372 results on '"Castilla, Joaquín"'
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2. Understanding the key features of the spontaneous formation of bona fide prions through a novel methodology that enables their swift and consistent generation
3. A tetracationic porphyrin with dual anti-prion activity
4. Description of the first Spanish case of Gerstmann–Sträussler–Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization
5. Bona fide atypical scrapie faithfully reproduced for the first time in a rodent model
6. Laboratory Identification of Prion Infections
7. Biosemiotics comprehension of PrP code and prion disease
8. A Protein Misfolding Shaking Amplification-based method for the spontaneous generation of hundreds of bona fide prions
9. Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease
10. Detection of chronic wasting disease in mule and white-tailed deer by RT-QuIC analysis of outer ear
11. Detection of amyloid fibrils in Parkinson’s disease using plasmonic chirality
12. A Single Amino Acid Substitution, Found in Mammals with Low Susceptibility to Prion Diseases, Delays Propagation of Two Prion Strains in Highly Susceptible Transgenic Mouse Models
13. Insights into the Bidirectional Properties of the Sheep–Deer Prion Transmission Barrier
14. Prion replication without host adaptation during interspecies transmissions
15. Autoantibodies against the prion protein in individuals with PRNP mutations
16. Protein misfolding cyclic amplification corroborates the absence of PrPSc accumulation in placenta from foetuses with the ARR/ARQ genotype in natural scrapie
17. Prpsc Prions : State of The Art
18. An Amino Acid Substitution Found in Animals with Low Susceptibility to Prion Diseases Confers a Protective Dominant-Negative Effect in Prion-Infected Transgenic Mice
19. iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology
20. Cofactors influence the biological properties of infectious recombinant prions
21. Animal models for prion-like diseases
22. Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy
23. Analysis of a large case series of fatal familial insomnia to determine tests with the highest diagnostic value
24. Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy
25. Presymptomatic Detection of Prions in Blood
26. A Quick Method to Evaluate the Effect of the Amino Acid Sequence in the Misfolding Proneness of the Prion Protein
27. Cyclic Amplification of Prion Protein Misfolding
28. Analysis of a large case series of fatal familial insomnia to determine tests with the highest diagnostic value.
29. Rabbits are not resistant to prion infection
30. Interference of Coronavirus Infection by Expression of IgG or IgA Virus Neutralizing Antibodies
31. Prion Strain Mutation Determined by Prion Protein Conformational Compatibility and Primary Structure
32. Unfolded Protein Response Transcription Factor XBP-1 Does Not Influence Prion Replication or Pathogenesis
33. Development of Protection against Coronavirus Induced Diseases : A Review
34. Induction of an Immune Response to Transmissible Gastroenteritis Coronavirus Using Vectors with Enteric Tropism
35. Sporadic creutzfeldt-jakob disease with extremely long fourteen-year survival period
36. Solid state NMR reveals a parallel in register architecture for an infectious recombinant prion
37. Human prion protein sequence elements impede cross-species chronic wasting disease transmission
38. Sporadic Creutzfeldt–Jakob disease with extremely long 14‐year survival period
39. Cerebrospinal Fluid and Plasma Small Extracellular Vesicles and miRNAs as Biomarkers for Prion Diseases
40. Improving the Pharmacological Properties of Ciclopirox for Its Use in Congenital Erythropoietic Porphyria
41. Homozygous R136S mutation in PRNP gene causes recessive inherited early onset prion disease
42. Evaluation of the Influence of Astrocytes on In Vitro Blood-Brain Barrier Models
43. Prion-Associated Neurodegeneration Causes Both Endoplasmic Reticulum Stress and Proteasome Impairment in a Murine Model of Spontaneous Disease
44. Coenzyme Q and protein/lipid oxidation in a BSE-infected transgenic mouse model
45. A Novel, Reliable and Highly Versatile Method to Evaluate Different Prion Decontamination Procedures
46. Evaluation of the Influence of Astrocytes on In Vitro Blood–Brain Barrier Models
47. Structural features of an infectious recombinant PrPSc prion using solid state NMR
48. Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases
49. Dogs are resistant to prion infection, due to the presence of aspartic or glutamic acid at position 163 of their prion protein
50. A molecular switch controls interspecies prion disease transmission in mice
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