Nebraska Center for Molecular Target Discovery and Development
Nebraska Center for Molecular Target Discovery and Development
批准号:
10714236
负责人:
Robert E. Lewis
金额:
$230.25万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
未结题
起止时间:
2018-03-16 至 2028-06-30
关键词:
AppointmentAwardAwarenessBasic ScienceBeliefBiologicalBiological ModelsBiologyBiomedical ResearchCareer MobilityCellsCenters of Research ExcellenceChemicalsClassificationClinicalCollaborationsDataData AnalysesData SetDedicationsDevelopmentDisciplineDiseaseEvaluationFacultyFinancial SupportFundingFutureGenerationsGenomicsGoalsGrantHealthHomeostasisHumanInfrastructureInstitutionInvestmentsJournalsMedical centerMentorsModernizationMolecularMolecular AnalysisMolecular TargetNebraskaOrganoidsPhasePre-Clinical ModelProtacReagentResearchResearch PersonnelResearch Project GrantsResearch SupportResource SharingResourcesSystemTaxesTeacher Professional DevelopmentTechniquesTechnologyTherapeuticTimeTrainingUniversitiesValidationVisionanalytical methodbench to bedsidecollegecostdata acquisitionexpectationexperiencefaculty supportgenetic analysisimprovedinhibitorinsightinterestmembernovelnovel therapeuticsoperationpreclinical developmentprogramsresearch and developmentskill acquisitionsmall moleculesuccesstechnology developmenttherapeutic developmenttherapeutic targettranscriptomicsundergraduate student
中文摘要
项目概要:总体
内布拉斯加州分子靶标发现和开发中心 (CMTDD) 的目标是建立和
扩大内布拉斯加大学医学中心 (UNMC) 的体力和智力资源以及
内布拉斯加大学系统促进方法的识别、验证和开发
操纵与临床重要疾病有关的分子靶标。我们察觉到越来越多的
期刊和资助机构对日益复杂的模型系统和数据集的期望。
获取这些系统和生成高内容数据通常需要大量时间投资
以及对有限的研究资源征税的资金。提升CMTDD研究项目的竞争力
CMTDD 最近投资于第二阶段的领导者 (RPL) 和其他大学教职人员
开发技术以提高研究者研究的复杂性,同时最大限度地降低研究成本
访问。这些技术:单细胞和空间转录组分析、类器官生成和
操作、抑制剂和蛋白水解靶向嵌合体(PROTAC)的合成将被整合为三个
第 2 阶段 CMTDD 核心。这些投资将增强该机构的研究能力,扩大
其教师的翻译能力,促进有前途的新人的培训、指导和职业发展
教师,并有效地推动发现和发展,以改善内布拉斯加州和
国家。第二阶段 RPL 为 CMTDD 带来了广泛的尖端专业知识。有指导并做好准备
访问 CMTDD 支持的核心,我们的 RPL 将成为对社会无价的自给自足的教职人员
UNMC 未来的成功。我们的 2 期 RPL 都对探索基本生物学原理充满热情
细胞稳态的基础,并相信许多疾病可以有效地分类和表征
通过详细的基因组、遗传和分子分析来识别驱动因素和脆弱性
将会出现独特的治疗方法。为了实现这一愿景,CMTDD 将: 1) 维持行政管理
核心和指导计划在最初四年内成功毕业,除了其中一个初始 RPL 之外的所有项目
支持; 2)通过新建立的最先进的单细胞科学核心提高研究能力
空间转录组学、类器官开发以及抑制剂和 PROTAC 合成和验证;和 3)
提供低成本或无成本获取这些技术和试剂,作为增加
研究者研究的影响。
英文摘要
Project Summary: Overall
The goal of the Nebraska Center for Molecular Target Discovery and Development (CMTDD) is to establish and
expand physical and intellectual resources at the University of Nebraska Medical Center (UNMC) and the
University of Nebraska system to catalyze the identification, validation, and development of approaches for
manipulation of molecular targets implicated in clinically important diseases. We perceive an increasing
expectation by journals and granting agencies for progressively sophisticated model systems and data sets.
Acquisition of these systems and generation of high-content data often requires a substantial investment in time
and money that taxes limited research resources. To enhance the competitiveness of CMTDD Research Project
Leaders (RPLs) and other university faculty members during Phase 2, the CMTDD recently invested in the
development of technologies to enhance the sophistication of investigator research while minimizing the cost of
access. These technologies: single-cell and spatial transcriptomic analysis, organoid generation and
manipulation, and inhibitor and proteolysis-targeting chimera (PROTAC) synthesis will be integrated into three
Phase 2 CMTDD cores. These investments will enhance the research capabilities of the institution, expand the
translational capacity of its faculty, facilitate the training, mentoring, and career advancement of promising new
faculty, and efficiently drive discovery and development for the improvement of human health in Nebraska and
the nation. Phase 2 RPLs bring a breadth of cutting-edge expertise to the CMTDD. With mentoring and ready
access to CMTDD-supported cores, our RPLs will become self-supporting faculty members invaluable to the
future success of UNMC. Our Phase 2 RPLs share both a passion for exploration of the basic biologic principles
that underly cell homeostasis and a belief that many diseases can be effectively classified and characterized
through detailed genomic, genetic, and molecular analyses that identify drivers and vulnerabilities from which
will emerge unique therapeutic approaches. To realize this vision, the CMTDD will: 1) maintain an Administrative
Core and mentoring program that successfully graduated all but one of its initial RPLs in the first four years of
support; 2) increase research capacity through newly established state-of-the-art scientific cores for single-cell
and spatial transcriptomics, organoid development, and inhibitor and PROTAC synthesis and validation; and 3)
provide low- or no-cost access to these technologies and reagents as an affordable means for increasing the
impact of investigator research.
期刊论文(13)
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会议论文
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Ubiquitin E3 ligase FBXO21 regulates cytokine-mediated signaling pathways, but is dispensable for steady-state hematopoiesis.
泛素 E3 连接酶 FBXO21 调节细胞因子介导的信号通路,但对于稳态造血来说是可有可无的。
DOI:
10.1016/j.exphem.2022.08.002
发表时间:
2022
期刊:
Experimental hematology
影响因子:
2.6
作者:
[Wittorf,KarliJ, Weber,KasidyK, Swenson,SamanthaA, Buckley,ShannonM]
通讯作者:
Buckley,ShannonM
DOI:
10.7554/elife.76497
发表时间:
2022-06-17
期刊:
ELIFE
影响因子:
7.7
作者:
[Ray, Suhita, Chee, Linda, Zhou, Yichao, Schaefer, Meg A., Naldrett, Michael J., Alvarez, Sophie, Woods, Nicholas T., Hewitt, Kyle J.]
通讯作者:
Hewitt, Kyle J.
Isolation and Immunodetection of Enzymatic DNA-Protein Crosslinks by RADAR Assay.
通过 RADAR 测定法分离和免疫检测酶促 DNA-蛋白质交联。
DOI:
10.1007/978-1-0716-3373-1_8
发表时间:
2023
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
[Perry,Megan, Ghosal,Gargi]
通讯作者:
Ghosal,Gargi
Interactome Profiling of DNA Damage Response (DDR) Mediators with Immunoprecipitation-Mass Spectrometry.
使用免疫沉淀-质谱法对 DNA 损伤反应 (DDR) 介质进行相互作用组分析。
DOI:
10.1007/978-1-0716-3373-1_12
发表时间:
2023
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
[Law,HenryC-H, Noe,Dragana, Woods,NicholasT]
通讯作者:
Woods,NicholasT
DOI:
10.1021/acsinfecdis.9b00527
发表时间:
2020-07-10
期刊:
ACS infectious diseases
影响因子:
5.3
作者:
[Rosenthal MR, Ng CL]
通讯作者:
Ng CL
共 7 条
Pancreatic cancer variant analysis of the All of Us cohort
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批准号:10660291
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资助金额:$11.51万
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财政年份:2022
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负责人:Robert E. Lewis
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依托单位:
Novel Mechanisms Controlling SCLC Tumor Initiation
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依托单位:
Novel Mechanisms Controlling SCLC Tumor Initiation
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批准号:10453763
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项目类别:
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资助金额:$20.84万
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财政年份:2021
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依托单位:
Nebraska Center for Molecular Target Discovery and Development
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批准号:9920161
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项目类别:
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资助金额:$227.02万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Nebraska Center for Molecular Target Discovery and Development
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批准号:10392932
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项目类别:
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资助金额:$227.02万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Administrative Core
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批准号:10392933
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项目类别:
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资助金额:$116.89万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Administrative Core
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批准号:10714237
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项目类别:
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资助金额:$50.02万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
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批准号:10117095
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项目类别:
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资助金额:$79.33万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Nebraska Center for Molecular Target Discovery and Development
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批准号:10117079
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项目类别:
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资助金额:$227.02万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Development of Spatial Transcriptomics Capability
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批准号:10582415
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项目类别:
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资助金额:$25.0万
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财政年份:2018
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负责人:Robert E. Lewis
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依托单位:
Novel Effectors of Colon Tumorigenesis
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批准号:9034446
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项目类别:
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资助金额:$30.96万
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财政年份:2012
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负责人:Robert E. Lewis
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依托单位:
Novel Effectors of Colon Tumorigenesis
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批准号:8627963
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项目类别:
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资助金额:$30.03万
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财政年份:2012
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负责人:Robert E. Lewis
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依托单位:
Novel Effectors of Colon Tumorigenesis
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批准号:8827270
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项目类别:
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资助金额:$30.96万
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财政年份:2012
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负责人:Robert E. Lewis
-
依托单位:
Novel Effectors of Colon Tumorigenesis
-
批准号:8458937
-
项目类别:
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资助金额:$29.26万
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财政年份:2012
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负责人:Robert E. Lewis
-
依托单位:
PILOT PROJECT 1 UBIQUITIN-MEDIATED REGULATION OF KINASE SUPPRESSOR OF RAS1
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批准号:8168392
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项目类别:
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资助金额:$3.36万
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财政年份:2010
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负责人:Robert E. Lewis
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依托单位:
KSR, a Modifier of Ras Mediated Cell Transformation
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批准号:6430333
-
项目类别:
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资助金额:$25.44万
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财政年份:2002
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负责人:Robert E. Lewis
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依托单位:
KSR, a Modifier of Ras-Mediated Cell Transformation
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批准号:7525658
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项目类别:
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资助金额:$26.59万
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财政年份:2002
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负责人:Robert E. Lewis
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依托单位:
KSR, a Modifier of Ras-Mediated Cell Transformation
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批准号:7686623
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项目类别:
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资助金额:$4.05万
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财政年份:2002
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负责人:Robert E. Lewis
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依托单位:
KSR, a Modifier of Ras Mediated Cell Transformation
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批准号:6621074
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项目类别:
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资助金额:$26.17万
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财政年份:2002
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负责人:Robert E. Lewis
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依托单位:
KSR, a Modifier of Ras-Mediated Cell Transformation
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负责人:Robert E. Lewis
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依托单位:
海外基金