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Trends in Cardiovascular Medicine|January 18, 2011
Defining the molecular genetic basis of idiopathic dilated cardiomyopathyT M Olson, M T Keating
The Journal of Clinical Investigation|January 15, 1996
Mapping a cardiomyopathy locus to chromosome 3p22-p25T M Olson, M T Keating
Biotechnology and Bioengineering|November 1, 1986
Kinetics and mechanism of dissimilative Fe(III) reduction by Pseudomonas sp. 200R G Arnold, T M Olson, M R Hoffmann
Journal of Molecular and Cellular Cardiology|March 29, 2001
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathyT M Olson, N Y Kishimoto, F G Whitby, et al.
Environmental Science & Technology|May 18, 2001
Pathogen filtration, heterogeneity, and the potable reuse of wastewaterJ A Redman, S B Grant, T M Olson, et al.
Journal of Muscle Research and Cell Motility|September 12, 2002
Functional studies of yeast actin mutants corresponding to human cardiomyopathy mutationsW W Wong, T C Doyle, P Cheung, et al.
Clinical Pharmacology and Therapeutics|December 23, 2006
Aminoglycoside-induced translational read-through in disease: overcoming nonsense mutations by pharmacogenetic therapyL V Zingman, S Park, T M Olson, et al.
Science (New York, N.Y.)|May 23, 1998
Actin mutations in dilated cardiomyopathy, a heritable form of heart failureT M Olson, V V Michels, S N Thibodeau, et al.
Clinical Pharmacology and Therapeutics|December 23, 2006
A common polymorphism in SCN5A is associated with lone atrial fibrillationL Y Chen, J D Ballew, K J Herron, et al.
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