Dissociation of pathological and molecular phenotype of variant Creutzfeldt–Jakob disease in transgenic human prion protein 129 heterozygous mice

All neuropathologically confirmed cases of variant Creutzfeldt–Jakob disease (vCJD), characterized by abundant florid plaques and type 4 disease-related prion protein (PrP(Sc)) in the brain, have been homozygous for methionine at polymorphic residue 129 of PRNP. The distinctive neuropathological and...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Asante, Emmanuel A., Linehan, Jacqueline M., Gowland, Ian, Joiner, Susan, Fox, Katie, Cooper, Sharon, Osiguwa, Olufumilayo, Gorry, Michelle, Welch, Julie, Houghton, Richard, Desbruslais, Melanie, Brandner, Sebastian, Wadsworth, Jonathan D. F., Collinge, John
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 2006
Gaiak:
Biological Sciences
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1502304/
https://ncbi.nlm.nih.gov/pubmed/16809423
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0604292103
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