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Titlebook: DNA Polymorphisms as Disease Markers; D. J. Galton,G. Assmann (Director) Book 1991 Springer Science+Business Media New York 1991 DNA.Lipid

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书目名称DNA Polymorphisms as Disease Markers
编辑D. J. Galton,G. Assmann (Director)
视频video
丛书名称NATO Science Series A:
图书封面Titlebook: DNA Polymorphisms as Disease Markers;  D. J. Galton,G. Assmann (Director) Book 1991 Springer Science+Business Media New York 1991 DNA.Lipid
描述The purpose of this workshop was to assess the value of DNA polymorphisms for the prediction, diagnosis or elucidation of aetiology for common metabolic diseases such as diabetes, hyperlipidaemia and atherosclerosis. The advent of recombinant DNA techniques has produced an explosion in knowledge of restriction site polymorphisms and hypervariable sequences around candidate genes for such common metabolic diseases as atherosclerosis, hyperlipidaemia and diabetes mellitus. These diseases are the major causes of morbidity and mortality in Western societies today. Since 1983 it has become apparent that there is much more variation in the frequency and sites of these DNA polymorphisms in human populations than was initially appreciated and that the majority of these DNA polymorphisms are only linkage markers for the disease. Consequently it was considered timely for laboratories involved in the mapping of these DNA mutations to meet together to discuss the implications of their studies. The main issues are whether such DNA polymorphisms will lead to an identification of major aetiological loci and which are the best techniques to achieve this? What is the cause of the differences in fre
出版日期Book 1991
关键词DNA; Lipid; atherosclerosis; coronary heart disease; genes; genetics; heart; heart disease; high-density lip
版次1
doihttps://doi.org/10.1007/978-1-4615-3690-1
isbn_softcover978-1-4613-6640-9
isbn_ebook978-1-4615-3690-1
copyrightSpringer Science+Business Media New York 1991
The information of publication is updating

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A Candidate Gene Approach to the Genetics of Normal Lipid Variation: DNA Association Studies and Genors combined. In addition, the contributing genes do not act alone; rather they are interacting with other genes and environmental factors in determining disease risk. Therefore, the effect of a gene measured in one environment or population may be very different from its effect in another.
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https://doi.org/10.1007/978-1-4020-9787-4 large aberrations in the DNA primary structure. A much more complicated situation is present in common disease where important roles for disease expression have been attributed to endogenous as well as exogenous factors (1).
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S. Z. Husain,V. H. Heywood,K. R. Markhamecretes VLDL particles and, similar to chylomicrons in the bloodstream, VLDLs are partly lipolyzed by LPL and the VLDLremnants or IDL particles formed are taken up with high affinity by the hepatic LDL receptors.
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Two Concepts of Opposition, Multiple Squareswo apo B abnormalities that cause hypercholesterolemia were investigated. The case of a family affected with defective apo B-100 and of a woman with severe hypercholesterolemia and hyperapobetalipoproteinemia are presented.
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Molecular Genetics Approach to Polygenic Disease—Initial Results from Atherosclerosis Research large aberrations in the DNA primary structure. A much more complicated situation is present in common disease where important roles for disease expression have been attributed to endogenous as well as exogenous factors (1).
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