Academic literature on the topic 'Escherichia coli Genetics'

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Journal articles on the topic "Escherichia coli Genetics"

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Lorenz, E., M. D. Plamann, and G. V. Stauffer. "Escherichia coli." MGG Molecular & General Genetics 250, no. 1 (1996): 81. http://dx.doi.org/10.1007/s004380050053.

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Gottesman, S. "Genetics of Proteolysis in Escherichia Coli." Annual Review of Genetics 23, no. 1 (December 1989): 163–98. http://dx.doi.org/10.1146/annurev.ge.23.120189.001115.

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Milkman, Roger. "Recombination and Population Structure in Escherichia coli." Genetics 146, no. 3 (July 1, 1997): 745–50. http://dx.doi.org/10.1093/genetics/146.3.745.

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Reynolds, Mary G. "Compensatory Evolution in Rifampin-Resistant Escherichia coli." Genetics 156, no. 4 (December 1, 2000): 1471–81. http://dx.doi.org/10.1093/genetics/156.4.1471.

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Abstract This study examines the intrinsic fitness burden associated with RNA polymerase (rpoB) mutations conferring rifampin resistance in Escherichia coli K12 (MG1655) and explores the nature of adaptation to the costs of resistance. Among 28 independent Rifr mutants, the per-generation fitness burden (in the absence of rifampin) ranged from 0 to 28%, with a median of 6.4%. We detected no relationship between the magnitude of the cost and the level of resistance. Adaptation to the costs of rif resistance was studied by following serial transfer cultures for several Rifr mutants both in the p
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Thaler, D. S., G. Tombline, and K. Zahn. "Short-patch reverse transcription in Escherichia coli." Genetics 140, no. 3 (July 1, 1995): 909–15. http://dx.doi.org/10.1093/genetics/140.3.909.

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Abstract Chimeras of RNA and DNA have distinctive physical and biological properties. Chimeric oligonucleotides that contained one, two or three ribonucleotides whose phosphodiester backbone was covalently continuous with DNA were synthesized. Site-directed mutagenesis was used to assess genetic information transfer from the ribonucleotide positions. Transfer was scored by the formation or reversion of an ochre site that also corresponded to a restriction cleavage site. This allowed physical as well as genetic assay of mutational events. Bases attached to the ribonucleotides were able to accur
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Friedman-Ohana, Rachel, Iris Karunker, and Amikam Cohen. "Chi-Dependent Intramolecular Recombination in Escherichia coli." Genetics 148, no. 2 (February 1, 1998): 545–57. http://dx.doi.org/10.1093/genetics/148.2.545.

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Abstract Homologous recombination in Escherichia coli is enhanced by a cis-acting octamer sequence named Chi (5′-GCTGGTGG-3′) that interacts with RecBCD. To gain insight into the mechanism of Chi-enhanced recombination, we recruited an experimental system that permits physical monitoring of intramolecular recombination by linear substrates released by in vivo restriction from infecting chimera phage. Recombination of the released substrates depended on recA, recBCD and cis-acting Chi octamers. Recombination proficiency was lowered by a xonA mutation and by mutations that inactivated the RuvABC
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Volkert, Michael R., Dinh C. Nguyen, and K. Christopher Beard. "ESCHERICHIA COLI GENE INDUCTION BY ALKYLATION TREATMENT." Genetics 112, no. 1 (January 1, 1986): 11–26. http://dx.doi.org/10.1093/genetics/112.1.11.

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ABSTRACT Searches for alkylation-inducible (aid) genes of Escherichia coli have been conducted by screening random fusions of the Mu-dl(ApR lac) phage for fusions showing increased β-galactosidase activity after treatment with methylating agents, but not after treatments with UV-irradiation. In this report we describe gene fusions that are specifically induced by alkylation treatments. Nine new mutants are described, and their properties are compared with the five mutants described previously. The total of 14 fusion mutants map at five distinct genetic loci. They can be further subdivided on t
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Cooke, E. Mary. "Escherichia coli – an overview." Journal of Hygiene 95, no. 3 (December 1985): 523–30. http://dx.doi.org/10.1017/s022217240006065x.

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The isolation and description of Bacillus coli commune by Escherich a hundred years ago marked the start of a series of scientific investigations which have led to some of the most important discoveries in microbial pathogenicity and genetics that have been made since that time. It is not difficult to find the reasons why so much effort has been concentrated on this organism. Escherichia coli is present in the gut of all warm-blooded animals generally forming the predominant aerobic flora; it is of medical and veterinary importance being responsible for a variety of infections in the human and
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Lederberg, Joshua. "Genetic Recombination in Escherichia coli: Disputation at Cold Spring Harbor, 1946–1996." Genetics 144, no. 2 (October 1, 1996): 439–43. http://dx.doi.org/10.1093/genetics/144.2.439.

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Guttman, D. S., and D. E. Dykhuizen. "Detecting selective sweeps in naturally occurring Escherichia coli." Genetics 138, no. 4 (December 1, 1994): 993–1003. http://dx.doi.org/10.1093/genetics/138.4.993.

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Abstract The nucleotide sequences of the gapA and pabB genes (separated by approximately 32.5 kb) were determined in 12 natural isolates of Escherichia coli. Three analyses were performed on the data. First, the levels of polymorphism at the loci were compared within and between E. coli and Salmonella strains relative to their degrees of constraint. Second, the gapA and pabB loci were analyzed by the Hudson-Kreitman-Aguadé (HKA) test for selective neutrality. Four additional dispersed genes (crr, putP, trp and gnd) were added to the analysis to provide the necessary frame of reference. Finally
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Dissertations / Theses on the topic "Escherichia coli Genetics"

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Baldwin, Thomas John. "Disease mechanism of enteropathogenic Escherichia coli." Thesis, University of Leicester, 1990. http://hdl.handle.net/2381/34445.

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Colonization of gut mucosal surfaces by enteropathogenic Escherichia coli (EPEC) elicits a severe persistant diarrhoea in infants and young children without elaboration of enterotoxins or tissue invasion. The formation of a distinct ultrastructural lesion involving intimate adherence to cell surfaces, loss of microvilli and membrane perturbations, however, has for some time been recognized as an important component of pathogenesis, but the processes involved in lesion formation and its relevance to the disease state remained obscure. In this study intimate adherence of EPEC to surfaces of cult
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Lim, C. K. "Cloning of Streptomyces genes in Escherichia coli." Thesis, University of Leeds, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373850.

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Chua, K.-L. "Plasmid recombination in Escherichia coli K-12." Thesis, University of Cambridge, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383777.

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Morgan, Brian Alexander. "The regulation of rpoBC in Escherichia coli." Thesis, University of Edinburgh, 1986. http://hdl.handle.net/1842/15431.

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Agostinho, Juliana Maria Avanci [UNESP]. "Diversidade genética, fatores de virulência e perfis de susceptibilidade a antimicrobianos de isolados de Escherichia coli provenientes do útero, da boca e das fezes de cadelas com piometra." Universidade Estadual Paulista (UNESP), 2013. http://hdl.handle.net/11449/108413.

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Made available in DSpace on 2014-08-13T14:50:35Z (GMT). No. of bitstreams: 0 Previous issue date: 2013-07-26Bitstream added on 2014-08-13T18:01:12Z : No. of bitstreams: 1 000735330_20140826.pdf: 26004 bytes, checksum: 80491d16dd561bc066d6dacbdc900451 (MD5)<br>A piometra canina é uma enfermidade caracterizada pela inflamação do útero com acúmulo de exsudatos, acometendo principalmente fêmeas adultas. Ocorre na fase lútea do ciclo estral em decorrência de alterações hormonais e infecção bacteriana. É reconhecida como uma das principais causas de morte em cadelas e a Escherichia coli é o prin
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Sendy, Bandar. "Studies on transcription in Escherichia coli." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7576/.

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The expression of genes is tightly controlled, predominantly at the point of transcription. RNA polymerase (RNAP) must first bind to a deoxyribonucleic acid (DNA) promoter upstream of a gene to transcribe it. However, the ability of RNAP binding is dictated by the core promoter DNA sequence, the presence of transcription activator or repressor proteins and numerous other factors. The strength of promoters has been indirectly measured. Only a few studies have attempted to directly address the RNAP flux through transcription units, and further studies are still required. In the current study, th
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Ennis, Don Gregory. "Genetics of SOS mutagenesis." Diss., The University of Arizona, 1988. http://hdl.handle.net/10150/184602.

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Previous genetic evidence suggested that RecA was required in SOS mutagenesis for its regulatory role and perhaps some other nonregulatory role (Mount, 1977; Blanco et al., 1982). I undertook a genetic study which confirmed the above studies and provided further evidence that RecA protein appeared to have a dual "role in mutagenesis; first, the cleavage of LexA repressor for the derepression of specific SOS genes and second, one or more additional role(s). For these studies a new phage mutagenesis assay was developed which allows rapid scoring of SOS mutagenesis in a large number of host mutan
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Woodgate, R. "A mechanism for UV mutagenesis in Escherichia coli." Thesis, University of Sussex, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375858.

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Hallewell, Jennyka, and University of Lethbridge Faculty of Arts and Science. "Shiga toxin-producing bacteriophage in Escherichia coli O157:H7." Thesis, Lethbridge, Alta. : University of Lethbridge, Deptartment of Biochemistry, 2008, 2008. http://hdl.handle.net/10133/776.

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Shiga toxin-producing E. coli (STEC) including E. coli O157:H7 are potential food and water borne zoonotic bacterial pathogens capable of causing outbreaks of severe illness in humans. The virulence of E. coli O157:H7 strains may be related to the type of Stx produced and several Stx2 variants have been identified which appear to differ in their ability to cause disease. Two lineages exist within O157 strains where lineage I is associated mainly with human and bovine isolates and lineage II is associated mainly with bovine isolates. The goal of this study was to identify and characterize a lin
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Miao, Yuanying, and 缪元颖. "The localization of E. coli persistent gene products." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B45554791.

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Books on the topic "Escherichia coli Genetics"

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Molecular genetics of Escherichia coli. New York, NY: Guilford Press, 1989.

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Smith-Keary, P. F. Genetic elements in Escherichia Coli. Basingstoke: Macmillan Education, 1988.

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Trempy, Janine. Fundamental bacterial genetics. Oxford: Blackwell, 2004.

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Ohman, Dennis E. Experiments in gene manipulation. Englewood Cliffs, N.J: Prentice Hall, 1988.

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Vaillancourt, Peter E. E. coli gene expression protocols. Totowa, N.J: Humana, 2011.

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E, Trempy J., ed. Fundamental bacterial genetics. Malden, MA: Blackwell Science, 2004.

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Mendelson, Itai. Mivneh ṿe-tafḳid ḥelbonim demuye hisṭonim be-ḥaidaḳe E. coli. [Israel: ḥ. mo. l., 1992.

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Polen, Tino. Genomweite Genexpressionsanalysen mit DNA-Chips zur Charakterisierung des Glucose-Überflussmetabolismus von Escherichia coli. Jülich: Forschungszentrum Jülich GmbH, Institut für Biotechnologie, 2003.

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Syväoja, Juhani. Factors involved in deoxyribonucleic acid ligation in Escherichia coli cells. Oulu: University of Oulu, 1987.

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Heterologous gene expression in E. coli: Methods and protocols. New York, NY: Humana Press, 2011.

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Book chapters on the topic "Escherichia coli Genetics"

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Birge, Edward A. "Conjugation in Escherichia coli." In Bacterial and Bacteriophage Genetics, 220–46. New York, NY: Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4757-1995-6_9.

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Teel, Louise D., Angela R. Melton-Celsa, and Alison D. O'Brien. "Shiga Toxin-Producing Escherichia coli." In Population Genetics of Bacteria, 199–223. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817114.ch12.

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Alm, Elizabeth W., Seth T. Walk, and David M. Gordon. "The Niche of Escherichia coli." In Population Genetics of Bacteria, 67–89. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817114.ch6.

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Hacker, J., and C. Hughes. "Genetics of Escherichia coli Hemolysin." In Current Topics in Microbiology and Immunology, 139–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70586-1_8.

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Orndorff, Paul E. "Escherichia coli Type 1 Pili." In Molecular Genetics of Bacterial Pathogenesis, 91–111. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555818340.ch7.

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Birge, Edward A. "Conjugation and the Escherichia coli Paradigm." In Bacterial and Bacteriophage Genetics, 277–303. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4757-2328-1_11.

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Birge, Edward A. "Conjugation and the Escherichia coli Paradigm." In Bacterial and Bacteriophage Genetics, 341–71. New York, NY: Springer New York, 2000. http://dx.doi.org/10.1007/978-1-4757-3258-0_11.

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Lloyd, Amanda L., and Harry L. T. Mobley. "Fitness Islands in Uropathogenic Escherichia coli." In Population Genetics of Bacteria, 157–79. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817114.ch10.

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McCarthy, John E. G. "Expression of atp Genes in Escherichia Coli." In Genetics of Translation, 451–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73139-6_37.

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Campbell, Allan, and Alice del Campillo-Campbell. "The Biotin Operon of Escherichia coli." In The Lure of Bacterial Genetics, 33–41. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555816810.ch5.

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Conference papers on the topic "Escherichia coli Genetics"

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Ishihama, Akira, Hiroshi Ogasawara, Tomohiro Shimada, Jun Teramoto, Akiko Hasegawa, Yoshimasa Umezawa, Koshiro Yabuki, et al. "Multi-Scale Genetics of Transcription Network: Understanding the Regulatory Roles of All 300 Transcription Factors from a Single Organism Escherichia coli." In 2007 International Symposium on Micro-NanoMechatronics and Human Science. IEEE, 2007. http://dx.doi.org/10.1109/mhs.2007.4420820.

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Trevizani, Raphael. "Genetic algorithm for deimmunization of Escherichia coli L-asparaginase." In IV International Symposium on Immunobiologicals & VII Seminário Anual Científico e Tecnológico. Instituto de Tecnologia em Imunobiológicos, 2019. http://dx.doi.org/10.35259/isi.sact.2019_32695.

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Daineko, A. V., A. B. Bulatovski, and A. I. Zinchenko. "STUDY ON POTENTIAL ENGINEERING OF ESCHERICHIA COLI XANTHOSE PHOSPHORYLASE STRAIN-PRODUCER." In SAKHAROV READINGS 2021: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2021. http://dx.doi.org/10.46646/sakh-2021-2-38-41.

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Genetic engineering is an actively developing branch of modern biotechnology. Using the methods of genetic engineering, it is possible to construct new forms of microorganisms that can synthesize a variety of substances, including enzymes. Xanthosine phosphorylase is the second purine nucleoside phosphorylase (PNP-II) in E. coli. This enzyme performs both reactions of phosphorolysis and the synthesis of purine deoxy / ribonucleosides. Due to this ability, xanthosine phosphorylase can catalyze the reaction of the formation of nicotinamide riboside. This substance is a precursor of the most impo
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Kazlouski, I., I. Belskaya, A. Soloveva, А. Zinchenko, O. Novikova, and Y. Lomako. "ENGINEERING OF A GENETIC CONSTRUCTION CONTAINING SUBUNIT B OF THERMOLABILE ESCHERICHIA COLI ANATOXIN." In SAKHAROV READINGS 2020: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. Minsk, ICC of Minfin, 2020. http://dx.doi.org/10.46646/sakh-2020-2-66-69.

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Hajimorad, Meghdad, and Jay D. Keasling. "Independence among synthetic genetic devices in the bacterium Escherichia coli extends to the time-domain." In 2014 IEEE Biomedical Circuits and Systems Conference (BioCAS). IEEE, 2014. http://dx.doi.org/10.1109/biocas.2014.6981652.

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Geethalakshmi, S., S. Narendran, S. Ramalingam, and N. Pappa. "Optimization of Fed-Batch Process for Recombinant Protein Production in Escherichia coli Using Genetic Algorithm." In 2011 International Conference on Process Automation, Control and Computing (PACC). IEEE, 2011. http://dx.doi.org/10.1109/pacc.2011.5978907.

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Wei, S., P. J. Richards, and Christine E. R. Dodd. "Genetic typing and heat resistance of Escherichia coli from pig carcasses during slaughter in a UK slaughterhouse." In Eighth International Symposium on the Epidemiology and Control of Foodborne Pathogens in Pork. Iowa State University, Digital Press, 2009. http://dx.doi.org/10.31274/safepork-180809-814.

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Kerouanton, A., V. Rose, B. Chidaine, I. Kempf, and Martin Denis. "Comparison of organic and conventional pig productions on prevalence, antibiotic resistance and genetic diversity of Escherichia coli." In 10th International Conference on the Epidemiology and Control of Biological, Chemical and Physical Hazards in Pigs and Pork. Iowa State University, Digital Press, 2013. http://dx.doi.org/10.31274/safepork-180809-930.

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Chinen, Isabel, Elizabeth Miliwebsky, Claudia Carolina Carbonari, Beatríz D´Astek, Gisela Zolezzi, Natalia Deza, Ariela Baschkier, Eduardo Manfredi, and Marta Rivas. "Characterization and Genetic Relationship of Shiga Toxin-Producing Escherichia Coli Strains Isolated From Food in Argentina, 1999-2013." In XII Latin American Congress on Food Microbiology and Hygiene. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/foodsci-microal-244.

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Pannekok, H., A. J. Van Zonneveid, C. J. M. de vries, M. E. MacDonald, H. Veerman, and F. Blasi. "FUNCTIONAL PROPERTIES OF DELETION-MUTANTS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643724.

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Over the past twenty-five years, genetic methods have generated a wealth of information on the regulation and the structure-function relationship of bacterial genes.These methods are based on the introduction of random mutations in a gene to alter its function. Subsequently, genetic techniques cure applied to localize the mutation, while the nature of the impairedfunction could be determined using biochemical methods. Classic examples of this approach is now considered to be the elucidation of the structure and function of genes, constituting the Escherichia coli lactose (lac) and tryptophan (
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Reports on the topic "Escherichia coli Genetics"

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Gutnick, David, and David L. Coplin. Role of Exopolysaccharides in the Survival and Pathogenesis of the Fire Blight Bacterium, Erwinia amylovora. United States Department of Agriculture, September 1994. http://dx.doi.org/10.32747/1994.7568788.bard.

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Fireblight, a disease of apples and pears, is caused by Erwinia amylovora. Mutants of E. amylovora that do not produce the extreacellular polysaccharide (EPS), amylovoran, are avirulent. A similar EPS, stewartan, is produced by E. stewartii, which caused Stewart's wilt of corn, and which has also been implicated in the virulence of this strain. Both stewartan and amylovoran are type 1 capsular polysaccharides, typified by the colanic acid slime produced by Escherichia coli. Extracellular polysaccharide slime and capsules are important for the virulence of bacterial pathogens of plants and anim
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Cahaner, Avigdor, Susan J. Lamont, E. Dan Heller, and Jossi Hillel. Molecular Genetic Dissection of Complex Immunocompetence Traits in Broilers. United States Department of Agriculture, August 2003. http://dx.doi.org/10.32747/2003.7586461.bard.

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Objectives: (1) Evaluate Immunocompetence-OTL-containing Chromosomal Regions (ICRs), marked by microsatellites or candidate genes, for magnitude of direct effect and for contribution to relationships among multiple immunocompetence, disease-resistance, and growth traits, in order to estimate epistatic and pleiotropic effects and to predict the potential breeding applications of such markers. (2) Evaluate the interaction of the ICRs with genetic backgrounds from multiple sources and of multiple levels of genetic variation, in order to predict the general applicability of molecular genetic marke
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Smiley, Daniel. A genetic and physiological study of an arsenite resistant, uncoupled mutant of Escherichia coli. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3124.

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Willis, C., F. Jorgensen, S. A. Cawthraw, H. Aird, S. Lai, M. Chattaway, I. Lock, E. Quill, and G. Raykova. A survey of Salmonella, Escherichia coli (E. coli) and antimicrobial resistance in frozen, part-cooked, breaded or battered poultry products on retail sale in the United Kingdom. Food Standards Agency, May 2022. http://dx.doi.org/10.46756/sci.fsa.xvu389.

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Frozen, breaded, ready-to-cook chicken products have been implicated in outbreaks of salmonellosis. Some of these outbreaks can be large. For example, one outbreak of Salmonella Enteritidis involved 193 people in nine countries between 2018 and 2020, of which 122 cases were in the UK. These ready-to-cook products have a browned, cooked external appearance, which may be perceived as ready-to-eat, leading to mishandling or undercooking by consumers. Continuing concerns about these products led FSA to initiate a short-term (four month), cross-sectional surveillance study undertaken in 2021 to det
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