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5. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark. Jensen HK Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167 [TBL] [Abstract][Full Text] [Related]
6. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB). Azian M; Hapizah MN; Khalid BA; Khalid Y; Rosli A; Jamal R Malays J Pathol; 2006 Jun; 28(1):7-15. PubMed ID: 17694954 [TBL] [Abstract][Full Text] [Related]
7. Molecular biology of human apolipoproteins B and E and associated diseases of lipoprotein metabolism. Zannis VI Adv Lipid Res; 1989; 23():1-64. PubMed ID: 2560890 [No Abstract] [Full Text] [Related]
9. Genetic causes of familial hypercholesterolaemia in a Malaysian population. Khoo KL; Van Acker P; Tan H; Deslypere JP Med J Malaysia; 2000 Dec; 55(4):409-18. PubMed ID: 11221151 [TBL] [Abstract][Full Text] [Related]
10. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia. Feussner G; Dobmeyer J; Nissen H; Hansen TS Am J Med Genet; 1996 Oct; 65(2):149-54. PubMed ID: 8911609 [TBL] [Abstract][Full Text] [Related]
11. Increased binding of LDL and VLDL to apo B,E receptors of hepatic plasma membrane of rats treated with Fibernat. Venkatesan N; Devaraj SN; Devaraj H Eur J Nutr; 2003 Oct; 42(5):262-71. PubMed ID: 14569407 [TBL] [Abstract][Full Text] [Related]
12. The role of lipoprotein receptors in lipid transport and in the pathogenesis of the hyperlipoproteinemias. Chait A Spec Top Endocrinol Metab; 1983; 5():1-53. PubMed ID: 6322371 [TBL] [Abstract][Full Text] [Related]
14. Familial defective apolipoprotein B-100. Hansen PS Dan Med Bull; 1998 Sep; 45(4):370-82. PubMed ID: 9777289 [TBL] [Abstract][Full Text] [Related]
15. Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664----leu mutation in the LDL receptor gene. Soutar AK; McCarthy SN; Seed M; Knight BL J Clin Invest; 1991 Aug; 88(2):483-92. PubMed ID: 1830890 [TBL] [Abstract][Full Text] [Related]
16. A receptor-mediated pathway for cholesterol homeostasis. Brown MS; Goldstein JL Science; 1986 Apr; 232(4746):34-47. PubMed ID: 3513311 [No Abstract] [Full Text] [Related]
17. Receptors in the regulation of lipoprotein metabolism. Packard CJ; Sheperd J Ann Biol Clin (Paris); 1988; 46(1):5-9. PubMed ID: 2839057 [TBL] [Abstract][Full Text] [Related]
18. Inherited disorders of lipid transport. Schonfeld G Endocrinol Metab Clin North Am; 1990 Jun; 19(2):229-57. PubMed ID: 2192872 [TBL] [Abstract][Full Text] [Related]
19. Aortic and coronary atheromatosis in a woman with severe hypercholesterolaemia without LDL receptor alterations. Sirtori CR; Catapano AL; Franceschini G; Corsini A; Noseda G; Fragiacomo C; Panzeri E; Vaccarino V; Guenzi S; Casari G Eur Heart J; 1991 Jul; 12(7):818-24. PubMed ID: 1889447 [TBL] [Abstract][Full Text] [Related]
20. The role of the LDL receptor in lipoprotein metabolism. Bilheimer DW; Grundy SM Adv Exp Med Biol; 1987; 210():123-30. PubMed ID: 3296682 [No Abstract] [Full Text] [Related] [Next] [New Search]