Relevant bibliographies by topics / Oorah

Academic literature on the topic 'Oorah'

Author: Grafiati
Published: 26 July 2024
Last updated: 27 July 2024

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Journal articles on the topic "Oorah"

1

Vranic, Valentino, and Milan Laslop. "Aspects and roles in software modeling: A composition based comparison." Computer Science and Information Systems 13, no. 1 (2016): 199–216. http://dx.doi.org/10.2298/csis151207065v.

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It?s intriguing how the work on inherent aspect-oriented modeling almost completely ignores the similarity between aspect-oriented and role based decomposition and composition. Ever since the notion of aspect entered the software development arena, it has been compared to the notion of role. Findings range from identifying greater similarities to more cautious observations that albeit aspects and roles are similar, they appear to be more as complimentary with a significant effort needed to really bring them together in programming. Even a cursory comparison of Theme/UML, which represents a design part of Theme, probably the best known and most comprehensive approach to aspect-oriented modeling, to OOram, a prominent representative of approaches to role based modeling that influenced UML, reveals striking similarities in both decomposition and composition. Within a more comprehensive effort of finding the principles of a sustainable approach to aspect-oriented modeling, this paper pursues further this observation by establishing a partially reversible transformation of a Theme/UML model to the corresponding OOram model that proves principal analogy of themes to OOram collaboration view diagrams accompanied by the corresponding scenario view and interface view diagrams. An important implication is that aspects have their counterpart not in roles themselves, but in role collaboration. Based on these results, a possibility of using UML composite structure diagrams for aspect-oriented design is sketched out in the paper.
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2

Graham, Ian. "Working with objects: The OOram software engineering method." Fuzzy Sets and Systems 82, no. 1 (August 1996): 130–31. http://dx.doi.org/10.1016/0165-0114(96)87709-8.

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3

Molina, Jesús García, María José Ortín, Begoña Moros, and Joaquín Nicolás. "Transforming the OOram Three-Model Architecture into a UML-based Process." Journal of Object Technology 1, no. 4 (2002): 119. http://dx.doi.org/10.5381/jot.2002.1.4.a2.

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4

Hughes, Nicky J., Chris L. Clayton, Peter A. Chalk, and David J. Kelly. "Helicobacter pylori porCDAB and oorDABCGenes Encode Distinct Pyruvate:Flavodoxin and 2-Oxoglutarate:Acceptor Oxidoreductases Which Mediate Electron Transport to NADP." Journal of Bacteriology 180, no. 5 (March 1, 1998): 1119–28. http://dx.doi.org/10.1128/jb.180.5.1119-1128.1998.

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ABSTRACT Helicobacter pylori, a major cause of human gastric disease, is a microaerophilic bacterium that contains neither pyruvate nor 2-oxoglutarate dehydrogenase activity. Previous studies (N. J. Hughes, P. A. Chalk, C. L. Clayton, and D. J. Kelly, J. Bacteriol. 177:3953–3959, 1995) have indicated that the major routes for the generation of acetyl coenzyme A (acetyl-CoA) and succinyl-CoA are via pyruvate:flavodoxin oxidoreductase (POR) and 2-oxoglutarate:acceptor oxidoreductase (OOR), respectively. The purified POR is a heterotetrameric protein, with subunits of 48 (PorA), 36 (PorB), 24 (PorC), and 14 (PorD) kDa. In this study OOR has been purified, and it is similarly composed of polypeptides of 43 (OorA), 33 (OorB), 24 (OorC), and 10 (OorD) kDa. Both POR and OOR are oxygen labile and are likely to be major contributors to the microaerophilic phenotype of H. pylori. Unlike POR, OOR was unable to use a previously identified flavodoxin (FldA) as an electron acceptor. Although the purified enzymes were unable to reduce NAD(P), electrons from both pyruvate and 2-oxoglutarate could reduce NADP in cell extracts, consistent with a role for these oxidoreductases in the provision of NADPH as a respiratory electron donor. The H. pylori por,oor, and fldA genes were cloned and sequenced. The deduced por gene products showed significant sequence similarity to archaeal four-subunit 2-oxoacid:acceptor oxidoreductases. However, the amino acid sequences of OorA and -B were more closely related to that of the two-subunit POR of the aerobic halophile Halobacterium halobium. BothporD and oorD encode integral ferredoxin-like subunits. POR and OOR are probably essential enzymes in H. pylori, as insertion inactivation of porB andoorA appeared to be lethal.
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Feinleib, Jessica, and Arthur French. "Standardization of US Veterans Health Administration system non-OR airway management through the OORAM educational program." Trends in Anaesthesia and Critical Care 30 (February 2020): e174-e175. http://dx.doi.org/10.1016/j.tacc.2019.12.428.

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6

Mulder, J. A., R. F. Berry, J. A. Halpin, S. Meffre, and J. L. Everard. "Depositional age and correlation of the Oonah Formation: refining the timing of Neoproterozoic basin formation in Tasmania." Australian Journal of Earth Sciences 65, no. 3 (February 15, 2018): 391–407. http://dx.doi.org/10.1080/08120099.2018.1426629.

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7

Sampath, Prabakaran, Sowmyapriya Rajalingam, Sharmila Murugesan, Rakesh Bhardwaj, and Veena Gupta. "Evaluation of Chemical Composition among the Multi Colored Germplasm of Abrus precatorius L." Plants 13, no. 14 (July 18, 2024): 1963. http://dx.doi.org/10.3390/plants13141963.

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The medicinal plant Abrus precatorius L. was traditionally used in the Siddha and Ayurvedic systems of medicine in India. The Indian center of origin holds a vast variability in its seed color. The objective of this study was to assess the total monomeric anthocyanin, flavonol, as well as the antioxidative potential, protein content and ash content among the accessions. A total of 99 accessions conserved in the Indian National Genebank were used in this study. The methods used for the estimation of total monomeric anthocyanin, flavonol, as well as the antioxidative potential, protein content and ash content were the pH differential method, Oomah method, Ferric Reducing Antioxidant Potential, Dumas method and gravimetric method, respectively. The completely black colored accession was recorded with highest total monomeric anthocyanin (51.95 mg/100 g of cyanidin 3-glucoside equivalent) and flavonol content (66.41 mg/g of quercetin equivalent). Red + black colored accessions have recorded the maximum value with respect to antioxidants (14.18 mg/g of gallic acid equivalent). The highest amount of protein content was found in a completely white colored accession (20.67%) and the maximum ash content was recorded in red + black colored accession (4.01%). The promising accessions identified can be used by pharmaceutical companies in drug development and in curing degenerative diseases.
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8

Knill, C. "Herbs, botanicals and teas G. Mazza, B.D. Oomah (Eds.); Technomic Publishing Co., Lancaster, PA, 2000, xvii+416 pp, ISBN 1-56676-851-9 (£77.00)." Carbohydrate Polymers 49, no. 4 (September 1, 2002): 516–17. http://dx.doi.org/10.1016/s0144-8617(01)00361-7.

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9

Takai, Ken, Barbara J. Campbell, S. Craig Cary, Masae Suzuki, Hanako Oida, Takuro Nunoura, Hisako Hirayama, et al. "Enzymatic and Genetic Characterization of Carbon and Energy Metabolisms by Deep-Sea Hydrothermal Chemolithoautotrophic Isolates of Epsilonproteobacteria." Applied and Environmental Microbiology 71, no. 11 (November 2005): 7310–20. http://dx.doi.org/10.1128/aem.71.11.7310-7320.2005.

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ABSTRACT The carbon and energy metabolisms of a variety of cultured chemolithoautotrophic Epsilonproteobacteria from deep-sea hydrothermal environments were characterized by both enzymatic and genetic analyses. All the Epsilonproteobacteria tested had all three key reductive tricarboxylic acid (rTCA) cycle enzymatic activities—ATP-dependent citrate lyase, pyruvate:ferredoxin oxidoreductase, and 2-oxoglutarate:ferredoxin oxidoreductase—while they had no ribulose 1,5-bisphosphate carboxylase (RubisCO) activity, the key enzyme in the Calvin-Benson cycle. These results paralleled the successful amplification of the key rTCA cycle genes aclB, porAB, and oorAB and the lack of success at amplifying the form I and II RubisCO genes, cbbL and cbbM. The combination of enzymatic and genetic analyses demonstrates that the Epsilonproteobacteria tested use the rTCA cycle for carbon assimilation. The energy metabolisms of deep-sea Epsilonproteobacteria were also well specified by the enzymatic and genetic characterization: hydrogen-oxidizing strains had evident soluble acceptor:methyl viologen hydrogenase activity and hydrogen uptake hydrogenase genes (hyn operon), while sulfur-oxidizing strains lacked both the enzyme activity and the genes. Although the energy metabolism of reduced sulfur compounds was not genetically analyzed and was not fully clarified, sulfur-oxidizing Epsilonproteobacteria showed enzyme activity of a potential sulfite:acceptor oxidoreductase for a direct oxidation pathway to sulfate but no activity of AMP-dependent adenosine 5′-phosphate sulfate reductase for a indirect oxidation pathway. No activity of thiosulfate-oxidizing enzymes was detected. The enzymatic and genetic characteristics described here were consistent with cellular carbon and energy metabolisms and suggest that molecular tools may have great potential for in situ elucidation of the ecophysiological roles of deep-sea Epsilonproteobacteria.
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10

Gilbreath, Jeremy J., Abby L. West, Oscar Q. Pich, Beth M. Carpenter, Sarah Michel, and D. Scott Merrell. "Fur Activates Expression of the 2-Oxoglutarate Oxidoreductase Genes (oorDABC) in Helicobacter pylori." Journal of Bacteriology 194, no. 23 (September 21, 2012): 6490–97. http://dx.doi.org/10.1128/jb.01226-12.

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ABSTRACTHelicobacter pyloriis a highly successful pathogen that colonizes the gastric mucosa of ∼50% of the world's population. Within this colonization niche, the bacteria encounter large fluctuations in nutrient availability. As such, it is critical that this organism regulate expression of key metabolic enzymes so that they are present when environmental conditions are optimal for growth. One such enzyme is the 2-oxoglutarate (α-ketoglutarate) oxidoreductase (OOR), which catalyzes the conversion of α-ketoglutarate to succinyl coenzyme A (succinyl-CoA) and CO2. Previous studies from our group suggested that the genes that encode the OOR are activated by iron-bound Fur (Fe-Fur); microarray analysis showed that expression ofoorD,oorA, andoorCwas altered in afurmutant strain ofH. pylori.The goal of the present work was to more thoroughly characterize expression of theoorDABCgenes inH. pylorias well as to define the role of Fe-Fur in this process. Here we show that these four genes are cotranscribed as an operon and that expression of the operon is decreased in afurmutant strain. Transcriptional start site mapping and promoter analysis revealed the presence of a canonical extended −10 element but a poorly conserved −35 element upstream of the +1. Additionally, we identified a conserved Fur binding sequence ∼130 bp upstream of the transcriptional start site. Transcriptional analysis using promoter fusions revealed that this binding sequence was required for Fe-Fur-mediated activation. Finally, fluorescence anisotropy assays indicate that Fe-Fur specifically bound this Fur box with a relatively high affinity (dissociation constant [Kd] = 200 nM). These findings provide novel insight into the genetic regulation of a key metabolic enzyme and add to our understanding of the diverse roles Fur plays in gene regulation inH. pylori.
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Books on the topic "Oorah"

1

Brunstetter, Bekah. Oohrah! New York: Samuel French, 2010.

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2

Reenskaug, Trygve. Working with objects: The OORAM software engineering method. Greenwich: Manning, 1996.

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Reenskaug, Trygve. Working with objects: The OOram software engineering method. Greenwich: Manning, 1996.

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Walker, S. C. Oorah: Story of a Marine. Independently Published, 2019.

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Oorah!: The Adventures of a Brave Girl. Archway Publishing, 2023.

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Michael, J., and D. Steele. OoRah Leadership and Tip-Of-the-Spear Transformation. Balboa Press, 2017.

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Michael, J., and D. Steele. OoRah Leadership and Tip-Of-the-Spear Transformation. Balboa Press, 2017.

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8

Mintz, Rachel. U. S. Marines Coloring Book: Oorah! American Soldiers in Military Action and Combat Scenes - Patriotic Coloring. Independently Published, 2019.

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Oorakh Khozooguh (Eastern Armenian). Kids Reading Armenian, 2023.

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10

Reenskaug, T. Working With Object: The Ooram Software Engineeringmethod. Prentice Hall, 1995.

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Book chapters on the topic "Oorah"

1

Lu, Ruqian, and Zhi Jin. "OORA: Ontology Oriented Requirement Analysis." In Domain Modeling-Based Software Engineering, 167–99. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4487-6_5.

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Vestli, H. "Using Actors as a computational model for OOram." In IFIP Advances in Information and Communication Technology, 170–77. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-0-387-35082-0_12.

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3

"TASKON/OOram." In SDL '95 with MSC in Case, 391–93. Elsevier, 1995. http://dx.doi.org/10.1016/b978-0-444-82269-7.50043-5.

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"oojah, n." In Oxford English Dictionary. 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/1041430836.

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"ooyah, int." In Oxford English Dictionary. 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/6630760273.

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"oojah capivvy, n." In Oxford English Dictionary. 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/8325501848.

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"oojah-cum-spiff, adj." In Oxford English Dictionary. 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/9083396660.

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Reports on the topic "Oorah"

1

Crowley, Nancy L. OORA Automated Knowledge System (OAKS) Code. Fort Belvoir, VA: Defense Technical Information Center, September 1993. http://dx.doi.org/10.21236/ada270709.

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