Pages that link to "Q37179619"
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The following pages link to Prion agent diversity and species barrier. (Q37179619):
Displaying 50 items.
- The physical relationship between infectivity and prion protein aggregates is strain-dependent (Q27315010) (← links)
- Transgenic Rabbits Expressing Ovine PrP Are Susceptible to Scrapie (Q27318296) (← links)
- Prion disease susceptibility is affected by -structure folding propensity and local side-chain interactions in PrP (Q27665543) (← links)
- Porcine prion protein amyloid (Q28606524) (← links)
- Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prions (Q28607285) (← links)
- Is the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic? (Q30357614) (← links)
- Biochemical characterization of prion strains in bank voles (Q33456970) (← links)
- Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata) (Q33487702) (← links)
- Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitro (Q33769143) (← links)
- Tracing conformational transition of abnormal prion proteins during interspecies transmission by using novel antibodies (Q33782462) (← links)
- Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells (Q33821808) (← links)
- PrP(Sc)-specific antibodies do not induce prion disease or misfolding of PrP(C) in highly susceptible Tga20 mice (Q34051202) (← links)
- Accelerated, spleen-based titration of variant Creutzfeldt-Jakob disease infectivity in transgenic mice expressing human prion protein with sensitivity comparable to that of survival time bioassay (Q34057924) (← links)
- Occurrence, transmission, and zoonotic potential of chronic wasting disease (Q34257676) (← links)
- Experimental oral transmission of chronic wasting disease to reindeer (Rangifer tarandus tarandus) (Q34283527) (← links)
- Individual factors associated with L- and H-type Bovine Spongiform encephalopathy in France (Q34286785) (← links)
- Sequence-dependent prion protein misfolding and neurotoxicity. (Q34299277) (← links)
- Molecular pathology of human prion disease (Q34462913) (← links)
- Review: contribution of transgenic models to understanding human prion disease. (Q34474868) (← links)
- Current evidence on the transmissibility of chronic wasting disease prions to humans-A systematic review (Q34550317) (← links)
- Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line (Q34580839) (← links)
- Strain typing of classical scrapie by transgenic mouse bioassay using protein misfolding cyclic amplification to replace primary passage (Q34614503) (← links)
- Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein (Q34641947) (← links)
- In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies (Q34929959) (← links)
- Quaternary structure of pathological prion protein as a determining factor of strain-specific prion replication dynamics. (Q35018090) (← links)
- Signal transduction by a fungal NOD-like receptor based on propagation of a prion amyloid fold (Q35130900) (← links)
- White-tailed deer are susceptible to the agent of sheep scrapie by intracerebral inoculation (Q35420475) (← links)
- The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species (Q35488786) (← links)
- Proteinase K-resistant material in ARR/VRQ sheep brain affected with classical scrapie is composed mainly of VRQ prion protein. (Q35531568) (← links)
- Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice (Q35844725) (← links)
- Did the prion protein become vulnerable to misfolding after an evolutionary divide and conquer event? (Q36010061) (← links)
- Genetic and Pathological Follow-Up Study of Goats Experimentally and Naturally Exposed to a Sheep Scrapie Isolate. (Q36080879) (← links)
- W8, a new Sup35 prion strain, transmits distinctive information with a conserved assembly scheme (Q36147463) (← links)
- Use of murine bioassay to resolve ovine transmissible spongiform encephalopathy cases showing a bovine spongiform encephalopathy molecular profile (Q36421690) (← links)
- Mutated but Not Deleted Ovine PrP(C) N-Terminal Polybasic Region Strongly Interferes with Prion Propagation in Transgenic Mice (Q36481434) (← links)
- Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions (Q36550420) (← links)
- Transmission of atypical bovine prions to mice transgenic for human prion protein (Q37080870) (← links)
- Generating Bona Fide Mammalian Prions with Internal Deletions (Q37093469) (← links)
- Prion diseases as transmissible zoonotic diseases (Q37105925) (← links)
- Prion infectivity in fat of deer with chronic wasting disease (Q37333962) (← links)
- Polymorphism analysis of prion protein gene in 11 Pakistani goat breeds (Q37371907) (← links)
- Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice (Q37415429) (← links)
- Detection of infectivity in blood of persons with variant and sporadic Creutzfeldt-Jakob disease (Q37449009) (← links)
- The role of the unusual threonine string in the conversion of prion protein (Q37508301) (← links)
- Therapeutic interventions ameliorating prion disease (Q37557690) (← links)
- Divergent prion strain evolution driven by PrPC expression level in transgenic mice (Q37604337) (← links)
- Genetic resistance to scrapie infection in experimentally challenged goats (Q37644091) (← links)
- Procedures for identifying infectious prions after passage through the digestive system of an avian species (Q37675385) (← links)
- Atypical Prion Diseases in Humans and Animals (Q37877629) (← links)
- The role of genetics in chronic wasting disease of North American cervids (Q37998389) (← links)