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Amino acids 149 and 294 of human lecithin:cholesterol acyltransferase affect fatty acyl specificity.
Role of glutamic acid residues 154, 155, and 165 of lecithin:cholesterol acyltransferase in cholesterol esterification and phospholipase A2 activities.
Lysosomal acid lipase mutations that determine phenotype in Wolman and cholesterol ester storage disease.
Identification of the lipoprotein initiating domain of apolipoprotein B.
Vesicle-binding properties of wild-type and cysteine mutant forms of alpha(1) domain of apolipoprotein B.
An abundant dysfunctional apolipoprotein A1 in human atheroma.