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Army News Service May 27, 2005 WASHINTON - The Army announced today the design for the Combat Action Badge. The design was approved by Gen. Peter J. Schoomaker, Army chief of staff. The CAB, featuring both a bayonet and grenade, may be awarded to any Soldier performing assigned duties in an area where hostile fire pay or imminent danger pay is authorized, who is personally present and actively engaging or being engaged by the enemy, and performing satisfactorily in accordance with the prescribed rules of engagement, according to its authorizing language. Award is not limited by one's branch or military occupational specialty. "Warfare is still a human endeavor, " Schoomaker said. "Our intent is to recognize Soldiers who demonstrate and live the Warrior Ethos." "The Global War on Terrorism and its associated operations will be the first era of conflict considered for this award, " said Lt. Col. Bill Johnson, Human Resources Command chief of military awards. "September 18, 2001, is the effective date for the new award. That is when President Bush signed Senate Joint Resolution 23, authorizing the use of military force against those responsible for the recent attacks launched against the United States." The CAB will go into immediate production and should be available late this summer or early fall through unit supply and military clothing sales stores. In the case of acetylsalicylic acid, sodium salicylate and magnesium salicylate, 325 mg; and in the case of choline salicylate, 435 mg. 2 ; The children's standard dosage unit of a salicylate shall be!

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Subjects underwent thoracic CT scans. BAL. and pulmonary function tests PFT ; . In three subjects. the C'!' scans were judged to be of unacceptable.

Lysozymes muramidases ; are a group of enzymes that are especially effective against certain Gram-positive bacterial cell walls. An apparent low level presence and atypical bioactivity in cattle may be significant in causing susceptibility to infectious bovine pulmonary disease 272.
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READ, P.J. & HIDE, G.A. 1995. Effects of fungicides on the growth and conidial germination of Colletotrichum coccodes and on the development of black dot disease of potatoes. Annals of Applied Biology 126: 437-447. REPUBLIC OF SOUTH AFRICA, 1998. Gazette, 15 May 1998, 395: 2-27. RICE, E.L. 1984. Allelopathy. Academic Press, London. ROSS, S.A., EL-KELTAWI, N.E. & MEGALLA, S.E. 1981. Antimicrobial activity of some Egiptian aromatic plants. Fitoterapia 52: 201-205. ROUSSEAEU, A., BENHAMOU, N., CHAT, I. & PICH, Y. 1996. Mycoparasitism of the extramatical phase of Glomus intraradices by Trichoderma harzianum. Phytopathology 86: 434-443. SCHIPPERS, B., BAKKER, A.W. & BAKKER, P.A.H.M. 1987. Interactions of deleterious and beneficial rhizosphere microorganisms and the effect of cropping practices. Review of Phytopathology 25: 339-358. SCHMIEDEKNECHT, G. 1993. Biologische bekampfung von Rhizoctonia solani Khn an kartoffelpflanzen durch mikrobielle antagonisten. Archives Phytopathologische Pflanzenchutz 28: 311-320. SCHOLTE, K. & LOOTSMA, M. 1998. Effect of farmyard manure and green manure crops on populations of mycophagous soil fauna and Rhizoctonia stem canker of potato. Pedobiologia 42: 223-231. SCHREINER, R.P. & KOIDE, R.T. 1993a. Antifungal compounds from the roots of mycotrophic and non-mycotrophic plant species. New Phytologist 123: 99-105. SCHREINER, R.P. & KOIDE, R.T. 1993b. Mustards, mustard oils and mycorrhizas. New Phytologist 123: 107-113. SCRIVANTI, L.R., ZUNINO, M.P. & ZYGADLO, J.A. 2003. Tagetes minuta and Schinus areira essential oils as allelopathic agents. Biochemical Systematic and Ecology 31: 563573. SEYOUM, A., PALSSON, K., KUNG'A, S., KABIRU, E.W., LWANDE, W., KILLEEN, G.F., HASSANALI, A. & KNOLS, B.G.J. 2002. Traditional use of mosquito-repellent plants in western Kenya and their evaluation in semi-field experimental huts against Anopheles gambiae: ethnobotanical studies and application by thermal expulsion and direct burning. Transactions of the Royal Society of Tropical Medicine and Hygiene 96: 225-231. SMITH, R.L., SCHANK, S.C., MILAN, J.R. & BALTENSPERGER, A.A. 1984. Responses of sorghum and pennisetum species to the N2 fixing bacterium, Azospirillum brasilense. Applied and Environmental Microbiology 37: 1331-1336. SPECHT, L.P. & LEACH, S.S. 1987. Effects of crop rotation on Rhizoctonia disease of white potato. Plant Disease 71: 433-437.

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33. Schroff, 0., Newmann, 0., and Sarg, C. Transglutaminase as marker for subsets of munne macrophages. Eur. 1. Immunol. 11, 637, 1981. Sham, D.R., and Griffin, F.M., Jr. Antibody-dependent and antibody-independent phagocytosis. In Methods for Studying Mononuclear Phagocytes, Adam, D.O., Edelsen, P.J., and Karen, H., Eds. ; . New York: Academic Press, Inc., p. 511, 1987. Selkoe, D.J., Abraham, C., and Ihara, Y. Brain transglutaminase in vitro cross-linking of human neurofilament proteins into insoluble polymers. Proc. NatI. Acad. Sci. USA 79, 6070, 1982 and thalidomide. Workshop 2 in the Lunchbox Learning Series will be held on Wednesday 6 June. The guest speaker will be David Dart, who works in the e-commerce marketing area of Telstra Country Wide. He will speak on `The Communications Suite -- Including the New E-Members', covering the development of a communication plan, with the emphasis on the use of Web sites, portals, email and interactive mediums. In his Telstra position, Dart is responsible for strategy development and delivery of online solutions for regional and rural customers. At Telstra, he has developed e-commerce. 477 PROXIMITY TO MOSQUITO BREEDING SITES AS A RISK FACTOR FOR CLINICAL MALARIA EPISODES IN AN URBAN COHORT OF UGANDAN CHILDREN. Staedke SG, Nottingham EW, Cox J, Kamya MR, Rosenthal PJ, Dorsey G. University of California, San Francisco, CA, USA; Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine; Makerere University Medical School, Kampala, Uganda. Malaria transmission, parasite prevalence, and clinical illness may be heterogeneous within small geographic areas, particularly urban environments. Prior studies suggest greater transmission exposure increases risk of infection, but may decrease risk of clinical illness due to acquisition of immunity. The and thalomid. 4-9. Evaluating Effectiveness of Coral Reef Ecosystem Management. The T B monoclonal mice 17 9 DO11.10 RAG-1 ; were previously described 24 ; . T monoclonal mice harbor monoclonal populations of T and B lymphocytes that are specific for chicken OVA323339 and HA of influenza virus, respectively. BALB c Thy1.2 mice and BALB c IL-2 mice were purchased from The Jackson Laboratory Bar Harbor, ME ; . BALB c Thy1.1 mice were obtained from Dr. F. Zavala New York University, New York, NY ; . TCR -deficient mice were backcrossed to the BALB c background in our facility. All mice were bred and housed at the Skirball specific pathogen-free animal facility and thiabendazole.

Sequences. Methods: RT and PR genes were amplified using RT-PCR and sequenced by capillary electrophoresis using both proprietary and commercially available primer sets. Resistance predictions were determined by comparison to the consensus subtype B sequence HX2B ; . The codon usage was determined at RT sites associated with NNRTI resistance RT98, RT100, RT101, RT103, RT106, RT108, RT179, RT181, RT188, RT190, RT225, and RT236 ; . The mutation frequencies were expressed as a percentage of codons observed within each subtype. The subtype geographic distribution of each subtype was determined by demographic data provided for each of 160, 000 patients. Results: The prevalence of non-B HIV-1 subtypes was shown to have increased from 0.4% in 1998 to 1.9% by the end of 2004. The geographic distribution of subtypes showed that non-B subtypes were prevalent throughout the U.S., but that subtype C was found at a higher frequency in the Midwest p 0.0001 ; regions, while subtype AG was more common in the Eastern region p 0.0001 ; . Codon usage analysis revealed that many of the documented drug resistance mutations known to occur in subtype B were also frequently found in non-B strains, and indicated the potential for both synonymous and quasi-synonymous pathways to drug resistance in non-B strains. Conclusions: The prevalence of non-B subtypes has increased, but remains below 2%, and is broadly distributed throughout the U.S. There are alternative mutational pathways to acquiring resistance in non-B subtypes. Recognizing these pathways is an important step toward understanding the HIV-1 evolutionary process. Thus, further research may be applied for more specific interpretation. ID13. Evaluation of the Qiagen BioRobot Mdx and the Roche Amplicor HPV Microwell Plate Research Reagents and the Roche Linear Array HPV Genotyping Test RUO ; for the Extraction and Detection of HPV DNA from ThinPrep Specimens. S. Dodson, T. Kerr, R.A. Hubbard, N.T. Potter 1Molecular Pathology Laboratory Network, Inc., Maryville, TN. Background: This study was designed to evaluate the performance characteristics of 1 ; the QIAGEN BioRobot MDx for the automated extraction of DNA from ThinPrep specimens, 2 ; the Roche AMPLICOR HPV Microwell Plate research reagents HPV-MWP ; for the detection of 13 high risk HPV types and 3 ; the Roche LINEAR ARRAY HPV Genotyping Test RUO ; LA-HPV ; for the characterization of 13 high risk plus 24 low risk HPV types. Materials and Methods: 536 consecutive ThinPrep cervical specimens submitted to our clinical laboratory for HR HPV testing were sequentially analyzed by the Hybrid Capture hc2 ; High-Risk HPV DNA Test Digene Corporation, Gaithersburg MD and by PCR utilizing both the Roche AMPLICOR HPV Microwell Plate research reagents and LINEAR ARRAY HPV Genotyping Test RUO ; . Sample DNA for the PCR assays was extracted utilizing the QIAGEN BioRobot MDx and QIAamp Media MDx kits designed for use with liquid based cytology media. Results: The QIAGEN MDx had an extraction efficiency of 97.3% for the generation of DNA suitable for down stream analysis by PCR. Overall, concordant results between the hc2 and AMPLICOR HPV-MWP assays were generated for 85% of the specimens tested. hc2 HPV-MWP discordant results were resolved with the LA-HPV Genotyping Test RUO ; . Among this group were included hc2 "equivocal" specimens with an RLU CO ratio of 1.0 - 2.5. Overall, LA-HPV analysis was able to resolve 92% of these specimens and included all of the hc2 equivocal samples. Furthermore, LA-HPV was able to identify the presence of "LR only" HPV types in hc2 "HR positive" specimens, supporting published data on the existence of cross-hybridization of hc2 HR probes with LR HPV types. Conclusions: The QIAGEN BioRobot MDx appears to be a robust and dependable platform for the generation of PCR amplifiable DNA extracted from ThinPrep specimens for input into the Roche AMPLICOR HPV-MWP and LA-HPV assays. The HPV-MWP assay appears to compare favorably with the Digene hc2 test for the detection of HR-HPV types and, when used in combination with the LA-HPV assay, can unambiguously type stratify the majority of specimens analyzed. ID14. Comparison of HPV Microarray with Hybrid Capture II HPV Analysis. F.B. Thunnissen1, C.F. Prinsen2, B. Sciarone2, C.H. Klaassen2, H.V. Stel3 1CWZ Hospital, Nijmegen, Gelderland; 2Pathology C66, CWZ Hospital, Nijmegen, Gelderland; 3Gooi-Noord Hospital, Blaricum, Utrecht. Introduction: Recently, we introduced a DNA microarray format for the detection and subtyping of human Papillomavirus HPV ; . The aim of this study was to compare the HPV microarray with the hybrid capture II HC-II ; assay. Methods: Archival specimens n 214 ; which were prospectively analysed with the HC-II assay were used for retrospective analysis with PCR and microarray. The mean age of the patients was 38.7 years range 17-71 ; . In the laboratory of the Gooi-Noord Hospital cervical cytology specimens are routinely analysed for high-risk HR ; HPV status with HC-II assay. Samples.

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Three intervals: less than 60 seconds, less than 120 seconds or more than 120 seconds of ventricular fibrillation. In addition, three of the animal groups were defibrillated at 30 seconds and two at 90 seconds. All groups were fibrillated and fibrillation was continued for 30 seconds group 1, 2 and 3 ; , 60 seconds all groups ; , 90 seconds groups 4 and 5 ; and 120, 150 and 180 seconds all groups ; before defibrillation. In 13 dogs in EMD, we attempted to restore effective mechanical systole by intraventricular injection of atropine, 0.5 mg three dogs ; , isoproterenol, 1 mg one dog ; , epinephrine, 1 mg five dogs ; , and calcium chloride, 1 g four dogs ; . At the end of the experiments, an autopsy was performed and the position of the flexible wire in the right ventricle was recorded together with gross pathologic changes which were present on examination of the heart and lungs. The statistical analyses were performed using the t test for paired and unpaired data and thiamin!

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