lecithin-cholesterol acyltransferase
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)
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Original Article Advanced membranous nephropathy-like lesion in a Chinese patient with familial lecithin-cholesterol acyltransferase deficiency
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Markedly accelerated catabolism of apolipoprotein A II (ApoA II) and high density lipoproteins containing ApoA II in classic lecithin: cholesterol acyltransferase deficiency and fish eye disease
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Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency Six newly identified defective alleles further contribute to the structural heterogeneity in this disease
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Radioimmunoassay of human plasma lecithin cholesterol acyltransferase
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Hyperalphalipoproteinemia in human lecithin cholesterol acyltransferase transgenic rabbits In vivo apolipoprotein A I catabolism is delayed in a gene dose dependent manner
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Expression of human lecithin cholesterol acyltransferase in transgenic mice Effect of human apolipoprotein AI and human apolipoprotein all on plasma lipoprotein cholesterol metabolism
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Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: physical and chemical studies of low and high density lipoproteins
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Pre-Clinical Development Of Aav Mediated Gene Therapy For Familial Lecithin Cholesterol Acyltransferase Deficiency
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Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: structure of low and high density lipoproteins as revealed by electron microscopy
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Association of Lecithin Cholesterol Acyltransferase rs5923 Polymorphism in Iranian Individuals with Extremely Low High-Density Lipoprotein Cholesterol: Tehran Lipid and Glucose Study
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A frameshift mutation in the human apolipoprotein A I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol acyltransferase deficiency, and corneal opacities
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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
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The role of lecithin: cholesterol acyltransferase for lipoprotein (a) assembly Structural integrity of low density lipoproteins is a prerequisite for Lp(a) formation in human plasma
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Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia
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A comparative study of lipid profile in patients with and without infective hepatitis
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ZYGOPHYLLUM GAETULUM AQUEOUS EXTRACT PROTECTS AGAINST DIABETIC DYSLIPIDEMIA AND ATTENUATES LIVER AND KIDNEY OXIDATIVE DAMAGE IN STREPTOZOTOCIN INDUCED DIABETIC RATS
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IN VITRO AND IN VIVO EVALUATION OF DIRECTLY COMPRESSED TABLETS OF SIMVASTATIN WITH SOY LECITHIN
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A Comparative Study of the Lipids of the Vertebrate Central Nervous System
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A Comparative Study of the Lipids of the Vertebrate Central Nervous System
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