| P2093 | author name string | Didier Vilette | |
| | Hubert Laude | |
| | Annick Le Dur | |
| | Jean-Luc Vilotte | |
| | Fabienne Archer | |
| | Nathalie Besnard | |
| | Rachid Essalmani | |
| | Solange Soulier | |
| P2860 | cites work | Prions | Q24633319 |
| | Mice devoid of PrP are resistant to scrapie | Q28249108 |
| | Transcriptional activation by tetracyclines in mammalian cells | Q28303934 |
| | Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue | Q29615225 |
| | Neuronal polarity and the epithelial metaphor | Q33731011 |
| | Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein | Q33794942 |
| | Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp. | Q33842432 |
| | Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein | Q34294957 |
| | Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier | Q34393434 |
| | Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein | Q35053001 |
| | Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation | Q36581272 |
| | Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice | Q36806018 |
| | Prion protein and the transmissible spongiform encephalopathies | Q36914449 |
| | Scrapie-associated prion protein accumulates in astrocytes during scrapie infection | Q37368465 |
| | Cultured cell sublines highly susceptible to prion infection | Q39590907 |
| | Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy | Q39591398 |
| | Efficient transmission of two different sheep scrapie isolates in transgenic mice expressing the ovine PrP gene | Q39606216 |
| | Scrapie strain variation and mutation | Q40729976 |
| | Screening Congo Red and its analogues for their ability to prevent the formation of PrP-res in scrapie-infected cells | Q40892763 |
| | Establishment of astrocyte cell lines from sheep genetically susceptible to scrapie | Q40897993 |
| | Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. | Q41064177 |
| | A review of the epidemiology of scrapie in sheep. | Q41345754 |
| | Polarized sorting of viral glycoproteins to the axon and dendrites of hippocampal neurons in culture | Q41511408 |
| | PrP genetics in sheep and the applications for scrapie and BSE. | Q41570657 |
| | Mammalian cell lines can be efficiently established in vitro upon expression of the SV40 large T antigen driven by a promoter sequence derived from the human vimentin gene | Q41708578 |
| | Immortalization of hypothalamic GnRH neurons by genetically targeted tumorigenesis | Q41729068 |
| | Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein | Q43522858 |
| | PrP genotype and agent effects in scrapie: change in allelic interaction with different isolates of agent in sheep, a natural host of scrapie | Q43969509 |
| | Characterization of scrapie infection in mouse neuroblastoma cells | Q44079577 |
| | 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 |
| | Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 |
| | Cellular prion protein expressed by bovine squamous epithelia of skin and upper gastrointestinal tract | Q45195159 |
| | Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques. | Q45962479 |
| | Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins | Q46155239 |
| | Natural scrapie in a closed flock of Cheviot sheep occurs only in specific PrP genotypes | Q47636904 |
| | Evidence for the multiplication of scrapie agent in cell culture | Q47676327 |
| | PrP genotype contributes to determining survival times of sheep with natural scrapie. | Q48059613 |
| | Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. | Q48297442 |
| | Transgenic and knockout mice in research on prion diseases | Q48357484 |
| | Preliminary observations on the pathogenesis of experimental bovine spongiform encephalopathy (BSE): an update | Q48510790 |
| | In vitro replication of scrapie agent in a neuronal model: infection of PC12 cells | Q48595899 |
| | Immunodetection of PrPSc in spleens of some scrapie-infected sheep but not BSE-infected cows | Q48629530 |
| | Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. | Q54154878 |
| | The same prion strain causes vCJD and BSE | Q57092996 |
| | Doubts over ability to monitor risks of BSE spread to sheep | Q58994097 |
| | Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie | Q60895162 |
| | Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters | Q70345462 |
| | The unusual properties of CH1641, a sheep-passaged isolate of scrapie | Q70407076 |
| | Scrapie infection can be established readily through skin scarification in immunocompetent but not immunodeficient mice | Q71398221 |
| | Prp-c and Prp-Sc at the fetal-maternal interface | Q73684853 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 49-57 | |
| P577 | publication date | 2002-01-01 | |
| P1433 | published in | Comptes Rendus. Biologies | Q2092827 |
| P1476 | title | New in vivo and ex vivo models for the experimental study of sheep scrapie: development and perspectives | |
| P478 | volume | 325 | |