Mitochondrial Biogenesis and Dynamics in Health, Disease and Aging
Mitochondrial Biogenesis and Dynamics in Health, Disease and Aging
批准号:
8528297
负责人:
Giovanni Manfredi
金额:
$0.5万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-11 至 2014-05-31
关键词:
AgingAging-Related ProcessAlzheimer&aposs DiseaseAreaBasic ScienceBiogenesisBiologyCardiomyopathiesCell Differentiation processCellular biologyCollaborationsCommunicationCommunitiesComplexDefectDiabetes MellitusDiseaseFriedreich AtaxiaFunctional disorderGleanGoalsHealthHeart DiseasesHereditary Spastic ParaplegiaHumanImmune responseIncidenceInflammatory ResponseInheritedLeber&aposs Hereditary Optic NeuropathyLeigh DiseaseLinkLiver diseasesLongevityMalignant NeoplasmsMedicineMetabolicMetabolic DiseasesMetabolismMinorityMitochondriaMitochondrial DiseasesMontanaMorphologyNerve DegenerationNeurodegenerative DisordersNorth AmericaOralOrganellesOutcomeOxygenParkinson DiseasePathologyPathway interactionsPatientsPhysiological ProcessesPostdoctoral FellowProcessProductionProtein ImportPublic HealthRegulationResearchResearch PersonnelRespiratory ChainRoleScienceScientistSeminalSignal TransductionSiteStudentsTimeTranslational ResearchUniversitiesWomanWorkage relatedcell growthforgingfrontiergraduate studenthuman diseaseinsightinterestmedical schoolsmeetingsmitochondrial dysfunctionnovelposterspublic health relevancerespiratorysymposium
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Mitochondria are essential cellular organelles, long noted for their central function in ATP production, as well as many other anabolic and catabolic pathways. Exciting new breakthroughs in our understanding of basic biology and function of mitochondria have taken place in recent years. New research has identified mitochondria as key players in many aspects of cell biology and disease, well beyond their central role in metabolism, including control of cell growth and differentiation, oxygen sensing and ROS signaling, and as hubs of the innate immune and inflammatory responses. These advances have led to realization that the contribution of mitochondria to human disease and aging is multifaceted and more far-reaching than previously anticipated. Therefore, the importance of the 2013 FASEB conference "Mitochondrial Biogenesis and Dynamics in Health, Disease and Aging", for which this proposal seeks support, is clear. There is a growing need to create interactions between investigators that understand and study the basic biology of the organelle with those engaged at these new frontiers of mitochondria, with the goal of melding these activities into a better understanding of how mitochondrial dysfunction contributes to human disease and aging. This area is undoubtedly one of the most exciting research topics in contemporary biology and medicine. The major topics that will be covered in this meeting are: 1) Basic Mitochondrial Biology, 2) Mitochondrial Diseases; 3) Mitochondria in Aging and Longevity; 4) New Frontiers in Mitochondrial Biology and Medicine. The meeting will bring together scientists with a broad range of expertise, ranging from established investigators to graduate students, to present and discuss the most recent advances in the biology of mitochondria and its links to disease and aging. The conference will facilitate discussion of basic and biomedical science as well as stimulate translational research opportunities. The goals will be: 1) to organize and support a conference in the field of mitochondrial biology and dysfunction. The conference will be held June 16-21, 2013, at the FASEB conference site in Big Sky, Montana; 2) to promote the exchange of scientific ideas among basic and translational scientists interested in diverse aspects of mitochondrial biology and mitochondrial dysfunction in human disease and in aging, with a focus on stimulate collaborative approaches and cross-field stimulation; 3) to encourage and promote participation by junior investigators, women and minorities, with the goal of integrating them in this important and rapidly growing field.
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会议论文
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批准号:10403558
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资助金额:$110.18万
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批准号:10616130
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资助金额:$110.17万
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资助金额:$6.95万
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The role of the mitochondrial protein dimer CHCHD2/10 in health and disease
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资助金额:$25.43万
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负责人:Giovanni Manfredi
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依托单位:
Impaired amino acid metabolism in mitochondrial diseases
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批准号:8658872
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项目类别:
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资助金额:$20.98万
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财政年份:2013
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负责人:Giovanni Manfredi
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依托单位:
Modulation of Oxidative phosphorylation by mitochondrial soluble adenylyl cyclase
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批准号:8332758
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资助金额:$35.49万
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财政年份:2009
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依托单位:
Defects of mitochondrial dynamics in ALS
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批准号:8385580
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资助金额:$34.64万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Modulation of Oxidative phosphorylation by mitochondrial soluble adenylyl cyclase
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批准号:8203778
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项目类别:
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资助金额:$35.49万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Defects of mitochondrial dynamics in ALS
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批准号:8010933
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资助金额:$35.91万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Modulation of Oxidative phosphorylation by mitochondrial soluble adenylyl cyclase
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批准号:8727587
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项目类别:
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资助金额:$35.49万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Defects of mitochondrial dynamics in ALS
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批准号:7594948
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项目类别:
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资助金额:$38.07万
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负责人:Giovanni Manfredi
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依托单位:
Modulation of Oxidative phosphorylation by mitochondrial soluble adenylyl cyclase
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项目类别:
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资助金额:$34.25万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Defects of mitochondrial dynamics in ALS
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批准号:8197704
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项目类别:
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资助金额:$35.9万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Modulation of Oxidative phosphorylation by mitochondrial soluble adenylyl cyclase
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批准号:7924568
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项目类别:
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资助金额:$35.49万
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财政年份:2009
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负责人:Giovanni Manfredi
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依托单位:
Mitochondrial calcium homeostasis in SOD1-familial ALS
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项目类别:
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资助金额:$36.23万
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财政年份:2006
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负责人:Giovanni Manfredi
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依托单位:
Mitochondrial calcium homeostasis in SOD1-familial ALS
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批准号:7992700
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项目类别:
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财政年份:2006
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依托单位: