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1
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2Academic Journal
Authors: Мустафин, Р. Н., Хуснутдинова, Э. К.
Subject Terms: медицина, медицинская генетика, вирусная мимикрия, длинные некодирующие РНК, злокачественные новообразования, канцерогенез, микроРНК, мобильные генетические элементы, таргетная терапия, транспозоны
Availability: http://dspace.bsu.edu.ru/handle/123456789/62805
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3Academic Journal
Authors: Ageevets V.A., Ageevets I.V., Sidorenko S.V.
Contributors: 0, РНФ
Source: Russian Journal of Infection and Immunity; Vol 12, No 3 (2022); 450-460 ; Инфекция и иммунитет; Vol 12, No 3 (2022); 450-460 ; 2313-7398 ; 2220-7619
Subject Terms: Klebsiella sp., hypervirulence, multi-drug resistance, hybrid pathotype, mobile genetic elements, epidemiology, гипервирулентность, множественная резистентность, гибридный патотип, мобильные генетические элементы, эпидемиология
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Relation: https://iimmun.ru/iimm/article/view/1825/1453; https://iimmun.ru/iimm/article/view/1825/1510; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7300; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7301; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7302; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7339; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7341; https://iimmun.ru/iimm/article/downloadSuppFile/1825/7342; https://iimmun.ru/iimm/article/view/1825
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4Academic Journal
Source: Естественные и технические науки.
Subject Terms: микросателлиты, мобильные генетические элементы, mobile genetic elements, microsatellites, sand lizard, прыткая ящерица
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5
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6Academic Journal
Source: Vavilov Journal of Genetics and Breeding; Том 21, № 6 (2017); 742-749 ; Вавиловский журнал генетики и селекции; Том 21, № 6 (2017); 742-749 ; 2500-3259
Subject Terms: процессинг, introns, mobile genetic elements, noncoding RNA, RNA interference, transposons, processing, интроны, мобильные генетические элементы, некодирующие РНК, система РНК-интерференции, транспозоны
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Elements. 2011;1(1):8-17.; Bush S.J., Chen L., Tovar-Corona J.M., Urrutia A.O. Alternative splicing and the evolution of phenotypic novelty. Philos. Trans. R. Soc. Lond. B. Bilol. Sci. 2017;372(1713):pii:20150474.; Christie M., Croft L.J., Carroll B.J. Intron splicing suppresses RNA silencing in Arabidopsis. Plant. J. 2011;68(1):159-167.; Coufal N.G., Garcia-Perez J.L., Peng G.E., Yeo G.W., Mu Y., Lovci M.T., Morell M., O’Shea K.S., Moran J.V., Gage F.H. L1 retrotransposition in human neural progenitor cells. Nature. 2009; 460(7259):1127-1231.; de Koning A.P., Gu W., Castoe T.A., Batzer M.A., Pollock D.D. Repetitive elements may comprise over two-thirds of the human genome. PLoS Genet. 2011;7(12):e1002384.; Dimmeler S., Nicotera P. MicroRNAs in age-related diseases. EMBO Mol. Med. 2013;5(2):180-190.; Du Z., Yang C., Rothschild M.F., Ross J. Novel microRNA families expanded in the human genome. BMC Genomics. 2013;14:98-105.; Duan C.G., Wang X., Xie S., Pan L., Miki D., Tang K., Hsu C.C., Lei M., Zhong Y., Hou Y.J., Wang Z., Zhang Z., Mangrauthia S.K., Xu H., Zhang H., Dilkes B., Tao W.A., Zhu J.K. A pair of transpo-son-derived proteins function in a histone acetyltransferase complex for active DNA demethylation. Cell Res. 2017;27(2):226-240.; Dumesic P.A., Madhani H.D. The spliceosome as a transposon sensor. RNA Biol. 2013;10(11):1653-1660.; Dupressoir A., Lavialle C., Heidmann T. From ancestral infectious retroviruses to bona fide cellular genes: role of the captured syncytins in placentation. Placenta. 2012;33(9):663-671.; Elliott T.A., Gregory T.R. Do larger genomes contain more diverse transposable elements? BMC Evol. Biol. 2015;15(1):69-81.; Faulkner G.J. Retrotransposons: mobile and mutagenic from conception to death. FEBS Lett. 2011;585(11):1589-1594.; Feschotte C. The contribution of transposable elements to the evolution of regulatory networks. Nat. Rev. Genet. 2008;9(5):397-405.; Finatto T., de Oliveira A., Chaparro C., da Maia L.C., Farias D.R., Woyann L.G., Mistura C.C., Soares-Bresolin A.P., Llauro C., Panaud O., Picault N. Abiotic stress and genome dynamics: specific genes and transposable elements response to iron excess in rice. Rice. 2015; 8(13). DOI 10.1186/s12284-015-0045-6.; Garcia-Perez J.L., Marchetto M.C., Muotri A.R., Coufal N.G., Gage F.H., O’Shea K.S., Moran J.V. LINE-1 retrotransposition in human embryonic stem cells. Hum. Mol. Genet. 2007;16(13):1569-1577.; Gim J., Ha H., Ahn K., Kim D.S., Kim H.S. Genome-wide identification and classification of microRNAs derived from repetitive elements. Genomics Inform. 2014;12(4):261-267.; Guo W., Zhang M.Q., Wu H. Mammalian non-CG methylations are conserved and cell-type specific and may have been involved in the evolution of transposon elements. Sci. Rep. 2016;6:32207-32219.; Hadjiargyrou M., Delihas N. The Intertwining of transposable elements and non-coding RNAs. Int. J. Mol. Sci. 2013;14(7):13307-13328.; Huff J.T., Zilberman D., Roy S.W. Mechanism for DNA transposons to generate introns on genomic scales. Nature. 2016;538(7626):533-536.; Johnson R., Guigo R. The RIDL hypothesis: transposable elements as functional domains of long noncoding RNAs. RNA. 2014;20(7): 959-976.; Kiselev O.I. Endogenous retroviruses: structure and functions in the human genome. Voprosy virusologii = Problems of Virology. 2013; 1:102-115. (in Russian); Kitkumthorn N., Mutirangura A. Long interspersed nuclear element-1 hypomethylation in cancer: biology and clinical applications. Clin. Epigenet. 2011;2:315-330.; Klawitter S., Fuchs N.V., Upton K.R., Munoz-Lopez M., Shukla R., Wang J., Garcia-Canadas M., Lopez-Ruiz C., Gerhardt D.J., Sebe A., Grabundaija I., Merkert S., Gerdes P., Pulgarin J.A., Bock A., Held U., Witthuhn A., Haase A., Sarkadi B., Lower J., Wolve tang E.J., Martin U., Ivics Z., Izsvak Z., Garcia-Perez J.L., Faulkner G.J., Schumann G.G. Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells. Nat. Commun. 2016;7:10286-10301.; Kubiak M.R., Makalowska I. Protein-coding genes’ retrocopies and their functions. Viruses. 2017;9(4):pii:E80.; Lee K.H., Chiu S., Lee Y.K., Greenhalgh D.G., Cho K. Age-dependent and tissue-specific structural changes in the C57BL/6J mouse genome. Exp. Mol. Pathol. 2012;93(1):167-172.; Lee K.H., Yee L., Lim D., Greenhalgh D., Cho K. Temporal and spatial rearrangements of a repetitive element array on C57BL/6J mouse genome. Exp. Mol. Pathol. 2015;98(3):439-445.; Lee S., Stevens S.W. Spliceosomal intronogenesis. Proc. Natl. Acad.; Sci. USA. 2016;113(23):6514-6519.; Lei H., Vorechovsky I. Identification of splicing silencers and enhancers in sense Alus: a role for pseudoacceptors in splice site repression. Mol. Cell. Biol. 2005;25(16):6912-6920.; Lescale C., Deriano L. The RAG recombinase: Beyond breaking. Mech. Ageing Dev. 2016;16:30263-30269. DOI 10.1016/j.mad.2016.11.003. Liew Y.J., Aranda M., Carr A., Baumgarten S., Zoccola D., Tambutte S., Allemand D., Micklem G., Voolstra C.R. Identification of microRNA in the coral Styphora pistillata. PLoS One. 2014;9(3):e91101.; Llave C., Kasschau K.D., Rector M.A., Carrington J.C. Endogenous and silencing-associated small RNAs in plants. 2002;14(7):1605-1619.; Lu D., Davis M.P., Abreu-Goodger C., Wang W., Campos L.S., Siede J., Vigorito E., Skarnes W.C., Dunham I., Enright A.J., Liu P. MiR-25 regulates Wwp2 and Fbxw7 and promotes reprogramming of mouse fibroblast cells to iPSCs. PLoS One. 2012;7(8):e40938.; Luco R.F., Allo M., Schor I.E., Kornblihtt A.R., Misteli T. Epigenetics in alternative pre-mRNA splicing. Cell. 2011;144(1):16-26.; Macia A., Munoz-Lopez M., Cortes J.L., Hastings R.K., Morell S., Lucena-Aguilar G., Marchal J.A., Badge R.M., Garcia-Perez J.L. Epigenetic control of retrotransposons expression in human embryonic stem cells. Mol. Cell. Biol. 2011;31(2):300-316.; Marchetto M.C., Narvaiza I., Denli A.M., Benner C., Lazzarini T.A., Nathanson J.L., Paguola A.C., Desai K.N., Herai R.H., Weitz-man M.D., Yeo G.W., Muotri A.R., Gage F.H. Differential L1 regulation in pluripotent stem cells of humans and apes. Nature. 2013; 503(7477):525-529.; Miousse I.R., Chalbot M.G., Lumen A., Ferguson A., Kavouras I.G., Koturbash I. Response of transposable elements to environmental stressors. Mutat. Res. Rev. Mutat. Res. 2015;765:19-39.; Moran Y., Praher D., Fredman D., Technau U. The evolution of mi-croRNA pathway protein components in Cnidaria. Mol. Biol. Evol. 2013;30(12):2541-2552.; Morita S., Horii T., Kimura M., Ochiya T., Tajima S., Hatada I. miR-29 represses the activities of DNA methyltransferases and DNA demethylases. Int. J. Mol. Sci. 2013;14:14647-14658.; Muotri A.R., Chu V.T., Marchetto M.C., Deng W., Moran J.V., Gage F.H. Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition. Nature. 2005;435(7044):903-910.; Ong S., Lee W.H., Kodo K., Wu J.C. MicroRNA-mediated regulation of differentiation and trans-differentiation in stem cells. Adv. Drug Deliv. Rev. 2015;88:3-15.; Ostertag E.M., De Berardinis R.J., Goodier J.L., Zhang Y., Yang N., Gerton G.L., Kazazian H.H., Jr. A mouse model of human L1 retrotransposition. Nat. Genet. 2002;32(4):655-660.; Pastor T., Talotti G., Lewandowska M.A., Pagani F. An Alu-derived in-tronic splicing enhancer facilitates intronic processing and modulates aberrant splicing in ATM. Nucleic Acids Res. 2009;37(21):7258-7267.; Patrushev L.I., Minkevich I.G. The problem of the eukaryotic genome size. Uspekhi biologicheskoi khimii = Advances of Biological Chemistry. 2007;47:293-370. (in Russian); Piriyapongsa J., Marino-Ramirez L., Jordan I.K. Origin and evolution of human microRNAs from transposable elements. Genetics. 2007; 176(2):1323-1337.; Pizarro J.G., Cristofari G. Post-transcriptional control of LINE-1 retrotransposition by cellular host factors in somatic cells. Front. Cell. Dev. Biol. 2016;4:14-23.; Platt R.N., Vandeweqe M.W., Kern C., Schmidt C.J., Hoffmann F.G.; Ray D.A. Large number of novel miRNAs originate from DNA transposons and are coincident with a large species radiation in bats. Mol. Biol. Evol. 2014;31(6):1536-1545.; Prak E.T., Dodson A.W., Farkash E.A., Kazazian H.H. Jr. Tracking an embryonic L1 retrotransposition event. Proc. Natl. Acad. Sci. USA. 2003;100(4):1832-1837.; Qin S., Jin P., Zhou X., Chen L., Ma F. The role of transposable elements in the origin and evolution of microRNAs in human. PLoS One. 2015;10(6):e0131365.; Ramsay L., Marchetto M.C., Caron M., Chen S.H., Busche S., Kwan T.; Pastinen T., Gage F.H., Bourgue G. Conserved expression of trans-poson-derived non-coding transcripts in primate stem cells. BMC Genomics. 2017;18(1):214-226.; Richardson S.R., Morell S., Faulkner G.J. L1 retrotransposons and somatic mosaicism in the brain. Annu. Rev. Genet. 2014;48:1-27.; Samantarrai D., Dash S., Chhetri B., Mallick B. Genomic and epigenomic cross-talks in the regulatory landscape of miRNAs in breast cancer. Mol. Cancer Res. 2013;11(4):315-328.; Shabalina S.A., Koonin E.V. Origins and evolution of eukaryotic RNA interference. Trends Ecol. Evol. 2008;23(10):578-587.; Shen S., Guo X., Yan H., Lu Y., Ji X., Li L., Liang T., Zhou D., Feng X.H., Zhao J.C., Yu J., Gong X.G., Zhang L., Zhao B. A miR-130a-YAP positive feedback loop promotes organ size and tumoro-genesis. Cell Res. 2015;25:997-1012.; Singh D.K., Rath P.C. Long interspersed nuclear elements (LINEs) show tissue-specific, mosaic genome and methylation-unrestricted, widespread expression of noncoding RNAs in somatic tissues of the rat. RNA Biol. 2012;9(11):1380-1396.; Smalheiser N.R., Torvik V.I. Mammalian microRNAs derived from genomic repeats. 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(in Russian); Wissing S., Munoz-Lopez M., Macia A., Yang Z., Montano M., Col-lins W., Garcia-Perez J.L., Moran J.V., Greene W.C. Reprogramming somatic cells into iPS cell activates LINE-1 retroelement mobility. Hum. Mol. Genet. 2012;21(1):208-218.; Xu C., Tian J., Mo B. siRNA-mediated DNA methylation and H3K9 dimethylation in plants. Protein Cell. 2013;4(9):656-663.; Yuan Z., Sun X., Liu H., Xie J. MicroRNA genes derived from repetitive elements and expanded by segmental duplication events in mammalian genomes. PLoS One. 2011;6(3):e17666.; Zakrzewski F., Schmidt M., Van Lijsebettens M., Schmidt T. DNA methylation of retrotransposons, DNA transposons and genes in sugar beet (Beta vulgaris L.). Plant J. 2017; DOI 10.1111/tpj. 13526.; Zhang G., Esteve P., Chin H.G., Terragni J., Dai N., Correa Jr. I.R., Pradhan S. Small RNA-mediated DNA (cytosine-5) methyltransferase 1 inhibition leads to aberrant DNA methylation. Nucleic Acids Res. 2015;43(12):6112-6124.; Zhang H., Tao Z., Hong H., Chen Z., Wu C., Li X., Xiao J., Wang S. Transposon-derived small RNA is responsible for modified function of WRKY45 locus. Nat. Plants. 2016;2:16016-16023.; Zhou H., Kishima Y. Alternative plant host defense against transposon activities occurs at the post-translational stage. Plant Signal. Behav. 2017;e1318238. DOI 10.1080/15592324.2017.; https://vavilov.elpub.ru/jour/article/view/1196
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7Academic Journal
Contributors: Казанский (Приволжский) федеральный университет
Subject Terms: антибиотикорезистентность, мобильные генетические элементы
Access URL: https://openrepository.ru/article?id=190767
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8Academic Journal
Authors: M. V. Puzakov, L. V. Puzakova, I. K. Zakharov, М. В. Пузаков, Л. В. Пузакова, И. К. Захаров
Contributors: бюджетный проект «Разработка научных основ решения экологических и гидробиологических проблем интегрированного управления прибрежными зонами» (0012-2015-0001), О.В. Ваулин
Source: Vavilov Journal of Genetics and Breeding; Том 21, № 2 (2017); 269-283 ; Вавиловский журнал генетики и селекции; Том 21, № 2 (2017); 269-283 ; 2500-3259
Subject Terms: морские беспозвоночные, genome, mobile genetic elements, MGE, transposons, retrotransposons, variation, biological diversity, species, hydrobionts, marine invertebrates, геном, мобильные генетические элементы, транспозоны, ретротранспозоны, изменчивость, биологическое разнообразие, вид, гидробионты
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Relation: https://vavilov.elpub.ru/jour/article/view/783/771; Бубенщикова Е.В., Антоненко О.В., Васильева Л.В., Ратнер В.А. Индукция транспозиций МГЭ 412 раздельно тепловым и холодовым шоком в сперматогенезе у самцов дрозофилы. Генетика. 2002;38(1):46-55.; Васильева Л.А., Ратнер В.А., Антоненко О.В., Лопухова Е.Д., Бубенщикова Е.В. Индукция транспозиций МГЭ 412 различными дозами паров этанола в изогенной линии Drosophila melanogaster. Генетика. 2003;39(5):717-720.; Захаренко Л.П., Коваленко Л.В., Перепелкина М.П., Захаров И.К. Влияние γ-радиации на индукцию транспозиций hobo-элемента у Drosophila melanogaster. Генетика. 2006;42(6):763-767.; Иващенко Н.И., Гришаева Т.М. Современные представления о роли разных семейств мобильных элементов в геномах эукариот. Успехи современной биологии. 2009;129(2):115-123.; Коваленко Л.В., Захаренко Л.П., Волошина М.А., Карамышева Т.В., Рубцов Н.Б., Захаров И.К. Поведение транспозонов hobo и P в нестабильной линии yellow2-717 Drosophila melanogaster и ее производных после скрещиваний с лабораторной линией. Генетика. 2006;42(6):748-756.; Ратнер В.А., Васильева Л.А. Индукция транспозиций и эксцизий мобильных генетических элементов у дрозофилы в процессе изогенизации. Генетика. 1996;32(7):933-944.; Сергеева Е.М., Салина Е.А. Мобильные элементы и эволюция генома растений. Вавиловский журнал генетики и селекции. 2011;15(2):382-398.; Сормачева Н.Д., Блинов А.Г. LTR ретротранспозоны растений. Вавиловский журнал генетики и селекции. 2011;15(2):351-381.; Чересиз С.В., Юрченко Н.Н., Иванников А.В., Захаров И.К. Мобильные элементы и стресс. Информационный вестник ВОГиС. 2008;12(1/2):217-242.; Юрченко Н.Н., Коваленко Л.В., Захаров И.К. Мобильные генетические элементы: нестабильность генов и геномов. Вавиловский журнал генетики и селекции. 2011;15(2):261-270.; Albertin C.B., Simakov O., Mitros T., Wang Z.Y., Pungor J.R., Edsinger-Gonzales E., Brenner S., Ragsdale C.W., Rokhsar D.S. The octopus genome and the evolution of cephalopod neural and morphological novelties. Nature. 2015;524(7564):220-224. DOI 10.1038/nature14668.; Arkhipova I., Meselson M. Transposable elements in sexual and ancient asexual taxa. Proc. Natl Acad. Sci. USA. 2000;97(26):14473-14477. DOI 10.1073/pnas.97.26.14473.; Bao W., Jurka M.G., Kapitonov V.V., Jurka J. New superfamilies of eukaryotic DNA-transposons and their internal divisions. Mol. Biol. Evol. 2009;26(5):983-993. DOI 10.1093/molbev/msp013.; Baughman K.W., McDougall C., Cummins S.F., Hall M., Degnan B.M., Satoh N., Shoguchi E. Genomic organization of Hox and ParaHox clusters in the echinoderm, Acanthaster planci. Genesis. 2014;52(12):952-958. DOI 10.1002/dvg.22840.; Baumgarten S., Simakov O., Esherick L.Y., Liew Y.J., Lehnert E.M., Michell C.T., Li Y., Hambleton E.A., Guse A., Oates M.E., Gough J., Weis V.M., Aranda M., Pringle J.R., Voolstra C.R. The genome of Aiptasia, a sea anemone model for coral symbiosis. Proc. Natl Acad Sci U S A. 2015;112(38):11893-11898. DOI 10.1073/pnas.1513318112.; Bui Q.T., Delaurière L., Casse N., Nicolas V., Laulier M., Chénais B. Molecular characterization and phylogenetic position of a new mariner-like element in the coastal crab, Pachygrapsus marmoratus. Gene. 2007;396(2):248-256. DOI 10.1016/j.gene.2007.03.004.; Casse N., Bui Q.T., Nicolas V., Renault S., Bigot Y., Laulier M. Species sympatry and horizontal transfers of Mariner transposons in marine crustacean genomes. Mol. Phylogenet. Evol. 2006;40(2):609-619. DOI 10.1016/j.ympev.2006.02.005.; Chipman A.D., Ferrier D.E., Brena C., Qu J., Hughes D.S., Schröder R., Torres-Oliva M., Znassi N., Jiang H., Almeida F.C., Alonso C.R., Apostolou Z., Aqrawi P., Arthur W., Barna J.C., Blankenburg K.P., Brites D., Capella-Gutiérrez S., Coyle M., Dearden P.K., Du Pasquier L., Duncan E.J., Ebert D., Eibner C., Erikson G., Evans P.D., Extavour C.G., Francisco L., Gabaldón T., Gillis W.J., GoodwinHorn E.A., Green J.E., Griffiths-Jones S., P. Grimmelikhuijzen C. 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9Academic Journal
Subject Terms: ISSR-PCR-МАРКЕРЫ, ИНВЕРТИРОВАННЫЕ ПОВТОРЫ ДНК, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ЭНДОГЕННЫЕ РЕТРОВИРУСЫ
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10Academic Journal
Authors: Glazko, Valeriy, Bardukov, Nickolay, Pheophilov, Anton, Sipko, Taras, Elkina, Mariya, Glazko, Tatyana
Subject Terms: ОВЦЕБЫК, ГЕНОМНОЕ СКАНИРОВАНИЕ, ИНВЕРТИРОВАННЫЕ ПОВТОРЫ, МИКРОСАТЕЛЛИТЫ, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ЭНДОГЕННЫЕ РЕТРОВИРУСЫ
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11Academic Journal
Authors: Артемьева, А., Дубовская, А., Соловьева, А., Чесноков, Ю.
Subject Terms: ВИДЫ РОДА BRASSICA, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ АС, СОХРАНЯЕМОЕ ГЕНЕТИЧЕСКОЕ БИОРАЗНООБРАЗИЕ, MOBILE GENETIC ELEMENTS АС
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12Academic Journal
Authors: Михеева, Лидия, Карбышева, Елена, Шестаков, Сергей
Subject Terms: ЭВОЛЮЦИЯ, ЦИАНОБАКТЕРИИ, ГЕНОМЫ, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ТРАНСПОЗАЗЫ, ГЕНОМНЫЕ ПЕРЕСТРОЙКИ
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13Academic Journal
Authors: Голубовский, Михаил
Subject Terms: МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ИСТОРИЯ ОТРЫТИЯ
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14Academic Journal
Source: Вестник Казанского технологического университета.
Subject Terms: СТАТИСТИЧЕСКАЯ МОДЕЛЬ, МУТАГЕННЫЕ СТРЕССОВЫЕ ФАКТОРЫ, ИНТРОНИЗАЦИЯ, ЭКЗОНИЗАЦИЯ, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ
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15Academic Journal
Source: Известия Тимирязевской сельскохозяйственной академии.
Subject Terms: ISSR-PCR-МАРКЕРЫ, ИНВЕРТИРОВАННЫЕ ПОВТОРЫ ДНК, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ЭНДОГЕННЫЕ РЕТРОВИРУСЫ
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16Academic Journal
Source: Сельскохозяйственная биология.
Subject Terms: ВИДЫ РОДА BRASSICA, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ АС, СОХРАНЯЕМОЕ ГЕНЕТИЧЕСКОЕ БИОРАЗНООБРАЗИЕ, MOBILE GENETIC ELEMENTS АС
File Description: text/html
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17Academic Journal
Source: Ecological genetics.
Subject Terms: ЭВОЛЮЦИЯ, ЦИАНОБАКТЕРИИ, ГЕНОМЫ, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ТРАНСПОЗАЗЫ, ГЕНОМНЫЕ ПЕРЕСТРОЙКИ
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18Academic Journal
Source: Историко-биологические исследования.
Subject Terms: 0301 basic medicine, 0303 health sciences, 03 medical and health sciences, МОБИЛЬНЫЕ ГЕНЕТИЧЕСКИЕ ЭЛЕМЕНТЫ, ИСТОРИЯ ОТРЫТИЯ
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19Academic Journal
Authors: Старикова Елизавета Валентиновна, Манолов Александр Иванович, Федоров Дмитрий Евгеньевич, Ильина Елена Николаевна
Contributors: Казанский (Приволжский) федеральный университет
Subject Terms: антибиотикорезистентность, мобильные генетические элементы
Relation: В поисках моделей персонализированной медицины; http://rour.neicon.ru:80/xmlui/bitstream/rour/190767/1/nora.pdf; 579.254; https://openrepository.ru/article?id=190767
Availability: https://openrepository.ru/article?id=190767
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20Academic Journal
Authors: Григорьев, Д.С., Воробьева, Л.И.
Subject Terms: генетика, локомоторная активность, гибридологический анализ, Drosophila melanogaster, мобильные генетические элементы
Relation: Григорьев Д.С., Воробьёва Л.И. Локомоторная активность линий Drosophila melanogaster, полученных из популяций разного географического происхождения / Вісник Харківського національного університету імені В.Н.Каразіна. Серія: біологія. – 2010. – Вип. 11, №905. – С. 77–83; http://dspace.univer.kharkov.ua/handle/123456789/3784
Availability: http://dspace.univer.kharkov.ua/handle/123456789/3784
