The MADRC Neuropathology Core (NPC) provides systematic and standardized collection, pathologic characterization, storage, and distribution of human post-mortem material appropriate for the research requirements of investigators affiliated with the MADRC. The overall goal of the NPC is to facilitate research by MADRC and other investigators probling the dementias by providing access to human post-mortem material that is both clinically and pathologically well characterized using state-of-art techniques. NPC services support the needs of local researchers, as well as cooperative research across ADCs. Working in tandem with the Clinical Core, the NPC assists subjects and families of subjects followed by the Clinical Core with pre-arrangements for brain donatioa The NPC is responsible for rapid collection of post-mortem material, standardized preparation of fixed and frozen tissues for subsequent pathologic characterization and distribution to investigators, and storage of fixed and frozen material in brain bank. The NPC performs extensive pathologic characterization of harvested post-mortem material, distributes material to investigators, transmits data to the Data Management and Statistics Core, prepares post-mortem human material for investigators, assists investigators with use of human post-mortem material, and assists investigators with special staining methods. In a new initiative, the NPC is also assisting investigators with histologic evaluation of animal models of dementias. The NPC interacts extensively with other components of the MADRC. The NPC depends on the Administrative Core for crucial adminstrative oversight and support. The NPC works closely with the Clinical Core, Education Core, and Data Management and Statistics Core for subject recruitment, subject characterization, and data archiving. The NPC serves all projects, providing key histology services for Project 1, and crucial pathologic information for Projects 2 and 3. The NPC is a major resource for study of dementia on our campus and has been used by a number of investigators at other centers to further investigations of dementias and other neurodegenerations. The NPC will adhere to standard neuropathology procedures being developed by a neuropathology working group once those procedures have been issued.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG008671-18
Application #
7446636
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
18
Fiscal Year
2007
Total Cost
$248,565
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Sims, Rebecca (see original citation for additional authors) (2017) Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet 49:1373-1384
Michaud, Tzeyu L; High, Robin; Charlton, Mary E et al. (2017) Dependence Stage and Pharmacoeconomic Outcomes in Patients With Alzheimer Disease. Alzheimer Dis Assoc Disord 31:209-217
Monin, Joan K; Poulin, Michael J; Brown, Stephanie L et al. (2017) Spouses' daily feelings of appreciation and self-reported well-being. Health Psychol 36:1135-1139
Jun, Gyungah R; Chung, Jaeyoon; Mez, Jesse et al. (2017) Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimers Dement 13:727-738
Cary, Brian P; Brooks, Allen F; Fawaz, Maria V et al. (2016) Synthesis and Evaluation of [(18)F]RAGER: A First Generation Small-Molecule PET Radioligand Targeting the Receptor for Advanced Glycation Endproducts. ACS Chem Neurosci 7:391-8
Karch, Celeste M; Ezerskiy, Lubov A; Bertelsen, Sarah et al. (2016) Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci. PLoS One 11:e0148717
Mez, Jesse; Mukherjee, Shubhabrata; Thornton, Timothy et al. (2016) The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable. Neurobiol Aging 41:115-121
Ridge, Perry G; Hoyt, Kaitlyn B; Boehme, Kevin et al. (2016) Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiol Aging 41:200.e13-200.e20
Hohman, Timothy J; Bush, William S; Jiang, Lan et al. (2016) Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiol Aging 38:141-150
Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M et al. (2016) A novel Alzheimer disease locus located near the gene encoding tau protein. Mol Psychiatry 21:108-17

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