Administrative Core
行政核心
基本信息
- 批准号:10207345
- 负责人:
- 金额:$ 37.75万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-07-05 至 2023-06-30
- 项目状态:已结题
- 来源:
- 关键词:Administrative PersonnelAnimalsApplications GrantsAwardBioinformaticsCRISPR screenCRISPR/Cas technologyCaliberCellsClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsCommunicationCommunitiesConflict (Psychology)Conflict of InterestDataData AnalysesEnsureFundingGenetic ScreeningGoalsGrantGroup MeetingsGuidelinesHospitalsHumanHuman ResourcesHuman Subject ResearchImmunityIndividualInfrastructureInstitutesInstitutionLeadLeadershipManuscriptsMediatingMethodsMonitorOnline SystemsPilot ProjectsPreparationPrincipal InvestigatorProceduresProcessProgress ReportsPubMedPublic PolicyReportingResearch PersonnelResearch Project GrantsResearch SupportResolutionResource SharingScheduleScientistSecureServicesStructureSystemTeleconferencesTimeTravelUnited States National Institutes of HealthValidationacute infectionadaptive immune responsebasecareerconflict resolutiondata managementdata portaldata sharingin vivoinnovationinnovative technologiesmedical schoolsmeetingsmembermouse modelnoveloperationorganizational structureprogramsscreeningsuccessweb portal
项目摘要
The major objectives of the Administrative Core are to institute an infrastructure that facilitates
productive interactions among the U19 Program investigators of this grant application, “Defining
regulators of immunity to acute infection using CRISPR screens” and implements our Pilot Project
program. The Administrative Core will serve as a centralized, transparent organizational structure to
provide administrative support that enables the Principal investigators and their personnel to focus on
their experimental and scientific goals. Dr. Sharpe, Program Director of the overall U19 grant, will
provide leadership and direction for operations of the Administrative Core, which will be based at
Harvard Medical School. Dr. Haining, Co-Director of this U19 grant and Core A, will lead the Pilot Grant
Program. The Administrative Core will be responsible for carrying out the following functions: a) Provide
the infrastructure for overall management and co-ordination; b) Facilitate and promote interactions and
communication between program investigators, scientific advisors and administrative personnel; c) Plan
and coordinate annual External Scientific Advisory Group (ESAG) meetings; d) Organize and
coordinate travel for ESAG members; e) Assist the Program Directors and Principal Investigators with
oversight of scientific, fiscal, regulatory and compliance matters, and with preparation and review of
yearly progress reports and financial reports; f) Implement a plan for data management/sharing among
investigators; and g) Implement the Pilot Project Program. The Administrative Core will also resolve all
conflicts that may arise. To achieve these goals, Core A has the following specific aims: Aim 1: To
provide infrastructure for overall management and coordination. Core A will provide administrative
support and coordination to promote communication and interactions among Project and Core
investigators, including the scheduling of regular teleconferences/face-to-face meetings and annual
meetings, preparing and submitting annual progress reports, providing fiscal oversight and ensuring
institutional compliance with fiscal, regulatory and scientific issues, and conflict resolution. Aim 2: To
maintain a web-based portal for data sharing via a secure Dropbox. Core A will host and manage
a secure Dropbox portal for data sharing within the U19. This easy access to data will maximize
transparency, encourage collaboration, and aid in monitoring project progress and how collaborators
are utilizing core services. Aim 3: To implement the Pilot Project Program. Core A will develop an
effective process to solicit review and award high caliber innovative Pilot Projects that use our in vivo
CRISPR platform, and monitor their progress. We will encourage applications from early career
investigators. Through these specific Aims, we will create an Administrative Core structured to
implement processes/procedures to enable the success of this highly collaborative program.
行政核心的主要目标是建立一个便利的基础设施
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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Arlene H. Sharpe其他文献
The complexity of the B7-CD28/CTLA-4 costimulatory pathway.
B7-CD28/CTLA-4 共刺激途径的复杂性。
- DOI:
- 发表时间:
1998 - 期刊:
- 影响因子:0
- 作者:
Schweitzer An;Arlene H. Sharpe - 通讯作者:
Arlene H. Sharpe
Age-associated remodeling of T cell immunity and metabolism
T 细胞免疫和代谢的年龄相关重塑
- DOI:
10.1016/j.cmet.2022.11.005 - 发表时间:
2023-01-03 - 期刊:
- 影响因子:30.900
- 作者:
SeongJun Han;Peter Georgiev;Alison E. Ringel;Arlene H. Sharpe;Marcia C. Haigis - 通讯作者:
Marcia C. Haigis
Tumor cells dictate anti-tumor immune responses by altering pyruvate utilization and succinate signaling in CD8sup+/sup T cells
肿瘤细胞通过改变 CD8+T 细胞中的丙酮酸利用和琥珀酸盐信号来决定抗肿瘤免疫反应
- DOI:
10.1016/j.cmet.2022.06.008 - 发表时间:
2022-08-02 - 期刊:
- 影响因子:30.900
- 作者:
Ilaria Elia;Jared H. Rowe;Sheila Johnson;Shakchhi Joshi;Giulia Notarangelo;Kiran Kurmi;Sarah Weiss;Gordon J. Freeman;Arlene H. Sharpe;Marcia C. Haigis - 通讯作者:
Marcia C. Haigis
The B7:CD28 family and friends: Unraveling coinhibitory interactions
B7:CD28 家族及朋友:解开共抑制相互作用
- DOI:
10.1016/j.immuni.2024.01.013 - 发表时间:
2024-02-13 - 期刊:
- 影响因子:26.300
- 作者:
Kelly P. Burke;Apoorvi Chaudhri;Gordon J. Freeman;Arlene H. Sharpe - 通讯作者:
Arlene H. Sharpe
PD-L2 is a second ligand for PD-1 and inhibits T cell activation
PD-L2 是 PD-1 的第二种配体,可抑制 T 细胞活化
- DOI:
10.1038/85330 - 发表时间:
2001-03-01 - 期刊:
- 影响因子:27.600
- 作者:
Yvette Latchman;Clive R. Wood;Tatyana Chernova;Divya Chaudhary;Madhuri Borde;Irene Chernova;Yoshiko Iwai;Andrew J. Long;Julia A. Brown;Raquel Nunes;Edward A. Greenfield;Karen Bourque;Vassiliki A. Boussiotis;Laura L. Carter;Beatriz M. Carreno;Nelly Malenkovich;Hiroyuki Nishimura;Taku Okazaki;Tasuku Honjo;Arlene H. Sharpe;Gordon J. Freeman - 通讯作者:
Gordon J. Freeman
Arlene H. Sharpe的其他文献
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{{ truncateString('Arlene H. Sharpe', 18)}}的其他基金
Defining regulators of immunity to acute infection using CRISPR screens
使用 CRISPR 筛选定义急性感染免疫调节因子
- 批准号:
10210502 - 财政年份:2020
- 资助金额:
$ 37.75万 - 项目类别:
Abbreviated targeted therapy to improve anti-PD-1 inhibitor efficacy in melanoma
简化靶向治疗可提高抗 PD-1 抑制剂对黑色素瘤的疗效
- 批准号:
10153453 - 财政年份:2018
- 资助金额:
$ 37.75万 - 项目类别:
Project 2: Measuring and modeling the tumor and immune microenvironment before and during therapy and at the time of drug resistance
项目2:治疗前、治疗期间以及耐药时的肿瘤和免疫微环境的测量和建模
- 批准号:
10343840 - 财政年份:2018
- 资助金额:
$ 37.75万 - 项目类别:
Abbreviated targeted therapy to improve anti-PD-1 inhibitor efficacy in melanoma
简化靶向治疗可提高抗 PD-1 抑制剂对黑色素瘤的疗效
- 批准号:
9906872 - 财政年份:2018
- 资助金额:
$ 37.75万 - 项目类别:
Abbreviated targeted therapy to improve anti-PD-1 inhibitor efficacy in melanoma
简化靶向治疗可提高抗 PD-1 抑制剂对黑色素瘤的疗效
- 批准号:
9576657 - 财政年份:2018
- 资助金额:
$ 37.75万 - 项目类别:
Defining regulators of immunity to acute infection using CRISPR screens
使用 CRISPR 筛选定义急性感染免疫调节因子
- 批准号:
10207344 - 财政年份:2017
- 资助金额:
$ 37.75万 - 项目类别:
Project 1: CRISPR screens to discover regulators of CD8 and CD4 cell fates and function
项目 1:通过 CRISPR 筛选发现 CD8 和 CD4 细胞命运和功能的调节因子
- 批准号:
10207349 - 财政年份:2017
- 资助金额:
$ 37.75万 - 项目类别:
Defining regulators of immunity to acute infection using CRISPR screens
使用 CRISPR 筛选定义急性感染免疫调节因子
- 批准号:
9380804 - 财政年份:2017
- 资助金额:
$ 37.75万 - 项目类别:
Defining regulators of immunity to acute infection using CRISPR screens
使用 CRISPR 筛选定义急性感染免疫调节因子
- 批准号:
10266219 - 财政年份:2017
- 资助金额:
$ 37.75万 - 项目类别:
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