Article
Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations.
Molecular neurobiology - 1 Mar 2019
Jeon Gye Sun, Shim Yu-Mi, Lee Do-Yeon, Kim Jun-Soon, Kang MinJin, Ahn So Hyun, Shin Je-Young, Geum Dongho, Hong Yoon Ho, Sung Jung-Joon
Abstract excerpt
Amyotrophic lateral sclerosis (ALS) is a fatal, adult-onset, progressive neurodegenerative disorder with no known cure. Cu/Zn-superoxide dismutase (SOD1) was the first identified protein associated with familial ALS (fALS). Recently, TAR DNA-binding protein 43 (TDP-43) has been found to be a principal component of ubiquitinated cytoplasmic inclusions in neurons and glia in ALS. However, it remains unclear whether...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
