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7 publications mentioning bta-mir-96

Open access articles that are associated with the species Bos taurus and mention the gene name mir-96. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary.

[+] score: 31
Interestingly, ErbB signalling pathway was enriched by only target genes of miRNAs up-regulated in preovulatory dominant follicles (bta-miR-129-5p, bta-miR-221, bta-miR-339b and bta-miR-96) and suggests possible involvement of these miRNAs in modulating ErbB gene family during bovine follicular development. [score:7]
To experimentally validate the Insilco target gene prediction of differentially expressed miRNAs, we selected the miR-183 cluster miRNAs (bta-miR-183, bta-miR-182 and bta-miR-96); which are predicted to target the Forkhead box protein O1 (FOXO1) gene. [score:7]
Simultaneously, mutant FOXO1 3´-UTR constructs with mutations on target recognition sites of miR-183, miR-182 and miR-96 were generated. [score:4]
Expression pattern of members of the miR-183 cluster (bta-miR-182 and bta-miR-96) and miR-132 cluster (bta-miR-132 and bta-miR-212) in companion follicular cells of both preovulatory dominant and subordinate follicles using qPCR. [score:3]
Nine differentially expressed candidate miRNAs identified by NGS (bta-miR-132, bta-miR-212, bta-miR-21-3p, bta-miR-96, bta-miR-182, bta-miR-221, bta-miR-335, bta-miR-708 and bta-miR-214) were randomly selected for quantitative real time PCR (qPCR) validation. [score:3]
Members of the miR-183 cluster; bta-miR-96, bta-miR-182 and bta-miR-183 are transcribed from intergenic region of chromosome 4 of the bovine genome. [score:1]
All members of the miR-183 cluster (bta-miR-183, bta-miR-96 and bta-miR-182) were the top three miRNAs highly enriched in granulosa cells of preovulatory dominant follicles. [score:1]
However, 28 miRNAs including bta-miR-96 and bta-miR-122 were found to be specific to preovulatory dominant. [score:1]
However, 2 miRNAs (bta-miR-96 and bta-miR-375) enriched in preovulatory dominant follicles were uniquely detected in granulosa cells of preovulatory dominant follicles. [score:1]
For this we constructed plasmid DNA containing part of the 3′-UTR of bovine FOXO1 gene harbouring the putative miRNA binding sites for bta-miR-183, bta-miR-182 and bta-miR-96. [score:1]
In comparison with subordinate follicles, 34 matured miRNAs including miR-132 cluster (bta-miR-132 and bta-miR-212) and miR-183 cluster (bta-miR-183, bta-miR-182 and bta-miR-96) were significantly enriched in preovulatory dominant follicles (Table 4). [score:1]
Granulosa cells were transfected with or without bta-miR-183 mimic (B), with or without bta-miR-96 mimic (C), with or without bta-miR-182 mimic (D). [score:1]
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[+] score: 20
the eCL,) and miR-96 (Table 1, significantly upregulated in mCL, lCL, and rCL vs. [score:4]
However, in contrast to hLGC they could not show an inhibitory effect for miR-96 on P4 production in bovine CL. [score:3]
Our sequencing results provide the expression pattern for all three mRNAs: miR-96, -183-5p, and -182 in bovine CL also throughout the cycle and not only for the very early days of the cycle (d 1–4). [score:3]
Although, miR-96 was experimentally validated to also target FOXO1 both in human (Guttilla and White, 2009) and bovine (Gebremedhn et al., 2016), its role in bovine CL (luteal cells) has been partially explained. [score:3]
This observation suggests miR-96, -183-5p, and -182 to be involved not only during very early CL development in the process of follicle-luteal transition as suggested by Gebremedhn et al. (2016), but also in the steps thereafter when the CL becomes functional (mCL and lCL) and then regresses (rCL). [score:2]
Coordinate regulation of FOXO1 by miR-27a, mir-96, and miR-182 in breast cancer cells. [score:2]
Using human luteinized granulosa cells (hLGC) and bovine CL from day 1 to 4 of the cycle, (Mohammed et al., 2017) identified miR-96 as the key regulator of luteal cell survival by modulating the effect of FOXO1 on steroidogenesis (P4). [score:2]
The adequate corpus luteum: miR-96 promotes luteal cell survival and progesterone production. [score:1]
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[+] score: 10
From those identified under RS diet, three rumen DE miRNAs (up-regulated, miR-149-5p and -21-3p; down-regulated, miR-2419-5p) and two mammary gland up-regulated miRNAs (miR-96 and -99a-5p) were identified. [score:10]
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[+] score: 6
Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-mir-21, hsa-mir-26a-1, hsa-mir-27a, hsa-mir-28, hsa-mir-30a, hsa-mir-96, hsa-mir-98, hsa-mir-99a, hsa-mir-103a-2, hsa-mir-103a-1, hsa-mir-196a-1, hsa-mir-199a-1, hsa-mir-148a, hsa-mir-30d, hsa-mir-34a, hsa-mir-196a-2, hsa-mir-199a-2, hsa-mir-23b, hsa-mir-27b, hsa-mir-125b-1, hsa-mir-143, hsa-mir-145, hsa-mir-152, hsa-mir-125a, hsa-mir-125b-2, hsa-mir-194-1, hsa-mir-194-2, hsa-mir-200a, hsa-mir-99b, hsa-mir-26a-2, hsa-mir-378a, hsa-mir-342, hsa-mir-148b, hsa-mir-338, hsa-mir-335, hsa-mir-196b, hsa-mir-484, hsa-mir-486-1, hsa-mir-1271, hsa-mir-378d-2, bta-mir-26a-2, bta-mir-103-1, bta-mir-148a, bta-mir-21, bta-mir-27a, bta-mir-30d, bta-mir-484, bta-mir-99a, bta-mir-125a, bta-mir-125b-1, bta-mir-145, bta-mir-199a-1, bta-mir-27b, bta-mir-98, bta-mir-148b, bta-mir-200a, bta-mir-30a, bta-let-7a-1, bta-mir-342, bta-mir-23b, bta-let-7a-2, bta-let-7a-3, bta-mir-103-2, bta-mir-125b-2, bta-mir-34a, bta-mir-99b, hsa-mir-885, hsa-mir-103b-1, hsa-mir-103b-2, bta-mir-143, bta-mir-152, bta-mir-16a, bta-mir-194-2, bta-mir-196a-2, bta-mir-196a-1, bta-mir-196b, bta-mir-199a-2, bta-mir-26a-1, bta-mir-28, bta-mir-335, bta-mir-338, bta-mir-378-1, bta-mir-486, bta-mir-885, bta-mir-1271, bta-mir-2299, bta-mir-199c, bta-mir-1388, bta-mir-194-1, bta-mir-378-2, hsa-mir-378b, bta-mir-3431, hsa-mir-378c, hsa-mir-4286, hsa-mir-378d-1, hsa-mir-378e, hsa-mir-378f, hsa-mir-378g, hsa-mir-378h, hsa-mir-378i, bta-mir-4286-1, bta-mir-4286-2, hsa-mir-378j, bta-mir-378b, bta-mir-378c, hsa-mir-486-2, bta-mir-378d, bta-mir-194b, bta-mir-194b-2
When compared with the control period (day-14), we identified a total of 22 DE miRNAs at day+28 including 10 up-regulated (bta-miR-199c, miR-199a-3p, miR-98, miR-378, miR-21-5p, miR-148b, miR-34a, miR-152, miR-16a, and miR-28) and 12 down-regulated (bta-miR-200a, miR-145, miR-99a-5p, miR-125b, miR-99b, miR-125a, miR-96, miR-484, miR-1388-5p, miR-342, miR-486 and miR-1271) (Table  2). [score:6]
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[+] score: 4
Other significantly up-regulated miRNAs in frustrated larvae compared to unexposed larvae are rmi-miR-279, rmi-miR-190, rmi-miR-79*, rmi-miR-96, rmi-miR-5307 and rmi-miR-5308 (P < 9.62E-05) (Table 4 and Additional file 8). [score:3]
As anticipated this approach identified five (rmi-miR-71, rmi-miR-96, rmi-miR-153, rmi-miR-745b and rmi-miR-2001) evolutionary conserved miRNAs in R. microplus that were lost in the D. melanogaster genome. [score:1]
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[+] score: 2
Mencía et al. identified two mutations in the seed region of miR96 in two Spanish families, thereby resulting in autosomal-dominant and progressive hearing loss [48]. [score:2]
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[+] score: 1
The adequate corpus luteum: miR-96 promotes luteal cell survival and progesterone production. [score:1]
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