Molecular Mechanisms of Fibrosis: From Bench to Bedside
Molecular Mechanisms of Fibrosis: From Bench to Bedside
批准号:
7223388
负责人:
ANDREW D ROBERTSON
金额:
$1.5万
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
项目状态:
已结题
起止时间:
2007-03-01 至 2008-02-28
关键词:
AffectArchitectureAreaBone MarrowCaliforniaCardiacCerebrumChronicCitiesClinicalClinical Trials DesignConnective TissueDepositionDevelopmentDiseaseDisease regressionDrug IndustryElementsEndopeptidasesEpithelialExperimental ModelsExtracellular MatrixFibrosisGoalsGraft RejectionGrowth FactorHamman-Rich syndromeHeart DiseasesHumanIndividualInflammationInflammatoryInterstitial Lung DiseasesKidneyKidney DiseasesKnowledgeLiverLiver CirrhosisLungLymphocyteMalignant NeoplasmsMesenchymalModelingMolecularMorbidity - disease rateNeoplasm MetastasisNormal tissue morphologyNumbersPathway interactionsPeptide HydrolasesPeripheral Vascular DiseasesPharmaceutical PreparationsPreclinical Drug EvaluationProductionProgressive DiseaseResearch PersonnelRoleSkinStimulusSystemSystemic SclerodermaTissuesTransplant RecipientsVascular Diseasesbasebench to bedsidebody systemcytokinefibrogenesismembermonocytemortalitynovelresearch clinical testingsymposium
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
This proposal is to request support for a Keystone Symposium entitled "Molecular Mechanisms of Fibrosis: From Bench to Bedside", which will be held in Tahoe City, California from March 11-15, 2007. Fibrosis affects nearly all tissues and organ systems. Diseases in which fibrosis is a major cause of morbidity and mortality include the interstitial lung diseases, liver cirrhosis, kidney disease, heart disease, and systemic sclerosis, among others. Fibrotic tissue remodeling can also influence cancer metastasis and accelerate chronic graft rejection in transplant recipients. Current treatments for fibrotic disorders target the inflammatory cascade, but they have been widely unsuccessful, largely because the mechanisms that are involved in fibrogenesis are believed to be distinct from those involved in inflammation. Because mechanistic studies are difficult to carry out in humans, numerous experimental models have been developed over the past few years to dissect the immunological and molecular mechanisms of fibrosis. The first of new therapies based on these models are just beginning to approach clinical testing. The goal of this meeting is to bring together academic researchers, clinicians, and members of the pharmaceutical industry to discuss the most recent advances in the field and to identify common mechanistic themes of tissue fibrogenesis in various tissue systems. By bringing together a diverse group of researchers, the meeting will provide a more integrated perspective from basic disease mechanisms through to the more pragmatic challenges of clinical trial design in chronic progressive disease.
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批准号:8056942
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Hematopoiesis
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资助金额:$0.8万
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Tuberculosis: Immunology, Cell Biology and Novel Vaccination Strategies
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批准号:8055809
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资助金额:$1.5万
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NK and NKT Cell Biology: Specificity and Redundancy of Innate Responses
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批准号:8006107
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资助金额:$0.8万
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依托单位:
MicroRNAs and Human Disease - Olson, Chair
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批准号:8061929
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资助金额:$2.0万
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依托单位:
Inositide Signaling in Pharmacology and Disease
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批准号:8061909
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资助金额:$1.0万
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Autophagy
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批准号:8121906
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资助金额:$0.7万
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New Frontiers at the Interface of Immunity and Glycobiology
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依托单位:
HIV Evolution, Genomics, and Pathogenesis
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资助金额:$2.3万
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Protection from HIV: Targeted Intervention Strategies
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资助金额:$2.0万
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Immunologic Memory, Persisting Microbes and Chronic Disease
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Lipid Biology and Lipotoxicity
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Lung Development and Repair
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B Cells: New Insights into Normal versus Dysregulated Function
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海外基金