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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]