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Analysis of nucleic acid chaperoning by the prion protein and its inhibition by oligonucleotides

Prion diseases are unique neurodegenerative illnesses associated with the conversion of the cellular prion protein (PrP(C)) into the aggregated misfolded scrapie isoform, named PrP(Sc). Recent studies on the physiological role of PrP(C) revealed that this protein has probably multiple functions, not...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Guichard, Cécile, Ivanyi-Nagy, Roland, Sharma, Kamal Kant, Gabus, Caroline, Marc, Daniel, Mély, Yves, Darlix, Jean-Luc
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2011
Aiheet:
RNA
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3201874/
https://ncbi.nlm.nih.gov/pubmed/21737432
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr554
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