Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor.
暂无分享,去创建一个
[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.