165 results on '"Raymond, Gregory J."'
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2. Chaperone-Supervised Conversion of Prion Protein to Its Protease-Resistant Form
3. Scrapie Susceptibility-Linked Polymorphisms Modulate the in vitro Conversion of Sheep Prion to Protease-Resistant Forms
4. Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals
5. Early preclinical detection of prions in the skin of prion-infected animals
6. Cryo-EM of prion strains from the same genotype of host identifies conformational determinants
7. Prion Biochemistry and Therapeutics
8. Amplified Detection of Prions and Other Amyloids by RT-QuIC in Diagnostics and the Evaluation of Therapeutics and Disinfectants
9. Detection and Diagnosis of Prion Diseases Using RT-QuIC: An Update
10. RT-QuIC Assays for Prion Disease Detection and Diagnostics
11. Immunodetection of PrPSc Using Western Immunoblotting Techniques
12. Purification of the Pathological Isoform of Prion Protein (PrPSc or PrPres) from Transmissible Spongiform Encephalopathy-affected Brain Tissue
13. Protease-Resistant Prion Protein Formation
14. Heat Shock Factor 1 Regulates Lifespan as Distinct from Disease Onset in Prion Disease
15. Structure of anchorless RML prion reveals motif variation between strains
16. High-resolution structure and strain comparison of infectious mammalian prions
17. Subclinical Scrapie Infection in a Resistant Species: Persistence, Replication, and Adaptation of Infectivity during Four Passages
18. Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier
19. The most infectious prion protein particles
20. Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems: An update
21. Transmission of CJD from nasal brushings but not spinal fluid or RT‐QuIC product
22. Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry
23. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans
24. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms
25. Interactions and conversions of prion protein isoforms
26. Early preclinical detection of prions in the skin of prion-infected animals
27. [9] Assays of protease-resistant prion protein and its formation
28. Cell-free formation of protease-resistant prion protein
29. Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein
30. Antisense oligonucleotides extend survival of prion-infected mice
31. Non-genetic propagation of strain-specific properties of scrapie prion protein
32. PrP P102L and Nearby Lysine Mutations Promote Spontaneous In Vitro Formation of Transmissible Prions
33. Role of the central lysine cluster and scrapie templating in the transmissibility of synthetic prion protein aggregates
34. Structural organization of brain-derived mammalian prions as probed by hydrogen exchange
35. PrP Sc -Specific Antibody Reveals C-Terminal Conformational Differences between Prion Strains
36. Transcription of tRNA gene fragments by Hela cell extracts
37. Methods for Studying Prion Protein (PrP) Metabolism and the Formation of Protease-Resistant PrP in Cell Culture and Cell-Free Systems
38. Isolation of Novel Synthetic Prion Strains by Amplification in Transgenic Mice Coexpressing Wild-Type and Anchorless Prion Proteins
39. Time Course of Prion Seeding Activity in Cerebrospinal Fluid of Scrapie-Infected Hamsters after Intratongue and Intracerebral Inoculations
40. Reaction of complement factors varies with prion strains in vitro and in vivo
41. Effect of Glycans and the Glycophosphatidylinositol Anchor on Strain Dependent Conformations of Scrapie Prion Protein: Improved Purifications and Infrared Spectra
42. Structural organization of brain-derived mammalian prions examined by hydrogen-deuterium exchange
43. Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors
44. Hemin Interactions and Alterations of the Subcellular Localization of Prion Protein
45. Transmission and Adaptation of Chronic Wasting Disease to Hamsters and Transgenic Mice: Evidence for Strains
46. Inhibition of Protease-Resistant Prion Protein Formation in a Transformed Deer Cell Line Infected with Chronic Wasting Disease
47. Inactivation of Transmissible Spongiform Encephalopathy (Prion) Agents by Environ LpH
48. Inhibition of Protease-Resistant Prion Protein Accumulation In Vitro by Curcumin
49. Long-Term Subclinical Carrier State Precedes Scrapie Replication and Adaptation in a Resistant Species: Analogies to Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease in Humans
50. Strain-dependent Differences in β-Sheet Conformations of Abnormal Prion Protein
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