scholarly article | Q13442814 |
P50 | author | Mark W Head | Q55300123 |
Marcelo A Barria | Q57421550 | ||
James Ironside | Q29643044 | ||
P2860 | cites work | Prions | Q24633319 |
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein | Q39686522 | ||
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans. | Q43213691 | ||
Creutzfeldt-Jakob disease in unusually young patients who consumed venison | Q43215637 | ||
Predicting susceptibility and incubation time of human-to-human transmission of vCJD. | Q43220422 | ||
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 | ||
Chronic wasting disease and atypical forms of bovine spongiform encephalopathy and scrapie are not transmissible to mice expressing wild-type levels of human prion protein. | Q45826513 | ||
Trans-species amplification of PrP(CWD) and correlation with rigid loop 170N. | Q46096050 | ||
Spontaneous neurodegeneration in transgenic mice with mutant prion protein | Q46249938 | ||
The possible nature of the transmissible agent of scrapie | Q47709063 | ||
Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. | Q48793714 | ||
Atypical L-type bovine spongiform encephalopathy (L-BSE) transmission to cynomolgus macaques, a non-human primate | Q48923866 | ||
Cell-free formation of protease-resistant prion protein. | Q53204380 | ||
CHRONIC WASTING DISEASE OF CAPTIVE MULE DEER: A SPONGIFORM ENCEPHALOPATHY | Q56210460 | ||
The same prion strain causes vCJD and BSE | Q57092996 | ||
Colorado Surveillance Program for Chronic Wasting Disease Transmission to Humans | Q57204426 | ||
Horizontal prion transmission in mule deer | Q59098665 | ||
BSE transmission to macaques | Q59098670 | ||
Mice devoid of PrP are resistant to scrapie | Q28249108 | ||
Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate | Q28473442 | ||
Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype | Q28476285 | ||
Novel proteinaceous infectious particles cause scrapie | Q29547678 | ||
Infectious prions in pre-clinical deer and transmission of chronic wasting disease solely by environmental exposure | Q33468412 | ||
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism | Q33520832 | ||
Prion diseases in man. | Q33598395 | ||
Susceptibilities of nonhuman primates to chronic wasting disease | Q33644675 | ||
Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice | Q33893587 | ||
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding | Q34084209 | ||
Interspecies transmission of chronic wasting disease prions to squirrel monkeys (Saimiri sciureus) | Q34092718 | ||
Distinct molecular phenotypes in bovine prion diseases | Q34165722 | ||
Self-replication and scrapie | Q34225002 | ||
Cases of scrapie with unusual features in Norway and designation of a new type, Nor98. | Q34228022 | ||
Occurrence, transmission, and zoonotic potential of chronic wasting disease | Q34257676 | ||
A new variant of Creutzfeldt-Jakob disease in the UK. | Q34374893 | ||
A cellular gene encodes scrapie PrP 27-30 protein | Q34557641 | ||
Molecular model of prion transmission to humans | Q34603607 | ||
Generation of a new form of human PrP(Sc) in vitro by interspecies transmission from cervid prions | Q34606377 | ||
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein | Q34641947 | ||
Species-barrier-independent prion replication in apparently resistant species. | Q34685449 | ||
Transmission of elk and deer prions to transgenic mice | Q35024303 | ||
Bovine spongiform encephalopathy (BSE) and its epidemiology | Q35549007 | ||
Environmental sources of prion transmission in mule deer | Q35880452 | ||
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans | Q36782262 | ||
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease | Q36853707 | ||
Insights into prion strains and neurotoxicity | Q36856446 | ||
Review on the epidemiology and dynamics of BSE epidemics | Q37054499 | ||
Transmission of atypical bovine prions to mice transgenic for human prion protein | Q37080870 | ||
Crossing the species barrier by PrP(Sc) replication in vitro generates unique infectious prions. | Q37339448 | ||
Molecular barriers to zoonotic transmission of prions | Q37449082 | ||
Atypical prion diseases in humans and animals | Q37877629 | ||
Species-barrier phenomenon in prion transmissibility from a viewpoint of protein science. | Q38071276 | ||
P433 | issue | 1 | |
P921 | main subject | prion protein family | Q24724413 |
zoonosis | Q182672 | ||
zoonotic potential | Q88491917 | ||
P304 | page(s) | 85-91 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | Prion | Q26842757 |
P1476 | title | Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches | |
P478 | volume | 8 |
Q47158648 | Chronic wasting disease (CWD) in cervids |
Q34550317 | Current evidence on the transmissibility of chronic wasting disease prions to humans-A systematic review |
Q35193339 | Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversion |
Q30639674 | Human prion protein sequence elements impede cross-species chronic wasting disease transmission. |
Q27002571 | It's more than stamp collecting: how genome sequencing can unify biological research |
Q35859408 | Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012. |
Q30436588 | Preclinical detection of variant CJD and BSE prions in blood |
Q35546137 | Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications. |
Q47157217 | Scientific Opinion on a request for a review of a scientific publication concerning the zoonotic potential of ovine scrapie prions |
Q56559501 | Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions |
Q40800092 | The Risk of Prion Infection through Bovine Grafting Materials |
Q38213991 | The potential of mesenchymal stem cell in prion research. |
Q38492754 | The transmissible spongiform encephalopathies of livestock |
Q97072486 | Update on chronic wasting disease (CWD) III |
Search more.