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Although the microarray analysis indicates that metabolic rate may increase in response to excess Fe, plants still retain many responses common to different biotic and abiotic stresses.
Our microarray analysis indicates that the expression of Tfrc was not significantly changed in the duodenum of Hfe−/− mice, a result that agrees with a previous report [19].
Furthermore, our microarray analysis indicates that rosiglitazone did not upregulate important insulin-regulated glucose transporters such as Glut4 in the heart, a finding that has been reported previously in isolated rat cardiomyocytes [23].
While we cannot formally rule out some conversion of SP into B220+ DN T cells, the microarray analysis indicates that the transcript profile of gld DN T cells is complex and with significant qualitative difference from the transcript profile of gld SP T cells (Fig. 2).
In addition to NF-κB, our microarray analysis indicates that TWEAK affects the expression of several genes involved in different cell signaling pathways such as Wnt, MAPK, PI3K/Akt, TGF-β, interferon-γ (IFN-γ), and ubiquitin-proteasome system (Figure 6).
Microarray analysis indicates a small reduction in expression during the mid-trophozoite stage.
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The results of our microarray analysis indicated that a total of 8410 genes passed the quality control criteria and statistical significance tests to identify genes expressed in adult murine RPE Supplementary Dataa S1).
Additionally, microarray analysis indicated that TGF-β1 up-regulated MAPK signaling in contrast to C-ABC, which did not enrich genetic pathways.
Moreover, microarray analysis indicated that the YAP/TAZ target genes connective tissue growth factor (CTGF), ankyrin repeat domain 1 (ANKRD1), cysteine-rich angiogenic inducer 61 (CYR61), baculoviral IAP repeat containing 5 (BIRC5), AXL receptor tyrosine kinase (AXL), inhibin alpha subunit (INHA) and collagen type VIII alpha 1 chain (COL8A1) are not upregulated in TAM-treated ER-Src cells18.
Microarray analysis indicated that the expressions of testosterone synthesis-associated genes, i.e., Star, P450scc, 3β-Hsd, Abp, Cox7a2, Pcna, p450c17and17β-Hsd were significantly altered by linuron exposure, along with other genes involving in cell proliferation and apoptosis, such as c-myc, S6K, Apaf1, and TSC1.
Microarray analysis indicated that Brahma-related gene 1 (Brg1) and proliferation-related genes including proliferating cell nuclear antigen (Pcna), neurotrophin 3 (Ntf3) and platelet-derived growth factor subunit A (Pdgfα) were significantly downregulated by H2S in endothelin-1-stimulated proliferative vascular smooth muscle cells.
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