380 results on '"Béringue, Vincent"'
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2. The dynamics of prion spreading is governed by the interplay between the non-linearities of tissue response and replication kinetics
3. Prion assemblies: structural heterogeneity, mechanisms of formation, and role in species barrier
4. The Smallest Infectious Substructure Encoding the Prion Strain Structural Determinant Revealed by Spontaneous Dissociation of Misfolded Prion Protein Assemblies
5. Transmission of cervid prions to humanized mice demonstrates the zoonotic potential of CWD
6. Bona fide atypical scrapie faithfully reproduced for the first time in a rodent model
7. Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation
8. Species barrier as molecular basis for adaptation of synthetic prions with N‐terminally truncated PrP.
9. Conformation-dependent membrane permeabilization by neurotoxic PrP oligomers: The role of the H2H3 oligomerization domain
10. A seven-residue deletion in PrP leads to generation of a spontaneous prion formed from C-terminal C1 fragment of PrP
11. Characterization of the 263K‐derived microsomal fraction: a source of prions for nanofiltration validation studies
12. Crossing Species Barriers Relies on Structurally Distinct Prion Assemblies and Their Complementation
13. Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients
14. Review on PRNP genetics and susceptibility to chronic wasting disease of Cervidae
15. Assessment of the Zoonotic Potential of Atypical Scrapie Prions in Humanized Mice Reveals Rare Phenotypic Convergence but Not Identity With Sporadic Creutzfeldt-Jakob Disease Prions.
16. Epigenetic Control of the Notch and Eph Signaling Pathways by the Prion Protein: Implications for Prion Diseases
17. A Newly Identified Type of Scrapie Agent Can Naturally Infect Sheep with Resistant PrP Genotypes
18. Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains
19. The Prion-like protein Shadoo is involved in mouse embryonic and mammary development and differentiation
20. Mixtures of prion substrains in natural scrapie cases revealed by ovinised murine models
21. Transmission of the BSE Agent to Mice in the Absence of Detectable Abnormal Prion Protein
22. A farewell to outgoing Editor-in-Chief Michel Brémont
23. Prion strain-dependent tropism is maintained between spleen and granuloma and relies on lymphofollicular structures
24. Early stage prion assembly involves two subpopulations with different quaternary structures and a secondary templating pathway
25. Thermostability as a highly dependent prion strain feature
26. Pathogenicity, strain properties and interspecies transmission capacity of pure recombinant prion protein assemblies
27. Cerebellar compartmentation of prion pathogenesis
28. Pressure Reveals Unique Conformational Features in Prion Protein Fibril Diversity
29. Prion assemblies: structural heterogeneity, mechanisms of formation, and role in species barrier
30. Facilitated Cross-Species Transmission of Prions in Extraneural Tissue
31. Integrity of Helix 2-Helix 3 Domain of the PrP Protein Is Not Mandatory for Prion Replication
32. Polyene Antibiotics in Experimental Transmissible Subacute Spongiform Encephalopathies
33. Marked influence of the route of infection on prion strain apparent phenotype in a scrapie transgenic mouse model
34. Transmission of Cervid prions to Humanized Mice Demonstrates the Zoonotic Potential of CWD
35. Co-invalidation of Prnp and Sprn in FVB/N mice affects reproductive performances and highlight complex biological relationship between PrP and Shadoo
36. Risque associé à l’allègement du « feed ban »
37. Prion potentiation after life-long dormancy in mice devoid of PrP
38. Use of Murine Bioassay to Resolve Ovine Transmissible Spongiform Encephalopathy Cases Showing a Bovine Spongiform Encephalopathy Molecular Profile
39. Improving the Predictive Value of Prion Inactivation Validation Methods to Minimize the Risks of Iatrogenic Transmission With Medical Instruments
40. Host prion protein expression levels impact prion tropism for the spleen
41. PrPSc Binding Antibodies Are Potent Inhibitors of Prion Replication in Cell Lines
42. Correlation between Bioassay and Protein Misfolding Cyclic Amplification for Variant Creutzfeldt-Jakob Disease Decontamination Studies
43. PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors
44. Host prion protein expression levels impact prion tropism for the spleen
45. Complementation between pathological prion protein subassemblies to cross existing species barriers
46. Causative Links between Protein Aggregation and Oxidative Stress: A Review
47. Heterogeneity and Architecture of Pathological Prion Protein Assemblies: Time to Revisit the Molecular Basis of the Prion Replication Process?
48. Quaternary structural convergence and structural diversification of prion assemblies at the early replication stage
49. Issues and special features of animal health research
50. Brain transcriptional stability upon prion protein-encoding gene invalidation in zygotic or adult mouse
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