Current Views of Fatty Acid Oxidation and Ketogenesis : From Organelles to Point Mutations /
| Autor Corporativo: | |
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| Otros Autores: | , |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer US : Imprint: Springer,
2002.
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| Edición: | 1st ed. 2002. |
| Colección: | Advances in Experimental Medicine and Biology,
466 |
| Materias: |
Tabla de Contenidos:
- Biogenesis of the Rat Liver Mitochondrial Carnitine Palmitoyltransferase I
- Subcellular Distributuon of Mitochondrial Carnitine Palmitoyltransferase I in Rat Liver
- Topology of Hepatic Mitochondrial Carnitine Palmitoyltransferase I
- Possible Involvement of Cytoskeletal Components in the Control of Hepatic Carnitine Palmitoyltransferase I Activity
- Effects of 3-Thia Fatty Acids on ?-Oxidation and Carnitine Palmitoylatransferase I Activity in Cultured Rat Hepatocytes
- Carnitine Acyltransferases and Associated Transport Processes in the Endoplasmic Reticulum
- Reciprocal Enzymatic Interference of Carnitine Palmitoyltransferase I and Glycerol-3-Phosphate Acyltransferase in Purified Liver Mitochondria
- Characterization of a Response Element for Peroxisomal Proliferator Activated Receptor (PPRE) in Human Muscle-type Carnitine Palmitoyltransferase I
- Kinetic Investigation of Carnitine Palmitoyltransferases in Homogenates of Human Skeletal Muscle Using L-amino-Carnitine and Malonyl-CoA
- Processing of Carnitine Octanoyl Transferase pre-mRNAs by cis and trans-splicing
- Selective Modulation of Carnitine Long-chain Acyltransferase Activities
- Confocal Laser Scanning Microscopy of Human Skin Fibroblasts Showing Transient Expression of a Green Fluorescent Carnitine Palmitoyltransferase 1 Fusion Protein
- Carnitine Biosynthesis
- Hypolipidemic 3-Thia Fatty Acids
- Molecular Mechanisms of Fatty Acid ?-Oxidation Enzyme Catalysis
- Control of Mitochondrial ?-Oxidation at the Levels of [NAD+]/[NADH] and CoA Acylation
- Production and Export of Acylcarnitine Esters by Neonatal Rat Hepatocytes
- Tissue Specific Differences in Intramitochondrial Control of ?-Oxidation
- Endotoxin-Induced Changes in Very-Low-Density Lipoprotein and Myocardial Utilisation of Triacylglycerol from Abnormal VLDL in the Rat
- Effect of Valproic Acid on the Expression of Acyl-CoA Dehydrogenases in Various Tissues
- Formation of a Human “Electron Transferring Flavoprotein”
- Cloning and Regulation of Peroxisome Proliferator-Induced Acyl-CoA Thioesterases From Mouse Liver
- Metabolic Effects of 3-Thia Fatty Acid in Cancer Cells
- Poorly Oxidizable Fatty Acid Analogues Inhibit the Proliferation of Cancer Cells in Culture
- The Role of PPAR? as a“lipostat” Transcription Factor
- The Hypolipidaemic Effect of EPA is Potentiated by 2- and 3-Methylation
- Is it Time to Reconsider the Role of CPT I in Control of Hepatic Ketogenesis?
- Developmental Comparison of Human and Rat Hepatic Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase
- Regulation of the Ketogenic Enzyme Mitochondrial 3-Hydroxy-3-Methylglutaryl-COA Synthase in Astrocytes and Meningeal Fibroblasts
- Studies on Regulation of the Peroxisomal ?-Oxidation at the 3-Ketothiolase Step
- Role and Organization of Peroxisomal ?-Oxidation
- Hepatic ?-Oxidation of Phytanic Acid
- Functions and Dysfunctions of Peroxisomes in Fatty Acid ?- and ?-Oxidation
- Enzymology of ?-Oxidation of (Poly)unsaturated Fatty Acids
- The Effect of ?-Oxidable and Non-?-Oxidable Thia Fatty Acids on Fatty Acid Metabolism
- EPA and DHA Possess Different Metabolic Properties
- The Use of [9,10-3H]Myristate, [9,10-3H]Palmitate and [9,10-3H]Oleate for the Detection and Diagnosis of Medium and Long-Chain Fatty Acid Oxidation Disorders in Intact Cultured Fibroblasts
- Rapid Diagnosis of Organic Acidemias and Fatty-acid Oxidation Defects by Quantitative Electrospray Tandem-MS Acyl-Carnitine Analysis in Plasma
- Genetics of Carnitine Palmitoyltransferase II Deficiencies
- Identification of a Missense Mutation in a Patient with Lethal Carnitine Acyl-Carnitine Carrier Deficiency
- MCAD Deficiency
- D-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Phytanoyl-CoA Hydroxylase Deficiency
- Rationale for a Conditional Knockout Mouse Model to Study Carnitine Palmitoyltransferase I Deficiencies
- Biochemical Characterisation of Mutations of Human Medium-Chain Acyl-CoA Dehydrogenase
- Lessons Learned from The Mouse Model of Short-Chain Acyl-CoA Dehydrogenase Deficiency.