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"Phase 3 renal cell carcinoma data could be available by the end of 2005.
(E) TCGA breast carcinoma data set (n = 61 for USP33 low, n = 61 for USP33 high; P = 0.0188 with log-rank analysis); (F) Breast cancer data were analyzed by KM plotter.
I used SEER-17 colon carcinoma data from 2000 for both men and women.
In gastric carcinoma, data concerning the CXCL12-CXCR4 pareway are sparse [29].
I also compared the colon carcinoma data to the exact representation of the multi-stage hypothesis, Equation 1.
We found correlations between the beta values for these probes to be above 0.80 for the colon adenocarcinoma, lung adenocarcinoma, and lung squamous cell carcinoma data sets, but 0.73 for gliomas, 0.67 for rectal adenocarcinomas, 0.62 for ovarian carcinomas, and 0.25 for renal papillary cell carcinomas (Supplemental Fig. S6A).
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Apoptotic cells, as identified by the TUNEL assay, and loss of Ki67+ cells were observed in the regressing acinar cell carcinomas (data not shown).
Between the two measured endogenous control genes (PPIA (Alias: cyclophilin A) and MGB2), we chose PPIA for normalization across different genes based on the fact that this gene showed the most relatively constant expression in different breast carcinomas (data not shown).
Human papillomavirus detection rates were not different among those histological types of invasive carcinomas (data not shown in the table).
The 26 kDa fragment was also detected in two out of 36 (5.5%) of the breast carcinomas (data not shown).
There were no significant protein expression differences observed in serum between the various lung cancer subtypes examined (adenocarcinoma, squamous and small cell carcinomas: data not shown).
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