Human Apolipoprotein Mutants 2: From Gene Structure to Phenotypic Expression

Evolution and Control of Gene Expression.- Apolipoprotein Genes: Organization, Linkage and Evolution.- Apolipoprotein Variation: Effect on Plasma Lipid Variability.- Expression of Human Apo AI, AII and CII Genes in Pro- and Eucaryotic Cells.- Cis-Acting Elements and Trans-Acting Factors Involved in Cell Type Specific Expression of the Human Apolipoprotein AI Gene.- Human Apolipoprotein A-I: Studies on Gene Expression and Site-Directed Mutagenesis in E. Coli.- High Density Lipoproteins and Apo AI-Milano.- Apolipoprotein AI-Milano: Mechanisms for the Antiatherogenic Potential.- In Vivo Catabolism of Apolipoprotein A-I in Subjects with Familial Hypoalphalipoproteinemia.- Synthesis of Apolipoprotein A-I in the Skeletal Muscle of the Developing Chick.- Apolipoprotein-Specific High Density Lipoprotein Populations in Plasma of Carriers of the Apolipoprotein AI-Milano.- Apolipoprotein B.- Apo B Gene Variants Are Involved in Determining Serum Cholesterol Levels: towards Identifying these Variants.- Genetic Evidence that the Apolipoprotein Gene Is not Involved in Abetalipoproteinemia.- RFLPS of ApoB Gene.- Apolipoprotein B Genetic Deficiences.- Apolipoprotein C-II and C-III.- The Molecular Basis of Apo C-II Deficiency.- Familial Chylomicronemia Due to Mutations in Apolipoprotein CII: Apolipoprotein CII-Toronto and Apolipoprotein CII-St. Michael.- Apolipoprotein C-II Deficiency Syndrome: New Insights into the Molecular Mechanism Leading to the Disease in the Apo C-IIPadovaKindred.- Biochemical Aspects and Molecular Study a Case of Apo CII Deficit.- The Molecular Basis of the Defect in Familial Combined Apolipoproteins AI and CIII Deficiency.- Familial Apolipoprotein A-I, C-III and A-IV Deficiency.- Dyslipoproteinemias, Coronary Artery Disease and Diabetes.- Phenotypic Expression of Hepatic Lipase Deficiency.- Abnormal Processing of HDL Precursors in Tangier Monocyte Derived Macrophages.- Apo E Polymorphism in Relation to the Expression of Familial Dysbetalipoproteinemia.- Identification of an Italian Kindred with a Variant Apolipoprotein E (E1) Associated with Type III Hyperlipoproteinemia.- Normolipidemic Dyslipoproteinemia in Patients with Coronary Artery Disease.- Current Status on the Apo E-Receptor.- DNA Polymorphisms of the Glucose Transporter Gene in non-Insulin Dependent Diabetes Mellitus (NIDDM).- Lipoprotein Structure: Immunological Methods.- Computer-Modelling of Human Apolipoproteins and of their Mutants.- Monoclonal Antibodies to Human Apolipoprotein A-I.- Factors Affecting the Expression of Apolipoprotein A-I Epitopes and Screening for Mutants.- Characterization of Monoclonal Antibodies to Human Low Density Lipoprotein.- Apolipoprotein B: Immunological Methods for the Detection of Mutants.