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We then analyzed gene expression profiles in the treated cells using a cDNA microarray consisting of 18,432 genes.
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.
Using a cDNA microarray and a novel experimental approach to assess response to day length, we reveal the transcriptional regulation of genes involved in the early stages of post-diapause morphogenesis and metabolism and propose one particular gene as a strong candidate for involvement in the photoperiodic switch mechanism itself.
In view of accumulating evidence suggesting that prolonged application of high fluid shear recapitulates some of the earmarks of OA, we aimed to identify the differentially-regulated genes in human T/C-28a2 chondrocytes subjected to high fluid shear (20 dyn/cm2) versus static (control) conditions (0 dyn/cm2) for 48 h and 72 h, using a cDNA microarray technique.
Previously, OsCPK9 expression in response to abiotic stresses was examined using a cDNA microarray.
Total RNA was extracted and subjected to screening using a cDNA microarray as previously described [ 35].
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To prepare transcript profiles of field plants we used a cDNA microarray containing 3628 unique sequences derived from libraries enriched in stress-responsive cDNAs as described in Wong et al. [ 19].
Wang et al. (2008) used a cDNA microarray containing 1,920 suppression subtractive hybridization clones to detect transcript profile differences in resistant and susceptible cultivars under controlled BPH feeding (Wang et al. 2008).
To examine the gene expression profiles in the selected tissues, we used a cDNA microarray with 13907 cDNA clones.
In the original study, the authors used a cDNA microarray technology that allowed them to measure gene expression of several thousand genes on 112 samples, including 41 normal prostate specimens, 62 primary prostate tumours and 9 lymph node metastases.
We used a cDNA microarray with over 5000 cDNA subclones that represent various genes expressed in the adult honeybee brains to screen gene(s) that are expressed more strongly in the OLs than in the other regions of the honeybee brain (for details of the screening, see the Materials and Methods section) [35], [39].
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