Abstract
We hypothesize that the inhibition of HIF-1α degradation via short hairpin RNA (shRNA) knockdown of PHD2 using UTMD in rats would promote transgene expression, facilitate angiogenesis, improve myocardial function and provide a potential therapy for ischemic and reperfusion myocardial injury in rats
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have