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The activities in this output had the following intended outcomes: to establish the needs of all three tiers of the SADNET network, the rural communities, the NGO partners and the research organizations, using participatory methodologies when appropriate the different group's information needs collected and assessed, as well as any drought mitigation best practices identified. Community information needs and capacities identified A participatory approach was applied in the development of survey tools, methodology for data collection from rural communities and its analysis. These were translated into vernacular in both pilot countries. The participatory methodology agreed captured both qualitative and quantitative data on information needs. After the tools were developed, they were tested on two communities Chibombo in Zambia and Seke in Zimbabwe ; before finalization. Over 20 partner institutions actively participated in the surveys. A total of 18 communities were consulted in Zambia 8 ; and Zimbabwe 10 ; . In Zambia four districts were identified which were Gwembe, Luangwa, Mambwe and Sesheke. In Zimbabwe the selected districts were Buhera, Chimanimani, Chiredzi, Chipinge, Gwanda, Nyanga, Plumtree and Rushinga. The survey with its broadened approach did not only fulfill SADNET objectives but also met other objectives of its members as it identified other needs. This made the exercise more complimentary to the interests of its members. Selection of these survey sites was based on a criterion developed by the project partners. The criteria selected broad areas for implementation of the SADNET project. In Zimbabwe, ecological regions 4 and 5 were chosen Similarly, in Zambia, ecological regions 1 and 2 with identical characteristics with those in Zimbabwe's regions 4 and 5 were selected. Marginal rainfall, shallow soils and periodic experiences of droughts and floods characterize these selected regions. Of importance to note was that the Cinci Wa Babili project was provisionally identified as a potential focal point and implementer in the project document. However, it operates in a region, which does not meet the criteria. As a result it was excluded. Vegetation, livelihoods, soil and hydrological maps as well as satellite images were used in the selection process. Other relevant secondary data was also utilized. These included reports from established institutions like the Food and Agriculture Organization FAO ; , World Bank, Southern Africa Development Community Food Early Warning Network SADC FEWSNET ; and IUCN. This reduced bias. The findings of the information needs surveys were synthesized, packaged and widely distributed. The publication is entitled "Community Information needs and Communication Capacity of Organisations in Agriculture and Drought Mitigation", by SAFIRE, 2003. The publication provides a summary of findings details and prioritized ICT options for implementation during the pilot-testing phase. 6.
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Are Phytoestrogens Beneficial in Breast Cancer Patients? Use of a Newly Validated Biomarker to Assess Phytoestrogen Intake in Women With Breast Cancer and Controls. J. Mackinnon1, T. Rawjee1, A. Blake3, G. Spahn2, G. Dobos2, and M. Ritchie1, 1Bute Medical School, University of St. Andrews, Fife, Scotland, 2Dept. of Integrative Medicine, University Duisburg-Essen, Essen, Germany, 3Scottish Crop Research Institute, Dundee, Scotland, for example, anacin aspirin.
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Differential Expression of PEPT 1 and PEPT 2 in Caco-2 and SKPT Cells--Mammalian intestine expresses PEPT 1 and not PEPT 2. Mammalian kidney expresses both PEPT 1 and PEPT 2, but the predominant one is PEPT 2. One of the goals of the present study was to investigate the interaction of -lactam antibiotics, a group of peptidomimetic drugs with pharmacological and clinical importance, with PEPT 1 and PEPT 2, using cultured intestinal and renal cell lines. Caco-2 cells, which are of human intestinal origin, are known to possess a low-affinity H peptide cotransporter, resembling PEPT 1 15 ; . SKPT cells, which are of rat kidney origin, have been recently demonstrated to express a high-affinity H peptide cotransporter, resembling PEPT 2 14 ; . Even though the MDCK renal cell line possesses a peptide transport system, available kinetic data suggest that the transport system is most likely PEPT 1 rather than PEPT 2 19 ; . Therefore, Caco-2 cells and SKPT cells were used in the present study. To establish unequivocally that Caco-2 cells express PEPT 1 and SKPT cells express PEPT 2, we performed the following experiments. We determined the identity of the peptide transporter present in Caco-2 cells by RT-PCR using PEPT 1- and PEPT 2-specific primers 11, 12 ; . The specificity of each pair of primers was established by PCR using respective cDNAs as templates. RNA samples prepared from human intestine, human kidney, and Caco-2 cells were subjected to RT-PCR using these primers and the products were analyzed by agarose gel electrophoresis. The results of these experiments, given in Fig. 1, show that the PEPT 1-specific PCR product of expected size 1.2 kb ; was generated from all three RNA samples. In contrast, the PEPT 2-specific PCR product 0.9 kb in size ; was generated only from kidney RNA. RNA samples from Caco-2 cells and intestine were negative for this product Fig. 1 ; . These data demonstrate that Caco-2 cells express PEPT 1 and not PEPT 2. The nucleotide sequences of the rat homologs of PEPT 1 and PEPT 2 have not yet been determined. Therefore, we investigated the expression of PEPT 1 PEPT 2 in the SKPT cell line by Northern blot hybridization using the human PEPT 1 and PEPT 2 cDNAs as probes Fig. 2 ; . Poly A ; RNA prepared from SKPT cells and Caco-2 cells was size-fractionated and probed and panadol.
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The year 2002 will be, at least in the economy, remembered by the turmoil in pharmacy caused by the sale of Lek to Novartis of Switzerland at the end of a wave of strategic partnerships, mergers and takeovers in the global pharmaceutical industry. Krka has decided to take a different, independent way. We therefore remain the only Slovene pharmaceutical company, an important foundation for the development of the Slovene economy. Our business results, especially the profit to be divided among our owners, leave little to want for, especially if we compare them to the results of 2001, which was exceptional for Krka in many ways. Even in the increasingly predatory environment of the global market, caused to no small degree by our competition, as well as the rules and regulations of individual countries, we sold 77.7 billion SIT worth of products, 10% more than in 2001. We also increased our production. However, the target we set was not quite reached due to the negative influence of the US dollar, in which nearly half our sales are realised. Despite all this, we produced a net profit of over 10.4 billion SIT in 2002, which is 15% more than last year and represents one of the largest net profits in Slovenia's economy. As one of the foremost Slovene exporters, we sold products totalling 62.1 billion SIT to foreign markets. The strategy of expansion in eastern markets was reinforced by the penetration of western European markets, in which sales increased by 35%. In eastern European markets, sales were increased by 14%, whereas in Slovenia, our reference market where roughly a fifth of our sales are generated, the increase was 8%. In the past year Slovene legislation was changed, giving the inventor of a new drug an advantage over generics manufacturers. Krka adapted quickly by changing its development plan, accelerating some projects and continuing others, according to the legislation of other markets. In 2002, we were awarded the first marketing authorisation for 14 products, including 9 prescription pharmaceuticals. One of the most important amongst these was the first marketing authorisation awarded to Krka Polska, confirming our statement that in key markets, we will produce a new generic range of products locally, on our own production lines. Because of the strategic decision to invest in our own production and distribution centres in key export markets, we continued with intensive investments in 2002. We invested 11.9 billion SIT this year, most going to Notol, a new factory for the production of solid drug dosage forms. Besides this investment we opened the new Development and Control Centre II in Novo mesto which, according to European legislation, enables us to introduce new technologies in development, evaluation and production of generic products. The storage part of a new production and distribution centre was opened in the vicinity of Moscow, with the start of operation for all parts planned for 2003. We are also beginning the activities for building a new chemical synthesis facility. We are concluding a phase of intensive key investments in production and distribution capabilities, at home and in traditional markets, and entering a new phase when the strength of the company will be increased. In addition to investments in our own capabilities, by takeovers, joint ventures and joint appearances in markets, we create a synergistic effect in research, development, production, marketing and sales of our products -- of those which were registered in the last few years or are still being developed. To put it briefly, we are ready for a period of consolidation and strong growth in the global generic industry, in which we play an important part -- and we will keep on doing that. We realise that good business results depend not only on a quality generics manufacturing programme, but also on a strong and extensive marketing network, both domestically and globally. Therefore, we strengthened our presence and anafranil.
Collaborating on care lifestyle interventions, nutrition counseling, and medical intervention to treat metabolic abnormalities have all become important facets of pcos management, underscoring the need for gynecologists to familiarize themselves with these aspects of medical care and to collaborate with internists, primary care physicians, and medical endocrinologists where required.
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FREQUENCES RADIO, CODAGE LECTURE PAR TABLETTE NUMERISANTE 71 ; MOORE NORTH AMERICA, INC. [US US]; 300 Lang Boulevard, Grand Island, NY 14072 US ; . 72 ; GRABAU, Robert, E.; 1094 Bowen Drive West, North Tonawanda, NY 14120 US ; . 74 ; SIMPSON, Robert, P. et al. etc.; Simpson, Simpson & Snyder, L.L.P., 5555 Main Street, Williamsville, NY 14221-5406 US ; . 81 ; AE ZW. 84 ; AP GH, because nsaids.
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NOTE: Children with phenylketonuira PKU ; should not take Children's Anacin-3, Children's Tylenol, Double Strength Tempra, Junior Strength Tylenol and Tempra in the chewable form. These products, in this dosage form, contain aspartame, which is metabolized in the GI tract to phenylalanine following oral administration. Many children's hospitals have modified their approach to the febrile infant over the past year or two. The reasons are two-fold. First, the pneumococcal vaccine has now clearly been shown to have a dramatic effect on the incidence of pneumococcal disease in infancy. Secondly, there is increasing concern regarding missed UTIs in infancy. These infections are now known to cause significant renal scarring and to be the cause of kidney problems later in life. For these reasons the new fever guidelines at children's hospitals have been de-emphasizing blood cultures for high fever in infants immunized against pneumococcus and have been emphasizing urinalyses and cultures on infants with moderate fevers and selected high-risk criteria for UTI and leflunomide!
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