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• Sequence analysis of the PrP protein from two species of antelope susceptible to transmissible spongiform encephalopathy.

  Poidinger M, Kirkwood J, Almond W. Poidinger M, et al. Arch Virol. 1993;131(1-2):193-9. doi: 10.1007/BF01379091. Arch Virol. 1993. PMID: 8328913
• Attempts to restore scrapie prion infectivity after exposure to protein denaturants.

  Prusiner SB, Groth D, Serban A, Stahl N, Gabizon R. Prusiner SB, et al. Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2793-7. doi: 10.1073/pnas.90.7.2793. Proc Natl Acad Sci U S A. 1993. PMID: 8464892 Free PMC article.
• A Non-amyloid Prion Particle that Activates a Heritable Gene Expression Program.

  Chakravarty AK, Smejkal T, Itakura AK, Garcia DM, Jarosz DF. Chakravarty AK, et al. Mol Cell. 2020 Jan 16;77(2):251-265.e9. doi: 10.1016/j.molcel.2019.10.028. Epub 2019 Nov 19. Mol Cell. 2020. PMID: 31757755 Free PMC article.
• Detection of Pathognomonic Biomarker PrP^Sc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases.

  Eraña H, Charco JM, González-Miranda E, García-Martínez S, López-Moreno R, Pérez-Castro MA, Díaz-Domínguez CM, García-Salvador A, Castilla J. Eraña H, et al. Biomolecules. 2020 Mar 19;10(3):469. doi: 10.3390/biom10030469. Biomolecules. 2020. PMID: 32204429 Free PMC article. Review.
• De novo prion aggregates trigger autophagy in skeletal muscle.

  Joshi-Barr S, Bett C, Chiang WC, Trejo M, Goebel HH, Sikorska B, Liberski P, Raeber A, Lin JH, Masliah E, Sigurdson CJ. Joshi-Barr S, et al. J Virol. 2014 Feb;88(4):2071-82. doi: 10.1128/JVI.02279-13. Epub 2013 Dec 4. J Virol. 2014. PMID: 24307586 Free PMC article.