Low Density Lipoproteins

Low Density Lipoproteins by Charles Day, published by Springer US on March 22, 2012, is a comprehensive resource that delves into the significance of low-density lipoproteins (LDL) in relation to atherosclerosis, a leading cause of death in developed countries. This edition, spanning 446 pages, aims to consolidate a wealth of research on LDL, providing a detailed overview of its structure, function, and metabolism, which are critical for understanding and potentially controlling atherosclerosis.
Readers will find a thorough compilation of published information on LDL up to 1975, supported by over 1,500 references. The book employs the A, B, C apolipoprotein classification system, which simplifies the categorization of apolipoproteins compared to other methods. This work focuses on the pathophysiological importance of LDL and the ongoing research efforts surrounding it, making it a valuable reference for those interested in the fields of biochemistry and life sciences.
Official synopsis Publisher
Low density lipoproteins (LDL) are pathophysiologically important be cause of their central role in the disease atherosclerosis and because atherosclerosis is the leading cause of death in developed countries. Many researchers believe that a more detailed knowledge of the struc ture, function, and metabolism of LDL may eventually lead to a means to control atherosclerosis. For this reason a fairly large research effort has gone into the investigation of LDL over the past few years. The purpose of this book is to collect and summarize in one place most of the pub lished information on LDL through 1975. To this end more than 1500 references are cited in the papers that make up this volume. The A, B, C apolipoprotein classification system was adopted for use throughout this work. In addition to the A, B, C, and “D” families of apolipoproteins, apoE is used to designate the “arginine-rich” apolipo protein. This classification system is used because it is far less cumber some than other proposed classification schemes for apolipoproteins.
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