1,477 research outputs found

    Graphitization in chromium cast iron

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    peer reviewedSome trials with graphite Hi-Cr iron rolls have been done mainly in Japan, for the rolling of stainless steel. This material could lead to good compromise between oxidation, wear and thermal behaviour. By using thermal analysis and resistometry, the conditions for secondary graphite formation have been studied. The amount and volume of free graphite may be strongly increased by a suitable heat treatment, allowing a good thermal conductivity as well as high wear and mechanical properties

    Cellular mechanisms of prostaglandin E2 and vasopressin interactions in the collecting duct

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    As the final segment of the nephron, the collecting duct is the ultimate regulator of renal salt and water excretion. Balance between intake and renal excretion of salt and water is fine-tuned by the action of several hormones targeted to the collecting duct. Vasopressin is, perhaps, the prototypical example of such a hormone. As total body water decreases and plasma osmolality rises, vasopressin secretion from the posterior pituitary increases [1]. Picomolar concentrations of circulating vasopressin lead to increased water permeability of the apical membrane of the collecting duct cell, resulting in increased water reabsorption and increased total body water [2,3]. There is abundant evidence demonstrating that vasopressin's effect on water reabsorption in the collecting duct is mediated through the classic second messenger, cAMP [3]. V2 selective receptors are linked via a G protein, to stimulation of plasma membrane adenylyl cyclase, resulting in increased cell cyclic AMP levels [4, 5]. The increased cyclic AMP then leads to augmented water permeability of the apical membrane [6, 7].As one might expect with such an important biologic process, other hormones and autocoids provide a counter-regulatory influence to modulate vasopressin mediated increases in osmotic water permeability. There is good evidence that the arachadonic acid metabolite, prostaglandin E2 (PGE2) plays a critical physiologic and pathophysiologic role in inhibiting vasopressin action in the collecting duct [8, 9]. Not only is the collecting duct the major renal site of synthesis for this cyclo-oxygenase product of arachidonic acid but PGE2 production is stimulated by vasopressin itself [10–12]. PGE2 infusion significantly blunts water reabsorption and cycloxygenase inhibition augments vasopressin antidiuresis [9, 13]. Thus, there is good evidence that the autocoid PGE2 plays an important role in regulating vasopressin-stimulated osmotic water flow

    In Memoriam: Clark Byse

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    The editors of the Harvard Law Review respectfully dedicate this issue to Professor Clark Byse

    A major zebrafish polymorphism resource for genetic mapping

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    645,088 candidate polymorphisms in zebrafish were identified and positioned on genetic and physical maps as a resource for positional cloning
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