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18 miRNAs, including 6 up-regulated and 12 down-regulated miRNAs were identified by microarray in primary HCC samples of patients who had developed HCC recurrence (n = 5) compared to those with non-recurrence (n = 5) following OLT by using p < 0.05 as cutoff value.
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In a previous work it has been shown by microarray analysis in primary HPV16 and HPV18-infected cervical cancers and normal cervical epithelium similar results for genes related to cell cycle control [ 49].
The expression profiles of genes and microRNAs, regulated by the treatment of SST, were measured by using microarray analysis in primary mouse hepatocytes.
Using oligonucleotide microarrays in primary human CD34+ cells, a group of genes was identified whose dysregulation by NUP98-HOXA9 is attributable primarily to the NUP98 portion.
To investigate the possibility that the gene expression profile in PBMCs is a reflection of the genes expressed in the PC tissues itself, we also investigated if there was a similarity between the differentially expressed genes identified in our study and those identified by microarray analysis in pancreatic primary tumors.
As the association of GATA expression levels and the prognostic phenotype of neuroblastoma could not unequivocally be addressed by northern blot and real-time RT-PCR, we examined GATA expression levels by microarray analysis in a larger cohort of primary neuroblastoma (n=251).
By overlaying our ChIP dataset with the microarray dataset from this previous study, we identified 32 additional genes as directly regulated by p63 in primary keratinocytes (Table 1).
Fig. 1 MicroRNA that exhibit altered pulmonary expression identified by microarray studies in experimental bronchopulmonary dysplasia.
mRNA microarray was carried out by Microarray facility in Sanford-Burnham Institute.
We performed microarray analyses to identify genes regulated by the PI3K/Akt pathway in primary chondrocytes.
We screened among a pool of genes that we have previously found to be downregulated following miRNA-203 overexpression in primary human keratinocytes by microarray analysis.
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