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Research interests

I study the mechanisms of TDP-43 aggregate pathology, primarily in myopathy. My current focus is on the prion-like aggregate seeding that occurs in both myopathy patients and neurodegenerative patients with TDP-43 pathology. I am interested in characterizing similarities and differences in TDP-43 pathological mechanisms between the two tissue types and whether it is possible for TDP-43 aggregate seeds to spread between tissues.

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