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Preliminary microarray experiments showed that this library contains sufficient chemical diversity to identify lead peptides with measurable target binding affinity and specificity (CWD and SAJ unpublished data).
Principal component analysis (PCA) on a large number of heterogeneous microarray experiments showed that a maximum of 50 statistically independent transcriptional system regulators (TSRs) can explain the vast majority of biological variance in gene expression in human as well as in mouse.
The microarray experiments showed that expression of the hpdA gene was reduced in the xprGΔ1 mutant.
Tissue microarray experiments showed that the intensity of RCA-I staining is positively correlated with the TNM grades.
Results from the replicated microarray experiments showed high levels of consistence with minimum variations within each treatment.
Interestingly, competitive cross-species hybridization of microarray experiments showed that the brain microenvironment induces complete reprogramming of metastasized cancer cells [ 25].
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The large scale analysis of gene expression provided by our microarray experiments show that FGF signaling is required for the normal expression of a large number of organizer genes, including goosecoid, chordin, noggin, dkk1 and Frzb, and a number of genes, such as Sip1 and FoxD5, which are expressed in the dorsal neuroectoderm (See Table S14).
Our yeast microarray experiments show a suitable dynamic range, good reproducibility and sensitivity.
Data from microarray experiments show that GRCD1 is in fact upregulated in marginal flowers compared to disc flowers [ 43].
Statistical analysis of the correlation between protein and microarray experiments shows a consistent trend of correlation among the datasets.
In Arabidopsis, microarray experiments show modest increases (2-fold) in AtSUC2 expression in response to drought, abscisic acid (a drought induced hormone), or turgor stimulation [ 18].
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