Administrative supplement to Duke G20 award

杜克大学G20奖的行政补充

基本信息

  • 批准号:
    10626469
  • 负责人:
  • 金额:
    $ 326.48万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-09-23 至 2025-02-28
  • 项目状态:
    未结题

项目摘要

Project Summary/Abstract: The Duke Regional Biocontainment Laboratory (RBL) was constructed with funding from the National Institutes of Health (NIH) to support basic research necessary to develop drugs, diagnostics, and vaccines for emerging/reemerging infections and biodefense. The state-of-the-art biocontainment facility, designed to support lab and small animal research, was fully commissioned and opened for operation in 2007 on the Duke University Medical School Campus in Durham, NC. The Duke RBL facility supports grant/contract-funded investigators and also provides biocontainment labs, innovative host monitoring assays and small animal models through Core Service Center Units on a cost recovery basis. Fourteen years of use and time have rendered some of the Duke RBL facilities, systems and critical core research equipment obsolete, or in need of repair, replacement or modernization. Since award of the parent G20 we have identified additional critical deficiencies of the facility’s existing physical infrastructure that limit biosafety, security or threaten the provision of services it offers and research-related activities it supports. We will address these additional deficiencies through this supplement funding in our three original Specific Aims: 1) Modernize Building Control Systems – Replace and upgrade obsolete air compressor and the BACNet (Building Automation Control Network); 2) Modernize Biosafety and Security Systems - Replace aged/damaged PAPR units; and 3) Modernize Research Resources – Replace or add additional major equipment to the Duke RBL Research Service Cores - liquid handling automation equipment, ELISpot reader, next-generation Luminex reader, upgraded cell counter, replacement incubators, freezers and centrifuges, advanced fluorescence microscopy capability in BSL3, additional Allentown Biocontainment mouse caging, and live animal imaging with micro CT capability. These Aims/Goals will be accomplished by the highly integrated project management team assembled in the parent award with solid institutional support and trusted contractors/vendors that were part of the original design and construction of the facility.
项目总结/文摘:

项目成果

期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A Virion-Based Combination Vaccine Protects against Influenza and SARS-CoV-2 Disease in Mice.
  • DOI:
    10.1128/jvi.00689-22
  • 发表时间:
    2022-08-10
  • 期刊:
  • 影响因子:
    5.4
  • 作者:
  • 通讯作者:
H3N2 influenza hemagglutination inhibition method qualification with data driven statistical methods for human clinical trials.
  • DOI:
    10.3389/fimmu.2023.1155880
  • 发表时间:
    2023
  • 期刊:
  • 影响因子:
    7.3
  • 作者:
  • 通讯作者:
Targeted dose delivery of Mycobacterium tuberculosis in mice using silicon antifoaming agent via aerosol exposure system.
  • DOI:
    10.1371/journal.pone.0276130
  • 发表时间:
    2022
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
  • 通讯作者:
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Colin S. Duckett其他文献

Letter to the Editor: The C-terminal Domain of Viral IAP Associated Factor (cVIAF) is a Structural Homologue of Phosducin: Resonance Assignments and Secondary Structure of the C-Terminal Domain of VIAF
  • DOI:
    10.1023/b:jnmr.0000013820.43366.99
  • 发表时间:
    2004-02-01
  • 期刊:
  • 影响因子:
    1.900
  • 作者:
    Jaison Jacob;John M. Louis;B.W.M. Richter;Colin S. Duckett;Dennis A. Torchia
  • 通讯作者:
    Dennis A. Torchia
IAP proteins: blocking the road to death's door
IAP 蛋白:阻挡通往死亡之门的道路
Cloning of an NF-κB subunit which stimulates HIV transcription in synergy with p65
一种与 p65 协同刺激 HIV 转录的 NF-κB 亚基的克隆
  • DOI:
    10.1038/352733a0
  • 发表时间:
    1991-08-22
  • 期刊:
  • 影响因子:
    48.500
  • 作者:
    Roland M. Schmid;Neil D. Perkins;Colin S. Duckett;Philip C. Andrews;Gary J. Nabel
  • 通讯作者:
    Gary J. Nabel

Colin S. Duckett的其他文献

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{{ truncateString('Colin S. Duckett', 18)}}的其他基金

Resources and Workforce Development for the Regional Biocontainment Laboratories
区域生物防护实验室的资源和劳动力发展
  • 批准号:
    10791947
  • 财政年份:
    2023
  • 资助金额:
    $ 326.48万
  • 项目类别:
Core 1: Facility Management, Maintenance and Operations Core
核心 1:设施管理、维护和运营核心
  • 批准号:
    10791948
  • 财政年份:
    2023
  • 资助金额:
    $ 326.48万
  • 项目类别:
Core 3: Biocontainment Research Support Services Core
核心 3:生物防护研究支持服务核心
  • 批准号:
    10791950
  • 财政年份:
    2023
  • 资助金额:
    $ 326.48万
  • 项目类别:
Regional Biocontainment Laboratories Facility and Building System Upgrades Support
区域生物防护实验室设施和建筑系统升级支持
  • 批准号:
    10392181
  • 财政年份:
    2021
  • 资助金额:
    $ 326.48万
  • 项目类别:
Signal Transduction Pathways in CD30-positive Lymphomas
CD30 阳性淋巴瘤的信号转导途径
  • 批准号:
    8109947
  • 财政年份:
    2010
  • 资助金额:
    $ 326.48万
  • 项目类别:
Signal Transduction Pathways in CD30-positive Lymphomas
CD30 阳性淋巴瘤的信号转导途径
  • 批准号:
    8403989
  • 财政年份:
    2010
  • 资助金额:
    $ 326.48万
  • 项目类别:
Signal Transduction Pathways in CD30-positive Lymphomas
CD30 阳性淋巴瘤的信号转导途径
  • 批准号:
    7984372
  • 财政年份:
    2010
  • 资助金额:
    $ 326.48万
  • 项目类别:
Signal Transduction Pathways in CD30-positive Lymphomas
CD30 阳性淋巴瘤的信号转导途径
  • 批准号:
    8204634
  • 财政年份:
    2010
  • 资助金额:
    $ 326.48万
  • 项目类别:
Signal Transduction Pathways in CD30-positive Lymphomas
CD30 阳性淋巴瘤的信号转导途径
  • 批准号:
    8589578
  • 财政年份:
    2010
  • 资助金额:
    $ 326.48万
  • 项目类别:
Control of Apoptosis and Signaling by XIAP
XIAP 对细胞凋亡和信号传导的控制
  • 批准号:
    7917092
  • 财政年份:
    2009
  • 资助金额:
    $ 326.48万
  • 项目类别:

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