A study in human plasma demonstrated that hsa-miR-92a-3p was upregulated within the first 24 hours after traumatic brain injury (TBI) [Qin et al. DOI:10.1371/journal.pone.0204051], while another study in human formalin-fixed paraffin-embedded brain tissue utilized hsa-miR-92a-3p as a stable housekeeping gene for normalization in the geometric mean with hsa-miR-16-5p during the relative quantification of diagnostic miRNAs in fatal TBI cases [Bonin et al. DOI:10.3390/ijms241310836]. Another investigation in rats, mice, and rabbits reported that inhibition of miR-92a, delivered via a PEI-DA copolymer system, promotes angiogenesis and wound closure in burn injury models, with this inhibitor advancing to clinical trials for wound healing [Badanina et al. DOI:10.3390/ijms262010060].