
GBT440 Increases Hematocrit and Improves Biventricular Function in Berkeley Sickle Cell Disease Mice
/in Genetics, Hemodynamics, Pre-ClinicalEstrogen Receptor Alpha Prevents Right Ventricular Diastolic Dysfunction and Fibrosis in Female Rats
/in Fibrosis, Genetics, Hemodynamics, Pre-Clinical, RV Function, Sex & Maturation, StressEffects of Red Blood Cell Sickling on Right Ventricular Afterload
/in Arterial Mechanics, Genetics, Hemodynamics, Pre-Clinical, RV FunctionPBX transcription factors drive pulmonary vascular adaptation to birth
/in Arterial Mechanics, Genetics, Hemodynamics, In Vitro, Pre-Clinical, RV FunctionPulmonary vascular collagen content, not cross-linking, contributes to right ventricular pulsatile afterload and overload in early pulmonary hypertension.
/in Arterial Mechanics, Fibrosis, Genetics, Pre-Clinical, RV Function, 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, 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 & MaturationComparison 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
419 South Circle View Drive
6830 ISEB
Irvine, CA 92697
(949) 824-3941
nchesler@uci.edu