Core A: Administrative Core
核心A:行政核心
基本信息
- 批准号:10223992
- 负责人:
- 金额:$ 10.11万
- 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:2017-08-08 至 2023-07-31
- 项目状态:已结题
- 来源:
- 关键词:AftercareAreaBackBioinformaticsBiological MarkersBiostatistics CoreBiotechnologyBlood CellsClinicalClinical TrialsCollaborationsCommunicationCommunitiesContractsDataDecision MakingDoctor of PhilosophyEnsureExposure toFundingFutureGoalsGoldGrantHIVImmunologistImmunologyImpairmentInstitutesInstitutionInterruptionInterventionInvestigationLeadLogisticsMissionMonitorPathway interactionsPatientsPerformancePlasmaPrivatizationProcessProductivityResourcesRobin birdSamplingScheduleServicesSiteSpecimenStrategic PlanningStructureTestingTherapeuticTherapeutic InterventionTimeUnited States National Institutes of HealthVideoconferencingWorkbasecostdata exchangemeetingsmemberpredictive markerprogramssoundsuccessviral reboundvirologyvolunteerweb site
项目摘要
Project Summary/Abstract
The overall success of the proposed BioMark project team depends on an efficient and highly organized
Administrative Core that effectively coordinates the team's efforts. The central mission of the proposed
BioMark project is to identify a robust set of biomarkers predicting time to rebound following treatment
interruption in HIV infected patients. This core will sek to remove or reduce the obstacles that might impair the
team from achieving its experimental goals. Keys to success are the orchestration of lively and informative
team meetings and the nucleation of the team in a manner that promotes synergistic rather than additive
scientific collaboration. The Administrative Core is organized around three specific aims: Specific Aim 1: To
provide a sound, effective administrative structure for the BioMark team that maximizes scientific productivity,
promotes free and open communication among members, allows for strategic planning on a regular basis,
ensures the implementation of sound fiscal practices to maximize resources and productivity, and promotes
the appropriate sharing, collation, and analyses of the scientific data generated. Specific Aim 2: To conduct
an annual scientific review of progress of the BioMark team by a Scientific Advisory Board comprised of three
members (beginning in year 3). Specific Aim 3: To regularly evaluate internally the performance of all
scientific projects and cores and, based on need or performance, to reallocate resources in a manner that best
serves the overall goals of the BioMark team. Dr. Warner Greene will serve as Director of this Core. This core
will be based at the Gladstone Institute of Virology and Immunology (GIVI), an institution widely recognized for
the excellence of its administrative services. Additional administrative staff participating in BioMark will include
Julia Roudabush (Gladstone Grants and Contracts) and Robin Givens (Senior Executive Assistant, Office of
the Director, GIVI). The Administrative Core will schedule biweekly videoconferences of BioMark's Executive
Committee (Greene chair, Pillai, Roan, Siliciano) alternating with videoconferencing meetings of the entire
BioMark team for review of results and discussion of future experimentation. The Executive Committee will
function as the principal decision-making body within the program. The Administrative Core will also organize
an annual strategic planning process and be responsible for launching BioMark's website to include public and
private portals, the latter facilitating data exchange among team members. In Year 3, a Scientific Advisory
Board will be assembled with plans to invite a bioinformatician, HIV immunologist, and an HIV clinical trialist to
join as members and to conduct an annual review of the entire program. The Administrative Core will also take
the lead on ensuring smooth specimen acquisition for the four different collaborating ATI trial sites and
ensuring a smooth interface between the three projects and the Bioinformatics and Biostatistics Core.
项目总结/摘要
拟议的BioMark项目团队的整体成功取决于一个高效和高度组织化的团队。
有效协调团队工作的行政核心。拟议的《公约》的中心使命是
BioMark项目旨在确定一组可靠的生物标志物,预测治疗后反弹的时间
艾滋病病毒感染者中断治疗。这一核心将设法消除或减少可能损害
团队实现其实验目标。成功的关键是将生动活泼、内容丰富的
团队会议和团队的核心,以促进协同而不是添加剂的方式
科学合作。行政核心围绕三个具体目标组织:具体目标1:
为BioMark团队提供一个健全、有效的管理结构,最大限度地提高科学生产力,
促进成员之间的自由和开放的沟通,允许定期进行战略规划,
确保实施健全的财政做法,以最大限度地利用资源和提高生产力,并促进
适当分享、整理和分析所产生的科学数据。具体目标2:开展
由科学顾问委员会对BioMark团队的进展进行年度科学审查,
成员(从第三年开始)。具体目标3:定期在内部评估所有
科学项目和核心,并根据需要或业绩,以最佳方式重新分配资源,
服务于BioMark团队的总体目标。Warner格林博士将担任该核心的主任。这一核心
将设在格莱斯顿病毒学和免疫学研究所(GIVI),这是一个被广泛认可的机构,
卓越的行政服务。参与BioMark的其他行政人员包括
Julia Roudabush(Gladstone赠款和合同)和Robin Givens(高级执行助理,
主任)。行政核心将安排每两周一次的BioMark执行官视频会议
委员会(格林主席、皮莱、罗恩、西利西亚诺)交替举行全体会议视频会议
BioMark团队审查结果并讨论未来实验。执行委员会将
作为项目的主要决策机构。行政核心还将组织
一个年度战略规划过程,并负责推出BioMark的网站,包括公众和
私人门户网站,后者促进团队成员之间的数据交换。在第三年,科学咨询
委员会将召集一名生物信息学家、艾滋病毒免疫学家和一名艾滋病毒临床试验专家,
作为会员加入,并对整个计划进行年度审查。行政核心还将采取
负责确保四个不同合作ATI试验中心顺利采集标本,
确保这三个项目与生物信息学和生物统计学核心之间的顺利衔接。
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)
数据更新时间:{{ journalArticles.updateTime }}
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Warner C. Greene其他文献
Cytochalasin binding in lymphocytes and polymorphonuclear leukocytes.
淋巴细胞和多形核白细胞中的细胞松弛素结合。
- DOI:
- 发表时间:
1976 - 期刊:
- 影响因子:3.7
- 作者:
C. Parker;Warner C. Greene;Hanna H. MacDonald - 通讯作者:
Hanna H. MacDonald
Interleukin 2-induced tyrosine phosphorylation. Interleukin 2 receptor beta is tyrosine phosphorylated.
白细胞介素2诱导的酪氨酸磷酸化。
- DOI:
- 发表时间:
1990 - 期刊:
- 影响因子:4.8
- 作者:
Gordon B. Mills;Christopher May;Martha McGill;Marion Fung;Michael Baker;Robert Sutherland;Warner C. Greene - 通讯作者:
Warner C. Greene
A role for cytochalasin-sensitive proteins in the regulation of calcium transport in activated human lymphocytes
- DOI:
10.1016/s0006-291x(75)80169-0 - 发表时间:
1975-07-22 - 期刊:
- 影响因子:
- 作者:
Warner C. Greene;Charles W. Parker - 通讯作者:
Charles W. Parker
Analysis of Interleukin-2-dependent Signal Transduction through the Shc/Grb2 Adapter Pathway: INTERLEUKIN-2-DEPENDENT MITOGENESIS DOES NOT REQUIRE Shc PHOSPHORYLATION OR RECEPTOR ASSOCIATION
- DOI:
10.1074/jbc.270.48.28858 - 发表时间:
1995-12-01 - 期刊:
- 影响因子:
- 作者:
Gerald A. Evans;Mark A. Goldsmith;James A. Johnston;Weiduan Xu;Sarah R. Weiler;Rebecca Erwin;O. M. Zack Howard;Robert T. Abraham;J. O'Shea John;Warner C. Greene;William L. Farrar - 通讯作者:
William L. Farrar
A second human interleukin-2 binding protein that may be a component of high-affinity interleukin-2 receptors
一种可能是高亲和力白介素-2 受体成分的第二种人类白介素-2 结合蛋白
- DOI:
10.1038/327518a0 - 发表时间:
1987-06-11 - 期刊:
- 影响因子:48.500
- 作者:
Mitchell Dukovich;Yuji Wano;Le thi Rich Thuy;Paul Katz;Bryan R. Cullen;John H. Kehrl;Warner C. Greene - 通讯作者:
Warner C. Greene
Warner C. Greene的其他文献
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{{ truncateString('Warner C. Greene', 18)}}的其他基金
Exploring HIV-associated Neurocognitive Disorder (HAND) and HIV Latency at the Single Cell Level in Cerebral Organoids
在脑类器官的单细胞水平上探索 HIV 相关神经认知障碍 (HAND) 和 HIV 潜伏期
- 批准号:
10237149 - 财政年份:2019
- 资助金额:
$ 10.11万 - 项目类别:
Exploring HIV-associated Neurocognitive Disorder (HAND) and HIV Latency at the Single Cell Level in Cerebral Organoids
在脑类器官的单细胞水平上探索 HIV 相关神经认知障碍 (HAND) 和 HIV 潜伏期
- 批准号:
10006808 - 财政年份:2019
- 资助金额:
$ 10.11万 - 项目类别:
Assessing the root causes of chronic inflammation in HIV-infected individuals using drugs of abuse
评估使用滥用药物的艾滋病毒感染者慢性炎症的根本原因
- 批准号:
9761514 - 财政年份:2017
- 资助金额:
$ 10.11万 - 项目类别:
Project 2: Delineating virus and host cell-derived biomarkers predicting time to HIV rebound after treatment interruption
项目 2:描绘病毒和宿主细胞衍生的生物标志物,预测治疗中断后 HIV 反弹的时间
- 批准号:
10223996 - 财政年份:2017
- 资助金额:
$ 10.11万 - 项目类别:
Exploiting the Host-HIV Interface To Identify Biomarkers Predicting Time to Viral Rebound after Treatment Interruption
利用宿主-HIV 界面识别生物标志物,预测治疗中断后病毒反弹的时间
- 批准号:
9754763 - 财政年份:2017
- 资助金额:
$ 10.11万 - 项目类别:
HIV without AIDS: A Radically Different Approach to Help the Developing World
没有艾滋病的艾滋病毒:帮助发展中国家的完全不同的方法
- 批准号:
9503875 - 财政年份:2013
- 资助金额:
$ 10.11万 - 项目类别:
HIV without AIDS: A Radically Different Approach to Help the Developing World
没有艾滋病的艾滋病毒:帮助发展中国家的完全不同的方法
- 批准号:
8606334 - 财政年份:2013
- 资助金额:
$ 10.11万 - 项目类别:
HIV without AIDS: A Radically Different Approach to Help the Developing World
没有艾滋病的艾滋病毒:帮助发展中国家的完全不同的方法
- 批准号:
8856536 - 财政年份:2013
- 资助金额:
$ 10.11万 - 项目类别:
HIV-Induced CD4 T-Cell Depletion: An Innate Host Defense Gone Awry?
HIV 诱导的 CD4 T 细胞耗竭:先天宿主防御出了问题?
- 批准号:
8411054 - 财政年份:2012
- 资助金额:
$ 10.11万 - 项目类别:
HIV-Induced CD4 T-Cell Depletion: An Innate Host Defense Gone Awry?
HIV 诱导的 CD4 T 细胞耗竭:先天宿主防御出了问题?
- 批准号:
8500196 - 财政年份:2012
- 资助金额:
$ 10.11万 - 项目类别:
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