194 results on '"Windl, Otto"'
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2. Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue
3. Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degeneration
4. Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification
5. Animal Prion Diseases
6. A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson’s disease with dementia
7. PrP gene polymorphisms in Cyprus goats and their association with resistance or susceptibility to natural scrapie
8. Neurodegenerative diseases and lifetime seizure risk: A study of autopsy proven cases
9. Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene
10. Seizure prevalence in neurodegenerative diseases—a study of autopsy proven cases
11. Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene
12. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment
13. First symptom guides diagnosis and prognosis in neurodegenerative diseases—a retrospective study of autopsy proven cases
14. Loss of glycosylation associated with the T183A mutation in human prion disease
15. Animal Prion Diseases
16. 29. Introduction of Surveillance for Human Prion Diseases
17. Seizure prevalence in neurodegenerative diseases—a study of autopsy proven cases.
18. Transcriptome analysis reveals altered cholesterol metabolism during the neurodegeneration in mouse scrapie model
19. Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid
20. Iatrogenic Creutzfeldt-Jakob Disease with Florid Plaques
21. Clinical findings in sporadic Creutzfeldt–Jakob disease correlate with thalamic pathology
22. The Heidenhain Variant of Creutzfeldt-Jakob Disease
23. In vitro amplification of ovine prions from scrapie-infected sheep from Great Britain reveals distinct patterns of propagation
24. Caprine prion gene polymorphisms are associated with decreased incidence of classical scrapie in goat herds in the United Kingdom
25. Sporadic fatal insomnia in Europe: phenotypic features and diagnostic challenges
26. Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges
27. Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice
28. Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice
29. Effect of Polymorphisms at Codon 146 of the Goat PRNP Gene on Susceptibility to Challenge with Classical Scrapie by Different Routes
30. Generation of a Persistently Infected MDBK Cell Line with Natural Bovine Spongiform Encephalopathy (BSE)
31. Overexpression of chimaeric murine/ovine PrP (A136H154Q171) in transgenic mice facilitates transmission and differentiation of ruminant prions
32. Enzymatic Formulation Capable of Degrading Scrapie Prion under Mild Digestion Conditions
33. Transcriptional Analysis Implicates Endoplasmic Reticulum Stress in Bovine Spongiform Encephalopathy
34. Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cells
35. Infection of Cell Lines with Experimental and Natural Ovine Scrapie Agents
36. Transcriptional Changes in the Brains of Cattle Orally Infected with the Bovine Spongiform Encephalopathy Agent Precede Detection of Infectivity
37. High prevalence of scrapie in a dairy goat herd: tissue distribution of disease-associated PrP and effect ofPRNPgenotype and age
38. Ovine PRNP untranslated region and promoter haplotype diversity
39. Real-Time PCR Detection and Identification of Prohibited Mammalian and Avian Material in Animal Feeds
40. Prion Protein Amino Acid Determinants of Differential Susceptibility and Molecular Feature of Prion Strains in Mice and Voles
41. Correction: Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP
42. Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP
43. The German FFI Cases
44. Iatrogenic Creutzfeldt-Jakob Disease with Florid Plaques
45. Conversion Efficiency of Bank Vole Prion Protein in Vitro Is Determined by Residues 155 and 170, but Does Not Correlate with the High Susceptibility of Bank Voles to Sheep Scrapie in Vivo
46. Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob disease
47. Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survival
48. Clinical course in young patients with sporadic Creutzfeldt-Jakob disease
49. Genetic Mapping of Activity Determinants within Cellular Prion Proteins
50. Identification of Differentially Expressed Genes in Scrapie-Infected Mouse Brains by Using Global Gene Expression Technology
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