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OverviewFull Product DetailsAuthor: J. Neuwirt , P. PonkaPublisher: Springer Imprint: Kluwer Academic Publishers Edition: 1977 ed. Dimensions: Width: 21.00cm , Height: 1.20cm , Length: 29.70cm Weight: 1.040kg ISBN: 9789024719990ISBN 10: 9024719992 Pages: 197 Publication Date: 31 August 1977 Audience: General/trade , Professional and scholarly , General , Professional & Vocational Format: Hardback Publisher's Status: Active Availability: In Print ![]() This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of Contents1. Introduction.- 2. Substrate Supply for Haemoglobin Syntheses.- Iron Uptake.- Mechanism of iron supply to erythroid cells.- Factors influencing iron uptake by erythroid cells.- Iron and transferrin levels and transferrin saturation.- Metabolic state of crythroid cells.- The role of sulfhydryl groups in iron uptake.- Other factors which influence iron uptake.- Iron uptake from chelating agents.- Intracellular kinetics of iron.- Ferritin.- Other non-haem iron proteins and iron complexes.- Mitochondrial iron.- Inhibitors of haem synthesis as a tool in investigations of the intracellular kinetics of iron.- Regulation of iron supply for haemoglobin synthesis.- Effect of haem on iron uptake by reticulocytes.- Effort of inhibitors of haem and globin syntheses on iron uptake.- Mechanism of the effcct of haem on iron uptake.- Regulation of Uptake of Glycine and other Amino Acids.- 3. Haem Synthesis.- Biosynthesis of Haem.- General introduction.- ALA synthesis.- ALA synthetase.- Porphobilinogen (PBG) synthesis. ALA dehydrase enzyme.- Conversion of porphobilinogen (PBG) to uroporphyrinogen III.- Conversion of uroporphyrinogen to coproporphyrinogen by the enzyme uroporphyrinogen decarboxylase.- Conversion of coproporphynnogen lo protoporphyrinogen by the enzyme coproporphyrinogen oxidase.- Combination of iron with protoporphyrin.- Free protoporphyrin.- Regulation of Haem Biosynthesis.- Enzyme synthesis.- Changes in enzyme activity.- Regulation by substrate supply.- Metabolic and external factors.- Haem catabolism.- 4. Globin Synthesis.- Globin Biosynthesis.- General introduction.- Role of ribonucleic acids in globin synthesis.- Messenger RNA.- Isolation and identification of globin mRNA.- Methods used for the isolation of globin mRNA.- Detection of messenger RNA for globin.- Characteristics of globin mRNA.- Biosynthesis of globin mRNA.- Transfer RNA.- Ribosomes and globin synthesis.- Ribosome structure.- The role of polyribosomes.- The role of sub-units.- Membrane-bound ribosomes.- Function of the active ribosomal complex.- Initiation of the globin chain.- Initiation of globin synthesis by means of methionyl-tRNA.- Initiation factors of reticulocyte ribosomes.- Elongation of the globin chain.- Globin chain termination.- Regulation of Globin Synthesis.- Post-transcription control of globin synthesis.- Stability of globin mRNA.- Translation control.- Rate limiting step in the synthesis of the globin chain.- Synchronization of synthesis of different chains.- The role of haem in globin synthesis.- 5. Regulation of Haemoglobin Synthesis.- Coordination of Haem and Globin Syntheses.- Regulatory role of haem.- Mutual relations between haem and globin synthesis.- Haemoglobin Synthesis During Maturation.- 6. Differentiation of Erythroid Cells.- Erythroid Differentiation in Haematopoietic Tissue and the Initiation of Haemoglobin Synthesis.- Mechamun of erythropoietin action.- Erythroid Differentiation Without Erythropoietin.- 7. Anaemias Due to Disorders of Haemoglobinization.- Hypochromic Anaemias Due to Impaired Haem Synthesis.- Hypochromic anaemias caused by a reduced iron supply into erythroid tissue.- Iron deficiency anaemia.- Congenital atransferrinaemia.- Hypochromic anaemia as a result of reduced iron release from reticuloendothelial cells.- Copper defficiency.- Sideroblastic anaemias.- Hypochromic Anaemias Due to Impaired Globin Synthesis.- Thalassaemia.- ?-thalassaemia.- Haemoglobin Constant Spring and related mutants of the terminal portion of the chain.- ß- and ?ß-thalassaemia.- References.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |