BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 9043632)

  • 1. Regulation of cholesterol synthesis and esterification in primary cultures of macrophages following uptake of chylomicron remnants.
    Yu KC; Mamo JC
    Biochem Mol Biol Int; 1997 Jan; 41(1):33-9. PubMed ID: 9043632
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evidence that chylomicron remnants and beta-VLDL are transported by the same receptor pathway in J774 murine macrophage-derived cells.
    Ellsworth JL; Cooper AD; Kraemer FB
    J Lipid Res; 1986 Oct; 27(10):1062-72. PubMed ID: 3025323
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transport of beta-very low density lipoproteins and chylomicron remnants by macrophages is mediated by the low density lipoprotein receptor pathway.
    Ellsworth JL; Kraemer FB; Cooper AD
    J Biol Chem; 1987 Feb; 262(5):2316-25. PubMed ID: 3546288
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lipoprotein metabolism by rat hepatomas. Studies on the etiology of defective dietary feedback inhibition of cholesterol synthesis.
    Barnard GF; Erickson SK; Cooper AD
    J Clin Invest; 1984 Jul; 74(1):173-84. PubMed ID: 6330173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effects of chylomicron remnants and beta-VLDL on the class and composition of newly secreted lipoproteins by HepG2 cells.
    Craig WY; Cooper AD
    J Lipid Res; 1988 Mar; 29(3):299-308. PubMed ID: 2837527
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Differences in the processing of chylomicron remnants and beta-VLDL by macrophages.
    Ellsworth JL; Fong LG; Kraemer FB; Cooper AD
    J Lipid Res; 1990 Aug; 31(8):1399-411. PubMed ID: 2280181
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lipoproteins activate acyl-coenzyme A:cholesterol acyltransferase in macrophages only after cellular cholesterol pools are expanded to a critical threshold level.
    Xu XX; Tabas I
    J Biol Chem; 1991 Sep; 266(26):17040-8. PubMed ID: 1894601
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The actin cytoskeleton is important for the stimulation of cholesterol esterification by atherogenic lipoproteins in macrophages.
    Tabas I; Zha X; Beatini N; Myers JN; Maxfield FR
    J Biol Chem; 1994 Sep; 269(36):22547-56. PubMed ID: 8077203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cholesterol accumulation in J774 macrophages induced by triglyceride-rich lipoproteins. Comparison of very low density lipoprotein from subjects with type III, IV, and V hyperlipoproteinemias.
    Huff MW; Evans AJ; Sawyez CG; Wolfe BM; Nestel PJ
    Arterioscler Thromb; 1991; 11(2):221-33. PubMed ID: 1998641
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effect of removal of lipoproteins of different composition on hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and hepatic very low density lipoprotein secretion.
    Van Zuiden PE; Erickson SK; Cooper AD
    J Lipid Res; 1983 Apr; 24(4):418-28. PubMed ID: 6854151
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Receptor-mediated uptake of remnant lipoproteins by cholesterol-loaded human monocyte-macrophages.
    Van Lenten BJ; Fogelman AM; Jackson RL; Shapiro S; Haberland ME; Edwards PA
    J Biol Chem; 1985 Jul; 260(15):8783-8. PubMed ID: 2991220
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Failure of the intracellular itinerary of beta very low density lipoproteins to augment cholesterol esterification in macrophages from Watanabe heritable hyperlipidemic rabbits.
    Daugherty A; Rateri DL
    J Biol Chem; 1991 Sep; 266(26):17269-75. PubMed ID: 1894618
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The distal pathway of lipoprotein-induced cholesterol esterification, but not sphingomyelinase-induced cholesterol esterification, is energy-dependent.
    Skiba PJ; Zha X; Maxfield FR; Schissel SL; Tabas I
    J Biol Chem; 1996 Jun; 271(23):13392-400. PubMed ID: 8662777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. beta-VLDL and acetylated-LDL binding to pigeon monocyte macrophages.
    Henson DA; St Clair RW; Lewis JC
    Atherosclerosis; 1989 Jul; 78(1):47-60. PubMed ID: 2667527
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Endocytosed beta-VLDL and LDL are delivered to different intracellular vesicles in mouse peritoneal macrophages.
    Tabas I; Lim S; Xu XX; Maxfield FR
    J Cell Biol; 1990 Sep; 111(3):929-40. PubMed ID: 2391369
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Plasma very low density lipoprotein (VLDL) in cholesterol-fed rabbits: chylomicron remnants or liver lipoproteins?
    Thompson KH; Zilversmit DB
    J Nutr; 1983 Oct; 113(10):2002-10. PubMed ID: 6619979
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regulation of the hepatic removal of chylomicron remnants and beta-very low density lipoproteins in the rat.
    Jäckle S; Rinninger F; Greeve J; Greten H; Windler E
    J Lipid Res; 1992 Mar; 33(3):419-29. PubMed ID: 1569389
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lipoprotein degradation and cholesterol esterification in primary cell cultures of rabbit atherosclerotic lesions.
    Jaakkola O; Nikkari T
    Am J Pathol; 1990 Aug; 137(2):457-65. PubMed ID: 2201201
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The regulation of 3-hydroxy-3-methylglutaryl-CoA reductase activity, cholesterol esterification and the expression of low-density lipoprotein receptors in cultured monocyte-derived macrophages.
    Knight BL; Patel DD; Soutar AK
    Biochem J; 1983 Feb; 210(2):523-32. PubMed ID: 6305342
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Serum lipoproteins and cholesterol metabolism in two hypercholesterolaemic rabbit models.
    O'Meara NM; Devery RA; Owens D; Collins PB; Johnson AH; Tomkin GH
    Diabetologia; 1991 Mar; 34(3):139-43. PubMed ID: 1884884
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.