Ion Channels and Disease

Ashcroft, Frances M.

In stock
Regular price 53.750 KD inc. VAT
License
Table of contents
  • Copyright Pageiv
  • CONTENTSix
  • PREFACExix
  • CHAPTER 1. INTRODUCTION1
  • CHAPTER 2. FROM GENE TO PROTEIN3
  • Basic Genetics12
  • CHAPTER 3. HOW ION CHANNELS WORK21
  • Properties of Single-Channel Currents21
  • From Single Channels to Macroscopic Currents33
  • From Whole-Cell Currents to Membrane Potential Changes37
  • CHAPTER 4. STUDYING ION CHANNELS43
  • Investigating Ion Channel Function43
  • Obtaining the Primary Sequence51
  • Investigating Ion Channel Structure57
  • Genetic Analysis of Ion Channels and Disease60
  • CHAPTER 5. VOLTAGE-GATED Na+ CHANNELS67
  • Diseases of Muscle Na+ Channels79
  • Diseases of Neuronal Na+ Channels95
  • CHAPTER 6. VOLTAGE-GATED K+ CHANNELS97
  • KV Channels97
  • KV Channels and Disease109
  • KCNQ Channels111
  • KCNQ Channels and Disease113
  • Eag-Like KV Channels117
  • Eag-like KV Channels and Disease120
  • CHAPTER 7. Ca2+–ACTIVATED K+ CHANNELS125
  • Maxi KCa (BK) Channels127
  • Small KCa Channels130
  • Myotonic Muscular Dystrophy132
  • Intermediate KCa Channels133
  • CHAPTER 8. INWARDLY RECTIFYING K+ CHANNELS135
  • Diseases Associated with Kir Channels149
  • CHAPTER 9. VOLTAGE-GATED Ca2+ CHANNELS161
  • Diseases of Skeletal Muscle Ca2+ Channels172
  • Diseases of Neuronal Calcium Channels177
  • CHAPTER 10. VOLTAGE-GATED CL- CHANNELS185
  • Cl- Channel Diseases190
  • CHAPTER 11. CYCLIC NUCLEOTIDE-GATED CHANNELS199
  • Cyclic Nucleotide-Gated Channels199
  • CNG Channel Mutations Associated with Disease207
  • Hyperpolarization-Activated Cyclic-Nucleotide- Gated Channels208
  • CHAPTER 12. CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR211
  • Cystic Fibrosis218
  • CHAPTER 13. EPITHELIAL Na+ CHANNEL231
  • Diseases Associated with ENaC Channels238
  • CHAPTER 14. LIGAND-GATED Ca2+ CHANNELS249
  • Ryanodine Receptors249
  • Diseases Associated with Ryanodine257
  • IP3 Receptors260
  • Diseases Associated with IP3 Receptors264
  • CHAPTER 15. ACETYLCHOLINE RECEPTORS269
  • Diseases of Skeletal Muscle AChRs283
  • Diseases of Neuronal AChR288
  • CHAPTER 16. GLUTAMATE RECEPTORS291
  • Non-NMDA Receptors291
  • NMDA Receptors301
  • Glutamate Channels and Disease306
  • CHAPTER 17. GLYCINE RECEPTORS313
  • Glycine Receptors and Disease319
  • CHAPTER 18. GABAA RECEPTORS325
  • Diseases Associated with GABAA Channels332
  • CHAPTER 19. WATER CHANNELS337
  • CHAPTER 20. GAP JUNCTION CHANNELS347
  • Diseases of Gap Junction Channels354
  • CHAPTER 21. AUTOANTIBODIES TO ION CHANNELS361
  • Basic Immunology361
  • Autoantibodies Affecting Neuromuscular Transmission363
  • Autoantibodies to Ion Channels Not Involved in Neuromuscular Transmission375
  • CHAPTER 22. ION CHANNELS IN VIRUSES379
  • Influenza Virus379
  • Other Types of Viruses383
  • CHAPTER 23. ION CHANNELS AS LETHAL AGENTS385
  • Ion Channels of the Vertebrate Immune System385
  • Ion Channels of Bacteria, Fungi and Protozoans391
  • Venoms403
  • CHAPTER 24. A RAGBAG OF CHANNELS405
  • ATP-Gated Ion Channels405
  • Vanilloid Receptors407
  • Channels Involved in Programmed Cell Death410
  • β-Amyloid Peptide411
  • A LAST WORD413
  • BIBLIOGRAPHY419
  • INDEX465
Book details
  • Vendor Elsevier S & T
  • SKU 9780120653102
  • ISBN-13 9780080535210
  • Author Ashcroft, Frances M.
  • Category Medical
  • Subject Biochemistry

Do you have questions about this book?

Ask an expert!

Ion channels are membrane proteins that act as gated pathways for the movement of ions across cell membranes. They play essential roles in the physiology of all cells. In recent years, an ever-increasing number of human and animal diseases have been found to result from defects in ion channel function. Most of these diseases arise from mutations in the genes encoding ion channel proteins, and they are now referred to as the channelopathies.
Ion Channels and Disease provides an informative and up-to-date account of our present understanding of ion channels and the molecular basis of ion channel diseases. It includes a basic introduction to the relevant aspects of molecular biology and biophysics and a brief description of the principal methods used to study channelopathies. For each channel, the relationship between its molecular structure and its functional properties is discussed and ways in which genetic mutations produce the disease phenotype are considered.
This book is intended for research workers and clinicians, as well as graduates and advanced undergraduates. The text is clear and lively and assumes little knowledge, yet it takes the reader to frontiers of what is currently known about this most exciting and medically important area of physiology.

Key Features
* Introduces the relevant aspects of molecular biology and biophysics
* Describes the principal methods used to study channelopathies
* Considers single classes of ion channels with summaries of the physiological role, subunit composition, molecular structure and chromosomal location, plus the relationship between channel structure and function
* Looks at those diseases associated with defective channel structures and regulation, including mutations affecting channel function and to what extent this change in channel function can account for the clinical phenotype