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 *

134 related articles for article (PubMed ID: 4362800)

  • 1. Homozygous familial hypercholesterolemia: specificity of the biochemical defect in cultured cells and feasibility of prenatal detection.
    Goldstein JL; Harrod MJ; Brown MS
    Am J Hum Genet; 1974 Mar; 26(2):199-206. PubMed ID: 4362800
    [No Abstract]   [Full Text] [Related]  

  • 2. 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.
    Brown MS; Dana SE; Goldstein JL
    J Biol Chem; 1974 Feb; 249(3):789-96. PubMed ID: 4359767
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol.
    Goldstein JL; Brown MS
    Proc Natl Acad Sci U S A; 1973 Oct; 70(10):2804-8. PubMed ID: 4355366
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expression of the familial hypercholesterolemia gene in heterozygotes: mechanism for a dominant disorder in man.
    Brown MS; Goldstein JL
    Science; 1974 Jul; 185(4145):61-3. PubMed ID: 4366052
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism.
    Goldstein JL; Brown MS
    Am J Med; 1975 Feb; 58(2):147-50. PubMed ID: 163579
    [No Abstract]   [Full Text] [Related]  

  • 6. Familial hypercholesterolemia: genetic, biochemical and pathophysiologic considerations.
    Brown MS; Goldstein JL
    Adv Intern Med; 1975; 20():273-96. PubMed ID: 1090121
    [No Abstract]   [Full Text] [Related]  

  • 7. Hyperlipidemia in coronary heart disease: a biochemical genetic approach.
    Goldstein JL; Brown MS
    J Lab Clin Med; 1975 Jan; 85(1):15-25. PubMed ID: 49382
    [No Abstract]   [Full Text] [Related]  

  • 8. Expression of the familial hypercholesterolemia gene in heterozygotes: model for a dominant disorder in man.
    Goldstein JL; Brown MS
    Trans Assoc Am Physicians; 1974; 87():120-31. PubMed ID: 4376290
    [No Abstract]   [Full Text] [Related]  

  • 9. Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity.
    Brown MS; Goldstein JL
    Proc Natl Acad Sci U S A; 1974 Mar; 71(3):788-92. PubMed ID: 4362634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cholesterol synthesis by cultured fibroblasts: decreased feedback inhibition in familial hypercholesterolemia.
    Khachadurian AK; Kawahara FS
    J Lab Clin Med; 1974 Jan; 83(1):7-15. PubMed ID: 4855550
    [No Abstract]   [Full Text] [Related]  

  • 11. [Familial hypercholesterolemia: clinical findings and immunochemical studies of lipoproteins].
    Kobierska-Szczepańska A; Dziuba P; Szczepański Z
    Pediatr Pol; 1976 Dec; 51(12):1435-41. PubMed ID: 188008
    [No Abstract]   [Full Text] [Related]  

  • 12. Regulation of 3-hydroxy-3-methylglutaryl coenzyme-A reductase activity in type II hyperlipoproteinaemia.
    Betteridge DJ; Higgins MJ; Galton DJ
    Br Med J; 1975 Nov; 4(5995):500-2. PubMed ID: 172188
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial hyperlipoproteinemia type IIA with homozygotic manifestations in a heterozygote].
    Traurig J; Sobra J; Kvasilová M; Wildtová Z
    Vnitr Lek; 1978 Jul; 24(7):684-90. PubMed ID: 209627
    [No Abstract]   [Full Text] [Related]  

  • 14. Regulation of lipid synthesis by low density lipoproteins in cultured skin fibroblasts in homozygous familial hypercholesterolemia.
    Fung CH; Khachadurian AK; Wang CH; Durr IF
    Biochim Biophys Acta; 1977 Jun; 487(3):445-57. PubMed ID: 195625
    [No Abstract]   [Full Text] [Related]  

  • 15. [Differentiation characteristics for the identification of patients with familial hypercholesteremia - studies on skin fibroblasts].
    Wieczorek A; Zöllner N
    Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():381-2. PubMed ID: 206053
    [No Abstract]   [Full Text] [Related]  

  • 16. Prospects for the prenatal diagnosis of familial hypercholesterolemia.
    Khachadurian AK
    J Med Liban; 1973 Apr; 26(4):325-9. PubMed ID: 4206463
    [No Abstract]   [Full Text] [Related]  

  • 17. Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and the esterification of cholesterol in human long term lymphoid cell lines.
    Kayden HJ; Hatam L; Beratis NG
    Biochemistry; 1976 Feb; 15(3):521-8. PubMed ID: 1252410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Esterification of low density lipoprotein cholesterol in human fibroblasts and its absence in homozygous familial hypercholesterolemia.
    Goldstein JL; Dana SE; Brown MS
    Proc Natl Acad Sci U S A; 1974 Nov; 71(11):4288-92. PubMed ID: 4373706
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homozygous hypercholesteraemia and the portacaval shunt. The need for a concerted attack by surgeons and clinical researchers.
    Ahrens EH
    Lancet; 1974 Aug; 2(7878):449-51. PubMed ID: 4136785
    [No Abstract]   [Full Text] [Related]  

  • 20. Prenatal diagnosis of homoxygous familial hypercholesterolemia: investigation of a case at risk.
    Wienker TF; Utermann G; Ropers HH
    Clin Genet; 1976 Jun; 9(6):545-52. PubMed ID: 179742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.