| scholarly article | Q13442814 |
| P50 | author | Byron Caughey | Q87076179 |
| P2093 | author name string | Richard A Bessen | |
| Jason M Wilham | |||
| Harold Shearin | |||
| James A Wiley | |||
| Scott Martinka | |||
| Diana Lowe | |||
| Ryan Boharski | |||
| P2860 | cites work | Asymptomatic deer excrete infectious prions in faeces | Q24635252 |
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| The nasal cavity is a route for prion infection in hamsters | Q35857428 | ||
| Environmental sources of prion transmission in mule deer | Q35880452 | ||
| Experimental transmission of scrapie agent to susceptible sheep by intralingual or intracerebral inoculation | Q36226126 | ||
| Signal transduction in olfactory neurons | Q36422759 | ||
| Olfactory neurogenesis: genetic or environmental controls? | Q36601172 | ||
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| Role of the lymphoreticular system in prion neuroinvasion from the oral and nasal mucosa | Q37232900 | ||
| Human variant Creutzfeldt-Jakob disease and sheep scrapie PrP(res) detection using seeded conversion of recombinant prion protein | Q37285506 | ||
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| Olfactory system involvement in natural scrapie disease. | Q41936997 | ||
| Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie | Q42693681 | ||
| Transmission of prion diseases by blood transfusion | Q44186164 | ||
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| Isolation and characterization of rat olfactory marker protein | Q48356340 | ||
| Isolation of scrapie agent from the placenta of sheep with natural scrapie in Japan | Q48373302 | ||
| Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease | Q48384269 | ||
| Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease | Q48483487 | ||
| Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters | Q48540661 | ||
| Ablation of the olfactory bulb up-regulates the rate of neurogenesis and induces precocious cell death in olfactory epithelium | Q48555118 | ||
| Comparison of histological lesions and immunohistochemical staining of proteinase-resistant prion protein in a naturally occurring spongiform encephalopathy of free-ranging mule deer (Odocoileus hemionus) with those of chronic wasting disease of cap | Q48558348 | ||
| Coincident scrapie infection and nephritis lead to urinary prion excretion | Q48730761 | ||
| Chronic wasting disease in a Wisconsin white-tailed deer farm | Q48934644 | ||
| Neuroinvasion of the 263K scrapie strain after intranasal administration occurs through olfactory-unrelated pathways. | Q51782975 | ||
| Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking. | Q51790930 | ||
| Urinary excretion and blood level of prions in scrapie-infected hamsters. | Q51794689 | ||
| Evidence for the disproportionate mapping of olfactory airspace onto the main olfactory bulb of the hamster. | Q51825553 | ||
| Expression and localization of the prion protein PrP(C) in the olfactory system of the mouse. | Q51962065 | ||
| PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis. | Q54254632 | ||
| PrPSc in mammary glands of sheep affected by scrapie and mastitis | Q57083648 | ||
| Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease | Q59505845 | ||
| Elimination of natural scrapie in sheep by sire genotype selection | Q67465436 | ||
| Epizootiology of chronic wasting disease in free-ranging cervids in Colorado and Wyoming | Q73207885 | ||
| Scrapie: A transmissible and hereditary disease of sheep | Q79047277 | ||
| Epidemiology of chronic wasting disease in captive white-tailed and mule deer | Q80553962 | ||
| High incidence of subclinical infection of lymphoid tissues in scrapie-affected sheep flocks | Q80567595 | ||
| P275 | copyright license | Creative Commons CC0 License | Q6938433 |
| P6216 | copyright status | copyrighted, dedicated to the public domain by copyright holder | Q88088423 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | prion protein family | Q24724413 |
| P304 | page(s) | e1000837 | |
| P577 | publication date | 2010-04-01 | |
| P1433 | published in | PLOS Pathogens | Q283209 |
| P1476 | title | Prion shedding from olfactory neurons into nasal secretions | |
| P478 | volume | 6 |
| Q34293962 | A test for Creutzfeldt-Jakob disease using nasal brushings |
| Q35689662 | Accelerated shedding of prions following damage to the olfactory epithelium |
| Q36734911 | Antemortem Detection of Chronic Wasting Disease Prions in Nasal Brush Collections and Rectal Biopsy Specimens from White-Tailed Deer by Real-Time Quaking-Induced Conversion |
| Q34057962 | Axonal and transynaptic spread of prions |
| Q90597989 | Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases |
| Q36086340 | Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype |
| Q46251829 | How do PrPSc Prions Spread between Host Species, and within Hosts? |
| Q35735220 | Identification of novel putative-binding proteins for cellular prion protein and a specific interaction with the STIP1 homology and U-Box-containing protein 1. |
| Q37409418 | Intra-host mathematical model of chronic wasting disease dynamics in deer (Odocoileus). |
| Q34720600 | Intranasal inoculation of white-tailed deer (Odocoileus virginianus) with lyophilized chronic wasting disease prion particulate complexed to montmorillonite clay |
| Q35231240 | Lesion of the olfactory epithelium accelerates prion neuroinvasion and disease onset when prion replication is restricted to neurons |
| Q37006741 | Mucosal transmission and pathogenesis of chronic wasting disease in ferrets |
| Q37993987 | New generation QuIC assays for prion seeding activity |
| Q36159486 | Particle-size dependent effects in the Balb/c murine model of inhalational melioidosis |
| Q36326862 | PrPSc formation and clearance as determinants of prion tropism |
| Q30436588 | Preclinical detection of variant CJD and BSE prions in blood |
| Q46451539 | Prion Strain Diversity |
| Q35006294 | Prion disease blood test using immunoprecipitation and improved quaking-induced conversion |
| Q39330702 | Prion pathogenesis and secondary lymphoid organs (SLO): tracking the SLO spread of prions to the brain |
| Q37890298 | Prion seeded conversion and amplification assays. |
| Q28484853 | Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC |
| Q37800332 | Prion transmission: prion excretion and occurrence in the environment |
| Q40061694 | RT-QuIC Assays for Prion Disease Detection and Diagnostics |
| Q33769767 | Rapid end-point quantitation of prion seeding activity with sensitivity comparable to bioassays |
| Q36397542 | Rapid transepithelial transport of prions following inhalation |
| Q47294251 | Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies. |
| Q36734886 | Seeded Amplification of Chronic Wasting Disease Prions in Nasal Brushings and Recto-anal Mucosa-Associated Lymphoid Tissues from Elk by Real-Time Quaking-Induced Conversion |
| Q99726049 | The Role of Vesicle Trafficking Defects in the Pathogenesis of Prion and Prion-Like Disorders |
| Q92723815 | The cellular prion protein promotes neuronal regeneration after acute nasotoxic injury |
| Q52631854 | The cellular prion protein promotes olfactory sensory neuron survival and axon targeting during adult neurogenesis. |
| Q39052041 | The olfactory bulb as the entry site for prion-like propagation in neurodegenerative diseases |
| Q35137829 | The sheddase ADAM10 is a potent modulator of prion disease. |
| Q27311657 | Transmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamsters |
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