A study in human full-term newborns demonstrated that the mir-376c has lower levels reported in newborns with hypoxic-ischemic encephalopathy, as mentioned in the introductory literature [Lai et al. DOI:10.1016/j.pedneo.2024.05.002]. In a separate study of human left ventricular myocardium, the mir-376c was identified as one of the most abundant miRNAs in baseline and postischemic samples, and it was downregulated (-2.75 fold) in postischemic tissue following acute ischemia [Saddic et al. DOI:10.1152/physiolgenomics.00049.2015].