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PUBMED FOR HANDHELDS

Journal Abstract Search


214 related items for PubMed ID: 9717715

  • 1. Correction of hypoalphalipoproteinemia in LDL receptor-deficient rabbits by lecithin:cholesterol acyltransferase.
    Brousseau ME, Wang J, Demosky SJ, Vaisman BL, Talley GD, Santamarina-Fojo S, Brewer HB, Hoeg JM.
    J Lipid Res; 1998 Aug; 39(8):1558-67. PubMed ID: 9717715
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  • 4. Hyperalphalipoproteinemia in human lecithin cholesterol acyltransferase transgenic rabbits. In vivo apolipoprotein A-I catabolism is delayed in a gene dose-dependent manner.
    Brousseau ME, Santamarina-Fojo S, Zech LA, Bérard AM, Vaisman BL, Meyn SM, Powell D, Brewer HB, Hoeg JM.
    J Clin Invest; 1996 Apr 15; 97(8):1844-51. PubMed ID: 8621767
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  • 5. Plasma PCSK9 levels and lipoprotein distribution are preserved in carriers of genetic HDL disorders.
    Ruscica M, Simonelli S, Botta M, Ossoli A, Lupo MG, Magni P, Corsini A, Arca M, Pisciotta L, Veglia F, Franceschini G, Ferri N, Calabresi L.
    Biochim Biophys Acta Mol Cell Biol Lipids; 2018 Sep 15; 1863(9):991-997. PubMed ID: 29852278
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  • 6. Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met).
    Klein HG, Lohse P, Pritchard PH, Bojanovski D, Schmidt H, Brewer HB.
    J Clin Invest; 1992 Feb 15; 89(2):499-506. PubMed ID: 1737840
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  • 8. Alteration of plasma HDL cholesteryl ester composition with transgenic expression of a point mutation (E149A) of human LCAT.
    Furbee JW, Francone O, Parks JS.
    J Lipid Res; 2001 Oct 15; 42(10):1626-35. PubMed ID: 11590219
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  • 10. Plasma apolipoprotein concentrations in familial apolipoprotein A-I and A-II deficiency (Tangier disease).
    Alaupovic P, Schaefer EJ, McConathy WJ, Fesmire JD, Brewer HB.
    Metabolism; 1981 Aug 15; 30(8):805-9. PubMed ID: 6790903
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  • 11. Overexpression of lecithin:cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis.
    Hoeg JM, Santamarina-Fojo S, Bérard AM, Cornhill JF, Herderick EE, Feldman SH, Haudenschild CC, Vaisman BL, Hoyt RF, Demosky SJ, Kauffman RD, Hazel CM, Marcovina SM, Brewer HB.
    Proc Natl Acad Sci U S A; 1996 Oct 15; 93(21):11448-53. PubMed ID: 8876155
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  • 13. Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.
    Torres AL, Moorjani S, Vohl MC, Gagné C, Lamarche B, Brun LD, Lupien PJ, Després JP.
    Atherosclerosis; 1996 Sep 27; 126(1):163-71. PubMed ID: 8879444
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  • 17. Interrelationships between human apolipoprotein A-I and apolipoproteins B-48 and B-100 kinetics using stable isotopes.
    Welty FK, Lichtenstein AH, Barrett PH, Dolnikowski GG, Schaefer EJ.
    Arterioscler Thromb Vasc Biol; 2004 Sep 27; 24(9):1703-7. PubMed ID: 15242863
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  • 20. Effects of hepatic HDL-related mRNAs on plasma prebeta HDL in cholesterol-fed rabbits.
    Sugano M, Makino N, Yanaga T.
    Artery; 1997 Sep 27; 22(4):182-205. PubMed ID: 9576025
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