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TAR DNA binding protein-43 and fused in sarcoma/translocated in liposarcoma protein in two neurodegenerative diseases / 中国医学科学院学报
Acta Academiae Medicinae Sinicae ; (6): 286-292, 2012.
Article in English | WPRIM | ID: wpr-352913
ABSTRACT
TAR DNA binding protein-43(TDP-43) and fused in sarcoma/translocated in liposarcoma protein (FUS/TLS) have been found to be associated with two neurodegenerative diseases - amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Mutations in TDP-43 and FUS/TLS lead to abnormal protein expressions, which result in altered RNA processing. The pathological changes of TDP-43 and FUS/TLS-associated ALS and FTD are similar. Although the interactions between ALS and FTD remain unknown, it is speculated that TDP-43 and FUS/TLS-associated neurodegenerative diseases may share similar pathogenesis.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: RNA Processing, Post-Transcriptional / RNA-Binding Protein FUS / DNA-Binding Proteins / Frontotemporal Dementia / Genetics / Amyotrophic Lateral Sclerosis / Metabolism / Mutation Limits: Humans Language: English Journal: Acta Academiae Medicinae Sinicae Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: RNA Processing, Post-Transcriptional / RNA-Binding Protein FUS / DNA-Binding Proteins / Frontotemporal Dementia / Genetics / Amyotrophic Lateral Sclerosis / Metabolism / Mutation Limits: Humans Language: English Journal: Acta Academiae Medicinae Sinicae Year: 2012 Type: Article