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
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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
-
项目类别:
-
资助金额:$11.51万
-
财政年份:2022
-
负责人:Robert E. Lewis
-
依托单位:
Novel Mechanisms Controlling SCLC Tumor Initiation
-
批准号:10303538
-
项目类别:
-
资助金额:$18.93万
-
财政年份:2021
-
负责人:Robert E. Lewis
-
依托单位:
Novel Mechanisms Controlling SCLC Tumor Initiation
-
批准号:10453763
-
项目类别:
-
资助金额:$20.84万
-
财政年份:2021
-
负责人:Robert E. Lewis
-
依托单位:
Nebraska Center for Molecular Target Discovery and Development
-
批准号:9920161
-
项目类别:
-
资助金额:$227.02万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
依托单位:
Nebraska Center for Molecular Target Discovery and Development
-
批准号:10392932
-
项目类别:
-
资助金额:$227.02万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
依托单位:
Administrative Core
-
批准号:10392933
-
项目类别:
-
资助金额:$116.89万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
依托单位:
Administrative Core
-
批准号:10714237
-
项目类别:
-
资助金额:$50.02万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
依托单位:
Administrative Core
-
批准号:10117095
-
项目类别:
-
资助金额:$79.33万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
依托单位:
Nebraska Center for Molecular Target Discovery and Development
-
批准号:10117079
-
项目类别:
-
资助金额:$227.02万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
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:
-
资助金额:$25.0万
-
财政年份:2018
-
负责人:Robert E. Lewis
-
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:
-
资助金额:$30.96万
-
财政年份:2012
-
负责人:Robert E. Lewis
-
依托单位:
Novel Effectors of Colon Tumorigenesis
-
批准号:8627963
-
项目类别:
-
资助金额:$30.03万
-
财政年份:2012
-
负责人:Robert E. Lewis
-
依托单位:
Novel Effectors of Colon Tumorigenesis
-
批准号:8827270
-
项目类别:
-
资助金额:$30.96万
-
财政年份:2012
-
负责人:Robert E. Lewis
-
依托单位:
Novel Effectors of Colon Tumorigenesis
-
批准号:8458937
-
项目类别:
-
资助金额:$29.26万
-
财政年份:2012
-
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:
-
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
-
依托单位:
KSR, a Modifier of Ras Mediated Cell Transformation
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批准号:6430333
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项目类别:
-
资助金额:$25.44万
-
财政年份:2002
-
负责人:Robert E. Lewis
-
依托单位:
KSR, a Modifier of Ras-Mediated Cell Transformation
-
批准号:7525658
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项目类别:
-
资助金额:$26.59万
-
财政年份:2002
-
负责人:Robert E. Lewis
-
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:
-
资助金额:$4.05万
-
财政年份:2002
-
负责人:Robert E. Lewis
-
依托单位:
KSR, a Modifier of Ras Mediated Cell Transformation
-
批准号:6621074
-
项目类别:
-
资助金额:$26.17万
-
财政年份:2002
-
负责人:Robert E. Lewis
-
依托单位:
KSR, a Modifier of Ras-Mediated Cell Transformation
-
批准号:8305038
-
项目类别:
-
资助金额:$25.79万
-
财政年份:2002
-
负责人:Robert E. Lewis
-
依托单位:
海外基金