A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation
A. A. Geisterfer-Lowrance and others

Toll-like receptor 4 polymorphisms and atherogenesis
S. Kiechl and others

Prospects for whole-genome linkage disequilibrium mapping of common disease genes
L. Kruglyak

Genetic isolates: separate but equal?
L. Kruglyak

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy
R. Coral-Vazquez and others

A calcineurin-dependent transcriptional pathway for cardiac hypertrophy
J. D. Molkentin and others

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
M. E. Curran and others

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
H. C. Dietz and others

Molecular medicine. The cholesterol quartet
J. L. Goldstein and M. S. Brown

Myocyte-enriched calcineurin-interacting protein, MCIP1, inhibits cardiac hypertrophy in vivo
B. A. Rothermel and others