[HTML][HTML] Molecular mechanisms linking loss of TDP-43 function to amyotrophic lateral sclerosis/frontotemporal dementia-related genes
Y Koike - Neuroscience Research, 2024 - Elsevier
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are characterized by
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …
Molecular mechanisms linking loss of TDP-43 function to amyotrophic lateral sclerosis/frontotemporal dementia-related genes.
Y Koike - Neuroscience Research, 2024 - europepmc.org
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are characterized by
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …
Molecular mechanisms linking loss of TDP-43 function to amyotrophic lateral sclerosis/frontotemporal dementia-related genes
Y Koike - Neuroscience research - pubmed.ncbi.nlm.nih.gov
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are characterized by
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …
nuclear depletion and cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) …