Relevant bibliographies by topics / Mcy genes

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Mcy genes'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Mcy genes"

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Christiansen, Guntram, Jutta Fastner, Marcel Erhard, Thomas Börner, and Elke Dittmann. "Microcystin Biosynthesis in Planktothrix: Genes, Evolution, and Manipulation." Journal of Bacteriology 185, no. 2 (2003): 564–72. http://dx.doi.org/10.1128/jb.185.2.564-572.2003.

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ABSTRACT Microcystins represent an extraordinarily large family of cyclic heptapeptide toxins that are nonribosomally synthesized by various cyanobacteria. Microcystins specifically inhibit the eukaryotic protein phosphatases 1 and 2A. Their outstanding variability makes them particularly useful for studies on the evolution of structure-function relationships in peptide synthetases and their genes. Analyses of microcystin synthetase genes provide valuable clues for the potential and limits of combinatorial biosynthesis. We have sequenced and analyzed 55.6 kb of the potential microcystin synthe
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DONG, S. J., X. D. BI, J. Y. ZHANG, et al. "ANALYSIS OF THE MICROCYSTIN-LR PRODUCTION ABILITY OF METAGENOMIC MCY GENES IN FRESHWATER AQUACULTURE PONDS FOCUSING ON THE ABUNDANCE OF METAGENOMIC MCY GENES AND SNP." Applied Ecology and Environmental Research 19, no. 1 (2021): 237–48. http://dx.doi.org/10.15666/aeer/1901_237248.

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Christiansen, Guntram, Rainer Kurmayer, Qian Liu, and Thomas Börner. "Transposons Inactivate Biosynthesis of the Nonribosomal Peptide Microcystin in Naturally Occurring Planktothrix spp." Applied and Environmental Microbiology 72, no. 1 (2006): 117–23. http://dx.doi.org/10.1128/aem.72.1.117-123.2006.

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ABSTRACT The filamentous cyanobacteria Planktothrix spp. occur in the temperate region of the Northern hemisphere. The red-pigmented Planktothrix rubescens bacteria occur in deep, physically stratified, and less eutrophic lakes. Planktothrix is a known producer of the toxic heptapeptide microcystin (MC), which is produced nonribosomally by a large enzyme complex consisting of peptide synthetases and polyketide synthases encoded by a total of nine genes (mcy genes). Planktothrix spp. differ in their cellular MC contents as well as the production of MC variants; however, the mechanisms favoring
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Tanabe, Yuuhiko, Kunimitsu Kaya, and Makoto M. Watanabe. "Evidence for Recombination in the Microcystin Synthetase (mcy) Genes ofToxic Cyanobacteria Microcystis spp." Journal of Molecular Evolution 58, no. 6 (2004): 633–41. http://dx.doi.org/10.1007/s00239-004-2583-1.

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Kurmayer, Rainer, and Thomas Kutzenberger. "Application of Real-Time PCR for Quantification of Microcystin Genotypes in a Population of the Toxic Cyanobacterium Microcystis sp." Applied and Environmental Microbiology 69, no. 11 (2003): 6723–30. http://dx.doi.org/10.1128/aem.69.11.6723-6730.2003.

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ABSTRACT The cyanobacterium Microcystis sp. frequently develops water blooms consisting of organisms with different genotypes that either produce or lack the hepatotoxin microcystin. In order to monitor the development of microcystin (mcy) genotypes during the seasonal cycle of the total population, mcy genotypes were quantified by means of real-time PCR in Lake Wannsee (Berlin, Germany) from June 1999 to October 2000. Standard curves were established by relating cell concentrations to the threshold cycle (the PCR cycle number at which the fluorescence passes a set threshold level) determined
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Sipari, Hanna, Anne Rantala-Ylinen, Jouni Jokela, Ilona Oksanen, and Kaarina Sivonen. "Development of a Chip Assay and Quantitative PCR for Detecting Microcystin Synthetase E Gene Expression." Applied and Environmental Microbiology 76, no. 12 (2010): 3797–805. http://dx.doi.org/10.1128/aem.00452-10.

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ABSTRACT The chip and quantitative real-time PCR (qPCR) assays were optimized to study the expression of microcystin biosynthesis genes (mcy) with RNA samples extracted from cyanobacterial strains and environmental water samples. Both microcystin-producing Anabaena and Microcystis were identified in Lake Tuusulanjärvi samples. Microcystis transcribed the mcyE genes throughout the summer of 2006, while expression by Anabaena became evident later in August and September. Active mcyE gene expression was also detectable when microcystin concentrations were very low. Detection of Anabaena mcyE tra
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Cordeiro, Rita, Joana Azevedo, Rúben Luz, Vitor Vasconcelos, Vítor Gonçalves, and Amélia Fonseca. "Cyanotoxin Screening in BACA Culture Collection: Identification of New Cylindrospermopsin Producing Cyanobacteria." Toxins 13, no. 4 (2021): 258. http://dx.doi.org/10.3390/toxins13040258.

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Microcystins (MCs), Saxitoxins (STXs), and Cylindrospermopsins (CYNs) are some of the more well-known cyanotoxins. Taking into consideration the impacts of cyanotoxins, many studies have focused on the identification of unknown cyanotoxin(s)-producing strains. This study aimed to screen strains from the Azorean Bank of Algae and Cyanobacteria (BACA) for MCs, STX, and CYN production. A total of 157 strains were searched for mcy, sxt, and cyr producing genes by PCR, toxin identification by ESI-LC-MS/MS, and cyanotoxin-producing strains morphological identification and confirmation by 16S rRNA ph
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Tanabe, Yuuhiko, Tomoharu Sano, Fumie Kasai, and Makoto M. Watanabe. "Recombination, cryptic clades and neutral molecular divergence of the microcystin synthetase (mcy) genes of toxic cyanobacterium Microcystis aeruginosa." BMC Evolutionary Biology 9, no. 1 (2009): 115. http://dx.doi.org/10.1186/1471-2148-9-115.

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Mbukwa, Elbert A., Sammy Boussiba, Victor Wepener, et al. "PCR amplification and DNA sequence of mcyA gene: The distribution profile of a toxigenic Microcystis aeruginosa in the Hartbeespoort Dam, South Africa." Journal of Water and Health 11, no. 3 (2013): 563–72. http://dx.doi.org/10.2166/wh.2013.014.

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Using new polymerase chain reaction (PCR) primers, a once known to be under-transcribed microcystin synthetase A (mcyA) gene from the only known toxigenic cyanobacterium Microcystis aeruginosa dominating the Hartbeespoort Dam was consistently amplified from genomic DNA extracted from a set of algal and cell free water samples collected across this dam. In addition to this, five more mcy genes (mcyBCDEG) were also amplified during this study. The resultant mcyA PCR products (518 bp) were purified and sequenced and gave nucleotide sequence segments of 408 bp sizes. The obtained sequence was alig
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Pearson, Leanne A., Michael Hisbergues, Thomas B�rner, Elke Dittmann, and Brett A. Neilan. "Inactivation of an ABC Transporter Gene, mcyH, Results in Loss of Microcystin Production in the Cyanobacterium Microcystis aeruginosa PCC 7806." Applied and Environmental Microbiology 70, no. 11 (2004): 6370–78. http://dx.doi.org/10.1128/aem.70.11.6370-6378.2004.

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ABSTRACT The cyanobacterium Microcystis aeruginosa is widely known for its production of the potent hepatotoxin microcystin. Microcystin is synthesized nonribosomally by the thiotemplate function of a large, modular enzyme complex encoded within the 55-kb microcystin synthetase (mcy) gene cluster. Also encoded within the mcy gene cluster is a putative ATP binding cassette (ABC) transporter, McyH. This study details the bioinformatic and mutational analyses of McyH and offers functional predictions for the hypothetical protein. The transporter is putatively comprised of two homodimers, each wit
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Dissertations / Theses on the topic "Mcy genes"

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Crespim, Elaine. "Identificação e sequenciamento de genes envolvidos na biossíntese de microcistinas e saxitoxinas na cianobactéria Microcystis aeruginosa SPC777." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/64/64133/tde-22052013-112756/.

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As toxinas produzidas por cianobactérias em ecossistemas aquáticos de superfície utilizados para abastecimento público constituem uma preocupação mundial, com casos de intoxicação relatados em diversos países.Sérios problemas de saúde e até mesmo óbito podem ocorrer como consequência dessas intoxicações. Em ambientes de água doce eutrofizados, florações de espécies de Microcystis são frequentemente observadas e, devido à sua ampla distribuição geográfica e capacidade de produzir toxinas, este é um dos gêneros de cianobactérias mais extensivamente estudados. Microcystis spp. são conhecidas pela
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Peres, Raquel Mary Rodrigues 1983. "Instabilidade genômica em neoplasias malignas da mama em função da concentração de alumínio intracelular : Genomic instability association with intracellular aluminum concentration in breast tumors." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/310522.

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Orientador: Luis Otavio Zanatta Sarian<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-11-07T13:37:40Z (GMT). No. of bitstreams: 1 Peres_RaquelMaryRodrigues_D.pdf: 3497486 bytes, checksum: c509c5d08807f1a5bcd1b918eaf7d09d (MD5) Previous issue date: 2013<br>Resumo: Introdução: A hipótese de que os efeitos do alumínio em células humanas podem ter implicações clínicas tem sido levantada há algum tempo, especialmente no que concerne ao câncer de mama. As evidências laboratoriais mostrando altos níveis de alumínio nos teci
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Goldman, Jacki P. "Regulated accessibility of variable region genes may control developmentally ordered T cell receptor [gamma] gene rearrangement." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/32626.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 1995.<br>On t.p., "[gamma] appears as the lower case Greek letter.<br>Includes bibliographical references (leaves 155-172).<br>by Jacki P. Goldman.<br>Ph.D.
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Madisen, Linda. "Lymphoid specific elements deregulate c-myc transcription following chromosomal translocation in murine plasmacytoma and human Burkitt's lymphoma cells /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/6324.

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James, Leonard Philip. "Myc and Mad target genes /." Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/5093.

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Melkoumian, Zaroui K. "Pharmacological regulation of c-myc gene expression in human breast cancer cells." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2218.

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Thesis (Ph. D.)--West Virginia University, 2001.<br>Title from document title page. Document formatted into pages; contains x, 152 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 119-149).
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Abbas, Nasser. "Parthenogenesis in plants: putative functions of MCM genes." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964450941.

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Harrison, David. "MCP-dependent chemotaxis in Rhodobacter sphaeroides." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360292.

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Souza, Ana Carolina Mamana Fernandes de. "Comparação das técnicas de PCR em tempo real e PCR para o estudo dos genes MYCN, DDX1 e NAG em pacientes portadores de neuroblastoma." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/5/5136/tde-21062007-141525/.

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O neuroblastoma é o tumor sólido extra-cranial mais comum e mortal da infância, sendo o tempo de sobrevida nos casos mais agressivos ainda muito curto. Uma das esperanças nesses casos é que os estudos moleculares possam fornecer informações sobre os genes ou as vias moleculares que governam a patogênese dos neuroblastomas. Pois, há poucos genes como o MYCN, que foi descrito por estar diretamente ligado ao neuroblastoma. A amplificação deste oncogene ocorre em pouco mais de 25% dos neuroblastomas e é considerada como o mais importante marcador de prognóstico nestes tumores, sendo fortemente rel
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Vulcani-Freitas, Tânia Maria [UNIFESP]. "Perfil de expressão dos genes MYC, MYCN, TERT, ASPM e PRAME em Meduloblastoma." Universidade Federal de São Paulo (UNIFESP), 2010. http://repositorio.unifesp.br/handle/11600/9928.

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Made available in DSpace on 2015-07-22T20:50:35Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-04-28<br>Meduloblastoma (MB) é o tumor maligno de sistema nervoso central (SNC) mais comum em criança, compreendendo 20% dos tumores primários de SNC e 40% dos tumores cerebelares da infância. Devido sua forte tendência metastática, o tratamento padrão pós-operatório inclui radio e quimioterapia, cujo impacto causa distúrbios endócrinos e de crescimento, e disfunção neurocognitiva a longo prazo. Frente a esses efeitos negativos, muitas pesquisas em meduloblastoma têm sido realizadas com in
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Books on the topic "Mcy genes"

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Dobert, Raymond. Gene expression in cereal crops: June 1992 - May 1994. National Agricultural Library, 1994.

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Raymond, Dobert. Gene expression in cereal crops: June 1992-May 1994. National Agricultural Library, 1994.

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Fulton, Wong, ed. Molecular neuroscience: Expression of neural genes : proceedings of the Fourth Galveston Neuroscience Symposium, held at Galveston, Texas, May 8-10, 1986. A.R. Liss, 1987.

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Dobert, Raymond. Gene expression in oilseed, fiber and forage crops : January 1992 - May 1994. National Agricultural Library, 1994.

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Raymond, Dobert. Gene expression in oilseed, fiber and forage crops : January 1992 - May 1994. National Agricultural Library, 1994.

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Ion, Măndoiu, Sunderraman Rajshekhar, and Zelikovsky Alexander, eds. Bioinformatics research and applications: Fourth international symposium, ISBRA 2008, Atlanta, GA, USA, May 6-9, 2008 : proceedings. Springer, 2008.

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Dobert, Raymond. Gene expression in oilseed, fiber, and forage crops: January 1992 - May 1994. National Agricultural Library, 1994.

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Etienne, Pays, ed. The trypanosome surface: Proceedings of the Third Francqui Colloquium, 26-27 May 1997, Brussels. De Boeck Université, 1999.

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Gene therapy: Are patients any safer? : hearing before the Subcommittee on Public Health of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Sixth Congress, second session ... May 25, 2000. U.S. G.P.O., 2000.

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United States. Congress. Senate. Committee on Small Business. Research on childhood diseases by entrepreneurs: Hearing before the Committee on Small Business, United States Senate, One Hundred Third Congress, second session ... Thursday, May 26, 1994. U.S. G.P.O., 1995.

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Book chapters on the topic "Mcy genes"

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Dang, Chi V., and Linda A. Lee. "Retroviruses, Cancer Genes, and Tumor Suppressor Genes." In c-Myc Function in Neoplasia. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-662-22681-0_2.

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Piatigorsky, Joram. "Crystallin genes: specialization by changes in gene regulation may precede gene duplication." In Genome Evolution. Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0263-9_13.

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Sodir, Nicole M., and Laura Soucek. "The Myc World Within Reach." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_1.

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Song, Rui, Nicole Sponer, and Lin He. "Methods to Quantify microRNAs in the Myc Gene Network for Posttranscriptional Gene Repression." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_10.

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Jackstadt, Rene, Antje Menssen, and Heiko Hermeking. "Genome-Wide Analysis of c-MYC-Regulated mRNAs and miRNAs, and c-MYC DNA Binding by Next-Generation Sequencing." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_11.

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Grandori, Carla. "A High-Throughput siRNA Screening Platform to Identify MYC-Synthetic Lethal Genes as Candidate Therapeutic Targets." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_12.

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Cunningham, John T., Michael Pourdehnad, Craig R. Stumpf, and Davide Ruggero. "Investigating Myc-Dependent Translational Regulation in Normal and Cancer Cells." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_13.

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Le, Anne, and Chi V. Dang. "Studying Myc’s Role in Metabolism Regulation." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_14.

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Rakhra, Kavya, and Dean W. Felsher. "Generation of a Tetracycline Regulated Mouse Model of MYC-Induced T-Cell Acute Lymphoblastic Leukemia." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_15.

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Huels, David J., Patrizia Cammareri, Rachel A. Ridgway, Jan P. Medema, and Owen J. Sansom. "Methods to Assess Myc Function in Intestinal Homeostasis, Regeneration, and Tumorigenesis." In The Myc Gene. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-429-6_16.

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Conference papers on the topic "Mcy genes"

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Shaposhnikov, A. I., N. A. Vishnevskaya, V. Yu Shakhnazarova, et al. "Activation of protective reactions in barley plants during colonization of roots with the phytopathogenic fungus Fusarium culmorum in the presence of Pseudomonas fluorescens 2137." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2020. http://dx.doi.org/10.33952/2542-0720-2020-5-9-10-118.

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The expression of the PAL gene, one of the host protection genes, in sterile barley plants and colonized F. culmorum and P. fluorescens 2137 were assessed. The obtained results indicate that strain 2137 may cause a more active protective response (1.5-2.1 fold) in barley than a phytopathogenic fungus.
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Mikov, D. S., E. R. Davoyan, Yu S. Zubanova, V. Ya Kovtunenko, V. V. Panchenko, and A. P. Kalmysh. "Identification of triticale lines resistant to leaf rust in the National Center of Grain named after P.P. Lukyanenko." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2020. http://dx.doi.org/10.33952/2542-0720-2020-5-9-10-68.

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Creation of leaf rust resistant varieties is one of the main aims of breeding of this crop. 94 lines of triticale were screened on the presence of genes Lr10, Lr25, Lr26 and its combinations. Lr26 gene was identified in all samples, 3 lines are carriers of Lr10 gene and presence of Lr25 was established in 4 lines. Combination Lr10+Lr26 was identified in lines 13-15т2-6, 13-15т2-7, 13-99т5-7 and 10-205т3-31, combination Lr25+Lr26 was established in lines 13-159т1-17, 12-80т14-1, 12-т1т-5 and 12-80т14-10. Eighty-five lines are resistant to leaf rust and nine lines are susceptible. In four lines
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Pannekoek, H., M. Linders, J. Keijer, H. Veerman, H. Van Heerikhuizen, and D. J. Loskutoff. "THE STRUCTURE OF THE HUMAN ENDOTHELIAL PLASMINOGEN ACTIVATOR INHIBITOR (PAI-1) GENE: NON-RANDOM POSITIONING OF INTRONS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644767.

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The endothelium plays a crucial role in the regulation of the fibrinolytic process, since it synthesizes and secretes tissue-type plasminogen activator (t-PA) as well as the fast-acting plasminogen activator inhibitor (PAI-1). Molecular cloning of full-length PAI-1 cDNA, employing a human endothelial cDNA expression library, and a subsequent determination of the complete nucleotide sequence, allowed a prediction of the amino-acid sequence of the PAI-1 glycoprotein. It was observed that the amino-acid sequence is significantly homologous to those of members of the serine protease inhibitor ("Se
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Ong, Bruce A., Julian L. Allen, Jason Caboot, Oscar H. Mayer, Patrick Sleiman, and Hakon Hakonarson. "Gene Network Analysis Identifies Novel Lung Function Genes." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a6024.

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Giannelli, B. F. "MOLECULAR GENETICS OF HAEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643981.

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Haemophilia B, an X-linked recessive disease with an incidence of 1/30,000 newborn males, is due to defects in the gene for coagulation factor IX, which is on the long am of the X chromosome at band Xq27.1. This gene consists of approximately 34 Kb and contains 8 exons which specify a mRtfc of 2803 residues coding for a protein of 415 aa preceded by a prepro signal peptide of 46 aa. Coripanson of the functional domains of the factor IX protein with the exon structure of the gene supports the exon/protein domain hypothesis of gene evolution. The factor IX gene seems to be formed by a number of
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Polstein, Lauren R., and Charles A. Gersbach. "Photoregulated Gene Expression in Human Cells With Light-Inducible Engineered Transcription Factors." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80573.

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Systems for controlling gene expression in mammalian cells have a wide range of applications in medicine, biotechnology and basic science. An ideal gene regulatory system would allow for precise and specific control over the magnitude and kinetics of gene expression in space and time, while also exerting minimal influence on other genes and cellular components. Several gene regulatory systems have been developed in which orthogonal transcription machinery from prokaryotes or insects has been imported into mammalian cells and used to control the expression of a specific gene. Despite the transf
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Laug, Walter E. "HETEROGENOUS EXPRESSION OF PLASMINOGEN ACTIVATOR (PA) GENES IN THE HUMAN SARCOMA CELL LINE HT1080." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644395.

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Tumor cell derived PA activities are of crucial importance for tissue invasion and destruction by tumor cells. Therefore, we studied the expression of the PA genes in HT1080 cells using immunoenzymatic methods and specific PA gene probes.Immunenzymatic methods allowed only for the detection of urokinase like PA (u-PA) activities in HT1080 cells which was suppressed by treatment of the cells with dexamethasone (10-7 m). Despite the lack of u-PA activities, the cells still degraded extracellular tissue glycoproteins. Northern blot analysis with specific PA gene probe showed that HT1080 cells exp
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"In silico analysis of the R2R3-Myb, bHLH-Myc and WDR proathocyanidins regulatory genes in Gossypium genus." In SYSTEMS BIOLOGY AND BIOINFORMATICS (SBB-2020). Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences., 2020. http://dx.doi.org/10.18699/sbb-2020-23.

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Ong, Bruce A., Jason Caboot, Julian Allen, et al. "Gene Network Analysis In A Pediatric Cohort Identifies Novel Lung Function Genes." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3488.

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Bomfim, Isabela Maria Fortaleza Neves, Yanne Naara Teixeira De Carvalho, Joyce Hercília Jerônimo Lins, Amanda Viera Barros, and Renato Motta Neto. "CULTURAS DE VIGILÂNCIA DE RESISTÊNCIA DE PACIENTES INTERNOS EM UNIDADE DE TERAPIA INTENSIVA DO HOSPITAL REFERÊNCIA EM DOENÇAS INFECCIOSAS DO RIO GRANDE DO NORTE." In I Congresso Nacional de Microbiologia Clínica On-Line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1202.

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Introdução: As Infecções Relacionadas à Assistência à Saúde (IRAS) são infeções adquiridas no curso de uma internação em uma unidade hospitalar. As Unidades de Terapia Intensiva (UTI) são os locais onde frequentemente ocorrem surtos por bactérias multirresistentes, visto a pressão seletiva e a disseminação de genes de resistência nestes ambientes. As culturas de vigilância de resistência são um conjunto de técnicas de isolamento e identificação de microrganismos resistentes aos antimicrobianos em indivíduos colonizados com a finalidade de prevenir as IRAS. Objetivos: Este trabalho teve como me
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Reports on the topic "Mcy genes"

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Michelmore, R. Transposon tagging of disease resistance genes. Progress report, May 1, 1988--1992. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10179207.

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Melkoumian, Zaroui. Regulation of C-myc Gene Expression by Potassium Channel Blocker Quindine in MCF-7 Human Breast Cancer Cell Line. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada384096.

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Michelmore, R. Transposon tagging of disease resistance genes. Final report, May 1, 1988--April 30, 1993. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10179215.

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Doi, R. H. Characterization and expression of Clostridium cellulase genes. Progress report, May 1, 1987--April 30, 1989. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/10138103.

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Sheen, Joon-Ho. A Gene Amplification Phenotype in c-Myc-Induced Mammary Tumors Cells. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada396567.

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Sheen, Joon-Ho. A Gene Amplification Phenotype in c-Myc-Induced Mammary Tumors Cells. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada390716.

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Kuchka, M. R. Post transcriptional regulation of chloroplast gene expression by nuclear encoded gene products. Progress report, June 1, 1991--May 31, 1992. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10142165.

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Hutchinson, M. L., J. E. L. Corry, and R. H. Madden. A review of the impact of food processing on antimicrobial-resistant bacteria in secondary processed meats and meat products. Food Standards Agency, 2020. http://dx.doi.org/10.46756/sci.fsa.bxn990.

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For meat and meat products, secondary processes are those that relate to the downstream of the primary chilling of carcasses. Secondary processes include maturation chilling, deboning, portioning, mincing and other operations such as thermal processing (cooking) that create fresh meat, meat preparations and ready-to-eat meat products. This review systematically identified and summarised information relating to antimicrobial resistance (AMR) during the manufacture of secondary processed meatand meat products (SPMMP). Systematic searching of eight literature databases was undertaken and the resu
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Petz, Lawrence N. Expression of the Estrogen-Regulated pS2 Gene in MCF-7 Human Breast Cancer Cells. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada398062.

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Petz, Lawrence N. Expression of the Estrogen-Regulated pS2 Gene in MCF-7 Human Breast Cancer Cells. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada360028.

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