The Proline/Arginine Dipeptide from Hexanucleotide Repeat Expanded C9ORF72 Inhibits the Proteasome

An intronic hexanucleotide repeat expansion (HRE) mutation in the C9ORF72 gene is the most common cause of familial ALS and frontotemporal dementia (FTD) and is found in ∼7% of individuals with apparently sporadic disease. Several different diamino acid peptides can be generated from the HRE by nonc...

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Publicat a:eNeuro
Autors principals: Gupta, Rahul, Lan, Matthews, Mojsilovic-Petrovic, Jelena, Choi, Won Hoon, Safren, Nathaniel, Barmada, Sami, Lee, Min Jae, Kalb, Robert
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 2017
Matèries:
New Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5282547/
https://ncbi.nlm.nih.gov/pubmed/28197542
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0249-16.2017
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