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In this study, we directly compared acylcarnitine concentrations measured in DBS with those in the corresponding plasma sample.
Table 2 summarises the PCDH10 methylation rate of the 63 colorectal tumours and corresponding plasma sample, and their association with various clinicopathological factors.
The specificity of IgM and IgG detection from oral swabs was very high, and all "false positive" results were patients with laboratory-confirmed DENV infection in whom serology in the corresponding plasma sample was negative.
The recovery was determined for each sampling period as R = (Cout − Cin)/(Cpl − Cin), where Cin, Cout, and Cpl are the measured electrical conductivity in the perfusate, the effluent sample, and the corresponding plasma sample, respectively.
The recovery (or exchange efficiency) was determined for each sampling period as R = (Cout − Cin)/(Cpl − Cin), where Cin, Cout, and Cpl are the measured electrical conductivity in the perfusate, the effluent sample, and the corresponding plasma sample, respectively.
PCR was performed on enrollment oral swab samples from six participants in whom the corresponding plasma sample was PCR positive, but DENV RNA could not be amplified from any of these oral swabs so we did not continue with PCR on the remaining oral swab samples.
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Finally, the quantitation of estrogens after whole blood microsampling was compared with the results obtained with the corresponding plasma samples.
We evaluated a total of 36 frozen packed blood cell samples and 22 corresponding plasma samples from wild Hawaiian honeycreepers.
Metabolomics was applied for the study of PCa bone metastases (n = 20) in comparison with corresponding normal bone (n = 14), and furthermore of malignant (n = 13) and benign (n = 17) prostate tissue and corresponding plasma samples obtained from patients with (n = 15) and without (n = 13) diagnosed metastases and from men with benign prostate disease (n = 30).
In 201 patients with an unknown EGFR mutation status due to technical problems with tumour samples (see above), 12 mutations were identified in the corresponding plasma samples.
Among them, PPP1R3C and EFHD1 were rarely hypermethylated in peripheral blood cells, but frequently hypermethylated in 24 CRC tissue samples and their corresponding plasma samples.
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