We validated a time-resolved immunofluorometric assay (TRIFMA) using commercial human RAGE antibodies (DY1145, R&D Systems) [ 49] and found comparable sRAGE concentrations by TRIFMA and ELISA.
We recently derived and internally validated a time-dependent survival model for hospital death that could predict a patient's daily mortality risk via estimation of the hazard of death on each day [ 6].
In this section, in order to validate a time domain simulator, we simply expand our simulator to cover two different geometrical scenarios: the angular deviations of the platform and the moving target case.
Our aim is to develop and validate a time-dependent logistic regression model and nomogram suitable for the annual risk prediction of LRRs in individual breast cancer patients.
The objective of this study was to develop and validate a time-dependent logistic regression model for prediction of locoregional recurrence (LRR) of breast cancer and a web-based nomogram for clinical decision support.
In this study, we analyzed and validated a microarray time series experiment of cells expressing a regulated NF-κB dominant-negative inhibitor in response to TNF.
For statistical comparison, data were transferred into SPSS version 16 and validated a second time, with the exception of demographic comparison which was performed using StatsDirect.
Since then, of course, Birchbox has been validated a few times over.
Using extensive genomic data, we next designed and validated a real-time PCR assay targeting the fucP locus in H. influenzae, which provided 100%% specificity for this bacterium both in silico and across a diverse bacterial DNA panel.
Our group has developed and validated a tool the real-time random safety audits (in Spanish: Análisis Aleatorios de Seguridad en Tiempo Real, AASTRE and found it to be effective in detecting and remedying errors of omission in real time, thereby improving adherence to guidelines [10] and proving to be most useful in situations of high care load and in more severe patients [11].
We designed and validated a multiplex real-time PCR assay by adapting the ΔΔCt relative quantification method for the analysis of GSTT1 and GSTM1 markers to accurately differentiate the three genotypes (∗1/1, ∗1/0, and ∗0/0) in degraded DNA from formalin-fixed paraffin-embedded tissue.
