Mutations and polymorphisms in the prion protein gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference41 articles.
1. Aminoacid polymorphism in human prion protein and age at death in inherited prion disease
2. Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells.
3. The molecular genetics of familial Creutzfeldt-Jakob disease in France
4. Phenotypic characteristics of familial Creutzfeldt-Jakob disease assoicated with the codon 178AsnPRNP mutation
5. Atypical Creutzfeldt‐Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene
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2. Decoding the function of the N-terminal tail of the cellular prion protein to inspire novel therapeutic avenues for neurodegenerative diseases;Virus Research;2015-09
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4. The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease;Reviews in Medical Virology;2012-02-28
5. Infectious prion protein alters manganese transport and neurotoxicity in a cell culture model of prion disease;NeuroToxicology;2011-10
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