Nathan Shock Center of Excellence in Basic Biology of Aging
Nathan Shock Center of Excellence in Basic Biology of Aging
批准号:
10670087
负责人:
David J. Marcinek
金额:
$96.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
未结题
起止时间:
1997-07-15 至 2025-05-31
关键词:
AccelerationAgingAllyArtificial IntelligenceBioinformaticsBiological AssayBiology of AgingCollaborationsCommunicationCommunitiesDataData AnalysesDevelopmentEducational workshopEnvironmentExperimental DesignsFacultyGenesGenetic studyGerontologyGeroscienceGoalsGrowthInformaticsInstitutionInternationalInvertebratesLeadershipLongevityMethodologyMethodsMicrofluidicsMolecularOffice of Administrative ManagementPathway interactionsPhenotypePhilosophyPilot ProjectsPost-Translational Protein ProcessingProcessProteinsProteomicsResearchResearch ActivityResearch PersonnelResearch SupportResourcesRoboticsServicesShockStatistical Data InterpretationTechnologyTranscriptUniversitiesVariantWashingtonbioinformatics toolcareer developmentcell agecomputerized toolsdata disseminationdata sharinghealthspanhigh dimensionalityinsightmeetingsmetabolomicsmultiple omicsnoveloutreachoutreach servicesprogramsresearch and developmentsymposiumtooltrait
中文摘要
整体项目总结
这份申请是为了续期内森·休克老年基础生物学卓越中心
在华盛顿大学及其附属机构。该中心在过去的25年里
为研究衰老生物学的研究人员提供了关键资源。此应用程序
继续强调向最广泛的调查人员社区提供外展和服务的主题
在老年学中。最密切相关的是与衰老相关的表型的特征
长寿健寿。由于我们的中心服务必须便于外部用户访问,我们的
长寿和健康核心(核心E)专注于无脊椎动物测试,其中许多都是新奇的。二
其他资源核心侧重于与老龄化密切相关的高维度评估
表型:衰老的蛋白质表型(核心C)和代谢产物的老化表型(核心D)。
提供复杂的计算和生物信息学工具,用于数据分析和最佳洞察
人工智能和生物信息学核心F。这四个资源核心中的每一个都由
该领域备受尊敬的专家,包括Michael MacCoss和Judit Villen(Core C),Daniel
Promislow(核心D)、Matt Kaeberlein和Maitreya Dunham(核心E)以及李秀英(核心F)。每个人
将突破适当技术的界限,开发新的最先进的方法
最适用于老年学的评估,并使国家可获得这些评估
老龄化社区。研究开发核心(核心B)将继续支持试点和初级
教员研究,坚定地把重点放在向国家老年科学群体提供服务上。这个
行政和计划丰富核心(核心A)支持行政管理,以及
外部咨询小组、课程以及数据共享和传播。核心A的研讨会计划
专题讨论会将继续侧重于赞助和组织国家课程、会议
和会前,以及与我们的资源核心服务相关的领域的研讨会。在……里面
与其他内森休克中心协调,我们将支持一项新的老年病理学研究
主动权。
英文摘要
OVERALL PROJECT SUMMARY
This application is for renewal of the Nathan Shock Center of Excellence in the Basic Biology of Aging
at the University of Washington and affiliated institutions. This Center has over the past 25 years
provided key resources in support of investigators who study the biology of aging. This application
continues a theme that emphasizes outreach and service to the broadest community of investigators
in the gerosciences. Of proximal relevance is the characterization of aging-related phenotypes of
longevity and healthspan. As our Center services must be easily accessible to outside users, our
Longevity and Healthspan Core (Core E) focuses on invertebrate assays, many of them novel. Two
other Resources Cores focus on the high dimensional assessments that are closely related to aging
phenotypes: Protein Phenotypes of Aging (Core C) and Metabolite Phenotypes of Aging (Core D).
Sophisticated computational and bioinformatic tools for data analysis and optimal insight are provided
by the Artificial Intelligence and Bioinformatics Core F. Each of these four Resource Cores is led by
highly respected experts in that field, including Michael MacCoss and Judit Villen (Core C), Daniel
Promislow (Core D), Matt Kaeberlein and Maitreya Dunham (Core E) and Su-In Lee (Core F). Each
will push the envelope of appropriate technologies, developing new state-of-the art approaches for
assessments that are the most applicable to gerontology and making them accessible to the national
aging community. The Research Development Core (Core B) will continue to support pilot and junior
faculty studies, with a firm focus on outreach of service to the national geroscience constituency. The
Administrative and Program Enrichment Core (Core A) supports administrative management, an
external advisory panel, courses, and data sharing and dissemination. Core A’s program of seminars
and symposia will continue a focus on sponsorship and organization of national courses, meetings
and pre-meetings, as well as workshops in the fields allied to our Resource Core Services. In
coordination with other Nathan Shock Centers, we will support a new Geropathology Research
initiative.
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Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.
系统生物学方法对迟到的阿尔茨海默氏病基因组基因组关联研究确定了使用脑表达数据和秀丽隐杆线虫实验验证的新型候选基因。
DOI:
10.1016/j.jalz.2017.01.016
发表时间:
2017-10
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
[Mukherjee S, Russell JC, Carr DT, Burgess JD, Allen M, Serie DJ, Boehme KL, Kauwe JSK, Naj AC, Fardo DW, Dickson DW, Montine TJ, Ertekin-Taner N, Kaeberlein MR, Crane PK]
通讯作者:
Crane PK
DOI:
10.1161/circresaha.114.302153
发表时间:
2014-01-31
期刊:
Circulation research
影响因子:
20.1
作者:
[Wang Y, Wang GZ, Rabinovitch PS, Tabas I]
通讯作者:
Tabas I
DOI:
10.1371/journal.pgen.0030084
发表时间:
2007-05-25
期刊:
PLOS GENETICS
影响因子:
4.5
作者:
[Kaeberlein, Matt, Burtner, Christopher R., Kennedy, Brian K.]
通讯作者:
Kennedy, Brian K.
DOI:
10.1523/jneurosci.2458-21.2022
发表时间:
2022-05-11
期刊:
JOURNAL OF NEUROSCIENCE
影响因子:
5.3
作者:
[Gupta, Shweta, Moreno, Arturo J., Wang, Dan, Leon, Julio, Chen, Chen, Hahn, Oliver, Poon, Yan, Greenberg, Kenneth, David, Nathaniel, Wyss-Coray, Tony, Raftery, Daniel, Promislow, Daniel E. L., Dubal, Dena B.]
通讯作者:
Dubal, Dena B.
Interstitial pericytes decrease in aged mouse kidneys.
老年小鼠肾脏的间质周细胞减少。
DOI:
10.18632/aging.100756
发表时间:
2015-06
期刊:
Aging
影响因子:
--
作者:
[Stefanska A, Eng D, Kaverina N, Duffield JS, Pippin JW, Rabinovitch P, Shankland SJ]
通讯作者:
Shankland SJ
共 139 条
Redox stress resilience in aging skeletal muscle
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批准号:10722970
-
项目类别:
-
资助金额:$48.54万
-
财政年份:2023
-
负责人:David J. Marcinek
-
依托单位:
Increased Risk of Chronic Disease Due to Domoic Acid Exposure with Age
-
批准号:10438785
-
项目类别:
-
资助金额:$13.06万
-
财政年份:2018
-
负责人:David J. Marcinek
-
依托单位:
Increased Risk of Chronic Disease Due to Domoic Acid Exposure with Age
-
批准号:9702219
-
项目类别:
-
资助金额:$13.02万
-
财政年份:2018
-
负责人:David J. Marcinek
-
依托单位:
Increased Risk of Chronic Disease Due to Domoic Acid Exposure with Age
-
批准号:10205069
-
项目类别:
-
资助金额:$13.06万
-
财政年份:2018
-
负责人:David J. Marcinek
-
依托单位:
Preventing Skeletal and Cardiac Muscle Aging by Restoring Mitochondrial Function
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批准号:9564597
-
项目类别:
-
资助金额:$81.95万
-
财政年份:2017
-
负责人:David J. Marcinek
-
依托单位:
SS peptides: a new approach to improve mitochondrial and skeletal muscle function
-
批准号:8444893
-
项目类别:
-
资助金额:$26.75万
-
财政年份:2012
-
负责人:David J. Marcinek
-
依托单位:
SS peptides: improve mitochondrial and skeletal muscle function with age
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批准号:8554758
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项目类别:
-
资助金额:$21.29万
-
财政年份:2012
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负责人:David J. Marcinek
-
依托单位:
Mitochondrial fuction, oxidative damage, and aging
-
批准号:7022219
-
项目类别:
-
资助金额:$10.26万
-
财政年份:2005
-
负责人:David J. Marcinek
-
依托单位:
Mitochondrial function, oxidative damage, and aging
-
批准号:7198108
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项目类别:
-
资助金额:$10.26万
-
财政年份:2005
-
负责人:David J. Marcinek
-
依托单位:
Mitochondrial function, oxidative damage, and aging
-
批准号:6870808
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项目类别:
-
资助金额:$10.26万
-
财政年份:2005
-
负责人:David J. Marcinek
-
依托单位:
Mitochondrial function, oxidative damage, and aging
-
批准号:7369717
-
项目类别:
-
资助金额:$10.26万
-
财政年份:2005
-
负责人:David J. Marcinek
-
依托单位:
Mitochondrial function, oxidative damage, and aging
-
批准号:7575639
-
项目类别:
-
资助金额:$10.26万
-
财政年份:2005
-
负责人:David J. Marcinek
-
依托单位:
Mitochondrial Dysfunction in Aged Muscle
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批准号:7883405
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项目类别:
-
资助金额:$37.67万
-
财政年份:1988
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负责人:David J. Marcinek
-
依托单位:
Mitochondrial Dysfunction in Aged Muscle
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批准号:7642396
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项目类别:
-
资助金额:$38.34万
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财政年份:1988
-
负责人:David J. Marcinek
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依托单位:
Mitochondrial-targeted Antioxidants, Aging and AZT in Skeletal Muscle Dysfunction
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批准号:8046002
-
项目类别:
-
资助金额:$30.28万
-
财政年份:--
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负责人:David J. Marcinek
-
依托单位:
Project 2: Mitochondrial ROS in aging-related skeletal muscle aging
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批准号:9918233
-
项目类别:
-
资助金额:$29.97万
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财政年份:--
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负责人:David J. Marcinek
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依托单位:
海外基金