grant

The Phex Pathway: Mechanisms Underlying a Meniere's Disease Subtype

Organization MASSACHUSETTS EYE AND EAR INFIRMARYLocation BOSTON, UNITED STATESPosted 1 May 2025Deadline 31 Mar 2030
NIHUS FederalResearch GrantFY2025Animal ModelAnimal Models and Related StudiesAntibodiesAuditoryAutomobile DrivingAutopsyAutoregulationAwardBilateralBlood SerumBone GrowthCausalityCharacteristicsChromosome MappingChronicClinical TreatmentClinical Treatment MoabCochleaCochlear OrganCorti CellDNA mutationDataDegenerative DisorderDevelopmentDysfunctionEmbryoEmbryonicEndolymphatic HydropsEpithelial CellsEquilibrium Hair CellEtiologyExhibitsFailureFamilial hypophosphatemic bone diseaseFunctional disorderGene LocalizationGene MappingGene Mapping GeneticsGeneral RadiologyGenesGenetic ChangeGenetic defectGenetic mutationGenotypeGoalsGrantHair CellsHearing DisordersHearing LossHearing problemHereditaryHistologicHistologicallyHomeostasisHumanHypoacusesHypoacusisHypophosphatemic RicketsImpairmentInheritedInner Ear DisorderInstitutionInternal EarKnowledgeLaboratoriesLabyrinthLeadLinkLinkage MappingMeniere's DiseaseMeniere's DisorderMeniere's SyndromeMentorsMetabolic DiseasesMetabolic DisorderMiceMice MammalsModelingModern ManMolecularMonoclonal AntibodiesMorphologyMurineMusMutationMénière's diseaseOrphan DiseasePathway interactionsPatientsPb elementPeripheralPhenotypePhosphatesPhysiologicPhysiologicalPhysiological HomeostasisPhysiologyPhysiopathologyPlayProductionRadiographyRadiologyRadiology SpecialtyRare DiseasesRare DisorderResearchRicketsRoentgenographyRoleScientistSerumSignal PathwaySpinning SensationSubjective VertigoSurgeonSymptomsTemporal BoneTemporal bone structureTestingThesaurismosisTimeTotal Human and Non-Human Gene MappingTrainingTranscriptVIT DVertigoVestibularVestibular AqueductVestibular Hair CellsVestibular System ImpairmentVestibular defectVestibular dysfunctionVestibular lossVestibular problemsVitamin DVitamin D-Resistant RicketsWild Type MouseWorkX linked hypophosphatemia in ricketsX-Linked Hypophosphatemic RicketsX-linked hypophosphatemiaauditory diseaseauditory disorderauditory dysfunctionauditory problemcausationclinical diagnosisclinical diagnosticsclinical interventionclinical therapycohortdebilitating symptomdegenerative conditiondegenerative diseasedevelopmentaldiagnostic criteriadisabling symptomdisease causationdisease subgroupsdisease subtypedisorder subtypedrivingdysfunctional hearingear hair cellearly adulthoodemerging adultendolymphatic sacentire genomefamilial hypophosphatemia in ricketsfull genomefunctional lossfunctional mimicsgenetic mappinggenome mutationgenome sequencinghearing challengedhearing defecthearing deficienthearing deficithearing difficultyhearing diseasehearing dysfunctionhearing impairmentheavy metal Pbheavy metal leadhypophosphatemia in ricketsimprovedin uteroin vivoinner earinner ear diseasesinorganic phosphatelabyrinthine hydropslater in lifelater lifeloss of function mutationmAbsmedical diagnosticmetabolism disordermodel of animalmonoclonal Absmouse modelmurine modelnecropsyneuronal survivalorphan disorderpathophysiologypathwaypost-natal developmentpostmortempostnatalpostnatal developmentpreventpreventingprogressive hearing lossradiological imagingsocial rolespatial and temporalspatial temporalspatiotemporaltrial regimentrial treatmentvestibular deficitvestibular impairmentvestibular systemvestibular system dysfunctionwhole genomewildtype mouse
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Project Summary
Meniere’s disease (MD), a chronic inner ear disorder characterized by debilitating symptoms of

progressive hearing loss and episodic vertigo, arises from unclear etiology. Recent work from our institution

identified a distinct subtype of MD – designated MDhp – representing a group of patients with hypoplasia of the

endolymphatic…

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The Phex Pathway: Mechanisms Underlying a Meniere's Disease Subtype — MASSACHUSETTS EYE AND EAR INFIRMARY | UNITED STATE | Dev Procure