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Recently, Rajhi et al. (2011) identified genes associated with lysigenous aerenchyma formation in maize roots by using a microarray analysis combined with laser microdissection.
Here, we take advantage of the natural variation of sweet and grain sorghum to uncover genes that are conserved in rice, sorghum, and sugarcane but differently expressed in sweet versus grain sorghum by using a microarray platform and the syntenous alignment of rice and sorghum genomic regions containing these genes.
Thus, insertion or deletion events in the genome of clinical strains tested could affect the apparent transcript abundance measured by using a microarray designed from the genome sequence of the Malish strain (seven) of R. conorii [13].
By using a microarray approach, we analyzed DNA methylation in regulatory regions of 806 cancer-related genes in 28 breast cancer paired samples.
The influenza A viruses were then subtyped from swabs by using a microarray assay (Clondiag, Jena, Germany) that enabled the rapid identification of influenza virus A (H10N7).
By using a microarray, we analyzed the temporal changes of messenger RNA (mRNA) and microRNA expression in primary mouse hepatocytes after SST treatment.
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By using a microarray-based approach Manque and collaborators [ 27] demonstrated that the expression profile of murine cardiomyocytes was greatly affected during the early stages of invasion and infection by T. cruzi trypomastigotes.
Images of the microarrays were acquired by using a laser microarray scanner (GenePix 4100A, Axon Instruments Inc., Foster City, CA, USA) with an excitation wave length of 532 nm, an emission wavelength of 570 nm, and standardized measurement parameters.
To identify genes with altered expression levels before and after Oct4 overexpression in cultured ATSCs, transcriptional profiles were generated by using a cDNA microarray consisting of 20,000 resequenced and annotated clones.
We compared antibody responses to monkeypox virus infection and human smallpox vaccination by using a protein microarray covering 92 95% (166 192 proteins) of representative proteomes from monkeypox viral clades of Central and West Africa, including 92% coverage (250 proteins) of the vaccinia virus proteome as a reference orthopox vaccine.
The study by Hong and colleagues examined limited number of genes (i.e., 1152) by using a custom microarray.
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