Quantitative Changes in T2* Reflect Remodeling of Both Remote and Ischemic Myocardium in a Murine Heart Failure Model

Keywords

addition adverse aging apex arrows artery assess assessment assessments axis biomedical blue bottom burden cardiac cine clinical coded collagen collection color compute considerable consisted continued core coronary cover days decrease decreased degree deposition determined diastolic displayed distance dynamically dynamics ejection engineering enhancement exhibit exhibited explored failure fraction frames free function gadolinium gradient heart heterogeneous histological homogeneous identification include increasing induced infarct infarction infarctions infarcts injury inter interval inversion late lesser ligation likely location magma management mapping maps materials matrix maturation measured merely mice model mouse muscle myocardial myocardium note observations optimize papillary parallel patients permanent positioned previous progressive protocol quantitative readout recently recovery reflect relatively remained remodeling remote representative respectively retrospectively revealed scar segmented segments serial seven severe short significantly slice slices slight smaller societies society staining starting status structural substantial substantially suffering surgery surgically survival systolic technology tissue triggered valuable ventricle ventricular viable volume wall western whereas widely wise wolfram