477 results on '"Chesebro, Bruce"'
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2. Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein
3. Prion-induced photoreceptor degeneration begins with misfolded prion protein accumulation in cones at two distinct sites: cilia and ribbon synapses
4. Innate immune responses after stimulation with Toll-like receptor agonists in ex vivo microglial cultures and an in vivo model using mice with reduced microglia
5. CD11c is not required by microglia to convey neuroprotection after prion infection
6. Prion-Induced Amyloid Heart Disease with High Blood Infectivity in Transgenic Mice
7. Anchorless Priori Protein Results in Infectious Amyloid Disease without Clinical Scrapie
8. Efficacy of Wex-cide 128 disinfectant against multiple prion strains
9. RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
10. Transmission studies of chronic wasting disease to transgenic mice overexpressing human prion protein using the RT-QuIC assay
11. Immunity to Retroviral Infection: The Friend Virus Model
12. Microglia are not required for prion-induced retinal photoreceptor degeneration
13. Additional file 1 of Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein
14. Additional file 2 of Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein
15. A Fresh Look at BSE
16. Microglia have limited influence on early prion pathogenesis, clearance, or replication
17. Analysis of two monoclonal antibodies reactive with envelope proteins of murine retroviruses: One pan specific antibody and one specific for Moloney leukemia virus
18. Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
19. Lower specific infectivity of protease-resistant prion protein generated in cell-free reactions
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. Apobec3 Encodes Rfv3, a Gene Influencing Neutralizing Antibody Control of Retrovirus Infection
23. The Formation of Scrapie-Associated Prion Protein In Vitro
24. Chronic wasting disease agents in nonhuman primates
25. Subclinical Scrapie Infection in a Resistant Species: Persistence, Replication, and Adaptation of Infectivity during Four Passages
26. In Vivo and In Vitro Selection of Equine Infectious Anemia Virus Variants
27. Prion protein on astrocytes or in extracellular fluid impedes neurodegeneration induced by truncated prion protein
28. T-Lymphocyte Priming and Protection against Friend Leukemia by Vaccinia-Retrovirus env Gene Recombinant
29. Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier
30. Passive Immunotherapy for Retroviral Disease: Influence of Major Histocompatibility Complex Type and T-Cell Responsiveness
31. Identification of a non-H-2 Gene (Rfv-3) Influencing Recovery from Viremia and Leukemia Induced by Friend Virus Complex
32. Molecular Cloning and Complete Sequence of Prion Protein cDNA from Mouse Brain Infected with the Scrapie Agent
33. Antibody-Induced Modulation of Friend Virus Cell Surface Antigens Decreases Virus Production by Persistent Erythroleukemia Cells: Influence of the Rfv-3 Gene
34. Substitution of Leucine for Isoleucine in a Sequence Highly Conserved Among Retroviral Envelope Surface Glycoproteins Attenuates the Lytic Effect of the Friend Murine Leukemia Virus
35. In vitro Expression in Eukaryotic Cells of a Prion Protein Gene Cloned from Scrapie-Infected Mouse Brain
36. Deletion of Kif5c Does Not Alter Prion Disease Tempo or Spread in Mouse Brain
37. Role of Erk1/2 activation in prion disease pathogenesis: Absence of CCR1 leads to increased Erk1/2 activation and accelerated disease progression
38. Susceptibilities of nonhuman primates to chronic wasting disease
39. Additional file 5 of RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
40. Additional file 4 of RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
41. Additional file 2 of RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
42. Additional file 3 of RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
43. Additional file 1 of RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection
44. Levels of abnormal prion protein in deer and elk with chronic wasting disease
45. Scrapie pathogenesis in brain and retina: Effects of prion protein expression in neurons and astrocytes
46. Sulfated glycans and elevated temperature stimulate PrPSc‐dependent cell‐free formation of protease‐resistant prion protein
47. Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems: An update
48. Increased excitatory amino acid transport into murine prion protein knockout astrocytes cultured in vitro
49. Prion-associated cerebral amyloid angiopathy is not exacerbated by human phosphorylated tau aggregates in scrapie-infected mice expressing anchorless prion protein
50. Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility
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