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15. Distant homology modeling of LCAT and its validation through in silico targeting and in vitro and in vivo assays. Sensi C; Simonelli S; Zanotti I; Tedeschi G; Lusardi G; Franceschini G; Calabresi L; Eberini I PLoS One; 2014; 9(4):e95044. PubMed ID: 24736652 [TBL] [Abstract][Full Text] [Related]
16. Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism. Hill JS; O K; Wang X; Pritchard PH Biochim Biophys Acta; 1993 Jun; 1181(3):321-3. PubMed ID: 8318557 [TBL] [Abstract][Full Text] [Related]
17. In vitro expression of natural mutants of human lecithin:cholesterol acyltransferase. Qu SJ; Fan HZ; Blanco-Vaca F; Pownall HJ J Lipid Res; 1995 May; 36(5):967-74. PubMed ID: 7658168 [TBL] [Abstract][Full Text] [Related]
18. Structural differences between wild-type and fish eye disease mutant of lecithin:cholesterol acyltransferase. Reshetnyak Y; Tchedre KT; Nair MP; Pritchard PH; Lacko AG J Biomol Struct Dyn; 2006 Aug; 24(1):75-82. PubMed ID: 16780378 [TBL] [Abstract][Full Text] [Related]
19. Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn). Klein HG; Lohse P; Duverger N; Albers JJ; Rader DJ; Zech LA; Santamarina-Fojo S; Brewer HB J Lipid Res; 1993 Jan; 34(1):49-58. PubMed ID: 8445342 [TBL] [Abstract][Full Text] [Related]
20. Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis. Klein HG; Santamarina-Fojo S; Duverger N; Clerc M; Dumon MF; Albers JJ; Marcovina S; Brewer HB J Clin Invest; 1993 Jul; 92(1):479-85. PubMed ID: 8326012 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]