Beschreibung
InhaltsangabeEnzymes and Apolipoproteins in the Diagnosis of Disease.- Lipoprotein Lipase: Gene Variants and Coronary Atherosclerosis.- Apolipoproteins in the Diagnosis of Disease: Cerebral and Peripheral Atherosclerosis.- Structural and Functional Relationships in Apolipoproteins.- Functional Properties of Discoidal Apoprotein/Phospholipid Complexes: Cholesterol Efflux from Macrophages and Conversion by Lecithin-Cholesterol Acyl Tansferase.- Lipid Transport by Apolipoprotein AI: Structure and Function.- Characterization of Lipoprotein Particles Containing Apolipoprotein A-IV.- Structural and Functional Properties of Apo A-I Variants in Reconstituted HDL.- Structural Domains in Human Serum Low Density Lipoprotein Apolipoprotein B100.- Crystal Structures of the Common Apolipoprotein E Variants: Insights into Functional Mechanisms.- Analysis of Apolipoprotein E Function in Adrenal Cells: Effects on Cholesterol Metabolism and Signal Transduction Pathways.- Animal Models in the Apolipoprotein Mutant Research.- Spontaneous Hypercholesterolemia in Pigs.- The Apolipoprotein E Cys-142 Mutant: Role in Dominant Inheritance of Type III Hyperlipoproteinemia and Expression in Transgenic Mice.- Recombinant Apolipoproteins as Drugs.- Apolipoproteins as "Drugs": Current Status.- Non-Mammalian Host System for the Expression of Mammalian Apolipoproteins.- Recombinant Human Proapolipoprotein A-I: Experimental Strategies for the Production of an Authentic Molecule.- The Role of HDL Apolipoproteins in Mediating HDL Receptor Binding and Intracellular Cholesterol Efflux.- Molecular Abnormalities of Apolipoproteins.- The Metabolism of Truncated Forms of Apolipoprotein B in Hypobetalipoproteinemia.- Apolipoprotein B: Genetic Variants Provide Insight Into Structure and Function.- The Mutations of Apolipoprotein B Gene Causing Hypobetalipoproteinemia: Molecular and Functional Abnormalities in Apo B-87Padova.- Causes Underlying the Reduced Response to Simvastatin Treatment in Hypercholesterolemic Patients.- Molecular Genetics of the Familial Chylomicronemia Syndrome.- Rare Mutations in the Apo E Gene Associated with Dominant Mode of Inheritance of Familial Dysbetalipoproteinemia (FD).- Identification of Common Genetic Polymorphisms that Determine Plasma Levels of Apo Al and HDL-C.- Structure-Function Relationships of Apolipoprotein A-I Variants.- Sex-Related Differences in the Phenotypic Expression of the Apolipoprotein A-Imllano mutant.- Human Apolipoprotein A-IV.
