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E validity of real-time PCR results for respiratory virus investigations in community-based studies. Keywords: Nasal swab, Respiratory virus, Real-time polymerase chain reaction, Quality control, Mould, Community-based study* Correspondence: a.alsaleh@uq.edu.au 1 Queensland Children's Medical Research Institute, The University of Queensland, Brisbane Queensland 4029, Australia 2 Queensland Paediat
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Ssical culture and phenotypic-based methods and have led to the discovery of new respiratory viruses [2]. However, contemporary studies employing these new techniques have often used convenience samples obtained from patients admitted to hospital or attending Emergency Department clinics [3-5]. Understanding more fully the ARI disease burden in the community is important for developing public heal
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Riggering exocytosis, directly killing cells, or indirectly damaging Weibel alade bodies. Our cytotoxicity data above suggest that antibody to HLA class I does not kill endothelial cells directly (Figs. 1 D and E). To further show that antibody triggers regulated secretion of VWF from endothelialYamakuchi et al.Fig. 3. Effects of both C5a and antibody to HLA upon exocytosis. (A) C5a added to anti-
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Riggering exocytosis, directly killing cells, or indirectly damaging Weibel alade bodies. Our cytotoxicity data above suggest that antibody to HLA class I does not kill endothelial cells directly (Figs. 1 D and E). To further show that antibody triggers regulated secretion of VWF from endothelialYamakuchi et al.Fig. 3. Effects of both C5a and antibody to HLA upon exocytosis. (A) C5a added to anti-
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Agnostics, Siena, Italy.Neutralizing Epitope Guiding Bacterial ClearanceBacterial strains, media, and growth conditionsGBS strains used in this work are 515 (serotype Ia, expressing BP-2a-515 allele); CJB111 (serotype V, expressing BP-2a-CJB111); H36B (serotype II, expressing BP-2a-H36B); 3050 (type II, expressing BP-2a-2603); CDC84 (serotype II, expressing BP-2aDK21); and strain CDC89 (serotype I
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