECULAR IMMUNE CYTOCHEMISTRY,ELDERLY
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13Academic Journal
Authors: Гладчук, І. З., Рожковська, Н. М., Каштальян, Н. М., Gladchuk, I. Z., Rozhkovska, N. M., Kashtalian, N. M., Гладчук, И. З., Рожковская, Н. Н.
Subject Terms: дисплазія шийки матки, цервікальна інтраепітеліальна неоплазія, діагностика, імуноцитохімія, біомаркери, дисплазия шейки матки, цервикальная интраэпителиальная неоплазия, диагностика, иммуноцитохимия, биомаркеры, р16, Кі-67, cervical dysplasia, cervical intraepithelial neoplasia, diagnostics, immunocytochemistry, biomarkers
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Availability: https://repo.odmu.edu.ua:443/xmlui/handle/123456789/9938
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14Academic Journal
Authors: N. L. Deineko, T. I. Bulycheva, A. M. Kovrigina, A. A. Grigoriyv, Н. Л. Дейнеко, Т. И. Булычева, А. М. Ковригина, А. А. Григорьев
Source: Medical Immunology (Russia); Том 16, № 5 (2014); 437-442 ; Медицинская иммунология; Том 16, № 5 (2014); 437-442 ; 2313-741X ; 1563-0625 ; 10.15789/1563-0625-2014-5
Subject Terms: иммуноцитохимия, lymphoproliferative diseases, nucleoli, immunocytochemistry, лимфопролиферативные заболевания, ядрышки
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Relation: https://www.mimmun.ru/mimmun/article/view/730/723; Булычева Т.И., Дейнеко Н.Л., Артеменко Е.Г.,Самойлова Р.С. Диагностическое значение ядрышкового белка В23 – нуклеофозмина при хронических лимфопролиферативных заболеваниях // «Terra Medica», Лабораторная диагностика. 2006. № 2 (10). C. 6-9. [Bulycheva T.I., Deyneko N.L., Artemenko E.G., Samoylova R.S. Diagnosticheskoe znachenie yadryshkovogo belka V23 – nukleofozmina pri khronicheskikh limfoproliferativnykh zabolevaniyakh [Diagnostic significance of the nucleolar protein B23 – nucleophosmin during chronic lymphoproliferative diseases]. Terra Medica. Laboratornaya diagnostika = Terra Medica. Laboratory Diagnostic, 2006, Vol. 2, no. 10, pp. 6-9].; Булычева Т.И., Дейнеко Н.Л., Вольпина О.М.,Владимирова Н.М. Иммуноцитохимическая визуализация мономерных и олигомерных форм ядрышкового белка В23/ нуклеофозмина в лимфоцитах человека в процессе пролиферации // Иммунология. 2011. № 5. C. 231-236. [Bulycheva T.I., Deyneko N.L., Vol`pina O.M.,Vladimirova N.M. Immunotsitokhimicheskaya vizualizatsiya onomernykh i oligomernykh form yadryshkovogo belka V23/ nukleofozmina v limfotsitakh cheloveka v protsesse proliferatsii [Immunocytochemical visualization of monomeric and oligomeric forms of the nucleolar protein B23/nucleophosmin in human lymphocytes in the process of proliferation]. Immunologiya = Immunology, 2011, no. 5, pp. 231-236].; Булычева Т.И., Григорьев А.А., Зацепина О.В. Иммуноцитохимическое изучение природы ядрышкового белка, выявляемого новыми МКА А3 // Иммунология. 2009. № 5. C. 287-289. [Bulycheva T.I.,Grigor`ev A.A., Zatsepina O.V. Immunotsitokhimicheskoe izuchenie prirody yadryshkovogo belka, vyyavlyaemogo novymi MKA A3 [Immunocytochemical study of the nature of the nucleolar protein revealed with new monoclonal antibodies A3]. Immunologiya = Immunology, 2009, Vol. 5, pp. 287-289].; Булычева Т.И., Дейнеко Н.Л., Артеменко Е.Г., Самойлова Р.С., Зацепина О.В. Способ прогнозирования прогрессирования хронического лимфолейкоза по количественному содержанию ядрышкового белка В23/нуклеофозмина в лизатах лимфоидных клеток // Патент на изобретение РФ № 2310201 от 10.11.2007. [Bulycheva T.I., Deyneko N.L., Artemenko E.G., Samoylova R.S., Zatsepina O.V. Sposob prognozirovaniya progressirovaniya khronicheskogo limfoleykoza po kolichestvennomu soderzhaniyu yadryshkovogo belka V23/nukleofozmina v lizatakh limfoidnykh kletok [A method for prognostication of progression of the chronic lympholeukosys according to the levels of the nucleolar protein B23/ nucleophosmin in the lysates of lymphoid cells]. Patent RF № 2310201. 10.11.2007].; Булычева Т.И, Калинина И.А, Григорьев А.А, Зацепина О.В. Штамм культивируемых клеток мышиной гибридомы А3, используемый для получения моноклональных антител к антигену ядрышек клеток человека // Патент на изобретение № 2296159 от 27.03.2007. [Bulycheva T.I, Kalinina I.A, Grigor`ev A.A, Zatsepina O.V. Shtamm kul`tiviruemykh kletok myshinoy gibridomy A3, ispol`zuemyy dlya polucheniya monoklonal`nykh antitel k antigenu yadryshek kletok cheloveka [A strain of cultured cells of murine hybridome A3 used for production of monoclonal antibodies against an antigen from the nucleoli of human cells]. Patent RF № 2296159, 27.03.2007].; Булычева Т.И., Григорьев А.А., Дейнеко Н.Л. Способ иммуноцитохимической оценки пролиферации лимфоцитов человека с помощью нового маркера - ядрышкового белка А3 // Патент на изобретение РФ № 2431670 от 20.10.2011. [Bulycheva T.I., Grigor`ev A.A., Deyneko N.L. Sposob immunotsitokhimicheskoy otsenki proliferatsii limfotsitov cheloveka s pomoshch`yu novogo markera - yadryshkovogo belka A3 [A method of immunocytochemical assessment of proliferation of human lymphocytes using a new marker – nucleolar protein A3]. Patent RF № 2431670, 20.10.2011].; Самойлова Р.С., Булычева Т.И. 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15Academic Journal
Subject Terms: АНТИГЕН А3, ЛИМФОПРОЛИФЕРАТИВНЫЕ ЗАБОЛЕВАНИЯ, ЯДРЫШКИ, ИММУНОЦИТОХИМИЯ
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16Academic Journal
Source: Research'n Practical Medicine Journal.
Subject Terms: 03 medical and health sciences, 0302 clinical medicine, рак молочной железы, иммуноцитохимия, рецепторы эстрогенов, рецепторы прогестерона, онкопротеин HER2/ neu, пролиферативная активность Ki67, 3. Good health
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17Academic Journal
Authors: Дьячкова, Наталья, Ковынев, Игорь, Поспелова, Татьяна, Лямкина, Анна, Скворцова, Наталия, Тарновский, Родион
Subject Terms: ВТОРИЧНЫЙ МИЕЛОДИСПЛАСТИЧЕСКИЙ СИНДРОМ, ЛИМФОМЫ, ЭРИТРОПОЭЗ, РЕЦЕПТОРЫ К ЭРИТРО- ПОЭТИНУ, ИММУНОЦИТОХИМИЯ, ЦИТОЛОГИЯ ДИЗЭРИТРОПОЭЗА
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18Academic Journal
Authors: Линькова, Н., Умнов, Р., Проняева, В., Хавинсон, В.
Subject Terms: ПЕПТИДЫ, ПОЧЕЧНАЯ ПАТОЛОГИЯ, ФАКТОР РОСТА ФИБРОБЛАСТОВ, ИММУНОЦИТОХИМИЯ, СТАРЕНИЕ
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19Academic Journal
Authors: Прошина, Л., Антонова, Л., Федорова, Н., Быкова, О., Григорьева, М., Викторова, Е.
Subject Terms: АДАПТАЦИЯ, СТРЕСС, ГИСТОХИМИЯ, ИММУНОЦИТОХИМИЯ, КАРДИОМИОЦИТЫ, ЭКСПЕРИМЕНТАЛЬНЫЙ ДИАБЕТ
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20Academic Journal
Authors: Сахарова, А., Диденко, Л., Муравина, Т., Чайковская, Р., Кост, Е., Мир-касимов, М.
Subject Terms: НЕЙРОБОРРЕЛИОЗ, МЫШЕЧНЫЕ БИОПСИИ, МИКРОСКОПИЯ ПОЛУТОНКИХ СРЕЗОВ, ЭЛЕКТРОННАЯ МИКРО-СКОПИЯ, ЭЛЕКТРОННАЯ ИММУНОЦИТОХИМИЯ
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