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The Oskar Fischer Lecture Series features invited scholars working at the vanguard of new ideas on the mechanisms, diagnosis and treatment of dementing illnesses.
His discovery that defective genes encoding presenilins are a cause of familial AD led to presenilins becoming a new target for treatments. He went on to show that mutated presenilins contribute to the generation of the amyloid beta protein — deposition of which is the earliest sign of AD in those carrying such genes. His work on several other neurodegeneration-related genes and proteins (including SORLA, TREM2, FUS) has led to an understanding of the role of vesicular transport, inflammation and perturbed RNA granule biology. Read full bio
The February Oskar Fischer Lecture is hosted in partnership with the 2024 TARCC Scientific Symposium. If you have registered to attend the symposium, you do not need to register for the Oskar Fischer Lecture. If you are not attending the 2024 TARCC Scientific Symposium and would like to attend The Oskar Fischer Lecture Series, please register using the button above. This event has in-person and virtual attendance options. Registration is required to receive the livestream link.