| P2093 | author name string | Landsverk T | |
| | Sarradin P | |
| | Ulvund MJ | |
| | Espenes A | |
| | Ersdal C | |
| | Benestad SL | |
| P2860 | cites work | Mice devoid of PrP are resistant to scrapie | Q28249108 |
| | Novel proteinaceous infectious particles cause scrapie | Q29547678 |
| | Pregnancy status and fetal prion genetics determine PrPSc accumulation in placentomes of scrapie-infected sheep | Q34029006 |
| | Cases of scrapie with unusual features in Norway and designation of a new type, Nor98. | Q34228022 |
| | Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie | Q34392833 |
| | Cultured peripheral neuroglial cells are highly permissive to sheep prion infection | Q34553074 |
| | Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms | Q36763154 |
| | Early spread of scrapie from the gastrointestinal tract to the central nervous system involves autonomic fibers of the splanchnic and vagus nerves | Q39604168 |
| | PrP expression and replication by Schwann cells: implications in prion spreading | Q39682667 |
| | Oral inoculation of sheep with the agent of bovine spongiform encephalopathy (BSE). 1. Onset and distribution of disease-specific PrP accumulation in brain and viscera | Q40698989 |
| | Diversity in the neuropathology of scrapie-like diseases in animals | Q40729965 |
| | Early and late pathogenesis of natural scrapie infection in sheep | Q43684067 |
| | Transmission of prion diseases by blood transfusion | Q44186164 |
| | The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis | Q44535658 |
| | Scrapie prion protein contains a phosphatidylinositol glycolipid | Q46814773 |
| | Different scrapie-associated fibril proteins (PrP) are encoded by lines of sheep selected for different alleles of the Sip gene | Q47572251 |
| | Natural scrapie in a closed flock of Cheviot sheep occurs only in specific PrP genotypes | Q47636904 |
| | Determination of the frequency and distribution of vascular and parenchymal amyloid with polyclonal and N-terminal-specific PrP antibodies in scrapie-affected sheep and mice | Q47937396 |
| | Tonsillar biopsy and PrPSc detection in the preclinical diagnosis of scrapie. | Q47948764 |
| | PrP genotype contributes to determining survival times of sheep with natural scrapie. | Q48059613 |
| | Accumulation of pathogenic prion protein (PrPSc) in nervous and lymphoid tissues of sheep with subclinical scrapie | Q48364297 |
| | Distinction of scrapie phenotypes in sheep by lesion profiling | Q48478492 |
| | Rapid test for the preclinical postmortem diagnosis of BSE in central nervous system tissue | Q48699103 |
| | Neuropathology of scrapie: a study of the distribution patterns of brain lesions in 222 cases of natural scrapie in sheep, 1982-1991. | Q48798889 |
| | Onset and distribution of tissue prp accumulation in scrapie-affected suffolk sheep as demonstrated by sequential necropsies and tonsillar biopsies | Q48823413 |
| | Prion protein gene polymorphisms in sheep with natural scrapie and healthy controls in Norway. | Q53150304 |
| | Effects of agent strain and host genotype on PrP accumulation in the brain of sheep naturally and experimentally affected with scrapie. | Q53674706 |
| | Pathogenesis of the oral route of infection of mice with scrapie and bovine spongiform encephalopathy agents. | Q54306429 |
| | Positioning of follicular dendritic cells within the spleen controls prion neuroinvasion | Q57083661 |
| P433 | issue | 3 | |
| P304 | page(s) | 258-274 | |
| P577 | publication date | 2005-05-01 | |
| P1433 | published in | Veterinary Pathology | Q7923710 |
| P1476 | title | Mapping PrPSc propagation in experimental and natural scrapie in sheep with different PrP genotypes | |
| P478 | volume | 42 | |