Molecular Phenotyping Core
分子表型核心
基本信息
- 批准号:10656208
- 负责人:
- 金额:$ 12.13万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-01 至 2025-06-30
- 项目状态:未结题
- 来源:
- 关键词:Acyl Coenzyme AAddressAdipocytesAmino AcidsAnimalsAreaBasic ScienceBioinformaticsBiologicalBiological AssayCarnitineCellsCeramidesChromatographyClinicalClinical ResearchCollaborationsComplementComplexConsultationsConsumptionCost MeasuresCoupledCultured CellsDataData AnalysesData AnalyticsData SetDevelopmentDiseaseElectrospray IonizationEquipmentExerciseFatty AcidsFundingGas ChromatographyGene ExpressionGenus HippocampusGlycolysisHigh Pressure Liquid ChromatographyHuman ResourcesIn VitroInfrastructureLabelLaboratoriesLibrariesLipidsLiquid ChromatographyMeasurementMeasuresMetabolicMetabolismMethodsMichiganMitochondriaModelingMolecularMolecular AnalysisMultiomic DataMusNetwork-basedNucleic AcidsNutrition DisordersNutritional StudyObesityPhenotypePhospholipidsPhysiologicalPlasmaPostdoctoral FellowProceduresProcessProductionProtocols documentationProtonsResearchResearch PersonnelRespirationRodentSamplingSensitivity and SpecificityServicesShotgunsStandardizationSurveysSystemTechniquesTechnologyTestingTimeTissuesTrainingTrans Fatty AcidsTranslational ResearchUrineVisualizationWeight maintenance regimenanalytical toolbioinformatics toolbiological systemsbiomarker identificationcost effectivenessdata integrationdata pipelinedetection methodgraduate studenthigh throughput screeninghuman subjecthuman tissuein vivoinnovationinsightinstrumentinterestlarge datasetslipidomicsmetabolic abnormality assessmentmetabolomicsmolecular phenotypenovelnutritionobesity in childrenpre-clinicalprogramsresponseskillssmall moleculestable isotopestemtemporal measurement
项目摘要
Abstract/Summary - MPC
The Molecular Phenotyping Core will provide analytical tools to the MNORC investigators to
elucidate molecular mechanisms of disease relevant to obesity and nutritional disorders including
structural identification and quantification of metabolites, perform functional metabolic studies
and integrate multi-omic datasets to provide biological context. These include identifying
unknown metabolites, developing new methods for targeted metabolomics in a range of
biological matrices, validating new biological response indicators and providing biological
context to diverse metabolomic measurements by providing bioinformatics analysis and
developing new bioinformatics tools. In addition to providing instrumental infrastructure, the Core
staff will provide consultation and collaboration to apply metabolomics and data analytical
platforms in nutrition and obesity research. The Molecular Phenotyping Core will optimize the
efficiency and cost-effectiveness by providing these services to MNORC investigators through a
centralized laboratory. In the past five years the core has provided standardized analytical
techniques for the analysis of small molecule metabolites such as amino acid, lipid and nucleic
acid metabolites in samples from murine, rodent and human tissues, plasma, and urine, and
cultured cells. New offerings have included novel untargeted metabolomics platforms, metabolic flux
analysis and data interrogation and bioinformatics tools which will enhance the infrastructure available
for the MNORC investigators. Emphasis will also be placed on fulfilling the needs of Investigators
of the MNORC who will gain maximum benefit from the power of molecular analysis. We are
particularly interested in addressing three areas of need: first, applying the unique sensitivity and
specificity of molecular Phenotyping techniques to broaden understanding of nutritional
disorders ; second, the development of innovative techniques for the detection and structural
elucidation of nutrition-related biomolecules; third, provide data integration and bioinformatic tools
relevant to metabolomics studies; and fourt, providing training for graduate students and
postdoctoral fellows with an interest in nutrition research. By centralizing and standardizing
procedures, the Core provides a common set of analytical tools that will lead to a unified
understanding of molecular mechanisms involved in physiologic and pathophysiologic processes
underlying obesity and other nutrition related disorders.
摘要/总结 - MPC
分子表型核心将为 MNORC 研究人员提供分析工具
阐明与肥胖和营养失调相关的疾病的分子机制,包括
代谢物的结构鉴定和定量,进行功能代谢研究
并整合多组学数据集以提供生物学背景。这些包括识别
未知的代谢物,开发一系列靶向代谢组学的新方法
生物基质,验证新的生物反应指标并提供生物
通过提供生物信息学分析和不同代谢组学测量的背景
开发新的生物信息学工具。除了提供工具基础设施外,核心
工作人员将提供咨询和协作以应用代谢组学和数据分析
营养和肥胖研究平台。分子表型核心将优化
通过向 MNORC 调查人员提供这些服务来提高效率和成本效益
集中实验室。在过去的五年里,核心提供了标准化的分析
氨基酸、脂质和核酸等小分子代谢物分析技术
小鼠、啮齿动物和人体组织、血浆和尿液样本中的酸性代谢物,以及
培养的细胞。新产品包括新颖的非靶向代谢组学平台、代谢流
分析和数据询问以及生物信息学工具将增强可用的基础设施
供 MNORC 调查人员使用。重点还将放在满足调查人员的需求上
MNORC 的成员将从分子分析的力量中获得最大的利益。我们是
特别有兴趣解决三个领域的需求:首先,应用独特的敏感性和
分子表型技术的特异性扩大了对营养的理解
疾病;第二,开发检测和结构创新技术
阐明营养相关的生物分子;三、提供数据整合和生物信息工具
与代谢组学研究相关;第四,为研究生提供培训
对营养研究感兴趣的博士后研究员。通过集中化和标准化
程序,核心提供了一套通用的分析工具,这将导致统一的
了解生理和病理生理过程中涉及的分子机制
潜在的肥胖和其他营养相关疾病。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Subramaniam Pennathur其他文献
Subramaniam Pennathur的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Subramaniam Pennathur', 18)}}的其他基金
University of Michigan O'Brien Kidney Translational Resource Center (MKTC)
密歇根大学奥布莱恩肾脏转化资源中心 (MKTC)
- 批准号:
10746899 - 财政年份:2023
- 资助金额:
$ 12.13万 - 项目类别:
相似国自然基金
本体驱动的地址数据空间语义建模与地址匹配方法
- 批准号:41901325
- 批准年份:2019
- 资助金额:22.0 万元
- 项目类别:青年科学基金项目
时空序列驱动的神经形态视觉目标识别算法研究
- 批准号:61906126
- 批准年份:2019
- 资助金额:24.0 万元
- 项目类别:青年科学基金项目
针对内存攻击对象的内存安全防御技术研究
- 批准号:61802432
- 批准年份:2018
- 资助金额:25.0 万元
- 项目类别:青年科学基金项目
大容量固态硬盘地址映射表优化设计与访存优化研究
- 批准号:61802133
- 批准年份:2018
- 资助金额:23.0 万元
- 项目类别:青年科学基金项目
IP地址驱动的多径路由及流量传输控制研究
- 批准号:61872252
- 批准年份:2018
- 资助金额:64.0 万元
- 项目类别:面上项目
相似海外基金
Them1 Inhibitors for the Management of Non-Alcoholic Fatty Liver Disease
Them1 治疗非酒精性脂肪肝的抑制剂
- 批准号:
10666090 - 财政年份:2023
- 资助金额:
$ 12.13万 - 项目类别:
Molecular and cellular analysis of the ABHD5/PNPLA3 metabolon in lipid homeostasis
ABHD5/PNPLA3 代谢在脂质稳态中的分子和细胞分析
- 批准号:
10453590 - 财政年份:2021
- 资助金额:
$ 12.13万 - 项目类别:
Molecular and cellular analysis of the ABHD5/PNPLA3 metabolon in lipid homeostasis
ABHD5/PNPLA3 代谢在脂质稳态中的分子和细胞分析
- 批准号:
10296888 - 财政年份:2021
- 资助金额:
$ 12.13万 - 项目类别:
Molecular and cellular analysis of the ABHD5/PNPLA3 metabolon in lipid homeostasis
ABHD5/PNPLA3 代谢在脂质稳态中的分子和细胞分析
- 批准号:
10296888 - 财政年份:2021
- 资助金额:
$ 12.13万 - 项目类别:
Multisite phosphorylated S6K1 directs a regulatory module determining adipocyte lipid metabolism
多位点磷酸化 S6K1 指导决定脂肪细胞脂质代谢的调节模块
- 批准号:
10349543 - 财政年份:2020
- 资助金额:
$ 12.13万 - 项目类别: