grant

Signaling mechanisms of the cerebral cavernous malformations protein complex

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 1 Jun 2024Deadline 31 May 2029
NIHUS FederalResearch GrantFY202520S Catalytic Proteasome20S Core Proteasome20S Proteasome20S ProteosomeAddressAnimal ModelAnimal Models and Related StudiesAnkyrin Repeat-Containing Protein KRIT1ApoplexyAssayBMK1BMK1 KinaseBeliefBig MAP Kinase 1BindingBioassayBiochemicalBiologic ModelsBiological AssayBiological ModelsBlood VesselsBrachydanio rerioBrain Vascular AccidentCCM1CCM1 geneCell Communication and SignalingCell SignalingCell modelCellular modelCerebral StrokeCerebrovascular ApoplexyCerebrovascular StrokeCirculationComplexCryo-electron MicroscopyCryoelectron MicroscopyCrystallographiesCrystallographyDNA mutationDanio rerioDataDefectDevelopmentDiseaseDisorderERK4ERK5ERK5 KinaseElectron CryomicroscopyEmbryoEmbryonicGenesGenetic ChangeGenetic defectGenetic mutationGoalsHeartIndividualIntracellular Communication and SignalingKO miceKRIT1KinasesKnock-outKnock-out MiceKnockoutKnockout MiceKnowledgeKrev Interaction Trapped 1LaboratoriesMAP Kinase CascadesMAP Kinase Kinase KinaseMAP Kinase ModulesMAP Kinase Signaling CascadesMAP kinaseMAP kinase 7MAP3 KinasesMAPK7MAPK7 Mitogen-Activated Protein KinaseMAPK7 geneMAPKKKsMacropainMacroxyproteinaseMitogen Activated Protein Kinase 7Mitogen-Activated Protein Kinase Kinase KinasesMitogen-Activated Protein KinasesModel SystemModelingMolecularMolecular InteractionMulticatalytic ProteinaseMutationN-terminalNH2-terminalNeurologicNeurologicalNon-sense Mediated DecayNonsense-Mediated DecayNull MouseOutcomePRKM7Pathway interactionsPeptide DomainPhenotypePhosphotransferase GenePhosphotransferasesProsomeProteasomeProteasome Endopeptidase ComplexProtein DeficiencyProtein DomainsProteinsProteosomeRecurrenceRecurrentRegulationResearchRoleSeizuresSignal PathwaySignal TransductionSignal Transduction SystemsSignalingSignaling Factor Proto-OncogeneSignaling Pathway GeneSignaling ProteinStrokeStructural ModelsStructureTertiary Protein StructureTestingTransphosphorylasesVascular EndotheliumZebra DanioZebra FishZebrafishbiochemical modelbiological signal transductionbiophysical analysisbiophysical characteristicsbiophysical characterizationbiophysical measurementbiophysical parametersbiophysical propertiesbiophysical studiesbrain attackcerebral cavernous malformationscerebral vascular accidentcerebrovascular accidentcryo-EMcryoEMcryogenic electron microscopydeficiency of proteindevelopmentalgenome mutationloss of functionloss of function mutationmembermodel of animalmulticatalytic endopeptidase complexpathwayprotein complexprotein functionprotein protein interactionrecruitscaffoldscaffoldingsocial rolestoichiometrystrokedstrokesvascularvascular abnormality
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Multi-PI: Titus J. Boggon and David A. Calderwood
TITLE: Signaling mechanisms of the cerebral cavernous malformations protein complex

ABSTRACT

Loss of function mutations in the genes encoding KRIT1 (CCM1), CCM2 (OSM), or CCM3 (PDCD10) cause

Cerebral Cavernous Malformations (CCM). The presentation of this disease includes dilated leaky blood…

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Signaling mechanisms of the cerebral cavernous malformations protein complex — YALE UNIVERSITY | UNITED STATES | Jun 202 | Dev Procure