183 results on '"Priola, Suzette A."'
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2. The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease
3. Efficacy of Wex-cide 128 disinfectant against multiple prion strains
4. Anchorless Priori Protein Results in Infectious Amyloid Disease without Clinical Scrapie
5. Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes
6. Interactions between Heterologous Forms of Prion Protein: Binding, Inhibition of Conversion, and Species Barriers
7. Porphyrin and Phthalocyanine Antiscrapie Compounds
8. Uptake and Degradation of Protease-Sensitive and -Resistant Forms of Abnormal Human Prion Protein Aggregates by Human Astrocytes
9. Lack of the immune adaptor molecule SARM1 accelerates disease in prion infected mice and is associated with increased mitochondrial respiration and decreased expression of NRF2
10. Rabbits are not resistant to prion infection
11. Disinfection and Sterilization of Prion‐Contaminated Medical Instruments
12. Susceptibility of Common Fibroblast Cell Lines to Transmissible Spongiform Encephalopathy Agents
13. Prophylactic and Therapeutic Effects of Phthalocyanine Tetrasulfonate in Scrapie-Infected Mice
14. Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier
15. Susceptibilities of nonhuman primates to chronic wasting disease
16. Additional file 1 of Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes
17. Toxicity and Protection in Prions
18. A View from the Top: Prion Diseases from 10,000 Feet
19. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans
20. Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation
21. Antiscrapie Drug Action
22. Cell-free formation of protease-resistant prion protein
23. Prions
24. Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation
25. Mitochondrial Respiration Is Impaired during Late-Stage Hamster Prion Infection
26. Prion strains depend on different endocytic routes for productive infection
27. Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity
28. Cellular prion protein is present in mitochondria of healthy mice
29. PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection
30. Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
31. The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients
32. Treatment of Prion Disease with Heterologous Prion Proteins
33. A Specific Population of Abnormal Prion Protein Aggregates Is Preferentially Taken Up by Cells and Disaggregated in a Strain-Dependent Manner
34. Lack of Prion Infectivity in Fixed Heart Tissue from Patients with Creutzfeldt-Jakob Disease or Amyloid Heart Disease
35. Recombinant Prion Protein Refolded with Lipid and RNA Has the Biochemical Hallmarks of a Prion but Lacks In Vivo Infectivity
36. Correction: Co-Infection with the Friend Retrovirus and Mouse Scrapie Does Not Alter Prion Disease Pathogenesis in Susceptible Mice
37. The role of the prion protein membrane anchor in prion infection
38. Cells Expressing Anchorless Prion Protein Are Resistant to Scrapie Infection
39. Acute cellular uptake of abnormal prion protein is cell type and scrapie-strain independent
40. Cyclic Tetrapyrrole Sulfonation, Metals, and Oligomerization in Antiprion Activity
41. Nonpsychoactive Cannabidiol Prevents Prion Accumulation and Protects Neurons against Prion Toxicity
42. Acute Formation of Protease-resistant Prion Protein Does Not Always Lead to Persistent Scrapie Infection in Vitro
43. Flexible N-terminal Region of Prion Protein Influences Conformation of Protease-resistant Prion Protein Isoforms Associated with Cross-species Scrapie Infection in Vivo and in Vitro
44. Multiple Amino Acid Residues within the Rabbit Prion Protein Inhibit Formation of Its Abnormal Isoform
45. Molecular Basis of Scrapie Strain Glycoform Variation
46. Therapeutic Potential of Prion Protein Peptides in the Transmissible Spongiform Encephalopathies
47. Deletion of β-Strand and α-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform
48. N-terminal Truncation of Prion Protein Affects Both Formation and Conformation of Abnormal Protease-resistant Prion Protein Generatedin Vitro
49. Efficient Conversion of Normal Prion Protein (PrP) by Abnormal Hamster PrP Is Determined by Homology at Amino Acid Residue 155
50. A Specific Population of Abnormal Prion Protein Aggregates Is Preferentially Taken Up by Cells and Disaggregated in a Strain- Dependent Manner.
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