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Abstract

Plasma high density lipoproteins (HDL) have been the focus of active research over the last two decades since HDL-cholesterol have been inversely associated with the risk of premature cardiovascular disease, respectively (1–4). HDL have been proposed to modulate the development of premature vascular disease by facilitating the removal of excess cholesterol from peripheral tissues and transporting the cholesterol directly back to the liver or transferring the cholesterol to VLDL or LDL by the cholesterol ester exchange protein (CETP) (5–7). The process of HDL mediated transport of cholesterol from peripheral tissues back to the liver has been termed reverse cholesterol transport (8,9) and remains to be definitively confirmed.

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© 1993 Springer-Verlag Berlin Heidelberg

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Brewer, H.B., Rader, D.J., Klein, HG., Ikewaki, K., Santamarina-Fojo, S. (1993). The Molecular Basis of Genetic Defects in HDL Metabolism. In: Schettler, G., Greten, H., Habenicht, A.J.R. (eds) Cellular Metabolism of the Arterial Wall and Central Nervous System. Sitzungsberichte der Heidelberger Akademie der Wissenschaften, vol 1993/94 / 1993/1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84949-7_5

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  • DOI: https://doi.org/10.1007/978-3-642-84949-7_5

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