17?-estradiol mediates superior adaptation of right ventricular function to acute strenuous exercise in female rats with severe pulmonary hypertension.
/in Arterial Mechanics, Fibrosis, Hemodynamics, Pre-Clinical, RV Function, Sex & Maturation, StressLimiting collagen turnover via collagenase-resistance attenuates right ventricular dysfunction and fibrosis in pulmonary arterial hypertension.
/in Fibrosis, Genetics, Hemodynamics, Pre-Clinical, RV Function, StressValidation of an arterial constitutive model accounting for collagen content and crosslinking.
/in Arterial Mechanics, Fibrosis, Genetics, In Silico, Pre-Clinical, Stress17?-estradiol attenuates conduit pulmonary artery mechanical property changes with pulmonary arterial hypertension.
/in Arterial Mechanics, Fibrosis, Pre-Clinical, Sex & Maturation, StressMitochondria DNA mutations cause sex-dependent development of hypertension and alterations in cardiovascular function.
/in Arterial Mechanics, Fibrosis, Genetics, Hemodynamics, Pre-Clinical, RV Function, Sex & MaturationDirect and Indirect protection of right ventricular function by estrogen in an experimental model of pulmonary arterial hypertension.
/in Arterial Mechanics, Fibrosis, Hemodynamics, Pre-Clinical, RV Function, Sex & Maturation, StressProgressive right ventricular function and structural changes in a mouse model of pulmonary arterial hypertension.
/in Arterial Mechanics, Fibrosis, Hemodynamics, Pre-Clinical, RV Function, StressChanges in large pulmonary arterial viscoelasticity in chronic pulmonary hypertension.
/in Arterial Mechanics, Fibrosis, Pre-Clinical, StressComparison of approaches to quantify arterial damping capacity from pressurization tests on mouse conduit arteries.
/in Arterial Mechanics, Fibrosis, Genetics, Pre-Clinical, StressChesler Lab
Professor Naomi C. Chesler
University of California, Irvine
2420 Engineering Hall
(949) 824-3941
nchesler@uci.edu