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We tested the expression profiles of the three markers (ACY1, SQSTM1, and GPC3) in a validation set of HGDN (n = 21) and WDHCC (n = 24).
Since gene expression differences could also result from responses to other deficient nutrients, we tested the expression profiles of the same selected candidate genes in root tissues grown under full N provided with 100% Hoagland solution (Additional file 5).
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Therefore, we tested the expression profile of GSK3ß-related genes (Figure 3B) in these hyper-proliferative PASMCs.
We then tested the expression profile of the tested genes in the strain χ3339 Δ island 4305 containing the R995 + island 4305 plasmid.
To address this question, we used a transcriptional inhibitor, rifampicin, to test the expression profile in the presence of DBMIB.
It was our intention to test the expression profile of one of the main cold markers genes defined for cold in other time points of fermentation and to know if NSR1 behaves similarly in both species.
For that, the immunohistochemical expression of a variety of metabolism-related proteins and VEGF family members was evaluated in a series of cervical adenocarcinomas, the possible co-expression between metabolism-related proteins and VEGF family members was tested and the expression profiles was associated with the clinicopathological tumor behavior.
A global test was applied to test whether the expression profiles differed between the classes by permuting the labels of which arrays corresponded to which classes.
Furthermore, we tested whether the expression profile of TRAIL-R1 and TRAIL-R2 could determine receptor preference, but failed to observe any clear correlation.
We further assessed their classification performance using receiver operator characteristic (ROC) curves and tested these with the expression profiles (GSE4172) from another cohort of DCM patients.
To test this hypothesis, the expression profiles of five transcripts were analyzed by qRT-PCR at 5, 8, 12, and 24 hPBM.
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