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Ryanodine Receptors: Structure, function and dysfunction in clinical disease 2005 ed. [Pehme köide]

  • Formaat: Paperback / softback, 330 pages, kõrgus x laius: 235x155 mm, kaal: 545 g, XXI, 330 p., 1 Paperback / softback
  • Sari: Developments in Cardiovascular Medicine 254
  • Ilmumisaeg: 01-Dec-2014
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1461498406
  • ISBN-13: 9781461498407
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  • Formaat: Paperback / softback, 330 pages, kõrgus x laius: 235x155 mm, kaal: 545 g, XXI, 330 p., 1 Paperback / softback
  • Sari: Developments in Cardiovascular Medicine 254
  • Ilmumisaeg: 01-Dec-2014
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1461498406
  • ISBN-13: 9781461498407
Teised raamatud teemal:

In recent years, the ryanodine receptor has emerged as a new and very promising target for the treatment of several cardiovascular disorders, including cardiac arrhythmias and heart failure. This volume is the most current publication devoted to the major intracellular calcium-release channel, the ryanodine receptor.

"In this series of brief but informative chapters, the contributions progress from the basic gene family and primary structure, through its 3D structure so far, to its regulation and physiology."

David E. Clapham, MD, PhD
Professor of Neurobiology and Pediatrics
Harvard Medical School

Dr. Xander H.T. Wehrens received his M.D. and Ph.D. degrees from Maastricht University in the Netherlands. His research has mainly concentrated on molecular mechanisms of cardiac arrhythmias, in particular in the setting of inherited arrhythmogenic syndromes and congestive heart failure. This work has led to the development of novel anti-arrhythmic therapies. He is currently a research scientist in the Department of Physiology and Cellular Biophysics at the College of Physicians and Surgeons of Columbia University.

Dr. Andrew R. Marks is the Chair and Professor of the Department of Physiology and Cellular Biophysics at Columbia University College of Physicians and Surgeons. Dr. Marks' research has focused on understanding how macromolecular signaling complexes regulate ion channel function in muscle and non-muscle systems, and on the regulation of vascular smooth muscle proliferation and migration. His work has contributed new understandings of fundamental mechanisms that regulate muscle contraction that have lead to the discovery of molecular defects that contribute to heart failure and fatal cardiac arrhythmias.

Evolution of the Ryanodine Receptor Gene Family.- Topology and
Transmembrane Organization of Ryanodine Receptors.- Three-Dimensional
Reconstruction of Ryanodine Receptors.- RYR-DHPR Relationships in Skeletal
and Cardiac Muscles.- The Pore of the Ryanodine Receptor Channel.-
Intra-Molecular Domain-Domain Interaction.- Regulation of Sarcoplasmic
Reticulum Calcium Release by Luminal Calcium.- Cytosolic Calcium Regulation
of Single Ryanodine Receptor Channels.- Elementary Ca2+ Release Events:
Ryanodine Receptor Ca2+ Sparks.- Ca2+ Release from the Sarcoplasmic Reticulum
in Intact Cardiomyocytes.- Stability and Instability of Ca2+ Release from the
SR.- Ryanodine Receptors in Smooth Muscle.- Functions of RYR3 Homologues.-
Knockout Mice Lacking RYR and Junctophilin Subtypes.- Regulation of Ryanodine
Receptor Ca2+ Release by Macromolecular Complexes.- RYR1 Modulation by
Calmodulin.- Ryanodine Receptor Function in Inflammation.- Ryanoids, Receptor
Affinity and RYR Channel Subconductance.- Scorpion Peptides as High-Affinity
Probes of Ryanodine Receptor Function.- Redox Sensing by the Ryanodine
Receptors.- Ryanodine Receptor Dysfunction in the Diabetic Heart.- Molecular
and Clinical Genetics of RYR1 Disorders.- Pathophysiology of Muscle Disorders
Linked to Mutations in the Skeletal Muscle Ryanodine Receptor.- The
Dantrolene Binding Site on RYR1.- Ryanodine Receptor Dysfunction in Heart
Failure and Arrhythmias.- Stabilization of Ryanodine Receptor as a Novel
Therapeutic Strategy Against Heart Failure.- Ryanodine Receptor Antibodies
and Myasthenia Gravis.