Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor.

FAMILIAL hypercholesterolemia, an example of a single-gene disorder that produces both hypercholesterolemia and atherosclerosis in man,1 2 3 is characterized by four cardinal features: hypercholest...

[1]  James G. Chandler,et al.  Paradoxical Increase in Rate of Catabolism of Low-Density Lipoproteins after Hepatectomy , 1974, Science.

[2]  M. Brown,et al.  Binding and degradation of low density lipoproteins by cultured human fibroblasts. Comparison of cells from a normal subject and from a patient with homozygous familial hypercholesterolemia. , 1974, The Journal of biological chemistry.

[3]  R. Havel Lipoproteins and lipid transport. , 1975, Advances in experimental medicine and biology.

[4]  A. Beaudet,et al.  Role of lysosomal acid lipase in the metabolism of plasma low density lipoprotein. Observations in cultured fibroblasts from a patient with cholesteryl ester storage disease. , 1975, The Journal of biological chemistry.

[5]  M. Brown,et al.  Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[6]  Marvin D. Siperstein,et al.  Regulation of cholesterol biosynthesis in normal and malignant tissues. , 1970 .

[7]  J. Dietschy,et al.  Regulation of cholesterol metabolism. I. , 1970, The New England journal of medicine.

[8]  R. Lees,et al.  Homozygous Familial Hypercholesterolemia , 1975 .

[9]  J. Goldstein,et al.  Release of low density lipoprotein from its cell surface receptor by sulfated glycosaminoglycans , 1976, Cell.

[10]  J. Glomset,et al.  The plasma lecithins:cholesterol acyltransferase reaction. , 1968, Journal of lipid research.

[11]  S. Grundy,et al.  Reduction in cholesterol and low density lipoprotein synthesis after portacaval shunt surgery in a patient with homozygous familial hypercholesterolemia. , 1975, The Journal of clinical investigation.

[12]  M. Brown,et al.  Use of mutant fibroblasts in the analysis of the regulation of cholesterol metabolism in human cells , 1975, Journal of cellular physiology.

[13]  D. Galton,et al.  A NEW TYPE OF FAMILIAL HYPERCHOLESTEROLÆMIA , 1975, The Lancet.

[14]  M. Brown,et al.  Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism. , 1975, The American journal of medicine.

[15]  Joseph L. Goldstein,et al.  Familial hypercholesterolemia: Defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme a reductase activity , 1974, Proceedings of the National Academy of Sciences.

[16]  M. Brown,et al.  Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured human fibroblasts. Comparison of cells from a normal subject and from a patient with homozygous familial hypercholesterolemia. , 1974, The Journal of biological chemistry.

[17]  L. Simons,et al.  The metabolism of the apoprotein of plasma low density lipoprotein in familial hyperbetalipoproteinaemia in the homozygous form. , 1975, Atherosclerosis.

[18]  M. Brown,et al.  Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[19]  M. Brown,et al.  Receptor-mediated control of cholesterol metabolism. , 1976, Science.

[20]  D. Steinberg,et al.  Binding, internalization, and degradation of low density lipoprotein by normal human fibroblasts and by fibroblasts from a case of homozygous familial hypercholesterolemia. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[21]  A. Khachadurian THE INHERITANCE OF ESSENTIAL FAMILIAL HYPERCHOLESTEROLEMIA. , 1964, The American journal of medicine.

[22]  J. Goldstein,et al.  Expression of the Familial Hypercholesterolemia Gene in Heterozygotes: Mechanism for a Dominant Disorder in Man , 1974, Science.