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Novel pharmacotherapies to abrogate postinfarction ventricular remodeling
Gerald W. Dorn
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Institute of Clinical and Translational Sciences (ICTS)
Department of Medicine
DBBS - Molecular Cell Biology
DBBS - Human and Statistical Genetics
DBBS - Molecular Genetics and Genomics
Hope Center for Neurological Disorders
Research output
:
Contribution to journal
›
Review article
›
peer-review
83
Scopus citations
Overview
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Keyphrases
Myocardial Infarction
100%
Post-infarction
100%
Ventricular Remodeling
100%
Novel Pharmacotherapy
100%
Cardiomyocytes
66%
Cell-based
33%
Apoptosis
33%
Human Disease
33%
Heart Failure
33%
Molecular Pathways
33%
Multiple Organs
33%
Infarction
33%
Dropout
33%
Cellular Pathways
33%
Kinase Inhibition
33%
Therapeutic Targeting
33%
Endothelial Nitric Oxide Synthase (eNOS)
33%
Pharmaceutics
33%
Putative Drug Targets
33%
Wall Thinning
33%
G Protein-coupled Receptor Kinase
33%
Therapeutic Window
33%
Inflammatory Fibrosis
33%
Erythropoietin
33%
Pharmacological Treatment
33%
Ventricular Geometry
33%
Active Processes
33%
Cardiac Outcomes
33%
Renin-angiotensin-aldosterone System
33%
Physiological Pathways
33%
Functional Compromise
33%
Direct Renin Inhibition
33%
Aldosterone Synthesis
33%
Pharmacology, Toxicology and Pharmaceutical Science
Heart Infarction
100%
Pharmacotherapy
100%
Heart Ventricle Remodeling
100%
Aldosterone
66%
Receptor
33%
Phosphotransferase
33%
Renin
33%
Angiotensin
33%
Inflammation
33%
Fibrosis
33%
Infarction
33%
Congestive Heart Failure
33%
Guanine Nucleotide Binding Protein
33%
Therapeutic Window
33%
Endothelial Nitric Oxide Synthase
33%
Erythropoietin
33%
Renin Inhibitor
33%
Diseases
33%