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Titlebook: Regulation of Smooth Muscle Contraction; Robert S. Moreland Book 1991 The Editor(s) (if applicable) and The Author(s), under exclusive lic

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Modulation of Ca2+ Sensitivity by Agonists in Smooth Muscleh electromechanical coupling and through pharmacomechanical coupling (Somlyo and Somlyo, 1968). The two components of pharmacomechanical coupling explored, until recently, are ligand-gated Ca. influx and G-protein coupled activation of the phosphatidylinositol cascade that results in inositol 1,4,5-
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Regulation of the Ca2+-Force Relationship in Permeabilized Arterial Smooth Musclequent phosphorylation of myosin light chain (MLC) by the Ca.-calmodulin dependent MLC kinase (for reviews see Kamm and Stull, 1985; Somlyo, 1985). However, simultaneous measurements of tension and [Ca.]. in intact tissues have shown that during continuous stimulation, although a-adrenergic agonist i
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Mechanical and Biochemical Events During Hypoxia-Induced Relaxations of Rabbit Aortaical or environmental changes such as exposure to high altitudes. A current challenge in medicine and physiology is to better understand how cellular functions can be preserved during hypoxic events. One of the primary and initial aspects of cellular function affected by hypoxia is energy production
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Calcium Homeostasis in Single Intact Smooth Muscle Cellstremendous effort directed at understanding Ca. homeostatic mechanisms, with experiments ranging the spectrum from isolated genes to intact cells. The work of the scientists in this laboratory has concentrated on the latter, Ca. regulation in intact, single smooth muscle cells that have been enzymat
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Mechanics of the Crossbridge Interaction in Living and Chemically Skinned Smooth Musclectin filament, which also determines the force by the elastic extension of the crossbridge. Particularly, “negative” strain on the crossbridge, giving rise to a force tending to oppose shortening of the muscle, is associated with a high rate constant for crossbridge detachment.
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