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