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Correspondence to:
Edward Kim.
Over the past five years, several laboratories have used a variety of transgenic and gene-targeted mice to study apoB. These studies have helped in 1) generating new mouse models suitable for investigating the genetic and environmental factors affecting atherogenesis; 2) providing systems for investigating apoB structure/function relationships; 3) understanding the regulation of apoB gene expression in the intestine; 4) delineating a critical role for apoB expression in mouse embryonic development; 5) yielding insights into the "physiologic rationale" for the existence of the two different forms of apoB, apoB-48 and apoB-100, in mammalian metabolism; and 6) providing basic insights into mechanisms involved in the human apoB deficiency syndrome, familial hypobetalipoproteinemia.Kim, E., and S. G. Young. Genetically modified mice for the study of apolipoprotein B. J. Lipid Res. 1998. 39: 703723.
Supplementary key words:
apolipoprotein B, lipids, cholesterol, triglycerides, atherosclerosis, mouse, transgenic, gene targeting, knockout
Copyright © 1998 by Lipid Research, Inc.
Review
Genetically modified mice for the study of apolipoprotein B
Edward Kima,b and
Stephen G. Younga,b
a Gladstone Institute of Cardiovascular Disease, San Francisco, CA 94141-9100
b Cardiovascular Research Institute and the Department of Medicine, University of California, San Francisco, CA 94143
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