Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have distinct clinical features but a common pathology-cytoplasmic inclusions rich in transactive response element DNA-binding protein of 43 kDa (TDP43). Rare TDP43 mutations cause ALS
Abnormal accumulation of TAR DNA-binding protein 43 (TDP-43) in the cytoplasm and its disappearance ...
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative di...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two neurodegenerative dise...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have distinct clinical feature...
Increasing biochemical and genetic evidence have suggested that Amyotrophic Lateral Sclerosis (ALS) ...
AbstractAmyotrophic lateral sclerosis (ALS) is a late-onset neurodegenerative disease characterized ...
Received: 2015.05.10; Accepted: 2015.06.18; Published: 2015.07.21 TAR DNA binding protein 43 (TDP-43...
Various pathophysiological mechanisms have been implicated in the ALS-FTLD clinicopathological spect...
Autophagy plays a major role in the elimination of cellular waste components, the renewal of intrace...
Autophagy is a catabolic mechanism where intracellular material is degraded by vesicular structures ...
TDP43 is one of the most important protein involved in the pathogenesis of amyotrophic lateral scler...
Amyotrophic lateral sclerosis (ALS) is a fatal, adult-onset degenerative disorder of motor neurons. ...
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease symptomatically char...
Increasing biochemical and genetic evidence have suggested that Amyotrophic Lateral Sclerosis (ALS) ...
Amyotrophic lateral sclerosis (ALS) is a lethal disease characterized by motor neuron degeneration a...
Abnormal accumulation of TAR DNA-binding protein 43 (TDP-43) in the cytoplasm and its disappearance ...
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative di...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two neurodegenerative dise...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have distinct clinical feature...
Increasing biochemical and genetic evidence have suggested that Amyotrophic Lateral Sclerosis (ALS) ...
AbstractAmyotrophic lateral sclerosis (ALS) is a late-onset neurodegenerative disease characterized ...
Received: 2015.05.10; Accepted: 2015.06.18; Published: 2015.07.21 TAR DNA binding protein 43 (TDP-43...
Various pathophysiological mechanisms have been implicated in the ALS-FTLD clinicopathological spect...
Autophagy plays a major role in the elimination of cellular waste components, the renewal of intrace...
Autophagy is a catabolic mechanism where intracellular material is degraded by vesicular structures ...
TDP43 is one of the most important protein involved in the pathogenesis of amyotrophic lateral scler...
Amyotrophic lateral sclerosis (ALS) is a fatal, adult-onset degenerative disorder of motor neurons. ...
Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease symptomatically char...
Increasing biochemical and genetic evidence have suggested that Amyotrophic Lateral Sclerosis (ALS) ...
Amyotrophic lateral sclerosis (ALS) is a lethal disease characterized by motor neuron degeneration a...
Abnormal accumulation of TAR DNA-binding protein 43 (TDP-43) in the cytoplasm and its disappearance ...
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative di...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two neurodegenerative dise...