Quantitative studies of lipoprotein-X in familial lecithin:Cholesterol acyltransferase deficiency and during cholesterol esterification
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
1. Identification of the abnormal cholestatic lipoprotein (LP-X) in familial lecithin:Cholesterol acyltransferase deficiency
2. FAMILIAL SERUM CHOLESTEROL ESTER DEFICIENCY
3. The Metabolic Role of Lecithin: Cholesterol Acyltransferase: Perspectives from Pathology
4. A method for the quantitative determination of the abnormal lipoprotein (LP-X) of obstructive jaundice
5. FAMILIAL LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
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2. Lipoprotein-X in cholestatic patients causes xanthomas and promotes foam cell formation in human macrophages;Journal of Clinical Lipidology;2017-01
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4. Lipoprotein X in a patient with cholestasis and hypertriglyceridaemia;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2013-02-21
5. Lecithin-cholesterol acyltransferase: role in lipoprotein metabolism, reverse cholesterol transport and atherosclerosis;Current Opinion in Lipidology;2000-06
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