Molecular Detection and Diagnostics Core
分子检测和诊断核心
基本信息
- 批准号:10664051
- 负责人:
- 金额:$ 17.38万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-03-10 至 2027-06-30
- 项目状态:未结题
- 来源:
- 关键词:APOL1 geneAddressAnalytical ChemistryBasic ScienceBiochemistryBiologyBiomedical EngineeringBiosensorBiotechnologyBlood PressureCardiometabolic DiseaseCellsCenters of Research ExcellenceChronicChronic DiseaseChronic Kidney FailureClinical ResearchClinical SciencesCollaborationsCommunicable DiseasesComplexConsultationsCore FacilityDetectionDevelopmentDiagnosisDiagnosticDiseaseDisease ProgressionDoctor of PhilosophyEarly DiagnosisEtiologyEvaluationExperimental DesignsFutureGenetic MarkersGoalsHuman ResourcesImageImmuneIndividualInfrastructureInstitutionIntakeInterdisciplinary StudyKnowledgeLouisianaMass Spectrum AnalysisMethodologyMethodsMolecularMolecular AnalysisMolecular BiologyMolecular DiagnosisMonitorNanotechnologyOverweightPathologicPhasePilot ProjectsPopulation SciencesPotassiumPreventionProcessProteomeProteomicsResearchResearch InfrastructureResearch PersonnelResearch Project GrantsResearch SupportSamplingServicesTechnologyTissuesTrainingTranslational ResearchUniversitiesWhole OrganismX Inactivationanalytical methodbiomarker discoverybiophysical techniquesblood pressure reductioncareer developmentearly detection biomarkersempowermentexperienceinnovationinnovative technologiesinstrumentinstrumentationmolecular diagnosticsmolecular markernovelnovel markerorgan on a chippersonalized diagnosticspersonalized medicinepoint of care testingprofessorprognosticprogramsreal time monitoringresearch and developmentscreeningsingle cell analysisskillsspecific biomarkerssustainable resourcesynergismtreatment response
项目摘要
PROJECT SUMMARY/ABSTRACT (Molecular Detection and Diagnostics Core)
The Tulane COBRE for Clinical and Translational Research in Cardiometabolic Diseases Phase 2 application
aims to further develop and strengthen the clinical and translational research infrastructure at Tulane University
and to continuously expand and support a critical mass of investigators with expertise in clinical and translational
research in cardiometabolic diseases. The newly proposed Molecular Detection and Diagnostics Core (MDDC)
will support the Research Project Leaders (RPLs), Pilot Project Leaders (PPLs), other COBRE investigators and
collaborators at Tulane University by providing cutting-edge instruments, innovative technologies and
methodologies, and expertise in multidisciplinary research including biochemistry, biomedical engineering,
analytical chemistry, proteomics, nanotechnology, and mass spectrometry (MS) to advance their clinical and
translational research in the etiology, prevention, diagnosis, and treatment of cardiometabolic disease. The
MDDC will develop and adapt integrated nanotechnology-based strategies and other innovative technologies to
identify novel biomarkers for early disease detection, prognostic evaluation, and the real-time monitoring of
treatment responses as well as to understand the molecular mechanisms of cardiometabolic disease. The MDDC
seeks to catalyze research that spans the analytical chemistry-biology interface, empowering investigators to
identify and solve important interdisciplinary research questions in the clinical and translational sciences of
cardiometabolic disease. Based on our team's expertise, the MDDC will provide COBRE investigators with
training and services in state-of-the-art analytical technologies such as MS and microarray-based proteomics
and organ-on-a-chip, among others, for the analysis of complex proteomes of tissue and biofluid samples. The
MDDC will also identify appropriate existing analytical methods as well as adapt newly developed methods, often
not available in the form of mature technologies. The MDDC will be housed within the Tulane University Center
for Cellular and Molecular Diagnostics, which has been well established for infectious and chronic disease
research. During the COBRE Phase 2, the MDDC will provide cutting-edge instruments and methodological
support for RPLs of Projects 2 and 3 to conduct their individual research projects. In addition, the MDDC will
provide expert consultation and state-of-the-art technologies for RPLs of Projects 1 and 4 to develop R01
applications to further investigate molecular mechanism of APOL1 on chronic kidney disease progression and
potassium intake on blood pressure reduction. The proposed MDDC will enhance the interactions and
collaborations among COBRE, non-COBRE and external investigators involved in molecular studies of
cardiometabolic disease. Since the MDDC is a critical component of the COBRE program, our long-term goal is
to grow MDDC into a sustainable resource that serves all phases of translational research, from basic science
to clinical science to population science at Tulane University by providing a broad range of state-of-the-art cellular
and molecular analytical services.
项目摘要/摘要(分子检测和诊断核心)
杜兰大学 COBRE 心脏代谢疾病临床和转化研究 2 期应用
旨在进一步发展和加强杜兰大学的临床和转化研究基础设施
并不断扩大和支持大量具有临床和转化专业知识的研究人员
心脏代谢疾病研究。新提出的分子检测和诊断核心(MDDC)
将支持研究项目负责人 (RPL)、试点项目负责人 (PPL)、其他 COBRE 研究人员和
杜兰大学的合作者提供尖端仪器、创新技术和
多学科研究的方法论和专业知识,包括生物化学、生物医学工程、
分析化学、蛋白质组学、纳米技术和质谱 (MS) 来推进其临床和
心脏代谢疾病的病因学、预防、诊断和治疗的转化研究。这
MDDC 将开发和调整基于纳米技术的综合战略和其他创新技术,以
识别用于早期疾病检测、预后评估和实时监测的新型生物标志物
治疗反应以及了解心脏代谢疾病的分子机制。 MDDC
寻求促进跨越分析化学-生物学界面的研究,使研究人员能够
识别并解决临床和转化科学中重要的跨学科研究问题
心脏代谢疾病。根据我们团队的专业知识,MDDC 将为 COBRE 调查人员提供
最先进的分析技术(例如 MS 和基于微阵列的蛋白质组学)的培训和服务
和器官芯片等,用于分析组织和生物流体样品的复杂蛋白质组。这
MDDC 还将确定适当的现有分析方法并采用新开发的方法,通常
无法以成熟技术的形式提供。 MDDC 将设在杜兰大学中心内
用于细胞和分子诊断,已在传染病和慢性疾病方面得到了很好的应用
研究。在 COBRE 第 2 阶段期间,MDDC 将提供尖端工具和方法论
支持项目 2 和 3 的 RPL 开展各自的研究项目。此外,MDDC 将
为项目1和4的RPL提供专家咨询和最先进的技术来开发R01
应用进一步研究APOL1对慢性肾脏病进展的分子机制和
钾摄入量对血压的降低。拟议的 MDDC 将加强互动和
COBRE、非 COBRE 和参与分子研究的外部研究人员之间的合作
心脏代谢疾病。由于 MDDC 是 COBRE 计划的重要组成部分,因此我们的长期目标是
将 MDDC 发展成为一个可持续的资源,服务于从基础科学到转化研究的各个阶段
杜兰大学通过提供广泛的最先进的细胞研究,从临床科学到人口科学
和分子分析服务。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Tony Y. Hu其他文献
Serum-Based Diagnosis of Pediatric Tuberculosis by Assay of Mycobacterium tuberculosis Factors: a Retrospective Cohort Study
通过结核分枝杆菌因子测定对小儿结核病进行血清诊断:一项回顾性队列研究
- DOI:
- 发表时间:
2020 - 期刊:
- 影响因子:9.4
- 作者:
Yifan He;Christopher J. Lyon;D. Nguyen;Chang Liu;W. Sha;E. Graviss;Tony Y. Hu - 通讯作者:
Tony Y. Hu
Microsoft Word-pbaa041.docx
Microsoft Word-pbaa041.docx
- DOI:
10.1038/leu.2014.102 - 发表时间:
2020 - 期刊:
- 影响因子:11.4
- 作者:
Xuerong Chen;Tony Y. Hu - 通讯作者:
Tony Y. Hu
IP-MS Analysis of ESX-5 and ESX-1 Substrates Enables Mycobacterial Species Identification
ESX-5 和 ESX-1 底物的 IP-MS 分析可实现分枝杆菌菌种鉴定
- DOI:
- 发表时间:
2020 - 期刊:
- 影响因子:0
- 作者:
Qingbo Shu;Meena U Rajagopal;Jia Fan;Lingpeng Zhan;Xiangxing Kong;Yifan He;Suwatchareeporn Rotcheewaphan;Christopher J. Lyon;W. Sha;A. Zelazny;Tony Y. Hu - 通讯作者:
Tony Y. Hu
2D metal carbides and nitrides (MXenes) for sensors and biosensors.
用于传感器和生物传感器的二维金属碳化物和氮化物 (MXene)。
- DOI:
10.1016/j.bios.2021.113943 - 发表时间:
2022-01-01 - 期刊:
- 影响因子:12.6
- 作者:
S. Alwarappan;N. Nesakumar;Da;Tony Y. Hu;Chen - 通讯作者:
Chen
Monocrystalline Labeling Enables Stable Plasmonic Enhancement for Isolation-Free Extracellular Vesicle Analysis.
单晶标记可实现稳定的等离子体增强,用于免分离的细胞外囊泡分析。
- DOI:
10.1002/smll.202204298 - 发表时间:
2022-11-10 - 期刊:
- 影响因子:13.3
- 作者:
Shu Wang;Wenshu Zheng;Ruixuan Wang;Lili Zhang;Li Yang;Tao Wang;Julian G. Saliba;Sutapa Ch;ra;ra;Chen;Christopher J. Lyon;Tony Y. Hu - 通讯作者:
Tony Y. Hu
Tony Y. Hu的其他文献
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{{ truncateString('Tony Y. Hu', 18)}}的其他基金
Multiplexed detection of cell-free M. Tuberculosis DNA and its drug-resistant variants in blood
血液中无细胞结核分枝杆菌 DNA 及其耐药变异体的多重检测
- 批准号:
10639855 - 财政年份:2023
- 资助金额:
$ 17.38万 - 项目类别:
A nanopore biosensor for leveling Mtb antigens in blood
用于平衡血液中 Mtb 抗原的纳米孔生物传感器
- 批准号:
10646134 - 财政年份:2022
- 资助金额:
$ 17.38万 - 项目类别:
Quantification of brain-derived extracellular vesicle microRNAs in blood by a liposome-mediated CRISPR assay for traumatic brain injury detection
通过脂质体介导的 CRISPR 测定对血液中脑源性细胞外囊泡 microRNA 进行定量,用于检测创伤性脑损伤
- 批准号:
10575436 - 财政年份:2022
- 资助金额:
$ 17.38万 - 项目类别:
Digital Nanoplasmonic Quantification of Tumor-derived Extracellular Vesicles in Plasma Microsamples
血浆微样品中肿瘤源性细胞外囊泡的数字纳米等离子体定量
- 批准号:
10461970 - 财政年份:2020
- 资助金额:
$ 17.38万 - 项目类别:
Digital Nanoplasmonic Quantification of Tumor-derived Extracellular Vesicles in Plasma Microsamples
血浆微样品中肿瘤源性细胞外囊泡的数字纳米等离子体定量
- 批准号:
10684737 - 财政年份:2020
- 资助金额:
$ 17.38万 - 项目类别:
Digital Nanoplasmonic Quantification of Tumor-derived Extracellular Vesicles in Plasma Microsamples
血浆微样品中肿瘤源性细胞外囊泡的数字纳米等离子体定量
- 批准号:
10269902 - 财政年份:2020
- 资助金额:
$ 17.38万 - 项目类别:
Digital Nanoplasmonic Quantification of Tumor-derived Extracellular Vesicles in Plasma Microsamples
血浆微样品中肿瘤源性细胞外囊泡的数字纳米等离子体定量
- 批准号:
10684737 - 财政年份:2020
- 资助金额:
$ 17.38万 - 项目类别:
Direct quantitation of the circulating Mtb-peptidome for pediatric TB management
直接定量循环 Mtb 肽组用于儿科结核病管理
- 批准号:
9333558 - 财政年份:2017
- 资助金额:
$ 17.38万 - 项目类别:
Detecting pathogen and host factors on extracellular vesicles for pediatric TB diagnosis and management
检测细胞外囊泡上的病原体和宿主因子,用于儿童结核病的诊断和管理
- 批准号:
10753281 - 财政年份:2017
- 资助金额:
$ 17.38万 - 项目类别:
Multiplexed quantification of circulating peptidomic signatures for EBOLA early diagnosis
用于埃博拉早期诊断的循环肽组特征的多重定量
- 批准号:
9387209 - 财政年份:2017
- 资助金额:
$ 17.38万 - 项目类别:
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