Related references
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C9orf72 nucleotide repeat structures initiate molecular cascades of disease
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C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
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Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
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hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations
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RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
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Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72
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Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
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p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
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Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
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