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Justin has 7 years in the architectural industry and has worked on residential, commercial, mixed-used, and cultural projects during his career. Detail-oriented by nature, Justin appreciates diving into the specifics on each project and tackling the challenges associated with the science of building construction. He prefers to work closely with the builders as a collaborative effort to bring the s
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Justin has 7 years in the architectural industry and has worked on residential, commercial, mixed-used, and cultural projects during his career. Detail-oriented by nature, Justin appreciates diving into the specifics on each project and tackling the challenges associated with the science of building construction. He prefers to work closely with the builders as a collaborative effort to bring the s
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Approximately 12 change in non-acute CRP (b = 1.17, SE = 0.42, P = 0.006, R2 = 0.09, Model 2, Table 2). This association was strengthened if CRP values above 2 mg/L were included in the model (b = 1.69, SE = 0.48, P
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Approximately 12 change in non-acute CRP (b = 1.17, SE = 0.42, P = 0.006, R2 = 0.09, Model 2, Table 2). This association was strengthened if CRP values above 2 mg/L were included in the model (b = 1.69, SE = 0.48, P
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Ed and sections were stained. (A) Photomicrographs of staining for VWF after 1 h. (B) Quantitation or VWF release after 1 h (n 8 SD; *, P 0.04). (C) Photomicrographs of staining for MPO in dermal vessels after 1 h. Clusters of cells in small vessels stain for MPO in antibody-treated grafts. (D) Quantitation of MPO-positive cells after 1 h (n 8 SD; *, P 0.03). (E) Quantitation of VWF release after
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Pressed by BldD. Based on a consensus sequence derived from these ChIP-chip data, BldD recognition?2013 The Author. FEMS Microbiology Reviews published by John Wiley Sons Ltd on behalf of the Federation of European Microbiological SocietiesG. Chandra K.F. Chatersequences were found upstream of many of the same genes not only in other streptomycetes, but also in other sporulating actinobacteria
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Scribed previously [72]. In Trial 2, 15 individuals of each species (approx. 40-70 g) were randomly allocated to 4 tanks. A total of 7,335 copepodids (163/fish) were added to each of two tanks as described above. In Trial 3, 12?5 individuals of each species (approx. 50-80 g) were randomly allocated to each of four tanks. A total of 8,900 copepodids (199/fish) were added to each of two tanks as des
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Scribed previously [72]. In Trial 2, 15 individuals of each species (approx. 40-70 g) were randomly allocated to 4 tanks. A total of 7,335 copepodids (163/fish) were added to each of two tanks as described above. In Trial 3, 12?5 individuals of each species (approx. 50-80 g) were randomly allocated to each of four tanks. A total of 8,900 copepodids (199/fish) were added to each of two tanks as des
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