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Prion disease susceptibility is affected by  -structure folding propensity and local side-chain interactions in PrP

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Targeted knock-down of cellular prion protein expression in myelinating Schwann cells does not alter mouse prion pathogenesis

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Transgenic Rabbits Expressing Ovine PrP Are Susceptible to Scrapie

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W8, a new Sup35 prion strain, transmits distinctive information with a conserved assembly scheme

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Quaternary Structure of Pathological Prion Protein as a Determining Factor of Strain-Specific Prion Replication Dynamics

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In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies

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Assessing Proteinase K Resistance of Fish Prion Proteins in a Scrapie-Infected Mouse Neuroblastoma Cell Line

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Generating Bona Fide Mammalian Prions with Internal Deletions

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The Glycosylation Status of PrPCIs a Key Factor in Determining Transmissible Spongiform Encephalopathy Transmission between Species

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Genetic Resistance to Scrapie Infection in Experimentally Challenged Goats

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Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice

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Mutated but Not Deleted Ovine PrPCN-Terminal Polybasic Region Strongly Interferes with Prion Propagation in Transgenic Mice

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Nonpathogenic Heterologous Prions Can Interfere with Prion Infection in a Strain-Dependent Manner

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The role of the unusual threonine string in the conversion of prion protein

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Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein

M. K. Sandberg, H. Al-Doujaily, C. J. Sigurdson, et al.
Journal of General Virology 91 (10) 2651 (2010)
DOI: 10.1099/vir.0.024380-0
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Molecular pathology of human prion disease

Jonathan D. F. Wadsworth and John Collinge
Acta Neuropathologica 121 (1) 69 (2011)
DOI: 10.1007/s00401-010-0735-5
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Prion Proteins

Michael A. Tranulis, Sylvie L. Benestad, Thierry Baron and Hans Kretzschmar
Topics in Current Chemistry, Prion Proteins 305 23 (2011)
DOI: 10.1007/128_2011_161
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Re-transmissibility of mouse-adapted ME7 scrapie strain to ovine PrP transgenic mice

Joshua Adekunle Babalola, Jong-Mu Kim, Yun-Jung Lee, et al.
Journal of Veterinary Science 20 (2) (2019)
DOI: 10.4142/jvs.2019.20.e8
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Improving the Predictive Value of Prion Inactivation Validation Methods to Minimize the Risks of Iatrogenic Transmission With Medical Instruments

Mohammed Moudjou, Johan Castille, Bruno Passet, et al.
Frontiers in Bioengineering and Biotechnology 8 (2020)
DOI: 10.3389/fbioe.2020.591024
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Use of different RT-QuIC substrates for detecting CWD prions in the brain of Norwegian cervids

Edoardo Bistaffa, Tram Thu Vuong, Federico Angelo Cazzaniga, et al.
Scientific Reports 9 (1) (2019)
DOI: 10.1038/s41598-019-55078-x
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Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation

Juan María Torres, Olivier Andreoletti, Sylvie L Benestad, et al.
The Journal of Infectious Diseases (2020)
DOI: 10.1093/infdis/jiz646
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Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice

Hiroyuki Okada, Kentaro Masujin, Kohtaro Miyazawa and Takashi Yokoyama
Veterinary Research 46 (1) (2015)
DOI: 10.1186/s13567-015-0211-2
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Characterization of atypical scrapie cases from Great Britain in transgenic ovine PrP mice

Peter C. Griffiths, John Spiropoulos, Richard Lockey, et al.
Journal of General Virology 91 (8) 2132 (2010)
DOI: 10.1099/vir.0.018986-0
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Transition of the prion protein from a structured cellular form (PrP C ) to the infectious scrapie agent (PrP Sc )

Pravas K. Baral, Jiang Yin, Adriano Aguzzi and Michael N. G. James
Protein Science 28 (12) 2055 (2019)
DOI: 10.1002/pro.3735
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Interventions to reduce the risk of surgically transmitted Creutzfeldt–Jakob disease: a cost-effective modelling review

Matt Stevenson, Lesley Uttley, Jeremy E Oakley, et al.
Health Technology Assessment 24 (11) 1 (2020)
DOI: 10.3310/hta24110
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Mixtures of prion substrains in natural scrapie cases revealed by ovinised murine models

Tomás Barrio, Hicham Filali, Alicia Otero, et al.
Scientific Reports 10 (1) (2020)
DOI: 10.1038/s41598-020-61977-1
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Prion Infectivity in Fat of Deer with Chronic Wasting Disease

Brent Race, Kimberly Meade-White, Richard Race and Bruce Chesebro
Journal of Virology 83 (18) 9608 (2009)
DOI: 10.1128/JVI.01127-09
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Experimental Infection of Cattle With a Novel Prion Derived From Atypical H-Type Bovine Spongiform Encephalopathy

Hiroyuki Okada, Kentaro Masujin, Kohtaro Miyazawa, et al.
Veterinary Pathology 54 (6) 892 (2017)
DOI: 10.1177/0300985817717769
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Met 166 ‐Glu 168 residues in human PrP β2‐α2 loop account for evolutionary resistance to prion infection

Juan Carlos Espinosa, Alba Marín‐Moreno, Patricia Aguilar‐Calvo and Juan María Torres
Neuropathology and Applied Neurobiology (2020)
DOI: 10.1111/nan.12676
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Sequence-dependent Prion Protein Misfolding and Neurotoxicity

Pedro Fernandez-Funez, Yan Zhang, Sergio Casas-Tinto, et al.
Journal of Biological Chemistry 285 (47) 36897 (2010)
DOI: 10.1074/jbc.M110.174391
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Tracing Conformational Transition of Abnormal Prion Proteins during Interspecies Transmission by Using Novel Antibodies

Yuko Ushiki-Kaku, Ryo Endo, Yoshifumi Iwamaru, et al.
Journal of Biological Chemistry 285 (16) 11931 (2010)
DOI: 10.1074/jbc.M109.058859
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