Editorials |
From the Departments of Pharmacology and Pediatrics, Center for Molecular Therapeutics, College of Physicians & Surgeons of Columbia University, New York, NY.
Correspondence to Michael R. Rosen, MD, College of Physicians & Surgeons of Columbia University, Department of Pharmacology, 630 W 168 St, PH7W-321, New York, NY 10032. E-mail mrr1@columbia.edu
Key Words: electrocardiography genetic translation molecular biology arrhythmia
| Introduction |
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Translational Research (formerly Physiology) provides a potent vehicle for associating experimental reality with The Real Thing. Yet all the models we use, whether computers, cells, tissues, or animals, can spew forth data that muddy the distinction between what is real and unreal. One example this statement applies to is mouse physiology. Since the advent of transgenic technology, we have learned a great deal about the mouse, all of it relevant to the mouse, and some of it relevant to other forms of animal life. But what is relevant, where is it relevant, and when?
The study by Guo et al1 in this issue of Circulation
Research is a case in point. The authors integrate molecular
determinism, cellular manifestation, and in vivo expression. The result
is an interesting counterpoint, incorporating
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