National Exposure Assessment Laboratory at Emory
National Exposure Assessment Laboratory at Emory
批准号:
9062183
负责人:
GARY W MILLER
金额:
$106.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-30 至 2021-08-31
关键词:
BehaviorBindingBiologicalBiological AssayBiological MarkersBiologyChemical ExposureChemicalsClientCoupledDNADNA DamageDatabasesDevelopmentDietEducational workshopEnvironmentEpigenetic ProcessEvaluationExposure toFingerprintGeneticGenetic TranscriptionGenetic VariationGenomeGenomicsGoalsHumanHuman GenomeIndividualLaboratoriesLeftLinkLongevityMeasurementMeasuresMethylationModificationMolecular ProfilingNational Institute of Environmental Health SciencesOutcomeOxidation-ReductionPathway AnalysisPathway interactionsPhysiologicalPredispositionProcessProductionProteinsResearch DesignResearch PersonnelResourcesSamplingScienceTargeted ResearchUpdateVariantWorkadductbiological systemscytokineeditorialepigenomicsflexibilityindexingmacromoleculemembermetabolomicsmicrobiomereceptorresponsetelomereworking group
中文摘要
生物反应资源(BRR)将研究外源和内源的相互作用
化学物质与我们的生物分子相互作用,因为它们是产生生物效应所必需的。其中一个
包括生物反应在内的最重要和最实际的原因是,绝大多数接触
都是短暂的。几周前、几个月前或几年前暴露的化学物质早已不复存在
从身体上。然而,这些过去的化学暴露往往会留下它们存在的分子指纹。
无论是DNA损伤,表观遗传修饰,还是蛋白质加合物形成,生物指纹
或许能够提供这些过去的短暂曝光的信息。如果没有具体包含
在曝光组的工作定义中,曝露的生物影响我们无法评估
在生物学水平上的先前暴露。生物响应资源BRR的总体目标是提供
专业知识和获得一套经过验证的生物反应测量方法。为了最大限度地提供
为了给潜在用户提供灵活性,我们的BRR提供了从基因组和
表观基因组提供氧化还原状态的测量、细胞因子的产生和途径分析。目标将是
通过下列目标进行追求:目标1.教育调查人员有关生物的益处
提供分析方法并协助研究设计和样品优化。目标2.提供最先进的
评估暴露在人类基因组上的生物效应和易感性的测量。
目标3.提供各种其他生物反应指数,如综合
氧化还原状态的简档、多重细胞因子评估和微生物组特征。目标4.达到
与非目标研究资源协作,以确定可测量的生物反应
非靶向(代谢组学)分析的一部分。目标5.与发展研究对接
资源和有针对性的研究资源,以确定与
具体的曝光。生物响应资源将与CHEAR客户、Neale同事和
整个CHEAR网络,以开发可靠和可重复的环境诱导指数
生物系统的扰动。
英文摘要
The Biological Response Resource (BRR) will examined the interactions of exogenous and endogenous
chemicals with our biological molecules as they are necessary for there to be a biological effect. One of the
most important and practical reasons to include the biological response is that the vast majority of exposures
are transient. The chemicals underlying exposures that occurred weeks, months, or years ago are long gone
from the body. However, these past chemical exposures often leave molecular fingerprints of their presence.
Whether this be damaged DNA, epigenetic modification, or protein adduct formation, the biological fingerprints
may be able to provide information of these transient exposures of the past. Without the specific inclusion of
the biological impact of exposures in the working definition of the exposome we are left with no way to assess
prior exposures at a biological level. The overall goal of the Biological Response Resource BRR is to provide
expertise and access to a suite of validated measures of biological responses. In order to offer maximal
flexibility to potential users, our BRR is offering a wide array of assays that range from genomic and
epigenomic offerings to measures of redox status, cytokine production, and pathway analysis. The goal will be
pursued through the following objectives: Objective 1. To educate investigators on the benefits of biological
assays available and assist in study design and sample optimization. Objective 2. To provide state-of-the-art
measurements that assess the biological effects of, and susceptibility to, exposures on the human genome.
Objective 3. To provide access to a variety of other indices of biological response, such as comprehensive
profiling of redox state, multiplexed cytokine assessment, and microbiome characterization. Objective 4. To
collaborate with the Untargeted Research Resource to identify biological responses that can be measured as
part of the untargeted (metabolomics) analysis. Objective 5. To interface with the Developmental Research
Resource and the Targeted Research Resource to identify biological markers which are highly associated with
specific exposures. The Biological Response Resource will work with CHEAR clients, NEALE colleagues, and
the entire CHEAR network to develop reliable and reproducible indices of environmentally-induced
perturbations of biological systems.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Vesicular Modulation of Dopamine Neuron Toxicity
-
批准号:9899567
-
项目类别:
-
资助金额:$40.89万
-
财政年份:2019
-
负责人:GARY W MILLER
-
依托单位:
Vesicular modulation of dopamine neuron toxicity
-
批准号:10210836
-
项目类别:
-
资助金额:$47.27万
-
财政年份:2014
-
负责人:GARY W MILLER
-
依托单位:
Vesicular modulation of dopamine neuron toxicity
-
批准号:9182820
-
项目类别:
-
资助金额:$34.85万
-
财政年份:2014
-
负责人:GARY W MILLER
-
依托单位:
Vesicular modulation of dopamine neuron toxicity
-
批准号:10374123
-
项目类别:
-
资助金额:$47.21万
-
财政年份:2014
-
负责人:GARY W MILLER
-
依托单位:
Vesicular modulation of dopamine neuron toxicity
-
批准号:9522240
-
项目类别:
-
资助金额:$2.44万
-
财政年份:2014
-
负责人:GARY W MILLER
-
依托单位:
Vesicular modulation of dopamine neuron toxicity
-
批准号:10540378
-
项目类别:
-
资助金额:$47.16万
-
财政年份:2014
-
负责人:GARY W MILLER
-
依托单位:
HERCULES: Health and Exposome Research Center at Emory
-
批准号:8838788
-
项目类别:
-
资助金额:$119.39万
-
财政年份:2013
-
负责人:GARY W MILLER
-
依托单位:
HERCULES: Health and Exposome Research Center at Emory
-
批准号:8736105
-
项目类别:
-
资助金额:$19.39万
-
财政年份:2013
-
负责人:GARY W MILLER
-
依托单位:
HERCULES: Health and Exposome Research Center at Emory
-
批准号:8427490
-
项目类别:
-
资助金额:$94.75万
-
财政年份:2013
-
负责人:GARY W MILLER
-
依托单位:
HERCULES: Health and Exposome Research Center at Emory
-
批准号:9070868
-
项目类别:
-
资助金额:$29.91万
-
财政年份:2013
-
负责人:GARY W MILLER
-
依托单位:
ADMINISTRATIVE CORE
-
批准号:8294765
-
项目类别:
-
资助金额:$13.72万
-
财政年份:2011
-
负责人:GARY W MILLER
-
依托单位:
PROGRAM AS INTEGRATED EFFORT - Research Development Core
-
批准号:8294764
-
项目类别:
-
资助金额:$9.48万
-
财政年份:2011
-
负责人:GARY W MILLER
-
依托单位:
PROJECT 1: EMORY PARKINSON'S DISEASE COLLABORATIVE ENVIRONMENTAL RESEARCH CENTER
-
批准号:8294760
-
项目类别:
-
资助金额:$37.16万
-
财政年份:2011
-
负责人:GARY W MILLER
-
依托单位:
ADMINISTRATIVE CORE
-
批准号:8099778
-
项目类别:
-
资助金额:$68.01万
-
财政年份:2010
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:7687587
-
项目类别:
-
资助金额:$130.15万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:8099779
-
项目类别:
-
资助金额:$126.21万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:8294766
-
项目类别:
-
资助金额:$130.67万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:8099234
-
项目类别:
-
资助金额:$7.74万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:8099324
-
项目类别:
-
资助金额:$11.63万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
Emory Parkinson's Disease Collaborative Environmental Research Center
-
批准号:8433593
-
项目类别:
-
资助金额:$2.27万
-
财政年份:2008
-
负责人:GARY W MILLER
-
依托单位:
国内基金
海外基金
登录
查看更多内容
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:32170319
-
项目类别:面上项目
-
资助金额:58.00万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:--
-
项目类别:--
-
资助金额:58万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
ID1 (Inhibitor of DNA binding 1) 在口蹄疫病毒感染中作用机制的研究
-
批准号:31672538
-
项目类别:面上项目
-
资助金额:62.0万元
-
批准年份:2016
-
负责人:孙跃峰
-
依托单位:
番茄EIN3-binding F-box蛋白2超表达诱导单性结实和果实成熟异常的机制研究
-
批准号:31372080
-
项目类别:面上项目
-
资助金额:80.0万元
-
批准年份:2013
-
负责人:杨迎伍
-
依托单位:
P53 binding protein 1 调控乳腺癌进展转移及化疗敏感性的机制研究
-
批准号:81172529
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2011
-
负责人:杨其峰
-
依托单位:
DBP(Vitamin D Binding Protein)在多发性硬化中的作用和相关机制的蛋白质组学研究
-
批准号:81070952
-
项目类别:面上项目
-
资助金额:35.0万元
-
批准年份:2010
-
负责人:刘师莲
-
依托单位:
研究EB1(End-Binding protein 1)的癌基因特性及作用机制
-
批准号:30672361
-
项目类别:面上项目
-
资助金额:24.0万元
-
批准年份:2006
-
负责人:徐宁志
-
依托单位: