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Titlebook: Cardiac Drug Development Guide; Michael K. Pugsley Book 2003 Springer Science+Business Media New York 2003

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发表于 2025-3-21 16:12:02 | 显示全部楼层 |阅读模式
书目名称Cardiac Drug Development Guide
编辑Michael K. Pugsley
视频videohttp://file.papertrans.cn/222/221754/221754.mp4
概述Includes supplementary material:
丛书名称Methods in Pharmacology and Toxicology
图书封面Titlebook: Cardiac Drug Development Guide;  Michael K. Pugsley Book 2003 Springer Science+Business Media New York 2003
描述Cardiac Drug Development Guide outlines, in detail, the therapeutics of cardiac medicine currently at the cutting edge of scientific research and development around the world. This volume integrates basic and clinical cardiac pharmacology by c- bining, for the first time, both classical and molecular aspects of therapeutic drug development. The chapters comprise a broad spectrum of therapeutic areas and hence involve a comprehensive discussion of molecular, biochemical, and electrophy- ological concepts based on years of in vitro as well as in vivo pharmacological st- ies. In addition, the latter part of the book includes comprehensive clinical cardiac chapters that describe important topics in molecular medicine. These chapters also discuss current clinical therapeutic trends in medicine and provide an evaluation of the efficacy of novel drugs in these areas. Cardiac Drug Development Guide has many distinctive and outstanding features that set it apart from other cardiac pharmacology books. This book introduces topics in an easily understandable format for researchers in many varying disciplines by integrating and thereby simplifying concepts not usually discussed across a broad r
出版日期Book 2003
版次1
doihttps://doi.org/10.1385/1592594042
isbn_softcover978-1-4899-3828-2
isbn_ebook978-1-59259-404-7Series ISSN 1557-2153 Series E-ISSN 1940-6053
issn_series 1557-2153
copyrightSpringer Science+Business Media New York 2003
The information of publication is updating

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J. Brindley,A. V. Holden,A. PalmerMAPKs found in cardiac tissue include the extracellular signal-regulated kinases (ERKs), the stress-activated/c-Jun NH2-terminal kinases (SAPK/JNKs), p38-MAPK, and ERK5/big MAPK 1 (BMK1). The ERKs are strongly activated by mitogenic and growth factors and by physical stress, SAPK/JNKs and p38-MAPK c
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V. S. Letokhov,A. A. Makarov,E. A. Ryabov function, providing additional targets for drug development. However, clinical experience has shown that the therapeutic index for the existing potent platelet inhibitors is narrow, suggesting that new and novel approaches to impairing platelet function will be required.
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V. S. Letokhov,A. A. Makarov,E. A. Ryabovdominance of NHE-1 in the myocardium is of some importance because pharmacological development of NHE inhibitors for cardiac therapeutics has concentrated specifically on those agents that are selective for NHE-1. These agents, as well as the earlier nonspecific amiloride derivatives have now been e
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The Role of Cardiac Pacemaker Currents in Antiarrhythmic Drug Discoveryas been a subject of much puzzlement. By the 1970s, it was clear that to provide a slow depolarization, there must be a slow increase in net inward current, although it was not clear whether this came about as a consequence of the slow inactivation of an outward current (presumed to be a carried by
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The Sodium-Hydrogen Exchange System in the Heartdominance of NHE-1 in the myocardium is of some importance because pharmacological development of NHE inhibitors for cardiac therapeutics has concentrated specifically on those agents that are selective for NHE-1. These agents, as well as the earlier nonspecific amiloride derivatives have now been e
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