Scientists develop lab model to study TDP-43 accumulation in neurodegeneration
The Rise of Prion-Like Proteinopathies in Neurodegenerative Research The recent advancements in understanding TDP-43 pathology revolutionize our approach to tackling neurodegenerative diseases like ALS and frontotemporal dementia. Researchers have emphasized the prion-like behavior of TDP-43, where misfolded proteins can induce further misfolding, creating a chain reaction leading to disease. This breakthrough opens avenues for innovative … Read more
