FAILED REGENERATION IN THE MUSCULAR DYSTROPHIES: INFLAMMATION, FIBROSIS AND FAT
FAILED REGENERATION IN THE MUSCULAR DYSTROPHIES: INFLAMMATION, FIBROSIS AND FAT
批准号:
9119600
负责人:
H Lee Sweeney
金额:
$153.37万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-25 至 2020-07-31
关键词:
AddressAnimal ModelBinding ProteinsBudgetsCardiacClinicalClinical TrialsClinical Trials DesignConnective TissueDepositionDiseaseDisease ProgressionDisease modelDuchenne muscular dystrophyEducational process of instructingFatty acid glycerol estersFibrosisFundingGenetic VariationGoalsGrantHeartHeart DiseasesHumanImageIndustryInfiltrationInflammationInflammation MediatorsInflammation ProcessInvestigationInvestigational DrugsLeadLegMagnetic Resonance ImagingMaintenanceMeasuresMonitorMuscleMuscular DystrophiesMyopathyNatural HistoryNatural regenerationNatureOutcome MeasurePathogenesisPathway interactionsPatientsPharmaceutical PreparationsPilot ProjectsPopulationProcessProtease InhibitorProtocols documentationResearchResearch PersonnelRespiratory MusclesRoleSafetySiteSkeletal MuscleStructureTestingTherapeuticTherapeutic AgentsTransforming Growth Factor betaTranslationsValidationVariantcell typedesigndrug efficacyimaging biomarkerimaging modalityimprovedinhibitor/antagonistinsightmdx mousemouse modelmuscle regenerationmuscular dystrophy mouse modelnew therapeutic targetnon-invasive imagingnovelosteopontinpreclinical studypreventpublic health relevancerepairedsuccesstherapeutic targettool
中文摘要
英文摘要
DESCRIPTION (provided by applicant): This MDCRC is organized around the central theme of improving muscle regeneration in a number of types of muscular dystrophy by inhibiting fibrosis and limiting fatty replacement of muscle, thus improving skeletal muscle repair and preserving cardiac function. Interacting and collaborative studies are proposed to address by what mechanisms muscle fibrosis and fat deposition occur. Project 1 is focused on understanding the pathways and cell types that contribute to inflammation, fibrosis, and fatty deposition. Project 1 will evaluate a number of potential therapeutics, utilizing an exciting new mouse model of DMD, the mdx mouse on the DBA background, which may greatly accelerate successful drug translation. Project 2 is focused on identifying and characterizing modifiers of cardiac disease, which in many cases will be modifiers of skeletal muscle disease as well. Project 3 will gain insights into how genetic variations in LTBP4 and Osteopontin impact imaging biomarkers of disease in the heart, respiratory muscles, and leg muscles of DMD patients. In doing so, Project 3 will develop MRI/MRS protocols for monitoring disease progression in the respiratory muscles.
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会议论文
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Development of novel small molecules for delaying the progression of muscular dy
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Protease Inhibition as Possible therapy for Muscular Dystrophy
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Administrative & Training Core
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资助金额:$19.45万
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财政年份:2007
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Development of novel small molecules for delaying the progression of muscular dy
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财政年份:2007
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Development of small molecules for delaying the progression of muscular dystrophy
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依托单位:
Regulation and Mechano-Chemistry of Myosins V and VI
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批准号:7504381
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项目类别:
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资助金额:$24.37万
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Development of novel small molecules for delaying the progression of muscular dy
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依托单位:
Understanding and Improving Therapies for the Muscular Dystrophies
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Core A - Admin Core
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批准号:10459579
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资助金额:$3.43万
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依托单位:
CO_FUND
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资助金额:$40.0万
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依托单位:
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项目类别:
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依托单位:
海外基金