Gotowa bibliografia na temat „H-246”

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Artykuły w czasopismach na temat "H-246"

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Ellegård, Alvar, Sabina Kielow, Arne Olofsson, et al. "Reviews and notices." Moderna Språk 93, no. 2 (1999): 238–55. http://dx.doi.org/10.58221/mosp.v93i2.9703.

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Includes the following reviews:
 p. 238. Alvar Ellegård. Svartvik, J., Engleska - öspråk, världsspråk, trendspråk.
 p. 239. Sabina Kielow. Ryan, M., Literary Theory. + Widdowson, P., Literature. The New Critical Idiom.
 p. 239-243. Arne Olofsson. Olsson, H., Språket - så fungerar det. Lärobok i allmän grammatik och lingvistik.
 p. 243-244. Ronald Paul. Ellegård, A., Jesus, One Hundred Years Before Christ: A Study in Creative Mythology.
 p. 244-245. Ted Tapper. Löfgre, H. & Shima, A. (eds), After Consensus: Critical Challende and Social Change in America.
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Jordan, Robert, Deborah Tien, Tove' C. Bolken, et al. "Single-Dose Safety and Pharmacokinetics of ST-246, a Novel Orthopoxvirus Egress Inhibitor." Antimicrobial Agents and Chemotherapy 52, no. 5 (2008): 1721–27. http://dx.doi.org/10.1128/aac.01303-07.

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ABSTRACT ST-246 is a novel, potent orthopoxvirus egress inhibitor that is being developed to treat pathogenic orthopoxvirus infections of humans. This phase I, double-blind, randomized, placebo-controlled single ascending dose study (first time with humans) was conducted to determine the safety, tolerability, and pharmacokinetics of ST-246 in healthy human volunteers. ST-246 was administered in single oral doses of 500, 1,000, and 2,000 mg to fasting healthy volunteers and 1,000 mg to nonfasting healthy volunteers. ST-246 was generally well tolerated with no serious adverse events, and no subj
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Quenelle, Debra C., R. M. L. Buller, Scott Parker, et al. "Efficacy of Delayed Treatment with ST-246 Given Orally against Systemic Orthopoxvirus Infections in Mice." Antimicrobial Agents and Chemotherapy 51, no. 2 (2006): 689–95. http://dx.doi.org/10.1128/aac.00879-06.

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ABSTRACT ST-246 was evaluated for activity against cowpox virus (CV), vaccinia virus (VV), and ectromelia virus (ECTV) and had an in vitro 50% effective concentration (EC50) of 0.48 μM against CV, 0.05 μM against VV, and 0.07 μM against ECTV. The selectivity indices were >208 and >2,000 for CV and VV, respectively. The in vitro antiviral activity of ST-246 was significantly greater than that of cidofovir, which had an EC50 of 41.1 μM against CV and 29.2 μM against VV, with selectivity indices of >7 and >10, respectively. ST-246 administered once daily by oral gavage to mice infecte
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Hosier, I. L., and D. C. Bassett. "A study of the morphologies and growth kinetics of three monodisperse n -alkanes: C 122 H 246 , C 162 H 326 and C 246 H 494." Polymer 41, no. 25 (2000): 8801–12. http://dx.doi.org/10.1016/s0032-3861(00)00223-8.

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Yang, Guangjun, Xiaoling Yang, and Ping Wang. "Hölder Derivative of the Koch Curve." Journal of Applied Mathematics and Physics 11, no. 01 (2023): 101–14. http://dx.doi.org/10.4236/jamp.2023.111008.

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Finger, Eduardo, Alessandra Finardi de Souza, Thaissa Galante Coimbra, and Daniel dos Santos. "Immunodominance of the Sm-p40 antigen contributes to the development of severe schistosomiasis mansoni (99.5)." Journal of Immunology 186, no. 1_Supplement (2011): 99.5. http://dx.doi.org/10.4049/jimmunol.186.supp.99.5.

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Abstract In murine schistosomiasis, H-2k CBA and C3H mice develop severe CD4 T cell(CD4) mediated liver pathology(LP) and a high Th1/17 response very focused on a single epitope of the parasite egg antigen Sm-p40(p234-246). Low pathology C57BL/6 mice do not recognize this antigen. A possible reason for this result is that p234-246 exacerbated dominance(ED) polarizes the anti-egg response causing severe LP. To test this hypothesis we: a)analyze the LP of SJL mice whose H-2 haplotype also exhibit ED of a single Sm-p40 epitope and b) analyze the LP of CBA mice whose p234-246 ED was neutralized by
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Waters, Jennifer C., Rey-Huei Chen, Andrew W. Murray, and E. D. Salmon. "Localization of Mad2 to Kinetochores Depends on Microtubule Attachment, Not Tension." Journal of Cell Biology 141, no. 5 (1998): 1181–91. http://dx.doi.org/10.1083/jcb.141.5.1181.

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A single unattached kinetochore can delay anaphase onset in mitotic tissue culture cells (Rieder, C.L., A. Schultz, R. Cole, G. Sluder. 1994. J. Cell Biol. 127:1301–1310). Kinetochores in vertebrate cells contain multiple binding sites, and tension is generated at kinetochores after attachment to the plus ends of spindle microtubules. Checkpoint component Mad2 localizes selectively to unattached kinetochores (Chen, R.-H., J.C. Waters, E.D. Salmon, and A.W. Murray. 1996. Science. 274:242–246; Li, Y., and R. Benezra. Science. 274: 246–248) and disappears from kinetochores by late metaphase, when
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Próchniak, Joanna, and Renata Płoska. "WIG-20 Warsaw Stock Exchange Companies: Are They Ready for Governance Matters Disclosures Based on EU Sustainable Reporting Standards?" Annales Universitatis Mariae Curie-Skłodowska, sectio H – Oeconomia 56, no. 5 (2023): 227–46. http://dx.doi.org/10.17951/h.2022.56.5.227-246.

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Theoretical background: In 2022, the European Commission’s intensive efforts to revise and enhance the Non-Financial Reporting Directive (NFRD) from 2014 resulted in the proposal of Corporate Sustainability Reporting Directive (CSRD) and the exposure draft on ESRS EDs (EFRAG Sustainable Reporting Standards Exposure Drafts). The ESRS drafts for public consultation presented the mandatory concepts and principles for sustainability reporting under the CSRD. The implementation of corporate sustainability is closely related to reporting that stimulates robustness of companies’ commitment to sustain
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İşcan, İmdat. "A new improvement of Hölder inequality via isotonic linear functionals." AIMS Mathematics 5, no. 3 (2020): 1720–28. http://dx.doi.org/10.3934/math.2020116.

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Danelli, Anderson Luiz Durante, and Erlei Melo Reis. "Quantification of incubation, latent and infection periods of Phakopsora pachyrhizi in soybean, according to chronological time and degree-days." Summa Phytopathologica 42, no. 1 (2016): 11–17. http://dx.doi.org/10.1590/0100-5405/1920.

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ABSTRACT In experiments conducted in a growth chamber, the chronological time and the accumulated degree-days were determined for the duration of incubation, latent and infectious periods of Phakopsora pachyrhizi cultivars BRSGO 7560 and BRS 246 RR. Detached soybean leaflets were placed in gerbox-type acrylic boxes and inoculated with 20 x 103 uredospores/mL. The study was conducted at 12-h photoperiod and temperatures of 10ºC, 15ºC, 22ºC, 25ºC and 30°C for 30 days. Lesions and uredia/cm2were evaluated and the number of uredia per lesion was quantified after the beginning of sporulation. The s
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