RC-BMAC
RC-BMAC
基本信息
- 批准号:10221537
- 负责人:
- 金额:$ 13.42万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2004
- 资助国家:美国
- 起止时间:2004-09-30 至 2025-06-30
- 项目状态:未结题
- 来源:
- 关键词:AdoptionAgingAmericanAnimal ModelAnimalsAreaBackBasic ScienceBiologicalBiological MarkersBiological ModelsBiological ProcessBiological ProductsBiological SciencesBiologyBiology of AgingCRISPR screenCapsicumChemicalsClinicalClinical TrialsClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsComplementConsultationsCore FacilityDevelopmentDoctor of PhilosophyDrosophila genusElderlyEquilibriumFacultyFosteringFoundationsFundingFutureGaitGenesGeneticGeriatricsGeroscienceGoalsHumanImpairmentIndividualInflammationInstitutesInternationalInterventionInvestmentsKnowledgeLaboratoriesLanguageLeadershipLinkMedicalMethodologyMissionMolecularMolecular TargetMuscle functionMuscle satellite cellNeurosciencesOrganismPharmacologyPhenotypePilot ProjectsPre-Clinical ModelProcessReagentResearch PersonnelResearch SupportResearch TrainingResourcesRodentScienceScientistSystemTechniquesTechnologyTranslatingTranslationsVisitWorkZebrafishage relatedbasebiomarker developmentclinical careclinical practicedesignexosomefirst-in-humangene therapyhealthspanhigh throughput analysishigh throughput screeningimprovedinnovationinsightinstrumentationmembermetabolomicsmicrobiomemolecular drug targetmolecular targeted therapiesmuscle physiologynovelnovel markernovel therapeuticspre-clinicalpreservationpreventrecruitscreeningsingle-cell RNA sequencingsmall molecule librariessquare foottargeted treatmenttooltranslational studytrendwhole genome
项目摘要
BMAC Summary/Abstract:
The impact of basic science is increasingly influencing medical practice. This trend will likely only accelerate in
the near future, as techniques including gene therapy and CRISPR-based gene editing begin to impact clinical
care. The continued progress of this approach, and its application to geriatrics, requires a seamless integration
of basic, translational and clinical researchers. In order to facilitate this integration, we are proposing creation
of a new Core for this application. Entitled, the Biology of Mobility and Aging Core (BMAC), this Core will foster
the work of clinicians and basic scientists by linking the tenets of `geroscience' to advance new treatments to
improve balance and mobility. These include the identification of new biomarkers, elucidating new molecular
targets for drug therapy, using in-depth animal phenotyping to assess new biologic agents, and generally
promoting back and forth translation between human and basic studies. This work will ultimately help catalyze
the ability of our Pepper Center to conduct first-in-human clinical trials of novel agents to preserve mobility and
balance in late life. Excitingly, some of these efforts have already been initiated. By supporting pilot,
developmental, and external projects, the BMAC also enhances the rigor, strength and quality of our OAIC.
Moreover, BMAC resources that include state-of-the-art instrumentation and methodologies, a range of
seminars and didactics, as well as laboratory visits, unique genetic reagents and in-depth consultations, will
become widely and easily accessible to Pepper investigators. The BMAC includes internationally renowned
faculty members who constitute a group of senior investigators with knowledge spanning neuroscience, muscle
physiology, pre-clinical animal phenotyping, metabolomics, translational pharmacology, the microbiome and
high throughput genetic and chemical screening platforms. All BMAC faculty operate state-of-the-art and well-
funded laboratories in areas relevant to the biology of mobility and aging.
BMAC摘要/摘要:
基础科学的影响越来越多地影响医学实践。这种趋势可能只会加速
不久的将来,随着包括基因疗法和基于CRISPR的基因编辑在内的技术开始影响临床
关心。这种方法的持续进展及其在老年医学上的应用需要无缝整合
基础,翻译和临床研究人员。为了促进这种整合,我们正在提议创建
该应用程序的新核心。该核心将促进流动性和衰老核心的生物学(BMAC),该核心将促进
临床医生和基础科学家的工作通过将“ Geroscience”的原则联系起来,以将新的治疗方法推向
提高平衡和流动性。这些包括识别新的生物标志物,阐明新分子
药物治疗的靶标,使用深入的动物表型来评估新的生物学剂,并且通常
在人类和基础研究之间来回促进。这项工作最终将有助于催化
我们的胡椒中心进行新型药物的首次人类临床试验的能力,以保留移动性和
晚年的平衡。令人兴奋的是,其中一些努力已经开始。通过支持飞行员
发展性和外部项目,BMAC还提高了我们OAIC的严格,力量和质量。
此外,包括最先进的仪器和方法论在内的BMAC资源,一系列
研讨会和教学品以及实验室访问,独特的遗传试剂和深入的咨询将
辣椒调查人员可以广泛易于使用。 BMAC包括国际知名
构成一群具有神经科学知识的高级调查员的教师
生理学,临床前动物表型,代谢组学,转化药理学,微生物组和
高通量遗传和化学筛选平台。所有BMAC的教师都经营最先进的教师
在与流动性和衰老生物学有关的领域的资助实验室。
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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{{ truncateString('TOREN FINKEL', 18)}}的其他基金
Comprehensive functional genomic analysis of the multi-disease associated CDKN2A/B locus
多种疾病相关 CDKN2A/B 基因座的综合功能基因组分析
- 批准号:
10672975 - 财政年份:2021
- 资助金额:
$ 13.42万 - 项目类别:
Comprehensive functional genomic analysis of the multi-disease associated CDKN2A/B locus
多种疾病相关 CDKN2A/B 基因座的综合功能基因组分析
- 批准号:
10491270 - 财政年份:2021
- 资助金额:
$ 13.42万 - 项目类别:
TriState SenNET (Lung and Heart) Tissue Map and Atlas consortium
TriState SenNET(肺和心脏)组织图谱和 Atlas 联盟
- 批准号:
10376488 - 财政年份:2021
- 资助金额:
$ 13.42万 - 项目类别:
Comprehensive functional genomic analysis of the multi-disease associated CDKN2A/B locus
多种疾病相关 CDKN2A/B 基因座的综合功能基因组分析
- 批准号:
10210579 - 财政年份:2021
- 资助金额:
$ 13.42万 - 项目类别:
The role of calcium entry through the mitochondrial uniporter in regulating cardiac metabolism and physiology
钙通过线粒体单转运蛋白进入在调节心脏代谢和生理学中的作用
- 批准号:
10320832 - 财政年份:2019
- 资助金额:
$ 13.42万 - 项目类别:
Vascular autophagy as a mediator of vascular aging and homeostasis
血管自噬作为血管衰老和稳态的介质
- 批准号:
9753359 - 财政年份:2018
- 资助金额:
$ 13.42万 - 项目类别:
Vascular autophagy as a mediator of vascular aging and homeostasis
血管自噬作为血管衰老和稳态的介质
- 批准号:
10186792 - 财政年份:2018
- 资助金额:
$ 13.42万 - 项目类别:
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