Molecular Cell and Analyitical Services Facility Core
Molecular Cell and Analyitical Services Facility Core
批准号:
9040176
负责人:
Max Costa
金额:
$14.98万
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:
已结题
起止时间:
至 2017-05-31
关键词:
Air PollutionApoptosisBioinformaticsBiological AssayCandidate Disease GeneCarcinogensCell CycleCellsCellular biologyConsultationsCore FacilityCulture MediaDNADNA MethylationDNA SequenceDataDiseaseDocumentationDoseEducationEducational workshopEmerging TechnologiesEnvironmentEnvironmental ExposureEnvironmental HealthEpigenetic ProcessEquipmentEvolutionFlow CytometryFluorescenceFluorescence Resonance Energy TransferFundingFunding AgencyGelGene ExpressionGenesGenomeGenomicsHealthHousingHumanHuman GenomeImageryImmune responseMetalsMethodologyMethylationMicroscopyMolecularMolecular BiologyMolecular Biology TechniquesOrganismOzoneParticulatePathway AnalysisPathway interactionsPlayPreparationPreventive InterventionReagentResearchResearch PersonnelResearch SupportResourcesRoentgen RaysRoleSentinelServicesSignal PathwaySignal TransductionSiteTechniquesTechnologyTestingTherapeutic InterventionTimeTissuesToxic Environmental SubstancesTrainingTraining and EducationWorkYeastsabsorptionbiomarker discoverycost efficientdesigndiscountenvironmental agentenvironmental stressorepigenetic regulationepigenomeepigenomicsfetal bovine serumgene environment interactioninstrumentinterdisciplinary approachmammalian genomememberpredictive markerprotein expressionpyrosequencingresearch studyresponsestatisticstissue culturetooltranscriptometranscriptome sequencingtrendwhole genome
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The overall objective of the Molecular Cell and Analytical Services Facility Core (MCASFC) is to provide
Center members with education on, and access to, state-of-the-art tools for assessing the effects of the
environment on human and mammalian genomes and epigenomes. The Core also provides analytical
services, particularly those for metals analysis in cells and tissues of exposed organisms, since metal effects
on the genome and epigenome are specialized research strengths of the Center. The rationale for, and
continuing evolution of, this Core reflects current trends in environmental health research, and in particular the
rapidly changing field of gene x environment interactions. Functionally important, dose-related perturbations to
human health from environmental stressors (e.g. metals, carcinogens, air pollution particulates) are being
actively analyzed by Center researchers who study changes in gene expression, epigenetic regulation at
candidate gene and whole genome levels, cell cycle perturbations, protein expression and signaling pathway
interactions. The MCASFC supports Center investigators' funded studies using genomics and epigenomics to
identify biomarkers and predictive sentinels of toxic challenges to health, as well as to identify targets for
preventive and therapeutic interventions. One new initiative implemented in 2008 and overseen by this core is
the collaborative yeast screen project involving analysis of global gene expression changes induced by metals
and ozone. This new project, supported in part by the Center Director's fund, involved multiple Center
investigators with Dr. Thomas Begley at the GeNYsis Center in Albany, NY. It has become increasingly
evident that the epigenome plays an enormous role in modulating the responses of organisms to
environmental exposures. Thus, other new initiatives that have developed for this Core since the last renewal
are the incorporation of ChlP-Chip, ChlP-Seq and RNA-Seq for epigenetic and transcriptome biomarker
discovery and for investigating mechanisms underlying toxic and disease responses to environmental agents.
Research on genome/epigenome x environment interactions requires multidisciplinary approaches and
utilization of highly sensitive molecular techniques supported by state-of-the-art instruments and emerging
technologies. The MCASFC provides Center investigators with evolving access to specialized methodologies
and equipment, either on-site or off-site, by taking advantage of regional resources involving intra- and interuniversity
research partnerships. The MCASFC acquires new equipment as deemed necessary, by continuing
to leverage funds from competitive and institutional funding sources. Furthermore, since genome/epigenome
studies require considerable training prior to implementation, the Facility Core provides Center investigators
with consultation services on the uses, applications, limitations and challenges ofthe latest techniques.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Persistent transcriptional changes induced by nickel through epigenetic alterations
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批准号:10077549
-
项目类别:
-
资助金额:$42.21万
-
财政年份:2020
-
负责人:Max Costa
-
依托单位:
Persistent transcriptional changes induced by nickel through epigenetic alterations
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批准号:9899647
-
项目类别:
-
资助金额:$45.4万
-
财政年份:2020
-
负责人:Max Costa
-
依托单位:
Persistent transcriptional changes induced by nickel through epigenetic alterations
-
批准号:10515635
-
项目类别:
-
资助金额:$41.39万
-
财政年份:2020
-
负责人:Max Costa
-
依托单位:
Persistent transcriptional changes induced by nickel through epigenetic alterations
-
批准号:10294236
-
项目类别:
-
资助金额:$42.16万
-
财政年份:2020
-
负责人:Max Costa
-
依托单位:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
-
批准号:10470848
-
项目类别:
-
资助金额:$39.9万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
MEG3 deletion drives lung tumorigenesis due to environmental nickel exposure
-
批准号:9852426
-
项目类别:
-
资助金额:$27.75万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Arsenic carcinogenesis and disruption of histone variant H3.3 assembly
-
批准号:10407027
-
项目类别:
-
资助金额:$54.15万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
-
批准号:10004646
-
项目类别:
-
资助金额:$41.77万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Arsenic carcinogenesis and disruption of histone variant H3.3 assembly
-
批准号:10631227
-
项目类别:
-
资助金额:$52.99万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
-
批准号:10681242
-
项目类别:
-
资助金额:$39.3万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Arsenic and Nickel Carcinogenesis in Human Lung Cells
-
批准号:10245059
-
项目类别:
-
资助金额:$40.1万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
MEG3 deletion drives lung tumorigenesis due to environmental nickel exposure
-
批准号:10357729
-
项目类别:
-
资助金额:$56.03万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
MEG3 deletion drives lung tumorigenesis due to environmental nickel exposure
-
批准号:10579842
-
项目类别:
-
资助金额:$54.87万
-
财政年份:2019
-
负责人:Max Costa
-
依托单位:
Epigenetic Stress and Chromate Carcinogenesis
-
批准号:10165716
-
项目类别:
-
资助金额:$46.6万
-
财政年份:2018
-
负责人:Max Costa
-
依托单位:
Epigenetic Stress and Chromate Carcinogenesis
-
批准号:10406986
-
项目类别:
-
资助金额:$46.1万
-
财政年份:2018
-
负责人:Max Costa
-
依托单位:
SESN2 and therapeutic effect of Isohapontigenin (ISO)
-
批准号:10265326
-
项目类别:
-
资助金额:$42.21万
-
财政年份:2018
-
负责人:Max Costa
-
依托单位:
SESN2 and therapeutic effect of Isohapontigenin (ISO)
-
批准号:10450132
-
项目类别:
-
资助金额:$41.36万
-
财政年份:2018
-
负责人:Max Costa
-
依托单位:
Epigenetic Stress and Chromate Carcinogenesis
-
批准号:9768470
-
项目类别:
-
资助金额:$49.05万
-
财政年份:2018
-
负责人:Max Costa
-
依托单位:
Arsenic Carcinogenesis and Interference With Histone mRNA
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批准号:8997324
-
项目类别:
-
资助金额:$38.14万
-
财政年份:2016
-
负责人:Max Costa
-
依托单位:
SATB2 and Nickel Carcingenesis
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批准号:8685083
-
项目类别:
-
资助金额:$38.14万
-
财政年份:2014
-
负责人:Max Costa
-
依托单位:
国内基金
海外基金
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项目类别:省市级项目
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Apoptosis signal-regulating kinase 1是七氟烷抑制小胶质细胞活化的关键分子靶点?
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批准年份:1995
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