Characterization of lecithin:cholesterol acyltransferase expressed in a human lung cell line
Author:
Publisher
Elsevier BV
Subject
Biotechnology
Reference18 articles.
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2. High density lipoprotein deficiency with xanthomas. A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene;Lackner;J. Clin. Invest.,1993
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4. Proposed architecture for lecithin:cholesterol acyltransferase. Identification of the catalytic triad and molecular modeling of LCAT;Peelman;Protein Sci.,1998
5. Characterization of functional residues in the interfacial recognition domain of lecithin cholesterol acyltransferase (LCAT);Peelman;Protein Eng.,1999
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1. Familial LCAT deficiency: from pathology to enzyme replacement therapy;Clinical Lipidology;2015-10-01
2. Recombinant human lecithin-cholesterol acyltransferase Fc fusion: Analysis of N- and O-linked glycans and identification and elimination of a xylose-based O-linked tetrasaccharide core in the linker region;Protein Science;2013-11-12
3. Effect of Recombinant Human Lecithin Cholesterol Acyltransferase Infusion on Lipoprotein Metabolism in Mice;Journal of Pharmacology and Experimental Therapeutics;2010-07-06
4. Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2003–2004;Mass Spectrometry Reviews;2008-09-29
5. Binding of 8-anilino-1-naphthalenesulfonate to lecithin:cholesterol acyltransferase studied by fluorescence techniques;Journal of Photochemistry and Photobiology B: Biology;2008-07
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