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Combination of COFRADIC and high temperature - extended column length conventional liquid chromatography: A very efficient way to tackle complex protein samples, such as serum
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Expression and activity of the nucleotide-binding domains of the human ABCA1 transporter
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Phosphorylation by protein kinase CK2 modulates the activity of the ATP binding cassette A1 transporter
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Characterization of the ABCA transporter subfamily: Identification of prokaryotic and eukaryotic members, phylogeny and topology
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Comparison of the aggregation properties, secondary structure and apoptotic effects of wild-type, Flemish and Dutch N-terminally truncated amyloid beta peptides.
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A hydrophobic cluster at the surface of the human plasma phospholipid transfer protein is critical for activity on high density lipoproteins.
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Effect of mutations of N- and C-terminal charged residues on the activity of LCAT.
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Characterization and functional studies of lipoproteins, lipid transfer proteins, and lecithin: cholesterol acyltransferase in CSF of normal individuals and patients with Alzheimer's disease.
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Relationship between structure and biochemical phenotype of lecithin: cholesterol acyltransferase (LCAT) mutants causing fish-eye disease.
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Headgroup specificity of lecithin cholesterol acyltransferase for monomeric and vesicular phospholipids.
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Characterization of recombinant wild type and site-directed mutations of apolipoprotein C-III: Lipid binding, displacement of ApoE, and inhibition of lipoprotein lipase.
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Apoptosis induced in neuronal cells by C-terminal amyloid beta-fragments is correlated with their aggregation properties in phospholipid membranes.
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Lipids, apolipoproteins and LCAT in cerebrospinal fluid of normal individuals and patients with Alzhelmer's disease
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Effects of natural mutations in lecithin:cholesterol acyltransferase on the enzyme structure and activity
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beta-amyloid peptide interacts specifically with the carboxy-terminal domain of human apolipoprotein E: Relevance to Alzheimer's disease.
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Characterisation of functional residues in the interfacial recognition domain of lecithin cholesterol acyltransferase.
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Contribution of the hydrophobicity gradient to the secondary structure and activity of fusogenic peptides.
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Characterization of functional residues in the interfacial recognition domain of lecithin cholesterol acyltransferase (LCAT).
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LCAT defects and low HDL levels.
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The nonfibrillar amyloid beta-peptide induces apoptotic neuronal cell death: Involvement of its C-terminal fusogenic domain.
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A proposed architecture for lecithin cholesterol acyl transferase (LCAT): Identification of the catalytic triad and molecular modeling.
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Enhanced efficiency of a targeted fusogenic peptide.
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Displacement of apo A-I from HDL by apo A-II or its C-terminal helix promotes the formation of pre-beta(1) migrating particles and decreases LCAT activation.
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Structural and functional properties of the 154-171 wild-type and variant peptides of human lecithin-cholesterol acyltransferase.