283 results on '"Priola, Suzette A."'
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2. Species Barriers in Prion Disease
3. Cell biology of prion strains in vivo and in vitro
4. The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease
5. β-Barrel proteins tether the outer membrane in many Gram-negative bacteria
6. Efficacy of Wex-cide 128 disinfectant against multiple prion strains
7. Processing of high-titer prions for mass spectrometry inactivates prion infectivity
8. Anchorless Priori Protein Results in Infectious Amyloid Disease without Clinical Scrapie
9. Full-length prion protein incorporated into prion aggregates is a marker for prion strain specific destabilization of aggregate structure following cellular uptake
10. Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes
11. Interactions between Heterologous Forms of Prion Protein: Binding, Inhibition of Conversion, and Species Barriers
12. Porphyrin and Phthalocyanine Antiscrapie Compounds
13. Cell biology of prion infection
14. Species Barriers in Prion Disease
15. Uptake and Degradation of Protease-Sensitive and -Resistant Forms of Abnormal Human Prion Protein Aggregates by Human Astrocytes
16. 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
17. Cell Biology Approaches to Studying Prion Diseases
18. Cell biology of prion strains in vivo and in vitro
19. Rabbits are not resistant to prion infection
20. Disinfection and Sterilization of Prion‐Contaminated Medical Instruments
21. Transgenic Mice with Neuron-Specific Expression of a Hamster Prion Protein Minigene Are Susceptible to Hamster Scrapie Agent
22. The Formation of Scrapie-Associated Prion Protein In Vitro
23. Susceptibility of Common Fibroblast Cell Lines to Transmissible Spongiform Encephalopathy Agents
24. Prophylactic and Therapeutic Effects of Phthalocyanine Tetrasulfonate in Scrapie-Infected Mice
25. Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier
26. Susceptibilities of nonhuman primates to chronic wasting disease
27. The Size and Stability of Infectious Prion Aggregates Fluctuate Dynamically during Cellular Uptake and Disaggregation
28. β-Barrel proteins tether the outer membrane in many Gram-negative bacteria
29. Additional file 1 of Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes
30. Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies
31. Species Barriers in Prion Disease
32. Antiaggregating Antibody Raised Against Human PrP 106-126 Recognizes Pathological and Normal Isoforms of the Whole Prion Protein
33. Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems: An update
34. Toxicity and Protection in Prions
35. A View from the Top: Prion Diseases from 10,000 Feet
36. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans
37. Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation
38. Antiscrapie Drug Action
39. Inhibition of scrapie-associated PrP accumulation: Probing the role of glycosaminoglycans in amyloidogenesis
40. Prions
41. Cell-free formation of protease-resistant prion protein
42. Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation
43. Mitochondrial Respiration Is Impaired during Late-Stage Hamster Prion Infection
44. Amyloid formation via supramolecular peptide assemblies
45. Prion strains depend on different endocytic routes for productive infection
46. Self-propagating, protease-resistant, recombinant prion protein conformers with or without in vivo pathogenicity
47. Cellular prion protein is present in mitochondria of healthy mice
48. PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection
49. Identification of possible animal origins of prion disease in human beings
50. Relative Abundance of apoE and Aβ1–42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes
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