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Recently Lagoutte et al. in a study that included patients undergoing elective colorectal surgery could not found differences between PCT and CRP for the detection of AL with a better AUC ROC for CRP on POD 4 [ 49].
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Thus, several studies have identified a role for routine post-operative CRP measurements in the detection of post-surgical complications [ 22, 25].
Au-MWNT-HB films were used as a good electrochemical transducer due to their excellent electrical properties and large surface areas for the signal transduction, while the genetically engineered fusion proteins, or 6His GBP SpA fusion proteins, specifically bind onto the surface of the Au-MWNT-HB films and efficiently immobilize bioreceptors for the detection of CRP.
Receiver operating characteristic (ROC) curve analyses were used to compare the sensitivity and specificity for the detection of CRP-SAA and total SAA.
For the detection of serum CRP, we chose the classic quantitative method.
We have demonstrated the fabrication of the biosensor platforms by means of the integration of the genetically engineered fusion proteins and the uniform gold nanoparticle-deposited multi-walled nanotube hybrid (Au-MWNT-HB) films for the detection of C-reactive protein (CRP).
We also investigated the expression levels of the CRP, HapR and RpoN proteins in the ΔrpoS and ΔrpoN derivatives by immunoblot analyses using the same samples that were used for the detection of Hcp (Fig. 7).
SAA concentrations were significantly increased in septic dogs which points to a possible higher clinical value for SAA in the detection of sepsis compared with CRP, and this potential deserves to be further investigated.
High serum levels of CRP are characteristic of an acute inflammatory condition; CRP measurement with a high sensitivity CRP (hs-CRP) between 0.5 and 10.00 mg/L facilitates the detection of low-intensity chronic inflammatory processes.
We investigated the value of PCT, comparing with C-reactive protein (CRP) and interleukin (IL -6, IL -6e detectinn of infecthen in the emergency detectiont (ED).
The ZnSe/CdS/ZnS QDs are used as fluorescent labels to exploit their application in fluorescence-linked immunosorbent assay (FLISA) for the first time in the detection of C-reactive protein (CRP) with a limit of detection (LOD) of 0.85 ng/mL, which is more sensitive than that of CdSe/ZnS type-I QDs based FLISA (1.00 ng/mL).
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