ALS and FTD are two degenerative diseases affecting the nervous system that cause quite different symptom patterns: ALS is an uncommon illness that leads to rapidly progressive muscular weakness. As the second-most common form of dementia after Alzheimer’s disease, FTD results in alterations in personality and social behavior. Despite these differences, however, both diseases appear to be based on a similar underlying mechanism. Several years ago, Manuela Neumann and her colleagues showed that changes in the DNA/RNA binding protein TDP-43 play a critical role in these degenerative diseases. In healthy individuals, most of this protein is found in the nuclei of nerve cells (neurons), where it is involved in processing genetic information (mRNA). In the neurons of patients with ALS or FTD, TDP-43 accumulates outside the nucleus, forming pathological deposits in the cytoplasm. This major discovery was published in 2006 in the renowned journal “Science”, and opened up a new area for research.