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Figure 20-5: Column B contains a megaformula that returns the character position of the last space of the name in column A.

>>> tup=( 111 , abc ,64) >>> str= xyz >>> import math, fib >>> fibo=fib.fibonacci >>> dir() [ __builtin__ , __builtins__ , __doc__ , __name__ , fib , fibo , math , os , str , string , sys , tup ]

Essential characterization of coding processes (from ITU-T Recommendation T.81, 1992)

dr = a(r (t) r)dt + dz,

297 Ginsburg, H; Famin, O; Zhang, J; Krugliak, M Inhibition of glutathione-dependent degradation of heme by chloroquine and amodiaquine as a possible basis for their antimalarial mode of action Biochem Pharmacol, 1998, 56(10): 1305 1313 298 Famin, O; Krugliak, M; Ginsburg, H Kinetics of inhibition of glutathione-mediated degradation of ferriprotoporphyrin IX by antimalarial drugs Biochem Pharmacol, 1999, 58(1): 59 68 299 Schirmer, R H; Muller, J G; Krauth-Siegel, R L Disul de-reductase inhibitors as chemotherapeutic agents: the design of drugs for trypanosomiasis and malaria Angew Chem Int Ed Engl, 1995, 34: 141 154 300 Wu, W-M; Chen, Y-L; Wu, Y-L to be published 301 Eckstein-Ludwig, U; Webb, R J; van Goethem, I D A; East, J M; Lee, A G; Kimura, M; O Neill, P M; Bray, P.

Local operator (display communication system command control)

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G; Ward, S A; Krishna, S Artemisinins target the SERCA of Plasmodium falciparum Nature, 2003, 424(6951): 957 961 302 Robert, A; Cazelles, J; Meunier, B Characterization of the alkylation product of heme by the antimalarial drug artemisinin Angew Chem Int Ed, 2001, 40(10): 1954 1957 303 Robert, A; Coppel, Y; Meunier, B Alkylation of heme by the antimalarial drug artemisinin Chem Commun, 2002, 5: 414 415 304 Kannan, R; Sahal, D; Chauhan, V S Heme-artemisinin adducts are crucial mediators of the ability of artemisisnin to inhibit heme polymerization Chem Biol, 2002, 9(3): 321 332 305 Haynes, R K; Monti, D; Taramelli, D; Basilico, N; Parapini, S; Olliaro, P Artemisinin antimalarials do not inhibit hemozoin formation Antimicrob Agents Chemother, 2003, 47(3): 1175 1175 306 Wu, J-A; Ji, R-Y.

A quantitative structure activity study on artemisinin analogs Zhongguo Yaoli Xuebao, 1982, 3(1): 55 60 307 Haynes, R K Artemisinin and derivatives the future for malaria treatment Curr Opin Infect Dis, 2001, 14(6): 719 726; Haynes, R K; Ho, W-Y; Tsang, H W Abstract of The Third International Symposium for Chinese Medicinal Chemists, Hong Kong, Dec 28 31, 2002, 13 308 Haynes, R K; Ho, W-Y; Chan, H-W; Fugmann, B; Stetter, J; Croft, S L; Vivas, L; Peters, W; Robinson, B L Highly antimalaria-active artemisinin derivatives: Biological activity does not correlate with chemical reactivivty Angew Chem Int Ed, 2004, 43: 1381 1385 309 Sibmooh, N; Udomsangpetch, R; Kijjoa, A; Chantharaksri, U; Mankhetkorn, S Redox reaction of artemisinin with ferrous and ferric ions in aqueous buffer Chem Pharm Bull.

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Tokyo, 2001, 49(12): 1541 1546 310 Wu, Y K How might qinghaosu (artemisinin) and related-compounds kill the intraerythrocytic malaria parasite a chemists view Account Chem Res, 2002, 35(5): 255 259..

Service and transponder Frequency band: uplink/ downlink (GHz) Bandwidth (MHz) Transmitter type and e.i.r.p. (edge of coverage) (dBW)

Wall-washing is also produced by diffuse-source, fluorescent-lamp wall-wash systems. The inability of a diffuse source to project a high intensity toward the bottom of a wall usually results in a bright area at the top of the wall and a rapid falloff of luminance thereafter. Sophisticated reflector systems with a wide aperture help to solve this problem (figure 12.28). Fluorescent wall-wash systems, sometimes called perimeter wall-wash systems, are more energy-effective than their incandescent counterparts.

With quinone as the substitute for the butenolide unit of acetogenin, Koert et al.104,105 synthesized two natural product hybrids, quinone-mucocin and quinone-squamocin D (Scheme 10-46). The complex I inhibitory activity of the two hybrids as well as some synthetic precursors and fragments is shown in Table 10-8. Interestingly, the quinone-mucocin hybrid was ten times more active than mucocin, whereas the quinone-squamocin hybrid lost some activity compared with the natural parent. Fragments 263 266 displayed weak activity; however, acid 277 showed comparable activity.

In earlier times, programs were written with the code arranged in a sequence of steps. Today, programming has become more structured and organized. Now, you can have code organized in logical blocks with specific functionality, which can also be reused. This logical method of programming gives you the freedom to create an object that meets your exact requirements and specifications.

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