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

  • Formaat: Hardback, 330 pages, kõrgus x laius: 235x155 mm, kaal: 1490 g, XXI, 330 p., 1 Hardback
  • Sari: Developments in Cardiovascular Medicine 254
  • Ilmumisaeg: 09-Nov-2004
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 0387231870
  • ISBN-13: 9780387231877
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  • Formaat: Hardback, 330 pages, kõrgus x laius: 235x155 mm, kaal: 1490 g, XXI, 330 p., 1 Hardback
  • Sari: Developments in Cardiovascular Medicine 254
  • Ilmumisaeg: 09-Nov-2004
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 0387231870
  • ISBN-13: 9780387231877
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.



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, PhDProfessor of Neurobiology and PediatricsHarvard Medical SchoolDr. 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.
Dedication v
Contributing Authors xi
Preface xv
Foreword xix
Evolution of the Ryanodine receptor gene family
1(8)
Alexander Kushnir
A.K.M.M. Mollah
Xander H.T. Wehrens
Topology and transmembrane organization of ryanodine receptors
9(16)
Guo Ghang Du
David H. MacLennan
Three-dimensional reconstruction of ryanodine receptors
25(10)
Zheng Liu
Terence Wagenknecht
RyR-DHPR relationships in skeletal and cardiac muscles
35(8)
Clara Franzini-Armstrong
The pore of the ryanodine receptor channel
43(10)
Alan J. Williams
S.R. Wayne Chen
William Welch
Inter-molecular domain-domain interaction: A key mechanism for calcium channel regulation of ryanodine receptors
53(14)
Noriaki Ikemoto
Regulation of sarcoplasmic reticulum calcium release by luminal calcium
67(10)
Sandor Gyorke
Dmitry Terentyev
Serge Viatchenko-Karpinski
Cytosolic calcium regulation of single ryanodine receptor channels
77(10)
Josefina Ramos-Franco
Michael Fill
Elementary calcium release events: ryanodine receptor Ca2+ sparks
87(12)
W.J. Lederer
Eric A. Sobie
Silvia Guatimosim
Long-Sheng Song
Ca2+ release from the sarcoplasmic reticulum in intact cardiomyocytes
99(12)
Donald M. Bers
Kenneth S. Ginsburg
Stability and instability of Ca2+ release from the SR
111(10)
Mary E. Diaz
Stephen C. O'Neill
Andrew W. Trafford
David A. Eisner
Ryanodine receptors in smooth muscle
121(10)
Steven O. Marx
Functions of RyR3 homologues
131(10)
Yasuo Ogawa
Takashi Murayama
Nagomi Kurebayashi
Knockout mice lacking RyR and junctophilin subtypes
141(10)
Hiroshi Takeshima
Regulation of ryanodine receptor Ca2+ release by macromolecular complexes
151(12)
Xander H.T. Wehrens
Stephan E. Lehnart
Andrew R. Marks
RyR1 modulation by calmodulin
163(6)
Paula Aracena
Cecilia Hidalgo
Susan L. Hamilton
Ryanodine receptor function in inflammation
169(10)
Edmond D. Buck
Barbara E. Ehrlich
Ryanoids, receptor affinity and RyR channel subconductance: Why the discordance?
179(12)
Henry R. Besch Jr.
Chun Hong Shao
Keshore R. Bidasee
Scorpion peptides as high-affinity probes of ryanodine receptor function
191(10)
Georgina R. Gurrola
Xinsheng Zhu
Hector H. Valdivia
Redox sensing by the ryanodine receptors
201(8)
Gerhard Meissner
Jonathan S. Stamler
Ryanodine receptor dysfunction in the diabetic heart
209(10)
Keshore R. Bidasee
Sarah Ingersoll
Chun Hong Shao
Molecular and clinical genetics of RyR1 disorders
219(10)
Tommie V. McCarthy
James J.A. Heffron
John Mackrill
Pathophysiology of muscle disorders linked to mutations in the skeletal muscle ryanodine receptor
229(14)
Robert T. Dirksen
Guillermo Avila
The dantrolene binding site on RyR1: Implications for clinical therapy
243(10)
Jerome Parness
Ryanodine receptor dysfunction in heart failure and arrhythmias
253(10)
Stephan E. Lehnart
Xander H.T. Wehrens
Andrew R. Marks
Stabilization of ryanodine receptor as a novel therapeutic strategy against heart failure
263(10)
Masafumi Yano
Takeshi Yamamoto
Masunori Matsuzaki
Ryanodine receptor antibodies and myasthenia gravis
273(8)
Frederik Romi
References 281(32)
Index 313