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In the XTT assay analysis in this study, the LNCaP cell line was most sensitive compared to PC3 and TSU-Pr1 cells.
With respect to EC50, sensitivity to each drug was cell-line specific, with neuroblastoma cells (NGP and SH-SY5Y) the most sensitive compared with the melanoma or glioblastoma cells.
However, it has been suggested that the technique using the TCZ1 and TCZ2 primers that amplify a 188 bp of a 195-bp repetitive nuclear sequence is the most sensitive compared with methods using S35 and S36 primers to amplify a 330-bp minicircle sequence [ 10, 19].
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Second, evaluation of P-gp function by assessment of [C]carvedilol uptake is most likely more sensitive compared to semi-quantitative measurement of P-gp expression by immunohistochemistry. Therefore, minor changes in P-gp expression levels might be missed by immunohistochemistry shortly after irradiation, which can already be detected with quantitative PET autoradiography.
A study of 128 lead workers in Singapore (Chia et al. 1995) showed that Uα1m appears to be the most sensitive parameter compared with Uβ2m and URBP.
A study of 128 lead workers (Chia et al. 1995) reported that Uα1m appears to be the most sensitive parameter compared with urinary β2-microglobulin (Uβ2m) and urinary retinol-binding protein (URBP).
The EPPO storage delayed radicle protrusion for both maturity fractions after only 1 week at 18 MPa pO2, and the less-mature seeds were more sensitive compared with the most-mature seeds (Fig. 5B).
The EC50 of the test organisms without submerged adaptation time is 135.1 μg/L, the most sensitive concentration value compared to the EC50 of the 7-day adapted plants (386.2 μg/L) and 28-day adapted plants (270.2 μg/L).
Therefore, nuclei micro-array FISH is the most sensitive technique when compared with immunohistochemistry and PCR.
Mickuvience et al. [ 32] compared several non-clonogenic assays for determining the effect of PDT on adherent cells in vitro and found that crystal violet staining for measuring the loss of monolayer adherence was the most sensitive assay, as compared to other non-clonogenic assays including [H]-thymidine incorporation, LDH-release, MTT, trypan blue exclusion and CyQUANT.
Histopathology, serology (ELISA), and molecular (PCR) methods tested for diagnosis of ocular toxocariasis caused by T. cati in experimentally infected Mongolian gerbils and Wistar rats revealed that molecular method was the most sensitive and superior compared to both histopathology and ELISA in the early diagnosis of ocular infection.
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