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miRBase |
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![]() 4 publications mentioning gga-mir-214Open access articles that are associated with the species Gallus gallus and mention the gene name mir-214. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary. |
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7d, hsa-let-7e, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-16-1, hsa-mir-21, hsa-mir-16-2, mmu-let-7g, mmu-let-7i, mmu-mir-9-2, mmu-mir-151, mmu-mir-10b, hsa-mir-192, mmu-mir-194-1, mmu-mir-199a-1, hsa-mir-199a-1, mmu-mir-122, hsa-mir-10a, hsa-mir-10b, hsa-mir-199a-2, hsa-mir-199b, hsa-mir-210, hsa-mir-214, mmu-let-7d, hsa-let-7g, hsa-let-7i, hsa-mir-122, hsa-mir-9-1, hsa-mir-9-2, hsa-mir-9-3, hsa-mir-194-1, mmu-mir-192, mmu-let-7a-1, mmu-let-7a-2, mmu-let-7b, mmu-let-7c-1, mmu-let-7c-2, mmu-let-7e, mmu-let-7f-1, mmu-let-7f-2, mmu-mir-16-1, mmu-mir-16-2, mmu-mir-21a, mmu-mir-10a, mmu-mir-210, mmu-mir-214, mmu-mir-199a-2, mmu-mir-199b, mmu-mir-9-1, mmu-mir-9-3, hsa-mir-194-2, mmu-mir-194-2, hsa-mir-365a, mmu-mir-365-1, hsa-mir-365b, hsa-mir-151a, gga-let-7i, gga-let-7a-3, gga-let-7b, gga-let-7c, gga-mir-16-1, gga-mir-194, gga-mir-10b, gga-mir-199-2, gga-mir-16-2, gga-let-7g, gga-let-7d, gga-let-7f, gga-let-7a-1, gga-mir-199-1, gga-let-7a-2, gga-let-7j, gga-let-7k, gga-mir-122-1, gga-mir-122-2, gga-mir-9-2, mmu-mir-365-2, gga-mir-9-1, gga-mir-365-1, gga-mir-365-2, hsa-mir-151b, mmu-mir-744, gga-mir-21, hsa-mir-744, gga-mir-199b, gga-mir-122b, gga-mir-10a, gga-mir-16c, sma-let-7, sma-mir-71a, sma-bantam, sma-mir-10, sma-mir-2a, sma-mir-3479, sma-mir-71b, mmu-mir-21b, mmu-let-7j, mmu-mir-21c, mmu-let-7k, gga-mir-365b, sma-mir-8437, sma-mir-2162, gga-mir-9-3, gga-mir-210a, gga-mir-9-4, mmu-mir-9b-2, mmu-mir-9b-1, mmu-mir-9b-3, gga-mir-9b-1, gga-mir-10c, gga-mir-210b, gga-let-7l-1, gga-let-7l-2, gga-mir-122b-1, gga-mir-9b-2, gga-mir-122b-2
In contrast, the miRNAs up-regulated in the liver (miR-199-3p, miR-199-5p, miR-21, miR-214 and miR-210) showed significantly higher levels in mouse serum at 12 weeks post infection (Fig. 2), however these failed to differentiate S. mansoni infected from uninfected humans (Fig. S4).
[score:4]
As shown in Fig. 2, the levels of miR-192, miR-194 and miR-122 in serum do not change between 4–12 weeks post infection, whereas five of the miRNAs that are up-regulated in the liver are also significantly elevated in serum at 12 weeks post infection (p<0.05), ranging from 2.6 fold (miR-21) to 4.7 fold (miR-214) (Table S2).
[score:4]
Temporal expression analysis of miR-199, miR-214, miR-21, miR-210, miR-122, miR-192 and miR-194 in the liver during S. mansoni infectionBetween weeks 6 and 12, female parasites continue to produce ∼300 eggs per day [51], resulting in an increase in the number of granulomas in the liver and the development of fibrosis [45].
[score:4]
The miRNAs that displayed the largest differential expression included miR-199a and miR-214, which are known to be altered in liver fibrosis caused by hepatitis C infection or induced by carbon tetrachloride [47], [48].
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Temporal expression analysis of miR-199, miR-214, miR-21, miR-210, miR-122, miR-192 and miR-194 in the liver during S. mansoni infection.
[score:3]
Thirty-three mouse miRNAs were differentially expressed in infected compared to naïve mice (>2 fold change, p<0.05) including miR-199a-3p, miR-199a-5p, miR-214 and miR-21, which have previously been associated with liver fibrosis in other settings.
[score:2]
Consistent with the array results, there was an increase in miR-199-5p, miR-199-3p, miR-214, miR-21, miR-210, and a reduction of miR-192, miR-194, miR-365, miR-122 and miR-151 in the liver tissue of S. mansoni infected mice as compared to naïve mice; miR-9 and miR-744 did not display differential expression and were not analysed further (Table 1).
[score:2]
The 5 host miRNAs were detectable in serum (miR-21, miR-199-3p, miR-199-5p, miR-210, miR-214) but showed variable abundance and failed to differentiate ‘egg -positive’ and ‘egg -negative’ participants (Fig. S4).
[score:1]
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Other miRNAs from this paper: gga-let-7i, gga-let-7a-3, gga-let-7b, gga-mir-99a, gga-let-7c, gga-mir-222a, gga-mir-221, gga-mir-20a, gga-mir-16-1, gga-mir-128-2, gga-mir-133a-1, gga-mir-1a-2, gga-mir-30d, gga-mir-30b, gga-mir-30a, gga-mir-30c-2, gga-mir-133b, gga-mir-206, gga-mir-103-2, gga-mir-203a, gga-mir-10b, gga-mir-128-1, gga-mir-181a-1, gga-mir-181b-1, gga-mir-199-2, gga-mir-16-2, gga-mir-15b, gga-mir-140, gga-let-7g, gga-let-7d, gga-let-7f, gga-let-7a-1, gga-mir-103-1, gga-mir-205b, gga-mir-130b, gga-mir-130a, gga-mir-181b-2, gga-mir-181a-2, gga-mir-126, gga-mir-199-1, gga-mir-1a-1, gga-mir-133a-2, gga-mir-200a, gga-mir-200b, gga-mir-1b, gga-mir-133c, gga-mir-30e, gga-mir-30c-1, gga-let-7a-2, gga-let-7j, gga-let-7k, gga-mir-101-1, gga-mir-27b, gga-mir-31, gga-mir-20b, gga-mir-499, gga-mir-367, gga-mir-429, gga-mir-21, gga-mir-460a, gga-mir-1329, gga-mir-460b, gga-mir-1c, gga-mir-1677, gga-mir-199b, gga-mir-101-2, gga-mir-10a, gga-mir-130c, gga-mir-15c, gga-mir-16c, gga-mir-2188, gga-mir-222b, gga-mir-203b, gga-mir-10c, gga-let-7l-1, gga-let-7l-2
For example, zebrafish miR-214 was reported to regulate the slow muscle phenotype by targeting suppressor of fused (Sufu), a negative regulator of hedgehog signaling [23].
[score:7]
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Other miRNAs from this paper: gga-mir-29a, gga-mir-29b-1, gga-let-7i, gga-let-7a-3, gga-let-7b, gga-let-7c, gga-mir-221, gga-mir-20a, gga-mir-16-1, gga-mir-15a, gga-mir-26a, gga-mir-148a, gga-mir-128-2, gga-mir-30d, gga-mir-30b, gga-mir-30a, gga-mir-30c-2, gga-mir-218-1, gga-mir-128-1, gga-mir-181a-1, gga-mir-181b-1, gga-mir-16-2, gga-mir-15b, gga-let-7g, gga-let-7d, gga-let-7f, gga-let-7a-1, gga-mir-146a, gga-mir-218-2, gga-mir-130b, gga-mir-130a, gga-mir-181b-2, gga-mir-181a-2, gga-mir-126, gga-mir-30e, gga-mir-30c-1, gga-let-7a-2, gga-let-7j, gga-let-7k, gga-mir-29c, gga-mir-29b-2, gga-mir-101-1, gga-mir-23b, gga-mir-24, gga-mir-122-1, gga-mir-7b, gga-mir-122-2, gga-mir-20b, gga-mir-146b, gga-mir-147, gga-mir-365-1, gga-mir-365-2, gga-mir-375, gga-mir-21, gga-mir-22, gga-mir-1456, gga-mir-1662, gga-mir-1786, gga-mir-122b, gga-mir-101-2, gga-mir-10a, gga-mir-130c, gga-mir-146c, gga-mir-15c, gga-mir-16c, gga-mir-365b, gga-let-7l-1, gga-let-7l-2, gga-mir-122b-1, gga-mir-122b-2
MiR-101-3p (−2.1-fold) and miR-15c-5p (−1.4-fold) had the most target genes followed by miR-15a, miR-16-5p, miR-214, miR-16c-5p, and miR-181b-5p (Supplementary Table S4), and these miRNAs were all down-regulated in L30 compared with L20.
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Other miRNAs from this paper: gga-mir-26a, gga-mir-30a, gga-mir-203a, gga-mir-10b, gga-mir-181a-1, gga-mir-184, gga-mir-140, gga-mir-205b, gga-mir-181a-2, gga-mir-126, gga-mir-205a, gga-mir-196-1, gga-mir-24, gga-mir-31, gga-mir-21, gga-mir-10a, gga-mir-2131, gga-mir-203b, gga-mir-205c
MiR-214 regulates skin morphogenesis and hair follicle cycling by targeting β-catenin [26, 27].
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