Molecular modeling of prion transmission to humans

scientific article

Molecular modeling of prion transmission to humans is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3390/V6103766
P932PMC publication ID4213560
P698PubMed publication ID25279820
P5875ResearchGate publication ID266577366

P50authorEtienne LevavasseurQ66360620
P2093author name stringThierry Baron
Nicolas Privat
Stéphane Haïk
Benoit Flan
Steve Simoneau
Juan-Carlos Espinosa Martin
Juan-Maria Torres
P2860cites workVariant CJD in an individual heterozygous for PRNP codon 129Q82681101
PrionsQ24633319
Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primateQ28473442
Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.Q30840051
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?Q33277907
Accelerated high fidelity prion amplification within and across prion species barriers.Q33366539
Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivoQ33449340
Transmission barriers for bovine, ovine, and human prions in transgenic miceQ33754930
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another proteinQ34294957
In vitro generation of infectious scrapie prions.Q34413661
In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc.Q34580924
Molecular model of prion transmission to humansQ34603607
Detection of new quantitative trait Loci for susceptibility to transmissible spongiform encephalopathies in miceQ34619306
Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic miceQ34693238
Lower specific infectivity of protease-resistant prion protein generated in cell-free reactionsQ35585904
Oral transmission of L-type bovine spongiform encephalopathy in primate modelQ35845923
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strainQ36498169
Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant formsQ36763154
Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic miceQ36806018
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob diseaseQ36853707
Cell-free propagation of prion strains.Q36936923
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
Susceptibility of sheep for scrapie as assessed by in vitro conversion of nine naturally occurring variants of PrP.Q39588310
Assessment of the genetic susceptibility of sheep to scrapie by protein misfolding cyclic amplification and comparison with experimental scrapie transmission studiesQ42113610
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.Q43213691
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strainQ44475863
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agentQ44592404
Risk factors for variant Creutzfeldt-Jakob disease: a case-control studyQ44908172
Human prion protein with valine 129 prevents expression of variant CJD phenotypeQ45147953
A bovine prion acquires an epidemic bovine spongiform encephalopathy strain-like phenotype on interspecies transmissionQ48124117
Variant or sporadic Creutzfeldt-Jakob disease?Q48273658
Early detection of PrPres in BSE-infected bovine PrP transgenic miceQ48351069
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue10
P921main subjectprion protein familyQ24724413
P304page(s)3766-3777
P577publication date2014-10-02
P1433published inVirusesQ7935305
P1476titleMolecular modeling of prion transmission to humans
P478volume6

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cites work (P2860)
Q40087612Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains
Q47157217Scientific Opinion on a request for a review of a scientific publication concerning the zoonotic potential of ovine scrapie prions
Q38492754The transmissible spongiform encephalopathies of livestock
Q92074937Tracking and clarifying differential traits of classical- and atypical L-type bovine spongiform encephalopathy prions after transmission from cattle to cynomolgus monkeys

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