Methylation of C9orf72 expansion reduces RNA foci formation and dipeptide-repeat proteins expression in cells
Author:
Funder
ALS Association Investigator Initiated Grant
Mayo Clinic Center for Regenerative Medicine
Publisher
Elsevier BV
Subject
General Neuroscience
Reference26 articles.
1. Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders;Lillo;J. Clin. Neurosci.,2009
2. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011
3. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;Renton;Neuron,2011
4. Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion;Waite;Neurobiol. Aging,2014
5. The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs;Levine;Bioinformatics,2013
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