Literature DB >> 28035501

Th Wichmann1,2, H -A Freye1, K Berndt3.   

Abstract

The significance of genetic factors contributing to the complex etiology of coronary heart disease is discussed using lipoprotein metabolism as an example. A radiochemical screening method was developed for precise biochemical diagnosis of autosomal monogenic hypercholesterolemia. In this method lymphocytes are used as test material.

Entities:  

Year:  1981        PMID： 28035501     DOI： 10.1007/BF00278946

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  29 in total

Review 1.  Genetic markers in atherosclerosis: a review.

Authors:  N E Morton
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

2.  Binding site on macrophages that mediates uptake and degradation of acetylated low density lipoprotein, producing massive cholesterol deposition.

Authors:  J L Goldstein; Y K Ho; S K Basu; M S Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

3.  Family study of serum lipids and lipoproteins in coronary heart-disease.

Authors:  E A Nikkilä; A Aro
Journal:  Lancet       Date:  1973-05-05       Impact factor: 79.321

4.  Serum cholesterol, lipoproteins, and the risk of coronary heart disease. The Framingham study.

Authors:  W B Kannel; W P Castelli; T Gordon; P M McNamara
Journal:  Ann Intern Med       Date:  1971-01       Impact factor: 25.391

5.  Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor.

Authors:  J L Goldstein; S E Dana; G Y Brunschede; M S Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1975-03       Impact factor: 11.205

6.  Regulation of low density lipoprotein receptors by adrenocorticotropin in the adrenal gland of mice and rats in vivo.

Authors:  P T Kovanen; J L Goldstein; D A Chappell; M S Brown
Journal:  J Biol Chem       Date:  1980-06-25       Impact factor: 5.157

7.  Some difficulties in the investigation of genetic factors in coronary artery disease.

Authors:  E A Murphy
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

8.  Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol.

Authors:  J L Goldstein; M S Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1973-10       Impact factor: 11.205

9.  The risk of atherosclerotic vascular disease in subjects with xanthomatosis.

Authors:  A Heiberg
Journal:  Acta Med Scand       Date:  1975-10

10.  Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity.

Authors:  M S Brown; J L Goldstein
Journal:  Proc Natl Acad Sci U S A       Date:  1974-03       Impact factor: 11.205
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