Bibliographies thématiques / S2008 at

Littérature scientifique sur le sujet « S2008 at »

Auteur : Grafiati
Publié le 27 juillet 2024
Mis à jour le 29 juillet 2024

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Articles de revues sur le sujet "S2008 at"

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Sajid, Muhammad, Muhammad Amjid, Hassan Munir, Muhammad Ahmad, Usman Zulfiqar, Muhammad Fraz Ali, Mohammad Abul Farah, Mohamed A. A. Ahmed et Arkadiusz Artyszak. « Comparative Analysis of Growth and Physiological Responses of Sugarcane Elite Genotypes to Water Stress and Sandy Loam Soils ». Plants 12, no 15 (25 juillet 2023) : 2759. http://dx.doi.org/10.3390/plants12152759.

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Stumpy irrigation water availability is extremely important for sugarcane production in Pakistan today. This issue is rising inversely to river flow due to inadequate water distribution and an uneven rainfall pattern. Sugarcane growth faces a shortage of available water for plant uptake due to the low water–holding capacity of sandy loam soil, particularly under conventional flood irrigation methods. To address this problem, sugarcane clones were evaluated for their agronomic and physiological traits under conditions of low water availability in sandy loam soil. Ten cane genotypes, HSF–240, SPF–213, CPF–249, CP 77–400, S2008–FD–19, S2006–US–469, S2007–AUS–384, S2003–US–633, S2003–US–127, and S2006–US–658, were exposed to four levels of water deficit created through skip irrigations. These deficit levels occurred during the 9th, 11th, 13th, and 16th irrigations at alternate deficit levels between 2020 and 2022. Physiological data were collected during the tillering and grand growth stages (elongation) in response to the water deficit. The sugarcane clones S2006–US–658, S2007–AUS–384, and HSF–240 exhibited resistance to low water availability at both the tillering and grand growth stages. Following them, genotypes S2006–US–658, S2007–AUS–384, and HSF–240 performed better and were also found to be statistically significant. Clones susceptible to water deficit in terms of growth and development were identified as CP 77–400, S2008–FD–19, S2006–US–469, and S2003–US–633. These genotypes showed reduced photosynthetic rate, transpiration rate, stomatal conductance, relative water content, cane yield, and proline content under stressed conditions. Therefore, genotypes S2006–US–658, S2007–AUS–384, and HSF–240 were better performers concerning physiological traits under water deficit and sandy loam soil in both years. Moreover, a significant positive correlation was assessed between agronomic traits and photosynthetic rats. This study highlights that sugarcane can sustain its growth and development even with less irrigation frequency or moisture availability, albeit with certain specific variations.
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Arshad, Waqas Raza, Muhammad Ehsan Khan et Zaheer Aslam. « EXPOLRING RATOON PROSPECTIVE OF SUGARCANE VARIEITES / CLONES AT TOBA TEK SINGH ». Pakistan Sugar Journal 34, no 3 (8 janvier 2020) : 12–15. http://dx.doi.org/10.35380/sugar.034.03.0147.

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Sugarcane is the crop that have the quality to sprout after its first harvesting, phenomenon known as ratooning. Among all other major crops, sugarcane ratooning is widely acceptable to farmers of the Punjab. The more the tillers grew, the higher are the chances of a greater number of stalks to be harvested. It is proven that more the number of stalks, the thinner is the diameter, finally results in more stalks and high production. Similarly, higher number of canes produce favorable ratoon. In this experiment, performance of Seven promising sugarcane varieties/clones along with the check variety CPF-246, were tested for their ratoon ability capacity at farmer’s field at Toba Tek Singh during the year 2017-18. It has been found that one of the varieties S2008-FD-19 produced that maximum ratoon yield, U2003-US-633 produced the maximum sugar recovery and S2003-US-133 produced maximum number of mill able canes. The observing of the current analysis also revealed that S2003-US-633 and S2003-US-133 have significant potential for boom sugar recovery through breeding programs and by improving the production techniques.
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Roulier, Christian. « Phytobase S2008 – vegetation database of Swiss floodplains (synusial plots) ». Biodiversity & ; Ecology 4 (10 septembre 2012) : 343. http://dx.doi.org/10.7809/b-e.00134.

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Tempera, Patrick, Maheep Sangha, Peter Ells et Mark P. Michael. « S2008 Unusual Case of Abdominal Pain - Medication Induced Biliary Colic ». American Journal of Gastroenterology 118, no 10S (octobre 2023) : S1475. http://dx.doi.org/10.14309/01.ajg.0000957672.15204.fd.

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Li, Andrew, et Joo Ha Hwang. « S2008 Endoscopic Strictureplasty and Stent Placement for a Recalcitrant Esophageal Peptic Stricture ». American Journal of Gastroenterology 116, no 1 (octobre 2021) : S875. http://dx.doi.org/10.14309/01.ajg.0000781564.50353.86.

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Bayoumi, Mahmoud, Nael Haddad, Wendy Z. Lamb, Sakolwan Suchartlikitwong et Hugo Pinillos. « S2008 Colonic Ischemia : When a Rare Etiology Leads to an Unusual Presentation ». American Journal of Gastroenterology 117, no 10S (octobre 2022) : e1379-e1380. http://dx.doi.org/10.14309/01.ajg.0000864672.21305.a8.

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Gonzaga, Ernesto Robalino, Irene T. Riestra Guiance, Richard Henriquez, Parikh Jignesh et Wojciech Blonski. « S2008 A Case of Esophageal Adenocarcinoma in a Young Male With Longstanding Untreated Eosinophilic Esophagitis ». American Journal of Gastroenterology 115, no 1 (octobre 2020) : S1050—S1051. http://dx.doi.org/10.14309/01.ajg.0000710080.88010.dc.

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Crombé, Valérie, Julia Salleron, Guillaume Savoye, Jean-Louis Dupas, Gwenola Vernier-Massouille, Eric Lerebours, Dominique Turck et al. « S2008 Long- Term Outcome of Treatment With Infliximab in Paediatric Crohn's Disease:a Population-Based Study ». Gastroenterology 138, no 5 (mai 2010) : S—300. http://dx.doi.org/10.1016/s0016-5085(10)61379-0.

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Huerta Espino, Julio, Rocío Torres García, María Florencia Rodríguez García, Héctor Eduardo Villaseñor Mir, Santos Gerardo Leyva Mir et Ernesto Solís Moya. « Resistencia a roya amarilla (Puccinia striiformis f. sp. tritici) en variedades de trigo harinero (Triticum aestivum L.) ». Revista Mexicana de Ciencias Agrícolas 3, no 5 (27 juin 2018) : 879–91. http://dx.doi.org/10.29312/remexca.v3i5.1381.

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Las variedades de trigo harinero Cortazar S94, Bárcenas S2002, Urbina S2007 y Maya S2007 fueron liberadas para siembras en condiciones de riego en “El Bajío”. Estas variedades mantienen resistencia a diferentes razas de roya amarilla que se encuentran en el país; sin embargo, se desconocen las bases genéticas de su resistencia. Para determinar la genética de la resistencia, estas variedades se cruzaron con el progenitor susceptible ‘Avocet- YrA’, y la determinación de similitud de genes se realizó mediante pruebas de alelismo. Las cuatro variedades y las familias F3 de cada cruza se evaluaron durante verano de 2009 en el Campo Experimental ‘Valle de México’ (INFAP-CEVAMEX) Chapingo, México, bajo una epifitia artificial creada con el aislamiento MEX96.11. Con los resultados de la evaluación de familias F3 se determinó que la resistencia de planta adulta a roya amarilla en Cortázar S94, Bárcenas S2002 y Maya S2007 está condicionada por dos ó tres genes de efectos aditivos, mientras que en Urbina S2007 la resistencia está condicionada por tres o cuatro genes de la misma naturaleza. La ausencia de familias completamente susceptibles en las cruzas entre las variedades resistentes indica la existencia de al menos un gen de resistencia en común.
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Raimondo, Massimo, Yoichi Matsuo, Timothy A. Woodward, Michael B. Wallace, Kanwar R. Gill, Nobuo Ochi, Zhimin Tong, Robert M. Strieter, Robert M. Hoffman et Sushovan Guha. « S2008 CXC-Chemokine/CXCR2 Biological Axis Promotes Angiogenesis In Vitro and In Vivo in Pancreatic Cancer ». Gastroenterology 136, no 5 (mai 2009) : A—312. http://dx.doi.org/10.1016/s0016-5085(09)61424-4.

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Thèses sur le sujet "S2008 at"

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Hamilton, Shanna. « Functional heterogeneity of CPVT-mutant human cardiac ryanodine receptors : evaluation of the influence of S2031 and S2808 phosphorylation sites ». Thesis, Cardiff University, 2017. http://orca.cf.ac.uk/111392/.

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Human cardiac ryanodine receptors (hRyR2) are calcium (Ca2+) release channels central to excitation-contraction coupling. Mutations in hRyR2 are linked to catecholaminergic polymorphic ventricular tachycardia (CPVT), a genetic disorder characterized by arrhythmia, occurring under adrenergic drive. Recent studies suggest gain-of-function mutant channels may undergo different mechanisms of dysfunction, with some showing altered Ca2+ release under basal conditions and others requiring an additional trigger (possibly in the form of β-adrenergic phosphorylation). This study evaluated whether mutants from different domains of hRyR2 (S2246L and N4104K) were functionally heterogeneous in a cellular setting and whether this was related to phosphorylation status. Cells (human embryonic kidney 293) expressing N4104K-hRyR2 displayed smaller, faster Ca2+ release events than those expressing the wild type (WT), while those of cells expressing S2246L-hRyR2 were similar to WT. However, a lower proportion of S2246L cells showed any kind of Ca2+ release functionality compared to those expressing WT or N4104K, reinforcing that these mutations cause different types of dysfunction. Assessment of phosphorylation status using site-specific antibodies for protein kinase A (PKA) target sites S2808 and S2031 showed that mutant phosphorylation levels were different to each other and to that of the WT, indicating a possible role of phosphorylation in this. Activation of PKA-mediated phosphorylation in cells using a cyclic AMP analogue resulted in changes to the kinetics of spontaneous Ca2+ release via WT hRyR2, but did not significantly affect that of mutants. Genetic phosphorylation at either PKA site (S2808D and S2031D) altered the Ca2+ release of mutants as well as WT hRyR2, but this was found to be due to changes in expression of sarco-endoplasmic reticulum Ca2+-ATPase (SERCa) pump, which also contributes to Ca2+ homeostasis. These findings reinforce the concept that phosphorylation is linked to dysfunction and contributes to our understanding of hRyR2 mutation in arrhythmia, highlighting that ‘gain-of-function’ does not necessarily equate to dysfunction via the same mechanism.
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Karakas, Mahir [Verfasser]. « Receptor-for-advanced-glycation-end-products-, (RAGE)-Genpolymorphismus bei Diabetikern und Prädiabetikern : von einer bevölkerungsbasierten Studie zur möglichen funktionellen Relevanz ; Ergebnisse der KORA-S2000-Studie / vorgelegt von Mahir Karakas ». 2009. http://d-nb.info/1000462935/34.

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Livres sur le sujet "S2008 at"

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Carney, Daniel F. Honda S2000. Osceola, Wis : MBI Pub. Co., 2001.

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Honda Giken Kōgyō Kabushiki Kaisha. S2000 : 2000 model series : body repair manual. [United States?] : Honda Motor Co., 1999.

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Sauber, Mary Anne. Staff training and recognition program : The lending process S200. 2e éd. Dubuque, Iowa : Kendall/Hunt Pub. Co., 1990.

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Sauber, Mary Anne. Staff training and recognition program : The lending process (S200). 4e éd. Dubuque, Iowa : Kendall/Hunt Pub. Co., 2002.

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Bible Notes (S200F 0827). Zoe Publications, 1999.

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Cuna. S200 Lending Process. Kendall Hunt Pub Co, 1994.

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Book of the Honda S2000. Veloce Publishing Limited, 2021.

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Long, Brian. Book of the Honda S2000. Veloce Publishing Limited, 2025.

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Bradley, Chris. Touring France with the Honda S2000. Independently Published, 2017.

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Bradley, Christopher. Touring France with the Honda S2000. Independently Published, 2017.

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Chapitres de livres sur le sujet "S2008 at"

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Gazhonova, Veronika. « 3D ABVS Technique on ACUSON S2000 ABVS ». Dans 3D Automated Breast Volume Sonography, 11–33. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-41971-8_3.

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Clark, Stephen. « S20098 ». Dans xPharm : The Comprehensive Pharmacology Reference, 1–2. Elsevier, 2007. http://dx.doi.org/10.1016/b978-008055232-3.62574-7.

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Goldman Schuyler, Kathryn, with Margaret Wheatley, Otto Scharmer, Ed Schein, Robert E. Quinn, et Peter Senge. « Visions of a Healthy World : Views from Thought Leaders ». Dans Building Leadership Bridges, 23–90. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016001.

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Eisler, Riane. « Reframing Organizational and Social Change : From Domination to Partnership ». Dans Building Leadership Bridges, 101–18. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016017.

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Jironet, Karin. « Use it or Lose it : About Leadership Ethics in the United Nations ». Dans Building Leadership Bridges, 143–60. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016018.

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Wilson, Samuel G. « Leadership for the Greater Good : Developing Indicators of Societal and Environmental Health ». Dans Building Leadership Bridges, 161–80. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016022.

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Wilson, Patricia A. « The Inner Practice of Community Development : Embracing Deep Democracy in Mexico ». Dans Building Leadership Bridges, 211–29. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016025.

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Bown, Carolina. « Sumak Kawsay among Indigenous Women Leaders of Ecuador ». Dans Building Leadership Bridges, 231–46. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016027.

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McCann, Jane. « Kiwi Ways of Leading : How 30 New Zealand Government Chief Executives Are Encouraging Healthier Cultures ». Dans Building Leadership Bridges, 247–63. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016033.

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Shuler, Barbara Rose. « “The Arts Are Not a Luxury” : The Arts as a Source of Community in California ». Dans Building Leadership Bridges, 265–77. Emerald Group Publishing Limited, 2016. http://dx.doi.org/10.1108/s2058-88012016034.

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Actes de conférences sur le sujet "S2008 at"

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Feng, Fang. « Philosophical Thinking on the Essence of Information ». Dans ISIS Summit Vienna 2015—The Information Society at the Crossroads. Basel, Switzerland : MDPI, 2015. http://dx.doi.org/10.3390/isis-summit-vienna-2015-s2008.

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Adams, Chris D., William W. Anderson, George T. Gray, William R. Blumenthal, Charles T. Owens, Franz J. Freibert, Johnny M. Montoya et al. « SPALL AND DAMAGE BEHAVIOR OF S200F BERYLLIUM ». Dans SHOCK COMPRESSION OF CONDENSED MATTER 2009 : Proceedings of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2009. http://dx.doi.org/10.1063/1.3295186.

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Otobe, Yutaka, Hiroshi Kawaguchi et Hideo Ueshima. « Development of the High-Power, Low-Emission Engine for the “Honda S2000” ». Dans SAE 2000 World Congress. 400 Commonwealth Drive, Warrendale, PA, United States : SAE International, 2000. http://dx.doi.org/10.4271/2000-01-0670.

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Wang, Cynthia, Patricia Plumb, Lana Harder et Benjamin Greenberg. « Distinguishing Features of MOG Positive and MOG Negative Pediatric Patients with ADEM (S2.008) ». Dans 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000204275.

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Eken, A., et M. Sahin. « A PARALLEL FULLY COUPLED APPROACH FOR LARGE-SCALE FLUID-STRUCTURE INTERACTION PROBLEMS ». Dans 3rd South-East European Conference on Computational Mechanics. Athens : Institute of Structural Analysis and Antiseismic Research School of Civil Engineering National Technical University of Athens (NTUA) Greece, 2014. http://dx.doi.org/10.7712/130113.4379.s2004.

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Gülçat, Ü. « FLAPPING THIN AIRFOIL INTERACTING WITH THE GROUND ». Dans 3rd South-East European Conference on Computational Mechanics. Athens : Institute of Structural Analysis and Antiseismic Research School of Civil Engineering National Technical University of Athens (NTUA) Greece, 2014. http://dx.doi.org/10.7712/130113.4380.s2006.

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Hollweg, F.-R., R.-C. Oliveski et M. Dalla Corte. « NUMERICAL ANALYSIS ABOUT THE INFLUENCE OF INAPPROPRIATE SHAPE OF THE CROSS-SECTION OF MICROCHANNELS IN LAMINAR FLOW ». Dans 3rd South-East European Conference on Computational Mechanics. Athens : Institute of Structural Analysis and Antiseismic Research School of Civil Engineering National Technical University of Athens (NTUA) Greece, 2014. http://dx.doi.org/10.7712/130113.4402.s2028.

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Sarris, E., et P. Papanastasiou. « THE INFLUENCE OF PUMPING PARAMETERS IN FLUID-DRIVEN FRACTURES ». Dans 3rd South-East European Conference on Computational Mechanics. Athens : Institute of Structural Analysis and Antiseismic Research School of Civil Engineering National Technical University of Athens (NTUA) Greece, 2014. http://dx.doi.org/10.7712/130113.4413.s2068.

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Allaire, G., F. Jouve et G. Michailidis. « STRUCTURAL AND MULTI-FUNCTIONAL OPTIMIZATION USING MULTIPLE PHASES AND A LEVEL-SET METHOD ». Dans 3rd South-East European Conference on Computational Mechanics. Athens : Institute of Structural Analysis and Antiseismic Research School of Civil Engineering National Technical University of Athens (NTUA) Greece, 2014. http://dx.doi.org/10.7712/130113.4414.s2009.

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Uçar, Kubilay, et Sait Engindeniz. « Economic aspects of fresh apricot production in Turkey ». Dans International Scientific days 2016 : : The Agri-Food Value Chain : Challenges for Natural Resources Management and Society. Slovak University of Agriculture in Nitra, 2016. http://dx.doi.org/10.15414/isd2016.s2.08.

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Rapports d'organisations sur le sujet "S2008 at"

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O' Neal, T., et M. Minard. SCADA S200 and S300 Project Sketches. Office of Scientific and Technical Information (OSTI), décembre 2018. http://dx.doi.org/10.2172/1491973.

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Martinez, B., et A. McGarrigle. S200 Roofing Map 2020 for TA. Office of Scientific and Technical Information (OSTI), août 2020. http://dx.doi.org/10.2172/1651185.

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Ficht, Thomas, Gary Splitter, Menachem Banai et Menachem Davidson. Characterization of B. Melinensis REV 1 Attenuated Mutants. United States Department of Agriculture, décembre 2000. http://dx.doi.org/10.32747/2000.7580667.bard.

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Brucella Mutagenesis (TAMU) The working hypothesis for this study was that survival of Brucella vaccines was directly related to their persistence in the host. This premise is based on previously published work detailing the survival of the currently employed vaccine strains S19 and Rev 1. The approach employed signature-tagged mutagenesis to construct mutants interrupted in individual genes, and the mouse model to identify mutants with attenuated virulence/survival. Intracellular survival in macrophages is the key to both reproductive disease in ruminants and reticuloendothelial disease observed in most other species. Therefore, the mouse model permitted selection of mutants of reduced intracellular survival that would limit their ability to cause reproductive disease in ruminants. Several classes of mutants were expected. Colonization/invasion requires gene products that enhance host-agent interaction or increase resistance to antibacterial activity in macrophages. The establishment of chronic infection requires gene products necessary for intracellular bacterial growth. Maintenance of chronic infection requires gene products that sustain a low-level metabolism during periods characterized little or no growth (1, 2). Of these mutants, the latter group was of greatest interest with regard to our originally stated premise. However, the results obtained do not necessarily support a simplistic model of vaccine efficacy, i.e., long-survival of vaccine strains provides better immunity. Our conclusion can only be that optimal vaccines will only be developed with a thorough understanding of host agent interaction, and will be preferable to the use of fortuitous isolates of unknown genetic background. Each mutant could be distinguished from among a group of mutants by PCR amplification of the signature tag (5). This approach permitted infection of mice with pools of different mutants (including the parental wild-type as a control) and identified 40 mutants with apparently defective survival characteristics that were tentatively assigned to three distinct classes or groups. Group I (n=13) contained organisms that exhibited reduced survival at two weeks post-infection. Organisms in this group were recovered at normal levels by eight weeks and were not studied further, since they may persist in the host. Group II (n=11) contained organisms that were reduced by 2 weeks post infection and remained at reduced levels at eight weeks post-infection. Group III (n=16) contained mutants that were normal at two weeks, but recovered at reduced levels at eight weeks. A subset of these mutants (n= 15) was confirmed to be attenuated in mixed infections (1:1) with the parental wild-type. One of these mutants was eliminated from consideration due to a reduced growth rate in vitro that may account for its apparent growth defect in the mouse model. Although the original plan involved construction of the mutant bank in B. melitensis Rev 1 the low transformability of this strain, prevented accumulation of the necessary number of mutants. In addition, the probability that Rev 1 already carries one genetic defect increases the likelihood that a second defect will severely compromise the survival of this organism. Once key genes have been identified, it is relatively easy to prepare the appropriate genetic constructs (knockouts) lacking these genes in B. melitensis Rev 1 or any other genetic background. The construction of "designer" vaccines is expected to improve immune protection resulting from minor sequence variation corresponding to geographically distinct isolates or to design vaccines for use in specific hosts. A.2 Mouse Model of Brucella Infection (UWISC) Interferon regulatory factor-1-deficient (IRF-1-/- mice have diverse immunodeficient phenotypes that are necessary for conferring proper immune protection to intracellular bacterial infection, such as a 90% reduction of CD8+ T cells, functionally impaired NK cells, as well as a deficiency in iNOS and IL-12p40 induction. Interestingly, IRF-1-/- mice infected with diverse Brucella abortus strains reacted differently in a death and survival manner depending on the dose of injection and the level of virulence. Notably, 50% of IRF-1-/- mice intraperitoneally infected with a sublethal dose in C57BL/6 mice, i.e., 5 x 105 CFU of virulent S2308 or the attenuated vaccine S19, died at 10 and 20 days post-infection, respectively. Interestingly, the same dose of RB51, an attenuated new vaccine strain, did not induce the death of IRF-1-/- mice for the 4 weeks of infection. IRF-1-/- mice infected with four more other genetically manipulated S2308 mutants at 5 x 105 CFU also reacted in a death or survival manner depending on the level of virulence. Splenic CFU from C57BL/6 mice infected with 5 x 105 CFU of S2308, S19, or RB51, as well as four different S2308 mutants supports the finding that reduced virulence correlates with survival Of IRF-1-/- mice. Therefore, these results suggest that IRF-1 regulation of multi-gene transcription plays a crucial role in controlling B. abortus infection, and IRF-1 mice could be used as an animal model to determine the degree of B. abortus virulence by examining death or survival. A3 Diagnostic Tests for Detection of B. melitensis Rev 1 (Kimron) In this project we developed an effective PCR tool that can distinguish between Rev1 field isolates and B. melitensis virulent field strains. This has allowed, for the first time, to monitor epidemiological outbreaks of Rev1 infection in vaccinated flocks and to clearly demonstrate horizontal transfer of the strain from vaccinated ewes to unvaccinated ones. Moreover, two human isolates were characterized as Rev1 isolates implying the risk of use of improperly controlled lots of the vaccine in the national campaign. Since atypical B. melitensis biotype 1 strains have been characterized in Israel, the PCR technique has unequivocally demonstrated that strain Rev1 has not diverted into a virulent mutant. In addition, we could demonstrate that very likely a new prototype biotype 1 strain has evolved in the Middle East compared to the classical strain 16M. All the Israeli field strains have been shown to differ from strain 16M in the PstI digestion profile of the omp2a gene sequence suggesting that the local strains were possibly developed as a separate branch of B. melitensis. Should this be confirmed these data suggest that the Rev1 vaccine may not be an optimal vaccine strain for the Israeli flocks as it shares the same omp2 PstI digestion profile as strain 16M.
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