These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 7137946)

  • 21. Diversity in expression of heterozygous familial hypercholesterolemia. Characterization of a unique kindred.
    Levy RA; Ostlund RE; Semenkovich CF; Witztum JL
    J Clin Invest; 1986 Jul; 78(1):96-101. PubMed ID: 3722389
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Receptor-mediated uptake of low density lipoprotein and utilization of its cholesterol for steroid synthesis in cultured mouse adrenal cells.
    Faust JR; Goldstein JL; Brown MS
    J Biol Chem; 1977 Jul; 252(14):4861-71. PubMed ID: 194897
    [No Abstract]   [Full Text] [Related]  

  • 23. Use of mutant fibroblasts in the analysis of the regulation of cholesterol metabolism in human cells.
    Brown MS; Brannan PG; Bohmfalk HA; Brunschede GY; Dana SE; Helgeson J; Goldstein JL
    J Cell Physiol; 1975 Apr; 85(2 Pt 2 Suppl 1):425-36. PubMed ID: 164479
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Presentation of the Kober Medal to Joseph L. Goldstein and Michael S. Brown.
    Foster DW; Wilson JD
    J Clin Invest; 2002 Dec; 110(12):S5-9. PubMed ID: 12506882
    [No Abstract]   [Full Text] [Related]  

  • 25. [HMG-CoA reductase : mechanism of reaction and physiological role (author's transl)].
    Tanzawa K
    Tanpakushitsu Kakusan Koso; 1981 May; 26(6):815-28. PubMed ID: 7031774
    [No Abstract]   [Full Text] [Related]  

  • 26. Effects of delipidated serum and lipoprotein-deficient serum on sterol biosynthesis and efflux in cultured skin fibroblasts - a comparison of the behaviour of cells from a control with those from a heterozygote and homozygote for familial hypercholesterolaemia.
    Giles PM; Andrews BJ; Cheshire J; Noble N; Muller DP; Slack J; Wolff OH
    Clin Chim Acta; 1981 Jun; 113(2):183-91. PubMed ID: 7249360
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial hypercholesterolaemia: effect of low density lipoproteins on esterification of cholesterol in lymphocytes from homozygous and heterozygous subjects.
    Hammond KD; Khan Q; Laminski NA; Mendelsohn D; Seftel HC
    Arch Int Physiol Biochim; 1987 Mar; 95(1):75-80. PubMed ID: 2441677
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor.
    Brown MS; Goldstein JL
    N Engl J Med; 1976 Jun; 294(25):1386-90. PubMed ID: 177875
    [No Abstract]   [Full Text] [Related]  

  • 29. Diagnosis of familial hypercholesterolemia by measurement of sterol synthesis in cultured skin fibroblasts.
    Khachadurian AK; Lipson M; Kawahara FS
    Atherosclerosis; 1975; 21(2):235-44. PubMed ID: 1131306
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Suppression of cholesterol synthesis in cultured fibroblasts from a patient with homozygous familial hypercholesterolemia by her own low density lipoprotein density fraction. A possible role of apolipoprotein E.
    Havekes L; Vermeer BJ; de Wit E; Emeis JJ; Vaandrager H; van Gent CM; Koster JF
    Biochim Biophys Acta; 1980 Mar; 617(3):529-35. PubMed ID: 7370293
    [No Abstract]   [Full Text] [Related]  

  • 31. The metabolic lesion in familial hypercholesterolaemia.
    Myant NB
    Expos Annu Biochim Med; 1977; 33():39-52. PubMed ID: 196909
    [No Abstract]   [Full Text] [Related]  

  • 32. Regulation of cholesterol synthesis in skin fibroblasts derived from old people.
    Shakespeare V; Postle AD
    Atherosclerosis; 1979 Jul; 33(3):359-64. PubMed ID: 226108
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human mutations affecting the low density lipoprotein pathway.
    Brown MS; Goldstein JL
    Curr Concepts Nutr; 1979; 8():173-8. PubMed ID: 230940
    [No Abstract]   [Full Text] [Related]  

  • 34. Activity of thrombocytes as a marker of sufficient intensity of LDL-apheresis in familial hypercholesterolaemia.
    Blaha M; Pecka M; Urbankova J; Blaha V; Maly J; Zadak Z; Blazek M
    Transfus Apher Sci; 2004 Apr; 30(2):83-7. PubMed ID: 15062743
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Biochemical genetics of LDL receptor mutations in familial hypercholesterolemia.
    Goldstein JL; Kottke BA; Brown MS
    Prog Clin Biol Res; 1982; 103 Pt B():161-76. PubMed ID: 6298809
    [No Abstract]   [Full Text] [Related]  

  • 36. A new type of familial hypercholesterolaemia.
    Higgins MJ; Lecamwasam DS; Galton DJ
    Lancet; 1975 Oct; 2(7938):737-40. PubMed ID: 52771
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The LDL receptor defect in familial hypercholesterolemia. Implications for pathogenesis and therapy.
    Goldstein JL; Brown MS
    Med Clin North Am; 1982 Mar; 66(2):335-62. PubMed ID: 6279983
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Lipoprotein receptors and genetic control of cholesterol metabolism in cultured human cells.
    Brown MS; Goldstein JL
    Naturwissenschaften; 1975 Aug; 62(8):385-9. PubMed ID: 172803
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Low-density lipoprotein receptor deficiency resulting in familial hypercholesterolaemia in a black man. A follow-up study.
    Coetzee GA; van Wingerden JJ; van der Westhuyzen DR
    S Afr Med J; 1985 Feb; 67(7):259-61. PubMed ID: 3983774
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial hypercholesterolaemia and platelet-activating factor acetylhydrolase: difference between the homozygous and heterozygous form.
    Napoli C
    Eur J Clin Invest; 1998 Jun; 28(6):506-9. PubMed ID: 9693945
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.