Pulmonary arterial hypertension (PAH) is a severe condition characterized by abnormally high mean pulmonary arterial pressure (mPAP) due to persistent vasoconstriction, proliferation, and inflammation of the pulmonary arteries (PAs) [1,2]. Potassium channels of the voltage-dependent (Kv) or K2P supe...
MN supplementation showed a 16% reducMtiMonNinsutphpelermiskenotaftdioinar, rchoemapaamreodntgo cIFhAild, wreans athgeeson6lmy coonmthpsartiosounnidnetrh-fiisvree,vwiehwentocionmclupdaered to IFA (astvuedriaesgethRaRt r0e.p8o4r;t9ed5%chCilId0d.7e6vetolop0.m92en; tstouudticeosm=...