grant

Biomarker Core

Organization CLEVELAND CLINIC LERNER COM-CWRULocation CLEVELAND, UNITED STATESPosted 1 Sept 2021Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY2025A β-42A β42A-beta 42A-beta42AD dementiaAD related dementiaADRDAbeta-42Abeta42AddressAfrican American groupAfrican American individualAfrican American peopleAfrican American populationAfrican AmericansAllelesAllelomorphsAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's and related dementiasAlzheimer's biomarkerAlzheimer's dementia and related dementiaAlzheimer's dementia or related dementiaAlzheimer's disease and related dementiaAlzheimer's disease and related disordersAlzheimer's disease biological markerAlzheimer's disease or a related dementiaAlzheimer's disease or a related disorderAlzheimer's disease or related dementiaAlzheimer's disease related dementiaAlzheimers DementiaAlzheimer’s biological markerAlzheimer’s disease biomarkerAmentiaAmyloid beta-42Amyloid beta42Amyloid β-42Amyloid β42Amyloidβ-42Amyloidβ42AssayAβ-42Aβ42BioassayBiological AssayBiological MarkersBloodBlood PlasmaBlood Reticuloendothelial SystemCCL2CCL2 geneCD183CKR-L2CMKAR3CRG-2CXCL10CXCL10 geneCXCR3CXCR3 geneCatalogingCatalogsCerebrospinal FluidChemokine (C-X-C Motif) Receptor 3Chemokine, CC Motif, Ligand 2Chemotactic CytokinesClinicClinicalClinical DataCognitive DiscriminationCollaborationsCollectionCommunitiesConsultationsDNADataData BasesData Management and Analysis CoreData Management and Statistical Analysis CoreData Management and Statistical CoreData SetData Storage and RetrievalDatabasesDegenerative Neurologic DisordersDementiaDementia with Lewy BodiesDeoxyribonucleic AcidDiagnosisDiscriminationDiseaseDisease ProgressionDisorderEnsureFoundationsFutureG Protein-Coupled Receptor 9GPR9Gene variantGeneticGenetic DiseasesGenotypeGoalsHeterogeneityHomologous Chemotactic CytokinesHumanHuman ResourcesIFI10INP10IP-10IP10IP10 ReceptorIP10-Mig receptorIP10-RImageInflammationInfrastructureIntercrinesInternationalInvestigatorsLightLinkMCAFMCP-1MCP1MOB-1MT-bound tauManpowerMedical centerMentorsMig ReceptorMig-RMigRMissionModern ManMolecularMolecular AnalysisMolecular GeneticsMonitorMonocyte Chemoattractant Protein-1Monocyte Chemotactic Protein-1Monocyte Chemotactic and Activating FactorMonocyte Chemotactic and Activating ProteinMonocyte Chemotactive and Activating FactorMonocyte Secretory Protein JENAC precursorNational Institute of AgingNational Institute on AgingNervous System Degenerative DiseasesNeural Degenerative DiseasesNeural degenerative DisordersNeurochipNeurodegenerative DiseasesNeurodegenerative DisordersNeurologic Degenerative ConditionsOther GeneticsPARK1 proteinPARK4 proteinPSEN1ParticipantPathogenicityPathologyPhotoradiationPlasmaPlasma SerumPopulationPopulation HeterogeneityPrimary Senile Degenerative DementiaProcessProtein AnalysisR-Series Research ProjectsR01 MechanismR01 ProgramResearchResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearch SpecimenResearchersReticuloendothelial System, Serum, PlasmaS182 proteinSCYA2SCYB10SIS cytokinesSNCASNCA proteinSalivaSamplingSecureSkinSmall Inducible Cytokine A2SpecimenSymptomsSystemTREM2TREM2 geneTherapeuticTimeTrainingTranslationsTriggering Receptor Expressed in Myeloid Cells 2Triggering Receptor Expressed on Myeloid Cells 2Underrepresented GroupsUnderrepresented PopulationsUnited States Department of Veterans AffairsUnited States Veterans AdministrationUniversitiesUniversity HospitalsUrineVeterans AdministrationVeterans Affairsa-syna-synucleinallelic variantalpha synucleinalpha synuclein genealphaSP22asynbio-markersbiobankbiologic markerbiological heterogeneitybiomarkerbiomarker discoverybiorepositorycatalogcerebral spinal fluidchemoattractant cytokinechemokineclinical relevanceclinically relevantconsultationcytokinedata basedata exchangedata retrievaldata storagedata transferdata transmissiondegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesdepositorydistributed datadiverse populationseducation researchgIP-10genetic analysisgenetic conditiongenetic disordergenetic variantgenomic variantheterogeneous populationimagingimprovedinnovateinnovationinnovativeinsoluble aggregatemicrotubule bound taumicrotubule-bound tauneurodegenerative illnessneurofilamentneuropathologicneuropathologicalneuropathologynon A-beta component of AD amyloidnon A4 component of amyloid precursorp-taup-τpersonnelphospho-tauphospho-τphosphorylated taupopulation diversitypost-translational modification of tauposttranslational modification of taupresenilin 1 proteinpresenilin-1primary degenerative dementiaprogramsprotein aggregateprotein aggregationprotein biomarkersprotein markersrepositorysenile dementia of the Alzheimer typespecific biomarkersspinal fluidsuccesstautau Proteinstau factortau phosphorylationtau posttranslational modificationtau-1translationtranslational therapeuticstranslational therapyunder representation of groupsunder represented groupsunder represented peopleunder represented populationsunderrepresentation of groupsunderrepresented peopleα synuclein geneα-synα-synucleinτ Proteinsτ phosphorylation
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Full Description

PROJECT SUMMARY
The mission of the Biomarker Core (BC) is to support Alzheimer's disease (AD) and AD-related dementias

(AD/ADRD) research projects by collecting, storing, tracking, sharing, and analyzing biospecimens and

associated clinical, genetic, and biomarker data. The collected clinical, genetic, and biomarker data on a

variety of human biospecimens will contribute to the understanding of AD/ADRD underlying heterogeneity by

cataloging the onset, progression, and disease symptoms of participant biospecimens currently stored in the

Cleveland Alzheimer's Disease Research Center (CADRC) BC. This information will contribute to improving

diagnosis in unique, understudied populations, as well as the population as a whole. Toward this mission, we

previously established and integrated biospecimen collection and research collaborations between Case

Western Reserve University, Cleveland Clinic, MetroHealth Systems, University Hospitals, and the Louis Stoke

Cleveland VA Medical Center. The aims of the BC are to 1) Facilitate research by leveraging and expanding

the CADRC BC infrastructure and biospecimens linked with participant clinical data in the integrated database

and continue to include longitudinal biospecimen collection, 2) Provide basic biomarker characterization to

facilitate AD/ADRD research, 3) Provide basic genetic characterization to facilitate AD/ADRD research, and 4)

Distribute biospecimens to neurodegenerative disease consortiums and coordinating centers, as well as to

internal and external investigators. Toward these aims, our team of experts will continue to contribute to

biospecimen collection for the CADRC. The establishment of the CADRC BC has provided an essential

infrastructure to facilitate and integrate the independent projects of unique and understudied populations, such

as African Americans, as well as understudied neurodegenerative disorders, including atypical AD and

dementia with Lewy bodies. Standard clinical data (the Uniform Data Set) from these diverse understudied

populations will continue to be linked with generated biomarker and genetic data. Genetic and biomarker data

linked to relevant clinical data in accordance with goals of the National Alzheimer's Project Act (NAPA) are

shared with the scientific community including the Alzheimer's Disease Genetic Consortium (ADGC), National

Alzheimer's Coordinating Center (NACC), and the National Institute on Aging Genetics of Alzheimer's Disease

Data Storage (NIAGADS). The already established CCLRCBH-Biobank and our highly trained personnel has

insured seamless creation of the CADRC BC. Importantly, the CADRC BC infrastructure is now in place to

facilitate future innovative AD/ADRD research projects that enhances our understanding of the heterogeneity

of AD/ADRD pathology.

Grant Number: 5P30AG072959-05
NIH Institute/Center: NIH

Principal Investigator: Lynn Bekris

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