Llwytho...
Genetic human prion disease modelled in PrP transgenic Drosophila
Inherited human prion diseases, such as fatal familial insomnia (FFI) and familial Creutzfeldt–Jakob disease (fCJD), are associated with autosomal dominant mutations in the human prion protein gene PRNP and accumulation of PrP(Sc), an abnormal isomer of the normal host protein PrP(C), in the brain o...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Biochem J |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Portland Press Ltd.
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5606059/ https://ncbi.nlm.nih.gov/pubmed/28814578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BCJ20170462 |
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