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Molecular Events in the Progression of Alzheimer’s Disease



Lee Makowski



Northeastern University



WEDNESDAY, October 20, 13:30 (EST)



Register in advance for this meeting:

https://bnl.zoomgov.com/meeting/register/vJIscuqgrD0vG8SVmZ49QwTrS8eGSZrs-1U



Abstract:

Fibrillar aggregates of Abeta peptides and tau protein are defining features of 
Alzheimer's disease (AD) but the role these structures play in the etiology of 
disease remains uncertain. Outstanding questions remain as to the distribution 
of polymorphs between and within cases.  We are using x-ray scanning 
microdiffraction on histological sections of human brain tissue in order to map 
the distribution and arrangement of fibrillar aggregates of these proteins in 
plaques and tangles.  The central hypothesis of the work is that the spatial 
distribution of structural polymorphs in brain tissue will provide important 
clues as to how fibrils contribute to disease.  Our goals are to assess whether 
or not different fibrillar polymorphs spread by a prion-like process during 
disease progression and to produce data that will provide insight into the 
structural basis by which different fibrillar strains are associated with 
different disease subtypes.




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