Pages that link to "Q44592404"
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The following pages link to Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent (Q44592404):
Displaying 50 items.
- Possible case of maternal transmission of feline spongiform encephalopathy in a captive cheetah (Q21091186) (← links)
- Pruritus is a common feature in sheep infected with the BSE agent (Q21203575) (← links)
- Insights into the management of emerging infections: regulating variant Creutzfeldt-Jakob disease transfusion risk in the UK and the US (Q24288772) (← links)
- The molecular biology of prion propagation. (Q24522314) (← links)
- Active surveillance for scrapie by third eyelid biopsy and genetic susceptibility testing of flocks of sheep in Wyoming (Q24531974) (← links)
- Chronic wasting disease and potential transmission to humans (Q24599755) (← links)
- Prions (Q24633319) (← links)
- A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea (Q24642582) (← links)
- Elimination of prions by branched polyamines and implications for therapeutics (Q24646752) (← links)
- Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice (Q24651920) (← links)
- Chronic wasting disease prions in elk antler velvet (Q24655021) (← links)
- Neuropathology of non-Alzheimer degenerative disorders (Q24657571) (← links)
- The role of the cellular prion protein in the immune system (Q24683862) (← links)
- A short purification process for quantitative isolation of PrPSc from naturally occurring and experimental transmissible spongiform encephalopathies. (Q24793769) (← links)
- (Q24795216) (← links)
- Updated projections of future vCJD deaths in the UK (Q24799671) (← links)
- vCJD risk in the Republic of Ireland (Q24801647) (← links)
- Microdissection: a method developed to investigate mechanisms involved in transmissible spongiform encephalopathy pathogenesis (Q24802935) (← links)
- Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease (Q24812893) (← links)
- Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles (Q25257725) (← links)
- Insights into Mechanisms of Chronic Neurodegeneration (Q26771732) (← links)
- Genetics of Prion Disease in Cattle (Q26783714) (← links)
- Calcineurin Inhibition at the Clinical Phase of Prion Disease Reduces Neurodegeneration, Improves Behavioral Alterations and Increases Animal Survival (Q27313215) (← links)
- Whole Blood Gene Expression Profiling in Preclinical and Clinical Cattle Infected with Atypical Bovine Spongiform Encephalopathy (Q27314189) (← links)
- Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes (Q27318658) (← links)
- Transgenic Mouse Bioassay: Evidence That Rabbits Are Susceptible to a Variety of Prion Isolates (Q27318898) (← links)
- PRNP haplotype associated with classical BSE incidence in European Holstein cattle (Q27320110) (← links)
- All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD (Q27324879) (← links)
- Evidence that bank vole PrP is a universal acceptor for prions (Q27330039) (← links)
- NMR structure of the bovine prion protein (Q27625390) (← links)
- NMR structure of the bank vole prion protein at 20 degrees C contains a structured loop of residues 165-171 (Q27652004) (← links)
- Florid plaques in ovine PrP transgenic mice infected with an experimental ovine BSE. (Q28360325) (← links)
- Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. (Q28363814) (← links)
- Protein folding pathology in domestic animals (Q28387663) (← links)
- Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathy (Q28469063) (← links)
- Molecular, biochemical and genetic characteristics of BSE in Canada (Q28473930) (← links)
- Ultra-efficient PrP(Sc) amplification highlights potentialities and pitfalls of PMCA technology (Q28478072) (← links)
- Histopathological studies of "CH1641-like" scrapie sources versus classical scrapie and BSE transmitted to ovine transgenic mice (TgOvPrP4) (Q28479008) (← links)
- Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy (Q28534276) (← links)
- Elements modulating the prion species barrier and its passage consequences (Q28540614) (← links)
- The Priority position paper: Protecting Europe's food chain from prions (Q28830533) (← links)
- Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP (Q28943533) (← links)
- Eliminating Trachoma in Areas with Limited Disease (Q29037878) (← links)
- Implications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge (Q30228914) (← links)
- Mammalian prion proteins. (Q30326201) (← links)
- Insights into Chronic Wasting Disease and Bovine Spongiform Encephalopathy Species Barriers by Use of Real-Time Conversion (Q30376453) (← links)
- New variant Creutzfeldt-Jakob disease and the blood supply: is it time to face the music? (Q30431733) (← links)
- Preclinical detection of variant CJD and BSE prions in blood (Q30436588) (← links)
- Proper calibration of ultrasonic power enabled the quantitative analysis of the ultrasonication-induced amyloid formation process (Q30459645) (← links)
- Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK. (Q30488585) (← links)