Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches.

scientific article published on January 2014

Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.4161/PRI.28124
P932PMC publication ID7030916
P698PubMed publication ID24549113
P5875ResearchGate publication ID260252947

P50authorMark W HeadQ55300123
Marcelo A BarriaQ57421550
James IronsideQ29643044
P2860cites workPrionsQ24633319
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinQ39686522
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.Q43213691
Creutzfeldt-Jakob disease in unusually young patients who consumed venisonQ43215637
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 agentQ44592404
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 proteinQ46249938
The possible nature of the transmissible agent of scrapieQ47709063
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 primateQ48923866
Cell-free formation of protease-resistant prion protein.Q53204380
CHRONIC WASTING DISEASE OF CAPTIVE MULE DEER: A SPONGIFORM ENCEPHALOPATHYQ56210460
The same prion strain causes vCJD and BSEQ57092996
Colorado Surveillance Program for Chronic Wasting Disease Transmission to HumansQ57204426
Horizontal prion transmission in mule deerQ59098665
BSE transmission to macaquesQ59098670
Mice devoid of PrP are resistant to scrapieQ28249108
Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primateQ28473442
Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotypeQ28476285
Novel proteinaceous infectious particles cause scrapieQ29547678
Infectious prions in pre-clinical deer and transmission of chronic wasting disease solely by environmental exposureQ33468412
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphismQ33520832
Prion diseases in man.Q33598395
Susceptibilities of nonhuman primates to chronic wasting diseaseQ33644675
Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic miceQ33893587
Sensitive detection of pathological prion protein by cyclic amplification of protein misfoldingQ34084209
Interspecies transmission of chronic wasting disease prions to squirrel monkeys (Saimiri sciureus)Q34092718
Distinct molecular phenotypes in bovine prion diseasesQ34165722
Self-replication and scrapieQ34225002
Cases of scrapie with unusual features in Norway and designation of a new type, Nor98.Q34228022
Occurrence, transmission, and zoonotic potential of chronic wasting diseaseQ34257676
A new variant of Creutzfeldt-Jakob disease in the UK.Q34374893
A cellular gene encodes scrapie PrP 27-30 proteinQ34557641
Molecular model of prion transmission to humansQ34603607
Generation of a new form of human PrP(Sc) in vitro by interspecies transmission from cervid prionsQ34606377
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion proteinQ34641947
Species-barrier-independent prion replication in apparently resistant species.Q34685449
Transmission of elk and deer prions to transgenic miceQ35024303
Bovine spongiform encephalopathy (BSE) and its epidemiologyQ35549007
Environmental sources of prion transmission in mule deerQ35880452
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humansQ36782262
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob diseaseQ36853707
Insights into prion strains and neurotoxicityQ36856446
Review on the epidemiology and dynamics of BSE epidemicsQ37054499
Transmission of atypical bovine prions to mice transgenic for human prion proteinQ37080870
Crossing the species barrier by PrP(Sc) replication in vitro generates unique infectious prions.Q37339448
Molecular barriers to zoonotic transmission of prionsQ37449082
Atypical prion diseases in humans and animalsQ37877629
Species-barrier phenomenon in prion transmissibility from a viewpoint of protein science.Q38071276
P433issue1
P921main subjectprion protein familyQ24724413
zoonosisQ182672
zoonotic potentialQ88491917
P304page(s)85-91
P577publication date2014-01-01
P1433published inPrionQ26842757
P1476titleExploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches
P478volume8

Reverse relations

cites work (P2860)
Q47158648Chronic wasting disease (CWD) in cervids
Q34550317Current evidence on the transmissibility of chronic wasting disease prions to humans-A systematic review
Q35193339Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversion
Q30639674Human prion protein sequence elements impede cross-species chronic wasting disease transmission.
Q27002571It's more than stamp collecting: how genome sequencing can unify biological research
Q35859408Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012.
Q30436588Preclinical detection of variant CJD and BSE prions in blood
Q35546137Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.
Q47157217Scientific Opinion on a request for a review of a scientific publication concerning the zoonotic potential of ovine scrapie prions
Q56559501Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions
Q40800092The Risk of Prion Infection through Bovine Grafting Materials
Q38213991The potential of mesenchymal stem cell in prion research.
Q38492754The transmissible spongiform encephalopathies of livestock
Q97072486Update on chronic wasting disease (CWD) III

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