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Since the first DNA microarray paper demonstrated that microarray technology can monitor multiple gene expression profile in 1995 [1], DNA microarray technology has been developed steadily.
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The results presented in this paper demonstrate that three common anomalies cited in the microarray literature can be explained by extraneous emission sources, reinforcing the urgent need for careful attention to detail to recognize the presence of extraneous emissions that reduce accuracy of existing microarray data.
This paper demonstrates the technique on some phantom tissues.
This paper demonstrates a single slice imaging technique.
We choose to analyse Cited2 for three reasons: 1. it was not present in our microarray slides; 2. it is an important negative regulator of Hif1α; 3. several papers demonstrated its role in cardiac looping and TGA [ 31].
The related microarray data of Eads et al. and Shaw et al. in companion papers demonstrate that most of the sequenced Daphnia genes are differentially transcribed in a manner consistent with their putative functions, thus reinforcing their provisional annotations based on sequence alignments to genes from model insects.
Our microarray data demonstrated a significant interaction between dietary fat and PCB exposure.
Indeed, studies using microarray tools demonstrated that there are much more upregulated than downregulated genes after exposure to a glucocorticoid.
Oligonucleotide microarray analysis demonstrated that GPC3 is over-expressed in tissues harvested from smokers with lung adenocarcinoma [28].
Gene expression microarray further demonstrated that a number of genes were potentially targeted by these differentially expressed novel miRNAs.
Overlapping of the unique GWAS and microarray genes demonstrated that 13,905 genes were assessed in both GWAS and microarray analyses.
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