Rubin E M, Tall A
Lawrence Berkeley National Laboratory, Genome Sciences Department, Berkeley, California 94720, USA.
Nature. 2000 Sep 14;407(6801):265-9. doi: 10.1038/35025236.
Diseases of the vascular system result from a complex mixture of genetic and environmental factors. Data sets, technologies and strategies emanating from the human genome programme have been applied to the analysis of both rare single-gene and common multigenic vascular disorders. Genomic approaches including inter- and intraspecies sequence comparisons, genotyping with dense marker sets spanning the genome, large-scale mutagenesis screens of model organisms, and genome-wide expression profiling have all begun to contribute to the identification of new genes and mechanisms that are central to cardiovascular disease processes.