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.
208 related articles for article (PubMed ID: 9007616)
61. A first British case of fish-eye disease presenting at age 75 years: a double heterozygote for defined and new mutations affecting LCAT structure and expression. Winder AF; Owen JS; Pritchard PH; Lloyd-Jones D; Vallance DT; White P; Wray R J Clin Pathol; 1999 Mar; 52(3):228-30. PubMed ID: 10450185 [TBL] [Abstract][Full Text] [Related]
63. A normal rate of cellular cholesterol removal can be mediated by plasma from a patient with familial lecithin-cholesterol acyltransferase (LCAT) deficiency. Bérard AM; Clerc M; Brewer B; Santamarina-Fojo S Clin Chim Acta; 2001 Dec; 314(1-2):131-9. PubMed ID: 11718688 [TBL] [Abstract][Full Text] [Related]
64. Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease. Calabresi L; Simonelli S; Gomaraschi M; Franceschini G Atherosclerosis; 2012 Jun; 222(2):299-306. PubMed ID: 22189200 [TBL] [Abstract][Full Text] [Related]
65. A novel pathogenic variant in LCAT causing FLD. A case report. Goñi Ros N; González-Tarancón R; Sienes Bailo P; Salvador-Ruperez E; Puzo Bayod M; Puzo Foncillas J Acta Clin Belg; 2022 Dec; 77(6):970-975. PubMed ID: 34789074 [TBL] [Abstract][Full Text] [Related]
66. 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]
67. A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency. Vitali C; Bajaj A; Nguyen C; Schnall J; Chen J; Stylianou K; Rader DJ; Cuchel M J Lipid Res; 2022 Mar; 63(3):100169. PubMed ID: 35065092 [TBL] [Abstract][Full Text] [Related]
68. An amino acid exchange in exon I of the human lecithin: cholesterol acyltransferase (LCAT) gene is associated with fish eye disease. Skretting G; Prydz H Biochem Biophys Res Commun; 1992 Jan; 182(2):583-7. PubMed ID: 1571050 [TBL] [Abstract][Full Text] [Related]
69. A novel TC deletion resulting in Pro(260)-->Stop in the human LCAT gene is associated with a dominant effect on HDL-cholesterol. Kasid A; Rhyne J; Zeller K; Pritchard H; Miller M Atherosclerosis; 2001 May; 156(1):127-32. PubMed ID: 11369005 [TBL] [Abstract][Full Text] [Related]
70. Familial plasma lecithin: cholesterol acyltransferase deficiency. A new family with partial LCAT activity. Sakuma M; Akanuma Y; Kodama T; Yamada N; Murata S; Murase T; Itakura H; Kosaka K Acta Med Scand; 1982; 212(4):225-32. PubMed ID: 7148518 [TBL] [Abstract][Full Text] [Related]
71. Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels. Miettinen HE; Gylling H; Tenhunen J; Virtamo J; Jauhiainen M; Huttunen JK; Kantola I; Miettinen TA; Kontula K Arterioscler Thromb Vasc Biol; 1998 Apr; 18(4):591-8. PubMed ID: 9555865 [TBL] [Abstract][Full Text] [Related]
72. Familial lecithin-cholesterol acyltransferase: identification of heterozygotes with half-normal enzyme activity and mass. Albers JJ; Chen C; Adolphson JL Hum Genet; 1981; 58(3):306-9. PubMed ID: 7327552 [TBL] [Abstract][Full Text] [Related]
73. Disturbed apolipoprotein A-I-containing lipoproteins in fish-eye disease are improved by the lecithin:cholesterol acyltransferase produced by gene-transduced adipocytes in vitro. Asada S; Kuroda M; Aoyagi Y; Bujo H; Tanaka S; Konno S; Tanio M; Ishii I; Aso M; Saito Y Mol Genet Metab; 2011 Feb; 102(2):229-31. PubMed ID: 21074466 [TBL] [Abstract][Full Text] [Related]
74. A kindred with fish eye disease, corneal opacities, marked high-density lipoprotein deficiency, and statin therapy. Dimick SM; Sallee B; Asztalos BF; Pritchard PH; Frohlich J; Schaefer EJ J Clin Lipidol; 2014; 8(2):223-30. PubMed ID: 24636183 [TBL] [Abstract][Full Text] [Related]
75. Current Status of Familial LCAT Deficiency in Japan. Kuroda M; Bujo H; Yokote K; Murano T; Yamaguchi T; Ogura M; Ikewaki K; Koseki M; Takeuchi Y; Nakatsuka A; Hori M; Matsuki K; Miida T; Yokoyama S; Wada J; Harada-Shiba M J Atheroscler Thromb; 2021 Jul; 28(7):679-691. PubMed ID: 33867422 [TBL] [Abstract][Full Text] [Related]
76. Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: evidence for functionally defective enzyme in homozygotes and obligate heterozygotes. Albers JJ; Chen CH; Adolphson J; Sakuma M; Kodama T; Akanuma Y Hum Genet; 1982; 62(1):82-5. PubMed ID: 7152525 [TBL] [Abstract][Full Text] [Related]
77. Effect of probucol in lecithin-cholesterol acyltransferase-deficient mice: inhibition of 2 independent cellular cholesterol-releasing pathways in vivo. Tomimoto S; Tsujita M; Okazaki M; Usui S; Tada T; Fukutomi T; Ito S; Itoh M; Yokoyama S Arterioscler Thromb Vasc Biol; 2001 Mar; 21(3):394-400. PubMed ID: 11231919 [TBL] [Abstract][Full Text] [Related]
78. Defective enzyme causes lecithin-cholesterol acyltransferase deficiency in a Japanese kindred. Albers JJ; Adolphson J; Chen CH; Murayama N; Honma S; Akanuma Y Biochim Biophys Acta; 1985 Jul; 835(2):253-7. PubMed ID: 4005283 [TBL] [Abstract][Full Text] [Related]
79. Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene. Owen JS; Wiebusch H; Cullen P; Watts GF; Lima VL; Funke H; Assmann G Hum Mutat; 1996; 8(1):79-82. PubMed ID: 8807342 [No Abstract] [Full Text] [Related]
80. Effects of natural mutations in lecithin:cholesterol acyltransferase on the enzyme structure and activity. Peelman F; Verschelde JL; Vanloo B; Ampe C; Labeur C; Tavernier J; Vandekerckhove J; Rosseneu M J Lipid Res; 1999 Jan; 40(1):59-69. PubMed ID: 9869650 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]