Dipeptide repeat (DPR) proteins are toxic in various models of FTD/ALS with GGGGCC (G4C2) repeat expansion. However, it is unclear whether nuclear G4C2 RNA foci also induce neurotoxicity. Here, we describe a Drosophila model expressing 160 G4C2 repeats (160R) flanked by human intronic and exonic sequences. Spliced intronic 160R formed nuclear G4C2 sense RNA foci in glia and neurons about ten times more abundantly than in human neurons; however, they had little effect on global RNA processing and neuronal survival. In contrast, highly toxic 36R in the context of poly(A)(+) mRNA were exported to the cytoplasm, where DPR proteins were produced at \u3e100-fold higher level than in 160R flies. Moreover, the modest toxicity of intronic 160R expre...
A GGGGCC hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of...
Hexanucleotide repeat expansions in C9orf72 are the most common cause of amyotrophic lateral scleros...
SummaryExpanded GGGGCC (G4C2) nucleotide repeats within the C9ORF72 gene are the most common genetic...
A GGGGCC hexanucleotide repeat expansion in the C9orf72 gene is the most common genetic cause of amy...
Abstract An intronic hexanucleotide repeat expansion in C9ORF72 causes familial and sp...
SummaryThe GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause o...
The most frequent genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia is a G4...
The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyot...
The most frequent genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia is a G(...
The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of spor...
Evidence for an RNA gain-of-function toxicity has now been provided for an increasing number of huma...
The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyot...
The pathogenic agent responsible for the expanded repeat diseases, a group of neurodegenerative dise...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by degenerati...
The exact mechanism underlying amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)...
A GGGGCC hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of...
Hexanucleotide repeat expansions in C9orf72 are the most common cause of amyotrophic lateral scleros...
SummaryExpanded GGGGCC (G4C2) nucleotide repeats within the C9ORF72 gene are the most common genetic...
A GGGGCC hexanucleotide repeat expansion in the C9orf72 gene is the most common genetic cause of amy...
Abstract An intronic hexanucleotide repeat expansion in C9ORF72 causes familial and sp...
SummaryThe GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause o...
The most frequent genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia is a G4...
The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyot...
The most frequent genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia is a G(...
The GGGGCC (G4C2) repeat expansion in a noncoding region of C9orf72 is the most common cause of spor...
Evidence for an RNA gain-of-function toxicity has now been provided for an increasing number of huma...
The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyot...
The pathogenic agent responsible for the expanded repeat diseases, a group of neurodegenerative dise...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by degenerati...
The exact mechanism underlying amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)...
A GGGGCC hexanucleotide repeat expansion within the C9orf72 gene is the most common genetic cause of...
Hexanucleotide repeat expansions in C9orf72 are the most common cause of amyotrophic lateral scleros...
SummaryExpanded GGGGCC (G4C2) nucleotide repeats within the C9ORF72 gene are the most common genetic...