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Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01132-7
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- Article
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1539, doi. 10.1093/brain/awad399
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- Article
Correction: A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 167, doi. 10.1007/s00401-023-02592-y
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- Article
A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 1, p. 121, doi. 10.1007/s00401-023-02581-1
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- Article