scholarly article | Q13442814 |
P356 | DOI | 10.1093/INFDIS/115.4.387 |
P698 | PubMed publication ID | 5891240 |
P2093 | author name string | Burger D | |
Hartsough GR | |||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 387-392 | |
P577 | publication date | 1965-10-01 | |
P1433 | published in | Journal of Infectious Diseases | Q4051141 |
P1476 | title | Encephalopathy of mink. I. Epizootiologic and clinical observations. | |
P478 | volume | 115 |
Q56830918 | A Review of the BSE Epidemic in British Cattle |
Q36731200 | A species barrier limits transmission of chronic wasting disease to mink (Mustela vison). |
Q42050127 | Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study. |
Q36078718 | Animal model of human disease: Kuru, Creutzfeldt-Jakob disease (slow virus infections). Animal model: transmissible mink encephalopathy, scrapie-like disease of mink |
Q40601771 | Animal spongiform encephalopathies--an update. Part 1. Scrapie and lesser known animal spongiform encephalopathies |
Q37810707 | Atypical Transmissible Spongiform Encephalopathies in Ruminants: A Challenge for Disease Surveillance and Control |
Q36849321 | BSE: a decade on--Part I. |
Q67278973 | Bovine spongiform encephalopathy |
Q34206657 | Bovine spongiform encephalopathy--food safety implications |
Q39798567 | Breaking an absolute species barrier: transgenic mice expressing the mink PrP gene are susceptible to transmissible mink encephalopathy |
Q31164848 | Comparative sequence analysis and expression of bovine PrP gene in mouse L-929 cells |
Q70263499 | Creutzfeld-Jakob disease: clinical, EEG and neuropathological findings in a cluster of eleven patients |
Q48472748 | Diagnosis of the first cases of scrapie in Poland |
Q91585620 | Differential gene expression in chronic wasting disease-positive white-tailed deer (Odocoileus virginianus) |
Q30420123 | Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy. |
Q37033343 | Epidemiology of Creutzfeldt-Jakob disease in England and Wales |
Q70978888 | Experimental infection of cattle with the agents of transmissible mink encephalopathy and scrapie |
Q34080450 | Experimental infection of sheep and goats with transmissible mink encephalopathy virus |
Q35863951 | From slow virus to prion: a review of transmissible spongiform encephalopathies |
Q45808123 | Immune and Autoimmune Reactions in the Pathogenesis of Slow Virus Disease |
Q35997610 | Infectious diseases of the central nervous system. |
Q47149313 | Joint Scientific Opinion on any possible epidemiological or molecular association between TSEs in animals and humans |
Q49128856 | Leucodystrophy in mink |
Q49053191 | Looking for a link |
Q36538997 | Molecular biology and transgenetics of prion diseases |
Q48512440 | Nonsuppurative meningoencephalomyelitis of unknown etiology in mink |
Q36549325 | Novel Properties and Biology of Scrapie Prions |
Q37610046 | Novel structure and genetics of prions causing neurodegeneration in humans and animals |
Q33823324 | Persistent or slow viral infections and related diseases |
Q33877843 | Phenotypic similarity of transmissible mink encephalopathy in cattle and L-type bovine spongiform encephalopathy in a mouse model |
Q37132966 | Physical and chemical properties of the transmissible mink encephalopathy agent |
Q72214592 | Prion diseases |
Q81229279 | Prion diseases |
Q37581303 | Prion liposomes |
Q48220367 | Prions and related neurological diseases |
Q40118928 | Prions: Novel Infectious Pathogens |
Q34462142 | Rapid prion neuroinvasion following tongue infection |
Q37677707 | Scrapie and Creutzfeldt-Jakob disease prion proteins share physical properties and antigenic determinants |
Q35122342 | Scrapie and chronic wasting disease |
Q35193162 | Scrapie: Report of an outbreak and brief review |
Q33587250 | Scrapie: a review of its relation to human disease and ageing |
Q44972596 | Serial ultrastructural study of experimental Creutzfeldt-Jacob disease in guinea pigs |
Q39620656 | Slow Infections of the Central Nervous System |
Q45808067 | Slow-Virus Infections of the Nervous System |
Q36078683 | Subacute spongiform virus encephalopathies. Scrapie, Kuru and Creutzfeldt-Jakob disease: a review |
Q47428130 | Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein. |
Q48460539 | Surveillance for lesions of bovine spongiform encephalopathy in US cattle |
Q36919315 | Temporal distribution of transmissible mink encephalopathy virus in mink inoculated subcutaneously |
Q36549298 | The Human Spongiform Encephalopathies: Kuru, Creutzfeldt-Jakob Disease, and the Gerstmann-Sträussler-Scheinker Syndrome |
Q39974461 | The control of viral diseases. Problems and prospects viewed in perspective |
Q48450985 | The distribution of scrapie-associated fibrils in neural and non-neural tissues of advanced clinical cases of natural scrapie in sheep |
Q37056332 | The search for scrapie agent nucleic acid |
Q36731460 | The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies |
Q70729709 | Thiamine deficiency encephalopathy in mink |
Q35219347 | Transmissible encephalopathy of mink in Ontario |
Q48374337 | Transmissible mink encephalopathy (TME) in Chinese hamsters: identification of two strains of TME and comparisons with scrapie |
Q34303175 | Transmissible mink encephalopathy: pathogenesis and nature of the aetiological agent |
Q41734530 | Transmissible spongiform encephalopathies in food animals. Human food safety and animal feed safety concerns for veterinarians. |
Q39603910 | Tropical disease and general medicine |
Q40308272 | Virus-induced subacute degenerative diseases of the central nervous system. |
Q79566803 | [The early history of transmissible spongiform encephalopathies exemplified by scrapie] |
Q56778732 | [Transmissible animal spongiform encephalopathies. Epidemiologic aspects] |
Search more.