Facility Core D: Biomarkers
Facility Core D: Biomarkers
批准号:
7529648
负责人:
Angeline Sanderson Andrew
金额:
$34.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Adverse effectsAreaArsenicBasic ScienceBioinformaticsBioinformatics Shared ResourceBiologicalBiological AssayBiological MarkersBiological ProcessCollaborationsComet AssayCore FacilityDNA RepairDataData AnalysesDevelopmentEnzyme-Linked Immunosorbent AssayEnzymesEquipmentExperimental DesignsExposure toGene ProteinsGenerationsGenomicsGoalsImmunoblottingImmunohistochemistryIndividualInvestmentsMethodologyMicroarray AnalysisMicroarray Shared ResourceMissionMolecularMolecular BiologyMolecular EpidemiologyNumbersPathway interactionsPolymerase Chain ReactionPopulationPredispositionPreparationProcessProgram Research Project GrantsProteinsProteomicsRNAReagentResearchResearch PersonnelResourcesRoleSamplingScreening procedureTechnical ExpertiseTimeToxicant exposureToxicogenomicsValidationWorkcostdata managementfield studyfollow-upinterestmedical specialtiesprogramsprotein expressionresponsetooltoxic metaltoxicant
中文摘要
毒理基因组学和蛋白质组学工具使研究人员能够快速筛选大细胞中的表达变化,
许多基因和蛋白质对有毒物质的暴露作出反应,从而能够有效地识别
暴露、生物效应和/或易感性的潜在分子生物标志物。但调查人员
传统上,他们的研究集中在特定分子途径中预先存在的假设上。
许多研究人员缺乏试剂、时间、生物信息学工具和技术专长来存储、管理、
分析、确认和跟踪通过毒理基因组学和蛋白质组学分析观察到的令人兴奋的变化,
生物学途径是他们的先验假设或专业领域之外。的主要作用
达特茅斯超级基金基础研究计划(SBRP)的一个新的生物标志物核心(核心D)将协助
SBRP研究人员使用这些毒理基因组学和蛋白质组学工具来识别潜在的分子
暴露、生物效应和/或易感性的生物标志物。我们将协助该计划的研究人员,
利用核心A(分子生物学和蛋白质组学核心)以及达特茅斯微阵列,
生物信息学共享资源为他们的个人项目。目标将是协助调查人员
这SBRP计划在实现其科学项目的具体目标,在最有效的,
在毒理基因组学、毒理蛋白质组学和生物标志物开发领域的生产方式,
应用程序.核心小组还将协助开发、验证和应用新的方法
可以用来评估暴露的功能效应。这些生物标志物可以应用于基础
机制研究或在分子流行病学和生态毒理学领域的研究,
与接触砷和其他有毒金属有关的影响。
英文摘要
Toxicogenomic and proteomic tools allow investigators to rapidly screen for expression changes in large
numbers of genes and proteins in response to toxicant exposures that enable efficient identification of
potential molecular biomarkers of exposure, biological effect, and/or susceptibility. However, investigators
have traditionally focused their research on pre-existing hypotheses within a specific molecular pathway.
Many researchers lack the reagents, time, bioinformatics tools, and technical expertise to store, manage,
analyze, confirm and follow-up on exciting changes observed through toxicogenomic and proteomic assays in
biological pathways that are outside of their a priori hypotheses or specialty areas. The principal role of the
new Biomarkers Core (Core D) of the Dartmouth Superfund Basic Research Program (SBRP) will be to assist
SBRP researchers in using these toxicogenomic and proteomic tools to identify potential molecular
biomarkers of exposure, biological effect, and/or susceptibility. We will assist the program's researchers in
utilizing Core A (Molecular Biology & Proteomics Core) as well as the Dartmouth Microarray and
Bioinformatics Shared Resources for their individual projects. The goal will be to assist the investigators of
this SBRP program in accomplishing the specific aims of their scientific projects in the most efficient and
productive manner in the area of toxicogenomics, toxicoproteomics and biomarkers development and
application. The Core will also assist in the development, validation and application of new methodologies
that can be used to assess the functional effects of exposures. These biomarkers can then be applied in basic
mechanistic studies or in molecular epidemiology and ecotoxicology field studies examining the adverse
effects associated with exposure to arsenic and other toxic metals.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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MicroRNA dysregulation and bladder cancer prognosis
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EGFR PATHWAY ALTERATIONS IN LUNG TUMORS
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EGFR PATHWAY ALTERATIONS IN LUNG TUMORS
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Comprehensive Assessment of Bladder Cancer Genetic Susceptibility
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依托单位:
Bladder Cancer Prognostic Indicators
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资助金额:$14.42万
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依托单位:
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财政年份:2005
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资助金额:$10.47万
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财政年份:2005
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依托单位:
Bladder Cancer Prognostic Indicators
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批准号:7113825
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资助金额:$14.26万
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财政年份:2005
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依托单位:
Bladder Cancer Prognostic Indicators
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批准号:7680246
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项目类别:
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资助金额:$14.42万
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依托单位:
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资助金额:$7.9万
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依托单位:
DNA Repair and Bladder Cancer
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资助金额:$7.9万
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财政年份:2003
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财政年份:--
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