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首页> 外文期刊>The American journal of clinical nutrition. >Scientific meeting held in Vina del Mar, Chile, in September 2007. Preface.
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Scientific meeting held in Vina del Mar, Chile, in September 2007. Preface.

机译:2007年9月在智利比尼亚德尔马举行的科学会议。前言。

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摘要

This supplement on copper biomarkers is the product of a scientific meeting held in Vina del Mar, Chile, in September 2007. The articles here provide a select update to the 1998 publication in this Journal addressing genetic and environmental determinants of copper metabolism.The individual articles partially overlap and therefore provide a comprehensive treatise of our current knowledge of copper metabolism, with special emphasis on elevated copper intakes. Beginning with genomics approaches, the reader will be provided insights about the homeostatic regulation of copper metabolism and its potential limitations. On the basis of the best available scientific evidence, we examine key indicators of copper homeostasis that serve as potential biomarkers for deficit and excess. The basis for a good biomarker is its ability to predict a given outcome, in this case, adverse consequences from deficit or excess. In doing so, we examined the basic molecular and cellular underpinnings of copper metabolism as well as the public health relevance of copper exposure. We have learned from bioinfor-matics the multiple dimensions and interrelations of putative copper proteins that could serve as biomarkers; in response to deficiency, the traditional biomarkers serve well to characterize the homeostatic response. However, the functional dimensions of various levels of copper exposure remain to be defined, especially as they relate to chronic disease and functional losses during aging.
机译:这种关于铜生物标志物的补充是2007年9月在智利Vina del Mar举行的一次科学会议的产物。本文对本刊1998年发表的文章进行了精选更新,该文章涉及铜代谢的遗传和环境决定因素。这些文章部分重叠,因此提供了我们目前对铜代谢知识的全面论述,特别强调了铜摄入量的增加。从基因组学方法开始,读者将获得有关铜代谢的稳态调节及其潜在局限性的见解。在现有最佳科学证据的基础上,我们研究了铜稳态的关键指标,这些指标可作为缺陷和过剩的潜在生物标志物。一个好的生物标志物的基础是它能够预测给定的结果,在这种情况下,是缺陷或过量的不良后果。在此过程中,我们研究了铜代谢的基本分子和细胞基础以及铜暴露的公共卫生相关性。我们从生物信息学中了解到可以作为生物标志物的假定铜蛋白的多个维度和相互关系;为了应对缺乏症,传统的生物标志物可以很好地表征稳态反应。然而,不同程度的铜暴露的功能维度仍有待定义,特别是因为它们与衰老过程中的慢性疾病和功能丧失有关。

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