CORE B: METABOLIC AND MOLECULAR PHYSIOLOGY CORE
核心 B:代谢和分子生理学核心
基本信息
- 批准号:9066636
- 负责人:
- 金额:$ 32.66万
- 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
- 起止时间:2003-05-01 至
- 项目状态:未结题
- 来源:
- 关键词:AdipocytesAnimalsAreaArterial Fatty StreakArtsBiological AssayBiologyBody CompositionCell RespirationCellsCollaborationsCommunitiesComplications of Diabetes MellitusConditioned Culture MediaConsultConsultationsCountryDataData AnalysesDatabasesDiabetes MellitusDietDiseaseDual-Energy X-Ray AbsorptiometryEnvironmentEpigenetic ProcessEvaluationExperimental DesignsFacultyFeeding behaviorsFosteringGene TargetingGeneticGenetically Engineered MouseGenomicsGlucoseGlycerolGlycerophospholipidsGoalsHormonesHumanHuman GeneticsIndirect CalorimetryInflammationInflammatoryInstitutesInstitutionInsulinInterventionKnockout MiceLaboratoriesLeadershipLiquid ChromatographyLos AngelesMagnetic Resonance ImagingMass FragmentographyMetabolicMetabolismMethodologyMicroscopyMissionMitochondriaMolecularMovementMusNuclear ReceptorsObesityOutcomeOxygen ConsumptionPathogenesisPatient CarePeptidesPharmacologic SubstancePhenotypePhysiologicalPhysiologyPlasmaPreparationProceduresProcessProductivityProtocols documentationPublicationsQuality ControlResearchResearch PersonnelResourcesRodentSamplingScientific Advances and AccomplishmentsSeriesServicesSignal TransductionSkeletal MuscleSphingolipidsStandardizationSterolsStrategic PlanningTechniquesTechnologyTimeTissuesTrainingTransgenic MiceTranslational ResearchTranslationsTravelUnited States National Institutes of HealthWorkadipokinesanimal tissueassay developmentbasebench to bedsidechemokinecostcost effectivecytokinedata integrationexperienceextracellularfatty acid metabolismflexibilityfunctional genomicsimprovedin vivoinsightinstrumentationinsulin sensitivityinsulin tolerancemacrophagemanmetabolic abnormality assessmentmetabolic phenotypemonocytenoveloutreachprenolpreventtherapeutic target
项目摘要
NIH-initiated efforts to centralize expertise, instrumentation, and facilities to promote comprehensive evaluation of genetically engineered mice, tissues and cells has improved our understanding of functional genomics and disease pathobiology. The Metabolic and Molecular Physiology Core (MMPC) provides investigators at UCLA, UCSD, Cedars-Sinai, and the Salk Institute with a series of state-of-the-art and cost-effective molecular and physiological assays not readily available from national phenotyping centers. The MMPC is divided into four sub-cores: A) Insulin sensitivity and metabolism, B) Oxidative metabolism and mitochondrial biology, C) LIPID MAPS-lipidomics, and D) Inflammatory siganling, and each sub-core offers extensive training and consultation on a variety of topics from experimental design to data interpretation and integration. Specifically, the MMPC provides services to assess: movement, feeding behavior, indirect calorimetry, body composition, glucose/insulin tolerance, insulin action, substrate metabolism and oxidative capacity, mitochondrial function, circulating and tissue lipids (lipidomics), circulating hormones / adipokines / cytokines, and diabetes complications. The MMPC maintains a tissue bio-bank as well as a comprehensive database of standard protocols for a vast number of phenotyping techniques, and phenotypic outcomes for a wide variety of genetically engineered mice. The MMPC leadership includes top investigators from the fields of nuclear receptor biology, lipid metabolism, inflammation, and adipocyte and skeletal muscle biology including: Peter Tontonoz, Andrea Hevener, Karen Reue, Rajendra Tangirala, Edward Dennis, Oswald Quehenberger. Strengths of the MMPC include the well-rounded and complementary expertise of its leadership and the exceptional track record of productivity and high impact scientific publications. The collaborative spirit ofthe MMPC team fosters a collegial environment and supports service well-coordinated with other DRC cores and institutional resources. The central goal ofthe MMPC is to advance the scientific capabilities ofthe DRC membership in leading-edge metabolic analysis to improve overall research quality with enhanced translation of research ideas from cell, tissue and mouse to man.
NIH引发的努力集中了专业知识,仪器和设施,以促进对基因工程小鼠,组织和细胞进行全面评估的全面评估,从而提高了我们对功能基因组学和疾病病理生物学的理解。代谢和分子生理学核心(MMPC)为UCLA,UCSD,Cedars-Sinai和Salk Institute提供了研究人员,并提供了一系列最先进的和具有成本效益的分子和生理测定法,而不容易从国家表型中心获得。 MMPC分为四个子核:a)胰岛素敏感性和代谢,b)氧化代谢和线粒体生物学,c)脂质图 - 脂肪组学,d)炎症性siganling以及每个子核提供了对实验性化诠释和集成的各种主题的广泛培训和咨询。 Specifically, the MMPC provides services to assess: movement, feeding behavior, indirect calorimetry, body composition, glucose/insulin tolerance, insulin action, substrate metabolism and oxidative capacity, mitochondrial function, circulating and tissue lipids (lipidomics), circulating hormones / adipokines / cytokines, and diabetes complications. MMPC维持组织生物银行以及针对多种表型技术的标准方案的全面数据库,以及各种基因工程小鼠的表型结果。 MMPC领导层包括来自核受体生物学领域,脂质代谢,炎症和脂肪细胞和骨骼肌生物学领域的顶级研究人员,包括:Peter Tontonoz,Andrea Hevener,Karen Reue,Rajendra Tangirala,Edward Dennis,Osward Dennis,Osward Queheld Quehenberger。 MMPC的优势包括其领导能力的全面和补充专业知识以及生产力和高影响力科学出版物的出色记录。 MMPC团队的协作精神促进了一个大学环境,并支持与其他刚果民主共和国核心和机构资源协调的服务。 MMPC的核心目的是提高DRC成员在领先的代谢分析中的科学能力,以增强从细胞,组织和小鼠到MAN的研究思想的翻译来提高整体研究质量。
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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Andrea L Hevener其他文献
Andrea L Hevener的其他文献
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{{ truncateString('Andrea L Hevener', 18)}}的其他基金
The impact of ERalpha on mitochondrial function in macrophages
ERα对巨噬细胞线粒体功能的影响
- 批准号:
10366022 - 财政年份:2021
- 资助金额:
$ 32.66万 - 项目类别:
The impact of ERalpha on mitochondrial function in macrophages
ERα对巨噬细胞线粒体功能的影响
- 批准号:
10597663 - 财政年份:2021
- 资助金额:
$ 32.66万 - 项目类别:
Systems-based approaches for investigating tissue communication during exercise
用于研究运动期间组织通讯的基于系统的方法
- 批准号:
10264084 - 财政年份:2020
- 资助金额:
$ 32.66万 - 项目类别:
Systems-based approaches for investigating tissue communication during exercise
用于研究运动期间组织通讯的基于系统的方法
- 批准号:
10438852 - 财政年份:2020
- 资助金额:
$ 32.66万 - 项目类别:
The impact of estrogen receptor alpha on cardiomyocellular metabolism and health
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10713760 - 财政年份:2018
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$ 32.66万 - 项目类别:
The Impact of Heat Shock Protein Expression on Inflammation and Insulin Action
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7837687 - 财政年份:2009
- 资助金额:
$ 32.66万 - 项目类别:
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