| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0959-4388(97)80091-8 |
| P698 | PubMed publication ID | 9384548 |
| P50 | author | Adriano Aguzzi | Q375410 |
| P2093 | author name string | Weissmann C | |
| P2860 | cites work | Sheep cloned by nuclear transfer from a cultured cell line | Q28275874 |
| Transmission dynamics and epidemiology of BSE in British cattle | Q28286643 | ||
| Does the agent of scrapie replicate without nucleic acid? | Q34224970 | ||
| Epidemiological observations on spongiform encephalopathies in captive wild animals in the British Isles | Q34315669 | ||
| A new variant of Creutzfeldt-Jakob disease in the UK. | Q34374893 | ||
| Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. | Q34403513 | ||
| Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein | Q35764516 | ||
| Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein | Q35823555 | ||
| Scrapie prions | Q38365719 | ||
| Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier | Q40624584 | ||
| An epidemiologist's view of bovine spongiform encephalopathy | Q40678364 | ||
| The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies | Q41017065 | ||
| Sleepless in Bologna: transmission of fatal familial insomnia | Q41052801 | ||
| Bovine spongiform encephalopathy: epidemiological features 1985 to 1990 | Q41115102 | ||
| Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease | Q42631333 | ||
| Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 | ||
| Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity | Q46433690 | ||
| Biochemical typing of scrapie strains | Q47622354 | ||
| Intracerebral transmission of scrapie to cattle | Q48145544 | ||
| Typing prion isoforms. | Q48762703 | ||
| Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice | Q48963662 | ||
| Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. | Q54154878 | ||
| NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231). | Q54559823 | ||
| A suspicious signature | Q57083722 | ||
| The same prion strain causes vCJD and BSE | Q57092996 | ||
| BSE transmission to macaques | Q59098670 | ||
| BSE a specific bovine disease? | Q60079637 | ||
| Predicting the CJD epidemic in humans | Q72988455 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 695-700 | |
| P577 | publication date | 1997-10-01 | |
| P1433 | published in | Current Opinion in Neurobiology | Q15763572 |
| P1476 | title | Bovine spongiform encephalopathy and early onset variant Creutzfeldt-Jakob disease | |
| P478 | volume | 7 |
| Q38439914 | Animal models for prion-like diseases. |
| Q35877214 | Antiprion immunotherapy: to suppress or to stimulate? |
| Q38579674 | Biochemical aspects of dementias |
| Q33860922 | Biological characteristics of Chinese hamster ovary cells transfected with bovine Prnp |
| Q33558398 | Cellular biology of prion diseases |
| Q57083643 | Chapter 7 A Neuropathologist's Diary |
| Q33889750 | Grafting mouse brains: from neurocarcinogenesis to neurodegeneration. |
| Q37569845 | Humoral immune response to native eukaryotic prion protein correlates with anti-prion protection. |
| Q43615251 | Imbalance of antioxidant defense in mice lacking cellular prion protein. |
| Q41831450 | Impact of methionine oxidation as an initial event on the pathway of human prion protein conversion |
| Q34389564 | Interventional strategies against prion diseases |
| Q31050944 | Isolation and characterization of a polymerized prion protein. |
| Q40569086 | Knock-down of the 37-kDa/67-kDa laminin receptor in mouse brain by transgenic expression of specific antisense LRP RNA. |
| Q33843281 | Paracrine inhibition of prion propagation by anti-PrP single-chain Fv miniantibodies |
| Q34202007 | Pathogenesis of prion diseases: a progress report |
| Q28349664 | Peripheral prion pursuit |
| Q57083708 | PrP expression in B lymphocytes is not required for prion neuroinvasion |
| Q33975800 | Prion diseases. |
| Q36577307 | Prion infections, blood and transfusions |
| Q35622996 | Prions and the immune system: a journey through gut, spleen, and nerves |
| Q44449351 | Reversible aggregation of mouse prion protein derivatives with PrPSC-like structural properties |
| Q34306690 | Spongiform encephalopathies: insights from transgenic models |
| Q39644598 | The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein |
| Q33705857 | The genetics of prions--a contradiction in terms? |
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