Activated Interstitial Myofibroblasts Express Catabolic Enzymes and Mediate Matrix Remodeling in Myxomatous Heart Valves
By E. Rabkin, M. Aikawa, J. R. Stone, Y. Fukumoto, Peter Libby, F. Schoen. Circulation, 2001
659 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/145c6da9d21797b88114cb9d789758337f9276db
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In Cardiology and Cardiovascular Medicine
In Molecular Biology
Citations in the corpus
- The emerging role of valve interstitial cell phenotypes in regulating heart valve pathobiology. (2007, background): “aVICs in mitral valve prolapse express excessive levels of catabolic enzymes.(68) Clinical disorders associated with increased serotonin 5-hydroxytryptamine (5-HT) levels, such as carcinoid syndrome, and the use of serotonin agonists, such as fenfluramine, have been associated with hyperplastic valv”
- Epidemiology of valvular heart disease in the adult (2011, background): “Although considered to be a degenerative valvular disease, mitral valve prolapse differs from AS by macroscopic and histological features, which further illustrates the heterogeneity of degenerative etiologies of valvular diseases”
- Engineering Complex Tissues (2006, positive): “Moreover, VIC in mitral valve leaflets from patients with myxomatous mitral valve degeneration also express features of myofibroblasts, suggesting that this disease comprises a nonequilibrium state, consistent with the progressive course of this condition in many patients.(167) ENGINEERING COMPLEX T”