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Results 1-10 of 11 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2019Recent developments in relaxin mimetics as therapeutics for cardiovascular diseasesLeo, C.H.; Jelinic, M.; Ng, H.H.; Parry, L.J.; Tare, M.
2019Relaxin reduces endothelium-derived vasoconstriction in hypertension: revealing new therapeutic insightsLeo, C.H.; Ng, H.H.; Marshall, S.A.; Jelinic, M.; Rupasinghe, T.; Qin, C.; Roessner, U.; Ritchie, R.H.; Tare, M.; Parry, L.J.
2016Serelaxin (recombinant human relaxin-2) prevents high glucose-induced endothelial dysfunction by ameliorating prostacyclin production in the mouse aortaNg, H.H.; Leo, C.H.; Parry, L.J.
2014Localization of relaxin receptors in arteries and veins, and region-specific increases in compliance and bradykinin-mediated relaxation after in vivo serelaxin treatmentJelinic, M.; Leo, C.H.; Post Uiterweer, E.D.; Sandow, S.L.; Gooi, J.H.; Wlodek, M.E.; Conrad, K.P.; Parkington, H.; Tare, M.; Parry, L.J.
2014Acute intravenous injection of serelaxin (recombinant human relaxin-2) causes rapid and sustained bradykinin-mediated vasorelaxationLeo, C.H.; Jelinic, M.; Parkington, H.C.; Tare, M.; Parry, L.J.
2016Serelaxin: a novel therapeutic for vascular diseasesLeo, C.H.; Jelinic, M.; Ng, H.H.; Tare, M.; Parry, L.J.
2017Vascular actions of relaxin: nitric oxide and beyondLeo, C.H.; Jelinic, M.; Ng, H.H.; Marshall, S.A.; Novak, J.; Tare, M.; Conrad, K.P.; Parry, L.J.
2018Relaxin as a therapeutic target for the cardiovascular complications of diabetesNg, H.H.; Leo, C.H.; Parry, L.J.; Ritchie, R.H.
2017Short-term (48 hours) intravenous serelaxin infusion has no effect on myogenic tone or vascular remodeling in rat mesenteric arteriesJelinic, M.; Leo, C.H.; Marshall, S.A.; Senadheera, S.N.; Parry, L.J.; Tare, M.
2016Time-dependent activation of prostacyclin and nitric oxide pathways during continuous i.v. infusion of serelaxin (recombinant human H2 relaxin)Leo, C.H.; Jelinic, M.; Ng, H.H.; Tare, M.; Parry, L.J.

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