Red Blood Cell Membranes

Structure: Function: Clinical Implications
Herausgeber: Agre, Peter

• Broschiertes Buch

Produktbeschreibung

This book is devoted to the red blood cell membrane, its structure and function, and abnormalities in disease states. It presents a well-documented and well-illustrated comprehensive picture of clinical manifestations of red blood cell disorders.

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Produktdetails

• Verlag: CRC Press
• Seitenzahl: 760
• Erscheinungstermin: 2. Dezember 2019
• Englisch
• Abmessung: 234mm x 156mm x 40mm
• Gewicht: 1132g
• ISBN-13: 9780367451141
• ISBN-10: 036745114X
• Artikelnr.: 58440309

Autorenporträt

Agre, Peter

Inhaltsangabe

1. Recently Identified Erythrocyte Membrane-Skeletal Proteins and
Interactions: Implications for Structure and Function 2. Structure and
Function of the Glucose Transporter 3. Intermediate Filament Expression in
Erythroid Differentiation and Morphogenesis 4. The Erythrocyte Cytoskeleton
in Hereditary Elliptocytosis and Spherocytosis 5. Spectrin Genes 6.
Na,K-ATPase Structure 7. Characterization of the Gene Coding for Human
Erythrocyte Protein 4.1: Implications for Understanding Hereditary
Elliptocytosis 8. Regulation of Protein 4.1-Membrane Associations by a
Phosphoinositide 9. Interaction of Native and Denatured Hemoglobins with
Band 3: Consequences for Erythrocyte Structure and Function 10.
Ultrastructure and Function of Membrane Skeleton 11. The Biochemistry of
the Antigens of the Red Blood Cell Membrane 12. The Transferrin Receptor
13. Red Blood Cell Membrane Protein and Lipid Diffusion 14. Red Blood Cell
Shape 15. Viscoelastic Properties and Rheology 16. Active Transport of
Sodium and Potassium 17. The Plasma Membrane Calcium Pump: The Red Blood
Cell as a Model 18. Passive Cation Transport 19. Anion Transport 20. The
Kinetics and Thermodynamics of Glucose Transport in Human Erythrocytes 21.
Nucleoside Transport 22. Regulated Transport: The Response of Ion Transport
Pathways to Physiological Stimuli 23. Ion Transport in Red Blood Cell
Disorders 24. Partial Deficiencies of Erythrocyte Spectrin in Hereditary
Spherocytosis