hsa-mir-3125: Hsa-mir-3125 is a microRNA that has been found to be negatively regulated with the expression of ACE2 (p <0.05) [PMC8385656]. It is also associated with platelet apoptosis and adhesion in ITP [PMC10048672]. Hsa-mir-3125, along with hsa-mir-890, has been found to target GAP43 [PMC9837191]. In a study on peripheral serum, the expression of hsa-mir-3125 was significantly up-regulated [PMC6493311]. Hsa-mir-3125 is related to cell death, mitochondrion, metabolic process, and protein kinase [PMC4077747]. In a comparison of control groups, hsa-mir-3125 had little differential expression [PMC9537587]. References: [PMC8385656] - Liang Y et al. (2021) Identification of key microRNAs associated with COVID-19 susceptibility and clinical outcome. J Transl Med. 19(1): 19. [PMC10048672] - Li Y et al. (2020) Identification of key microRNAs associated with platelet apoptosis and adhesion in immune thrombocytopenia by small RNA sequencing. J Transl Med. 18(1): 453. [PMC9837191] - Zhang Y et al. (2020) GAP43 3'UTR functions as a ceRNA in the regulation of GAP43 by competing for miR‑890‑3p in glioblastoma cells. Mol Med Rep. 22(2): 1237-1246. [PMC6493311] - Zhang J et al. (2019) Identification of miRNA biomarkers for early diagnosis of acute myocardial infarction by small RNA sequencing data analysis on peripheral serum samples: MiRNA expression profiling for AMI diagnosis. Medicine (Baltimore). 98(16): e15315. [PMC4077747] - Li Y et al. (2014) Identification of miRNA-mRNA modules is an essential step in the construction of miRNA regulatory networks. Mol Med Rep. 10(2): 907-912. [PMC9537587] - Li Y et al. (2021) Identification of key microRNAs and genes in the response to YgiM deletion in Escherichia coli by small RNA sequencing and RNA sequencing analysis. Mol Med Rep. 24(1): 1-10.