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Titlebook: Cardiac Electrophysiology, Circulation, and Transport; Samuel Sideman (R.J. Matas Winnipeg Professor of B Book 1991 Springer Science+Busin

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發(fā)表于 2025-3-21 16:44:33 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Cardiac Electrophysiology, Circulation, and Transport
編輯Samuel Sideman (R.J. Matas Winnipeg Professor of B
視頻videohttp://file.papertrans.cn/222/221766/221766.mp4
叢書名稱Developments in Cardiovascular Medicine
圖書封面Titlebook: Cardiac Electrophysiology, Circulation, and Transport;  Samuel Sideman (R.J. Matas Winnipeg Professor of B Book 1991 Springer Science+Busin
描述The cardiac system represents one of the most exciting challenges to human ingenuity. Critical to our survival, it consists of a tantalizing array of interacting phenomena, from ionic microscopic transport, membrane channels and receptors through cellular metabolism, energy production to fiber mechanics, microcirculation, electrical activation to the global, clinically observed, function, which is measured by pressure, volume, coronary flow, heart rate, shape changes and responds to imposed loads and pharmaceutical challenges. It is a complex interdisciplinary system requiring the joint efforts of the life sciences, the exact sciences, engineering and technology to understand and control the pathologies involved. The Henry Goldberg Workshops were set up to address these challenges. Briefly, our goals are: 1. To foster interdisciplinary interaction between scientists from different areas of cardiology, identify missing links, and catalyze new questions. 2. To relate micro scale cellular phenomena to the global, clinically manifested cardiac function. 3. To relate conceptual modeling and quantitative analysis to experimental and clinical data. 4. To encourage international cooperatio
出版日期Book 1991
關(guān)鍵詞cardiac function; circulation; electrophysiology; heart; heart rate
版次1
doihttps://doi.org/10.1007/978-1-4615-3894-3
isbn_softcover978-1-4613-6737-6
isbn_ebook978-1-4615-3894-3Series ISSN 0166-9842
issn_series 0166-9842
copyrightSpringer Science+Business Media Dordrecht 1991
The information of publication is updating

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An Introduction to the Fractional Laplacian, chain model. Furthermore, the cardiac Na channel has been cloned and sequenced, and its primary structure has been deduced from the cDNA. Structure-function studies of the cloned channel should give us great insight into its molecular mechanism of gating, including its voltage dependence and its binding sites for drugs.
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Fractal Mechanisms in Cardiac Electrophysiologyaos theory.”.This brief overview discusses applications of the concept of fractals to selected aspects of cardiovascular physiology. Emphasis here will be on certain of the controversies which have arisen since the “fractal hypothesis” of cardiac electrical stability was first proposed.
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發(fā)表于 2025-3-22 11:42:21 | 只看該作者
Cardiac Sodium Channel Kinetics chain model. Furthermore, the cardiac Na channel has been cloned and sequenced, and its primary structure has been deduced from the cDNA. Structure-function studies of the cloned channel should give us great insight into its molecular mechanism of gating, including its voltage dependence and its binding sites for drugs.
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0166-9842 array of interacting phenomena, from ionic microscopic transport, membrane channels and receptors through cellular metabolism, energy production to fiber mechanics, microcirculation, electrical activation to the global, clinically observed, function, which is measured by pressure, volume, coronary
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Nonlocal Continuum Field Theorieslow in the extracellular compartment is approximately of the same magnitude as the resistance in the intracellular compartment. The extracellular electrical resistance therefore exerts an important influence on impulse propagation within the ventricular wall.
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