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The microarray study allowed us to identify differential effects of the nsp11 protein on the cellular gene expression profiles.
This microarray study allowed us to identify a set of 270 DEGs in hypoxia (81 downregulated and 189 upregulated) common to three BC cell lines (fold change > |0.5 | and P < 0.05).
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The proposed method, by greatly enhancing the sensitivity of microarray studies, allows the identification of important aspects of genetic regulation networks and might be useful for the discrimination of the different players involved in regulation circuits.
Tissue microarray studies allow comprehensive assessment of the tumour expression of EpCAM.
In plant-pathogen interactions microarray studies allow a more comprehensive understanding of molecular responses in the infection process making the elucidation of mechanisms involved in resistance possible [ 20].
The present microarray study has allowed us to identify changes of expression (up-regulated and down-regulated) of many important oncogenesis-associated genes at the different stages of mycoplasma-mediated cell transformation.
The DNA microarray developed in this study allowed efficient detection of bacterial pathogens with the specificities of 100%.
Microarray analyses conducted in this study allowed us to gain insights into global gene expression changes in Arabidopsis associated with PPV infection, symptom development and defence responses.
The entire L. major genome is 32.8 Mbp, so the Nimblegen microarrays [ 41] used in this study allowed us to space 50-nucleotide probes every 85 bp across the entire genome.
Microarray studies have allowed us to examine temporal changes in mammary gene expression during secretory differentiation and activation in some detail [ 33].
Furthermore, this study allowed identification of more potentially differentially expressed transcripts than were discovered in the microarray study, because of the deeper sequencing done here.
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