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Gene Information
Gene symbol: MIRN145
Gene name: microRNA 145
HGNC ID: 31532
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | ADIPOQ | 1 hits |
| 2 | AKT1 | 1 hits |
| 3 | FABP4 | 1 hits |
| 4 | FSD1 | 1 hits |
| 5 | INS | 1 hits |
| 6 | LILRB1 | 1 hits |
| 7 | MIRN126 | 1 hits |
| 8 | MIRN128-1 | 1 hits |
| 9 | MIRN146A | 1 hits |
| 10 | MIRN195 | 1 hits |
| 11 | MIRN19A | 1 hits |
| 12 | MIRN21 | 1 hits |
| 13 | MIRN34A | 1 hits |
| 14 | MIRN375 | 1 hits |
| 15 | MIRN96 | 1 hits |
| 16 | PIK3CA | 1 hits |
| 17 | RORC | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 20948521 | Phosphoglycerate kinase-1 (PGK1) and peptidylprolyl isomerase A (PPIA) were identified as the most stable mRNAs across all tissues and panels. |
| 2 | 20948521 | We then tested the effect on expression of two established adipocyte-related transcripts (fatty acid binding protein 4 (FABP4) and microRNA-145 (miR-145)), either normalized to the optimal or a commonly used controls transcript. |
| 3 | 21441927 | Obesity-induced overexpression of miRNA-143 inhibits insulin-stimulated AKT activation and impairs glucose metabolism. |
| 4 | 21441927 | Induced transgenic overexpression of miR-143, but not miR-145, impairs insulin-stimulated AKT activation and glucose homeostasis. |
| 5 | 21441927 | Reduced ORP8 expression in cultured liver cells impairs the ability of insulin to induce AKT activation, revealing an ORP8-dependent mechanism of AKT regulation. |
| 6 | 23834149 | In this paper, an overview was depicted about the role of following miRNAs in pancreatic development and insulin secretion (miR-375, miR-7, miR-124a2, miR-195, miR-126, miR-9, miR-96, miR-34a); insulingrowth factor-1 receptor expression (miR-7, miR-139, miR-145, miR-1); the diabetes-associated pancreatic cancer pathway genes such as IRS, PI3K, AKT/PKB (miR-128a, miR-19a, miR-21, miR-29 a/b/c); mTOR protein regulation (miR- 99, miR-21, miR-126, and miR-146a) etc. |
| 7 | 23834149 | At last, we have also explained the role of miRNAs in diagnostic marker (miR- 200, miR-21, miR-103, miR-107, and miR-155) and as a therapeutic modulator (miR-34, miR-21, miR-221, and miR-101) in pancreatic cancer. |