Mouse Phenotype Core, Project 9 of 10
小鼠表型核心,项目 9(共 10 个)
基本信息
- 批准号:7883580
- 负责人:
- 金额:$ 37.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2007
- 资助国家:美国
- 起止时间:2007-09-30 至 2012-06-30
- 项目状态:已结题
- 来源:
- 关键词:AffectAmino Acid SequenceAnimal Disease ModelsAnimal ModelAntibody FormationAntigensArtsBehavioralBehavioral AssayBiological AssayBlood Chemical AnalysisBrainCollaborationsConsultCore FacilityCrystallographyDNA SequenceDataDetectionDiseaseElectronicsEnsureEquilibriumEquipmentFacultyFee-for-Service PlansFlow CytometryFundingGene ExpressionGene TargetingGlucoseGoalsGrantGuidelinesHealth Services AccessibilityHistologyHome environmentHormonesImageIn SituKineticsKnowledgeLaboratoriesLifeLipidsMagnetic ResonanceMass Spectrum AnalysisMeasurementMessenger RNAMetabolicMethodologyMethodsMicroarray AnalysisMissionMusNeuroanatomyObesityOrganismPatient CarePeptide Sequence DeterminationPhenotypePhysiologicalPhysiologyProceduresProductionQuality ControlRNA chemical synthesisResearchResearch PersonnelResourcesReverse Transcriptase Polymerase Chain ReactionRunningSamplingScientistSerumServicesSliceStagingStaining methodStainsStudy of magneticsSynaptic plasticityTestingTimeTransgenic AnimalsTranslatingWorkX-Ray Computed Tomographyadverse outcomeanalytical ultracentrifugationbasebody systemcellular imagingglucose toleranceinsightinterestlaser capture microdissectionmembernovelresearch studysmall moleculestructural biologysuccessweb site
项目摘要
The adverse consequences of obesity are pleiotrophic for the mammalian organism. Animal models of
obesity that allow careful characterization of the pervasive metabolic effects of the disease are vital to the
success of our mission. To enhance research into the causes and consequences of obesity, we established
a mouse phenotyping core. The primary goals of this core are to develop and provide standardized state-ofthe-
art methods for the analysis of animal models of disease. The core applies the analytical expertise of ten
laboratories to provide histology, neuroanatomy, gene expression, mass spectrometry, physiology, lipid,
glucose, metabokine, and behavioral assays. The core is directed by Russell, Elmquist, and Scherer and is
staffed by a dedicated team of skilled technicians who utilize existing equipment to perform optimized assays
on samples provided by TORS investigators. Currently available assays include histological staining and
antigen detection, in situ mRNA hybridization, real time reverse transcriptase-PCR, microarray analysis,
laser capture microdissection, small molecule mass spectrometry and metabolite profiling, metabolic cage
analyses, complete lipid balance studies, magnetic resonance and computed tomography imaging, glucose
tolerance and clamp analyses, serum hormone measurements, routine blood chemistries, exhaustive
behavioral analyses, and synaptic plasticity measurements in brain slices. As new research findings dictate,
novel methodologies are developed and made available by the core. For each experiment, results are
collected, calculated, and compiled in electronic format and returned to submitting investigators. The
availability of the services provided by this core accelerates the pace of our research, allows centralized
troubleshooting, and facilitates the efficient utilization of existing expertise and resources. The mouse
phenotyping core is a crucial component of our Roadmap effort that brings together a diverse team of
scientists and clinicians to ensure that discoveries made in obesity research are rapidly translated into
advances in patient care.
肥胖的不利后果对于哺乳动物来说是多效性的。动物模型
肥胖症可以仔细表征疾病的普遍代谢影响,这对于
我们的使命取得成功。为了加强对肥胖原因和后果的研究,我们建立了
小鼠表型核心。该核心的主要目标是开发和提供标准化的最新技术
用于分析疾病动物模型的艺术方法。核心应用了十位专家的分析专业知识
实验室提供组织学、神经解剖学、基因表达、质谱、生理学、脂质、
葡萄糖、代谢因子和行为测定。核心由 Russell、Elmquist 和 Scherer 执导,
拥有一支由熟练技术人员组成的专业团队,他们利用现有设备来执行优化的检测
由 TORS 调查员提供的样本。目前可用的检测方法包括组织学染色和
抗原检测、原位 mRNA 杂交、实时逆转录酶 PCR、微阵列分析、
激光捕获显微切割、小分子质谱和代谢物分析、代谢笼
分析、完整的脂质平衡研究、磁共振和计算机断层扫描成像、葡萄糖
耐受性和钳夹分析、血清激素测量、常规血液化学、详尽的
行为分析和大脑切片中的突触可塑性测量。新的研究结果表明,
核心开发并提供了新的方法。对于每个实验,结果是
以电子格式收集、计算和汇编并返回给提交调查人员。这
该核心提供的服务的可用性加快了我们研究的步伐,允许集中
故障排除,并促进现有专业知识和资源的有效利用。鼠标
表型分析核心是我们路线图工作的重要组成部分,该路线图汇集了多元化的团队
科学家和临床医生确保肥胖研究的发现能够迅速转化为
患者护理方面的进步。
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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DAVID W. RUSSELL其他文献
Strand segregation or recombination
链分离或重组
- DOI:
10.1038/329678b0 - 发表时间:
1987-10-22 - 期刊:
- 影响因子:48.500
- 作者:
DAVID W. RUSSELL - 通讯作者:
DAVID W. RUSSELL
DAVID W. RUSSELL的其他文献
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{{ truncateString('DAVID W. RUSSELL', 18)}}的其他基金
2009 Lipids, Molecular & Cellular Biology of Gordon Research Conference
2009 脂质,分子
- 批准号:
7743873 - 财政年份:2009
- 资助金额:
$ 37.01万 - 项目类别:
Cholesterol and Oxysterol Metabolism in Brain and Liver
脑和肝脏中的胆固醇和氧甾醇代谢
- 批准号:
7217721 - 财政年份:2007
- 资助金额:
$ 37.01万 - 项目类别:
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