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2005 Chronobiology Gordon Research Conference

2005 Chronobiology Gordon Research Conference
2005年时间生物学戈登研究会议
批准号:
6939852
负责人:
Martha U Gillette
金额:
$0.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2006-03-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):第14届戈登时间生物学研究会议将在罗得岛州纽波特的萨尔韦里贾纳大学举行。近年来,人体内部时钟(昼夜节律时钟)在调节和调节时间生理方面的重要性越来越明显,因此,许多人致力于分析昼夜节律过程的机制。认识到昼夜节律在人类健康和疾病中所起的关键作用,加上最近关于产生和调节昼夜节律系统的分子机制的具有里程碑意义的发现,导致了该领域的显著扩展。今天,时间生物学研究吸引了来自广泛学科的大量研究人员,包括分子遗传学,神经科学,光生物学,计算生物学和代谢,以及睡眠医学,精神病学,肿瘤学和老年学。戈登时间生物学会议的目的是:(1)为快速发展的时间生物学领域提供一个讨论和确定一般原则的论坛。(2)促进时间生物学各分支学科研究人员之间的互动,从而提高整个研究领域的一致性。(3)加强年轻和成熟研究人员之间的互动,从而维持高质量的时间生物学研究。(4)通过汇集来自许多不同研究小组和国家的科学家,促进国内和国际合作。(5)通过将使用模式生物的研究人员与在昼夜节律研究中研究人类受试者的研究人员聚集在一起,促进转化研究。会议将通过聚集来自不同国家、年龄、性别和使用不同研究模式的大约150名科学家来实现这些目标。我们将通过邀请个人和直接联系少数民族学院(如莫尔豪斯)的方式鼓励少数民族积极参与。该计划将侧重于关键研究领域的新发展和新兴发展(见暂定计划)。按照非常成功的戈登会议形式,讲座将分为9个上午和晚上的会议,并有充足的讨论时间。三个下午晚些时候的海报会议将允许参与者提交额外的数据。特别注意实现性别平衡和包括来自非常不同学科的专家,以实现对我们科学前沿的广泛理解和对未来机会的见解。结果将与改善睡眠、情感、认知、神经、代谢、内分泌和肿瘤紊乱等功能障碍的健康相关。
英文摘要
DESCRIPTION (provided by applicant): Partial support is requested for the 14th Gordon Research Conference on Chronobiology, to be held at Salve Regina University, Newport, Rhode Island. In recent years, the significance of internal body clocks (circadian clocks) in regulating and adjusting temporal physiology has become increasingly clear and, as a consequence, much effort has been devoted to the analysis of the mechanisms underlying circadian processes. Recognition of the key role played by circadian rhythms in human health and disease, combined with recent landmark discoveries regarding the molecular mechanisms that both generate and regulate the circadian system, has led to a remarkable expansion of the field. Today, chronobiological research attracts a host of researchers from a broad range of disciplines, including molecular genetics, neuroscience, photobiology, computational biology and metabolism, as well as sleep medicine, psychiatry, oncology and gerontology. The aims of the Gordon Conference on Chronobiology are: (1) To provide a forum for discussion and for identifying general principles in the rapidly expanding field of Chronobiology. (2) To stimulate interactions among researchers working in the various sub-disciplines of Chronobiology and thus enhance the coherence of the research field as a whole. (3) To intensify interactions between young and established researchers, and thus sustain high-quality chronobiological research. (4) To promote both national and international collaboration by bringing together scientists from many different research groups and countries. (5) To promote translational research by bringing together investigators employing model organisms with those studying human subjects in circadian research. The conference will achieve these goals by assembling approximately 150 scientists encompassing individuals from different countries, age groups, genders, and using different research models. We will encourage active participation of minority groups by inviting individuals and contacting minority colleges directly (e.g., Morehouse). The program will focus on new and emerging developments in key research areas (see Tentative Program). In accordance with the highly successful Gordon Conference format, lectures will be presented in 9 morning and evening sessions with ample time for discussion. Three late-afternoon poster sessions will allow participants to present additional data. Special attention has been given to achieving gender balance and to including experts from very diverse disciplines to achieve a broadly-based understanding of the frontier of our science and insights as to future opportunities. Outcomes will have health relevance for ameliorating dysfunctions that manifest as sleep, affective, cognitive, neurological, metabolic, endocrine and oncological disorders.
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会议论文
Dynamic Circadian Regulation of the Blood-Brain Interface in a Human Brain-mimicking Microfluid Chip
Dynamic Circadian Regulation of the Blood-Brain Interface in a Human Brain-mimicking Microfluid Chip
High Resolution Analysis of miR125b in Dendrites via Microfluidic Devices
Nano-Scale Processes of Dendrogenesis
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