Evidence from clinical and experimental heart failure studies indicates tha
t cardiac growth and morphogenesis are important determinants for morbidity
and mortality. Characterization of the myocardial gene expression patterns
that are associated with these processes may be useful in the search for n
ovel therapeutic strategies. Changes in tissue mRNA abundance have traditio
nally been monitored by a candidate gene approach, in which transcripts of
interest have been analyzed one or several at a time. New methodologies for
detecting differentially expressed genes, such as DNA microarrays, and res
triction fragment display, are now enabling molecular phenotyping to be per
formed on a much larger scale. Here ive describe our work on the applicatio
n of these methods and the insights gained into the biology and pathophysio
logy of the myocardium. (C) 2001, Elsevier Science Inc.