Biological Mechanisms Core-RC-2
Biological Mechanisms Core-RC-2
批准号:
10201466
负责人:
Peter M. Abadir
金额:
$25.53万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-06-01 至 2023-06-30
关键词:
AgingAmericanAngiotensinsAnimal ModelAnimalsAreaAttenuatedAutoantibodiesBiocompatible MaterialsBioinformaticsBiologicalBiological AssayBiologyBiology of AgingCellsChronicClinicalClinical ResearchCollaborationsCommunicationComputing MethodologiesData AnalysesDevelopmentDiagnosticElderlyEnzyme-Linked Immunosorbent AssayEtiologyFacultyFosteringFunctional disorderFundingGeneticGenomicsGerontologyGoalsInflammationInformation DisseminationInfrastructureInternationalInterventionKnowledgeLaboratoriesLeadershipLinkMeasurementMentorsMentorshipMitochondriaModalityMolecularMolecular ComputationsNanotechnologyPathway interactionsPhenotypePreventionPrevention strategyPreventive treatmentProteomicsPsychological TransferReceptor, Angiotensin, Type 1ResearchResearch DesignResearch PersonnelResourcesSamplingScienceSection 8SourceSystemTechnologyTechnology TransferTestingTherapeuticTrainingTranslatingTranslationsTweensVendorWorkage relatedaptamerbaseclinically relevantcost effectivedrug developmentfrailtyhuman subjectinsightinterestmetabolomicsmodel developmentmouse modelnext generationnovelphysical propertypreventtherapy developmenttooltreatment strategy
中文摘要
资源核心2(RC 2)生物机制核心:项目摘要
查明身体虚弱和与年龄有关的脆弱性的病因仍然是一项重大挑战,
老年学研究应对这一挑战的关键是更好地了解
导致脆弱性的潜在生物学基础以及关键生物学途径的识别
制定可能有助于预防或减轻脆弱和丧失独立性的干预措施。目标
约翰霍普金斯老年美国人独立中心(OAIC)的生物机制核心(RC-2)是
使下一代的弱点相关的病因学发现,并促进这些翻译
临床相关的诊断,预防和治疗模式的发现。核心实现了这一点
通过提供高质量的生物测量专业知识、技术和基础设施
必须实现这一目标。为了全面涵盖生物和测量
我们拥有研究虚弱相关病因学所需的专业知识,我们聘请了一个具有相当大的领导团队,
生物学和翻译专业知识以及几位内部顾问,他们带来了关键的额外知识,
专业知识、受训人员辅导和基础设施。RC-2的具体目标是:1)提供
先进的科学专业知识,基础设施和技术,以促进生物和
与虚弱相关的病因学研究,2)提供来自人类受试者和来自
测试与虚弱相关的假设所需的动物模型,3)促进生物学的翻译
将研究结果纳入干预措施或以预防为重点的临床研究,4)提供培训,指导,
指导有前途的初级研究人员了解影响脆弱性的生物学机制,以及5)提供
RC-2相关科学和活动的机构和外部可见度。这些宣传工作将
如第8节所述,新的信息传播核心(IDC)进一步促进了这一进程。我们的目标将
通过核心领导人与他们的实验室之间的密切沟通,
与其他OAIC核心建立合作伙伴关系,并聘请高度相关的专家顾问
线粒体测量、代谢组学、小鼠模型开发、
诊断目的,以及与药物开发相关的纳米技术。通过提供这些资源,RC-2
将促进高质量的研究,阐明临床相关的生物学途径,基础脆弱,
相关的干预措施,有望减轻脆弱,相关的条件,和独立性的丧失。
英文摘要
Resource Core 2 (RC2) Biological Mechanisms Core: Project Summary
The identification of the etiologies of frailty and age-related vulnerability remains a crucial challenge for
gerontological research. Key to this challenge are the development of a better understanding of the
underlying biological basis that contributes to frailty and the identification of key biological pathways for the
development of interventions that might help prevent or alleviate frailty and loss of independence. The goal
of Johns Hopkins Older Americans Independence Center (OAIC) Biological Mechanisms Core (RC-2) is to
enable the next generation of frailty-related etiological discovery and to promote the translation of these
discoveries into clinically relevant diagnostic, preventive, and treatment modalities. This core achieves this
through the provision of high-quality biological measurement expertise, technologies, and infrastructure
necessary to attain this goal. In order to comprehensively encompass the biological and measurement
expertise necessary to study frailty-related etiology, we have engaged a leadership team with considerable
biological and translational expertise as well as several internal consultants who bring crucial additional
expertise, mentorship for trainees, and infrastructure to RC-2. The specific aims of RC-2 are to: 1) provide
state of the art scientific expertise, infrastructure, and technology necessary to advance biological and
etiological research related to frailty, 2) provide access to biological samples from human subjects and from
animal models necessary to test hypotheses related to frailty, 3) facilitate the translation of biological
findings into interventions or prevention-focused clinical studies, 4) provide training, mentorship, and
guidance to promising junior investigators around biological mechanisms that impact frailty, and 5) provide
institutional and external visibility for RC-2 related science and activities. These visibility efforts will be
further facilitated by a novel Information Dissemination Core (IDC) as described in section 8. Our aims will
be accomplished through close communication between the core leaders and their laboratories, close
partnership with the other OAIC cores, and the engagement of expert consultants in the highly relevant
areas of mitochondrial measurement, metabolomics, mouse model development, nanotechnologies for
diagnostic purposes, and nanotechnology related to drug development. By providing these resources, RC-2
will foster high quality research that elucidates clinically relevant biological pathways that underlie frailty and
related interventions that hold promise to attenuate frailty, related conditions, and the loss of independence.
期刊论文(0)
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会议论文
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海外基金