POWRE: Structure and Function of an Apoptosis Domain in the 75 kDa Neurotropin Receptor
POWRE:75 kDa Neurotropin 受体中凋亡结构域的结构和功能
基本信息
- 批准号:9805771
- 负责人:
- 金额:$ 7.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-09-01 至 2002-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
9805771 CHAPMAN During development, different tissues and organs require different numbers of cells. Programmed cell death (or "apoptosis"), along with cell division, is a primary way that cell number is controlled. Apoptosis occurs as a series of cellular and biochemical events in which the cell, instead of dividing, involutes, falls apart, and is engulfed. Every normal cell appears to have the "program" for cell death, which can be activated in a number of ways. The neurotrophin receptor gp75NTR or NTR, expressed by neurons and some immune cells, is a member of a family of cytokine and growth factor receptors known to regulate many cellular decisions to undergo programmed cell death. The NTR contains an intracellular domain that is similar to the "death domain" of other receptors that can initiate apoptosis, but it has not yet been shown that the NTR's putative death domain functions in apoptotic signaling. The objective of Dr. Chapman's study are to establish whether the NTR's death domain interacts with elements of the apoptotic mechanism (caspases), and to demonstrate whether this receptor can induce programmed cell death when expressed ectopically in cultured mammalian cells. This project is particular suitable for a POWRE award. Dr. Chapman recently made the unusual transition from the biotechnology industry to take a faculty job at the new San Marcos campus of the California State University system. CSUSM emphasized hands-on laboratory experience with modern technology to prepare their students in the biological sciences for careers as researchers, science teachers and in the biotechnology industry. Dr. Chapman brings real world experience to her students, and will be able to actively engage them in research with this POWRE award, which will provide the funding for her to initiate this research project.
小行星9805771 在发育过程中,不同的组织和器官需要不同数量的细胞。 程序性细胞死亡(或“细胞凋亡”),沿着细胞分裂,是控制细胞数量的主要方式。 细胞凋亡作为一系列细胞和生物化学事件发生,其中细胞不是分裂,而是内卷、福尔斯分裂和被吞噬。 每个正常细胞似乎都有细胞死亡的“程序”,可以通过多种方式激活。 由神经元和一些免疫细胞表达的神经营养因子受体gp75NTR或NTR是已知调节许多细胞决定以经历程序性细胞死亡的细胞因子和生长因子受体家族的成员。 NTR含有一个细胞内结构域,它类似于可以启动细胞凋亡的其他受体的“死亡结构域”,但尚未显示NTR的推定死亡结构域在细胞凋亡信号传导中起作用。 Chapman博士研究的目的是确定NTR的死亡结构域是否与细胞凋亡机制的元件(半胱天冬酶)相互作用,并证明该受体在培养的哺乳动物细胞中异位表达时是否可以诱导程序性细胞死亡。 该项目特别适合获得POWRE奖。 查普曼博士最近从生物技术行业做出了不同寻常的转变,在加州州立大学系统的圣马科斯新校区担任教职。 CSUSM强调现代技术的实践实验室经验,以帮助生物科学的学生为研究人员,科学教师和生物技术行业做好准备。 查普曼博士带来了真实的世界经验,她的学生,并将能够积极从事他们的研究与此POWRE奖,这将提供资金,她发起这个研究项目。
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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Barbara Chapman其他文献
Maximizing Parallelism and GPU Utilization For Direct GPU Compilation Through Ensemble Execution
通过集成执行最大限度地提高并行度和 GPU 利用率以实现直接 GPU 编译
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
Shilei Tian;Barbara Chapman;Johannes Doerfert - 通讯作者:
Johannes Doerfert
Performance Evaluation of a Multi-Zone Application in Different OpenMP Approaches
- DOI:
10.1007/s10766-008-0074-5 - 发表时间:
2008-04-29 - 期刊:
- 影响因子:0.900
- 作者:
Haoqiang Jin;Barbara Chapman;Lei Huang;Dieter an Mey;Thomas Reichstein - 通讯作者:
Thomas Reichstein
Feasibility Study of Interventions to Reduce Medication Omissions Without Documentation: Recall and Check Study
在没有文件的情况下减少药物遗漏的干预措施的可行性研究:召回和检查研究
- DOI:
10.1097/ncq.0000000000000229 - 发表时间:
2017 - 期刊:
- 影响因子:1.2
- 作者:
Maree Johnson;P. Sanchez;Catherine Zheng;Barbara Chapman - 通讯作者:
Barbara Chapman
Comparison of human and chimpanzee ξ1 blobin genes
- DOI:
10.1007/bf02115686 - 发表时间:
1985-12-01 - 期刊:
- 影响因子:1.800
- 作者:
Cary Willard;Elsie Wong;John F. Hess;Che-Kun James Shen;Barbara Chapman;Allan C. Wilson;Carl W. Schmid - 通讯作者:
Carl W. Schmid
Experiences Developing the OpenUH Compiler and Runtime Infrastructure
- DOI:
10.1007/s10766-012-0230-9 - 发表时间:
2012-11-21 - 期刊:
- 影响因子:0.900
- 作者:
Barbara Chapman;Deepak Eachempati;Oscar Hernandez - 通讯作者:
Oscar Hernandez
Barbara Chapman的其他文献
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{{ truncateString('Barbara Chapman', 18)}}的其他基金
Collaborative Research: SHF: MEDIUM: Smart Integrated Tuning of Parallel Code for Multicore and Manycore Systems
合作研究:SHF:MEDIUM:多核和众核系统并行代码的智能集成调整
- 批准号:
2211983 - 财政年份:2022
- 资助金额:
$ 7.5万 - 项目类别:
Continuing Grant
SHF:Small:Performance Portable Parallel Programming on Extremely Heterogeneous Systems
SHF:Small:极端异构系统上的高性能便携式并行编程
- 批准号:
2113996 - 财政年份:2021
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
SPX: Collaborative Research: Cross-layer Application-Aware Resilience at Extreme Scale (CAARES)
SPX:协作研究:超大规模跨层应用程序感知弹性 (CAARES)
- 批准号:
1725499 - 财政年份:2017
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
Increasing Student Participation in Fifth PGAS Conference (PGAS11)
提高第五届 PGAS 会议 (PGAS11) 的学生参与度
- 批准号:
1158635 - 财政年份:2011
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
SHF:Small: Portable High-Level Programming Model for Heterogeneous Computing Based on OpenMP
SHF:Small:基于OpenMP的可移植异构计算高级编程模型
- 批准号:
0917285 - 财政年份:2009
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
Collaborative Research: Extreme OpenMP: A Programming Model for Productive High End Computing
协作研究:Extreme OpenMP:高效高端计算的编程模型
- 批准号:
0833201 - 财政年份:2008
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
Scalable Performance and Power-Aware Hybrid Compilation System for Multicores
适用于多核的可扩展性能和功耗感知混合编译系统
- 批准号:
0702775 - 财政年份:2007
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
CRI: Planning A Research Compiler Infrastructure Based on Open64
CRI:规划基于Open64的研究编译器基础设施
- 批准号:
0708797 - 财政年份:2007
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
Collaborative Research: Performance Toolset for Dynamic Optimization of High-End Hybrid Applications
协作研究:用于高端混合应用动态优化的性能工具集
- 批准号:
0444468 - 财政年份:2004
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
POWRE: Structure and Function of an Apoptosis Domain in the 75 kDa Neurotropin Receptor
POWRE:75 kDa Neurotropin 受体中凋亡结构域的结构和功能
- 批准号:
0227160 - 财政年份:2002
- 资助金额:
$ 7.5万 - 项目类别:
Standard Grant
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