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Image Search Results
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Table of Demographics for patients in this analysis
Article Snippet: Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV
Techniques:
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Spaghetti plots for ZIKV and DENV sIgG and sIgM among the three cohorts: ZIKV-sIgG (row 1), ZIKV-sIgM (row 2), DENV-sIgG (row 3) and DENV-sIgM (row 4) by study visit for each cohort: Definitive Dengue, Definitive Zika and Household. Each colored line represents the trajectory of one subject in the study. The horizontal black line represents the manufacturer-recommended cutoff for defining seropositivity.
Article Snippet: Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV
Techniques:
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Decision Tree results. In the flow diagram each level shows the decision criteria and variable to use to predict the disease group. The colored figures show the criteria diagrammatically. The left figure shows the cut points for the initial cutpoint of low DENV-sIgG SV 28. The purple area shows prediction of household patients with ZIKV-sIgG high and the red area shows the prediction of DENV infected patients. The dots show the true disease status of the people who would fall in the purple and red areas. Red dots are true DENV infected patients, green triangles are true ZIKV infected patients and purple squares are Household subjects. The figure on the right is for the initial cutpoint of high DENV-sIgG SV 28. The green area shows prediction of ZIKV infected patients with ZIKV-sIgM change high and the red area shows the prediction of DENV infected patients.
Article Snippet: Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV
Techniques: Infection
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Apply decision criteria to undefined fever events patients as an example. These are the results of applying both our decision tree model and the manufacturer recommended cutoffs to those subjects with unknown disease status.
Article Snippet: Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV
Techniques:
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Spaghetti plots for ZIKV and DENV sIgG and sIgM among the three cohorts: ZIKV-sIgG (row 1), ZIKV-sIgM (row 2), DENV-sIgG (row 3) and DENV-sIgM (row 4) by study visit for each cohort: Definitive Dengue, Definitive Zika and Household. Each colored line represents the trajectory of one subject in the study. The horizontal black line represents the manufacturer-recommended cutoff for defining seropositivity.
Article Snippet: Laboratory procedures Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV specific-IgM (ZIKV-sIgM) and IgG (ZIKV-sIgG) ELISA (EuroImmun®, Lübeck, Germany), anti-CHIKV
Techniques:
Journal: Antiviral research
Article Title: Serial Real-time RT-PCR and serology measurements substantially improve Zika and Dengue virus infection classification in a co-circulation area.
doi: 10.1016/j.antiviral.2019.104638
Figure Lengend Snippet: Decision Tree results. In the flow diagram each level shows the decision criteria and variable to use to predict the disease group. The colored figures show the criteria diagrammatically. The left figure shows the cut points for the initial cutpoint of low DENV-sIgG SV 28. The purple area shows prediction of household patients with ZIKV-sIgG high and the red area shows the prediction of DENV infected patients. The dots show the true disease status of the people who would fall in the purple and red areas. Red dots are true DENV infected patients, green triangles are true ZIKV infected patients and purple squares are Household subjects. The figure on the right is for the initial cutpoint of high DENV-sIgG SV 28. The green area shows prediction of ZIKV infected patients with ZIKV-sIgM change high and the red area shows the prediction of DENV infected patients.
Article Snippet: Laboratory procedures Serologies of the three arboviruses were measured using commercial Enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s instructions: anti-ZIKV specific-IgM (ZIKV-sIgM) and IgG (ZIKV-sIgG) ELISA (EuroImmun®, Lübeck, Germany), anti-CHIKV
Techniques: Infection
Journal: BMC Cancer
Article Title: Myc suppression of Nfkb2 accelerates lymphomagenesis
doi: 10.1186/1471-2407-10-348
Figure Lengend Snippet: Nfkb2 loss accelerates Myc-induced lymphomagenesis by impairing apoptosis . a) Effects of Nfkb2 deficiency on Myc-induced lymphomagenesis. The survival of Eμ- Myc transgenic littermates of the indicated Nfkb2 genotypes is shown. The differences in the rates of tumor incidence between the Nfkb2 +/+ and the Nfkb2 -/- littermates is statistically significant (p = 0.0307). b) Eμ- Myc transgenic littermates of the indicated Nfkb2 genotypes were injected with BrdU, and cells from bone marrow and spleen were harvested 12 hr later. BrdU-incorporation was analyzed using an antibody-dependent fluorescence assay. The bars show the mean percentage of cells in S phase ± SEM (three independent experiments). c) The apoptotic index of the indicated genotypes was analyzed using an antibody dependent fluorescence assay. Annexin V + B220 + cells of sIgM - or sIgM + phenotype are shown. The bars represent the mean ± SEM from three independent experiments. * indicates p < 0.05.
Article Snippet: Cells were then resuspended, incubated with antibody against B220 and
Techniques: Transgenic Assay, Injection, BrdU Incorporation Assay, Fluorescence