scholarly article | Q13442814 |
P819 | ADS bibcode | 2009PLoSO...4.5916M |
P356 | DOI | 10.1371/JOURNAL.PONE.0005916 |
P932 | PMC publication ID | 2691594 |
P698 | PubMed publication ID | 19529769 |
P5875 | ResearchGate publication ID | 26295103 |
P50 | author | Candace K. Mathiason | Q56994150 |
Edward A. Hoover | Q89717635 | ||
Jeanette Hayes-Klug | Q108759117 | ||
P2093 | author name string | David A Osborn | |
Jenny Powers | |||
Gary L Mason | |||
Robert J Warren | |||
Karl V Miller | |||
Sallie J Dahmes | |||
Sheila A Hays | |||
Julia Langenberg | |||
P2860 | cites work | Chronic wasting disease and potential transmission to humans | Q24599755 |
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Prion infection of oral and nasal mucosa | Q33239798 | ||
Transmission and detection of prions in feces | Q33579436 | ||
Chronic wasting disease in deer and elk in North America. | Q33958780 | ||
Extraneural prion neuroinvasion without lymphoreticular system infection | Q33987431 | ||
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding | Q34084209 | ||
Cases of scrapie with unusual features in Norway and designation of a new type, Nor98. | Q34228022 | ||
Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient | Q34339769 | ||
A new variant of Creutzfeldt-Jakob disease in the UK. | Q34374893 | ||
Infectious prions in the saliva and blood of deer with chronic wasting disease | Q34571835 | ||
Cyclic amplification of protein misfolding: application to prion-related disorders and beyond | Q34750237 | ||
Bovine spongiform encephalopathy, chronic wasting disease, scrapie, and the threat to humans from prion disease epizootics | Q34929408 | ||
Scrapie and experimental BSE in sheep | Q35549003 | ||
Chronic wasting disease of cervids. | Q35776144 | ||
Human prion disease and relative risk associated with chronic wasting disease | Q35792137 | ||
Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. | Q51037857 | ||
Spatial epidemiology of chronic wasting disease in Wisconsin white-tailed deer. | Q51718370 | ||
Urinary excretion and blood level of prions in scrapie-infected hamsters. | Q51794689 | ||
Prion diseases are efficiently transmitted by blood transfusion in sheep. | Q51872417 | ||
CHRONIC WASTING DISEASE OF CAPTIVE MULE DEER: A SPONGIFORM ENCEPHALOPATHY | Q56210460 | ||
The same prion strain causes vCJD and BSE | Q57092996 | ||
Colorado Surveillance Program for Chronic Wasting Disease Transmission to Humans | Q57204426 | ||
Horizontal prion transmission in mule deer | Q59098665 | ||
Epizootiology of chronic wasting disease in free-ranging cervids in Colorado and Wyoming | Q73207885 | ||
vCJD and blood transfusion in the United Kingdom | Q79450770 | ||
Demonstration of lateral transmission of scrapie between sheep kept under natural conditions using lymphoid tissue biopsy | Q79830508 | ||
Epidemiology of chronic wasting disease in captive white-tailed and mule deer | Q80553962 | ||
Chronic wasting disease | Q81169811 | ||
Environmental sources of prion transmission in mule deer | Q35880452 | ||
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Risks of transmission of variant Creutzfeldt-Jakob disease by blood transfusion | Q36370046 | ||
The transmissible spongiform encephalopathies: emerging and declining epidemics | Q36638973 | ||
Risk behaviors in a rural community with a known point-source exposure to chronic wasting disease | Q36755505 | ||
Fourth case of transfusion-associated vCJD infection in the United Kingdom. | Q36763881 | ||
Temporal distribution of transmissible mink encephalopathy virus in mink inoculated subcutaneously | Q36919315 | ||
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study | Q37097991 | ||
Projections of the future course of the primary vCJD epidemic in the UK: inclusion of subclinical infection and the possibility of wider genetic susceptibility | Q40306174 | ||
Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease | Q40370560 | ||
A case of chronic wasting disease in an elk imported to Korea from Canada | Q40572204 | ||
Detection of infectious prions in urine | Q41371006 | ||
PrPSc in salivary glands of scrapie-affected sheep | Q41769208 | ||
Experimental chronic wasting disease (CWD) in the ferret | Q42526425 | ||
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans. | Q43213691 | ||
An analysis of natural scrapie in suffolk sheep | Q43550724 | ||
Polymorphisms in the prion precursor functional gene but not the pseudogene are associated with susceptibility to chronic wasting disease in white-tailed deer | Q43859793 | ||
PrP(CWD) lymphoid cell targets in early and advanced chronic wasting disease of mule deer | Q44141188 | ||
Transmission of prion diseases by blood transfusion | Q44186164 | ||
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 | ||
Spongiform encephalopathy in free-ranging mule deer (Odocoileus hemionus), white-tailed deer (Odocoileus virginianus) and Rocky Mountain elk (Cervus elaphus nelsoni) in northcentral Colorado | Q44756050 | ||
The effect of homogenisation on the level of scrapie activity detected in cells from spleens of scrapie affected mice | Q44791005 | ||
Similar levels of infectivity in the blood of mice infected with human-derived vCJD and GSS strains of transmissible spongiform encephalopathy | Q44949376 | ||
Pathogenesis of Scrapie Virus Infection in the Mouse | Q44956310 | ||
Infectious agent of sheep scrapie may persist in the environment for at least 16 years | Q45141929 | ||
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Course of experimental scrapie virus infection in the goat | Q45825585 | ||
Epidemiology of chronic wasting disease in captive Rocky Mountain elk. | Q46357764 | ||
Prevalence of lymphoreticular prion protein accumulation in UK tissue samples. | Q47278870 | ||
Ultra-efficient replication of infectious prions by automated protein misfolding cyclic amplification. | Q47843274 | ||
Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease | Q48152236 | ||
Survey of Cattle in Northeast Colorado for Evidence of Chronic Wasting Disease: Geographical and High-Risk Targeted Sample | Q48316681 | ||
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report. | Q48340913 | ||
Evolution of a strain of CJD that induces BSE-like plaques | Q48660544 | ||
Additional cases of Chronic Wasting Disease in imported deer in Korea | Q48788134 | ||
Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. | Q48793714 | ||
In vitro amplification of PrPSc derived from the brain and blood of sheep infected with scrapie | Q48827827 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | chronic wasting disease | Q1087811 |
prion protein family | Q24724413 | ||
P304 | page(s) | e5916 | |
P577 | publication date | 2009-06-16 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Infectious prions in pre-clinical deer and transmission of chronic wasting disease solely by environmental exposure | |
P478 | volume | 4 |
Q36630654 | Absolute quantification of prion protein (90-231) using stable isotope-labeled chymotryptic peptide standards in a LC-MRM AQUA workflow |
Q27324879 | All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD |
Q47590330 | Amyloidosis-inducing activity of blood cells in mouse AApoAII amyloidosis |
Q35586642 | An overview of animal prion diseases |
Q41276056 | Aspects of the husbandry and management of captive cervids |
Q35845872 | Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob disease |
Q47423726 | Assessment of Chronic Wasting Disease Prion Shedding in Deer Saliva with Occupancy Modeling |
Q33826801 | B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease |
Q31012349 | Bayesian Modeling of Prion Disease Dynamics in Mule Deer Using Population Monitoring and Capture-Recapture Data |
Q34585664 | Behavior of prions in the environment: implications for prion biology |
Q34039829 | Can plants serve as a vector for prions causing chronic wasting disease? |
Q36116896 | Chronic Wasting Disease Drives Population Decline of White-Tailed Deer. |
Q47158648 | Chronic wasting disease (CWD) in cervids |
Q102059036 | Chronic wasting disease (CWD) prion detection in blood from pre-symptomatic white-tailed deer harboring PRNP polymorphic variants |
Q34641947 | Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein |
Q30829414 | Clay Components in Soil Dictate Environmental Stability and Bioavailability of Cervid Prions in Mice |
Q47112380 | Clay content and pH: soil characteristic associations with the persistent presence of chronic wasting disease in northern Illinois |
Q64060892 | Comparison of conventional, amplification and bio-assay detection methods for a chronic wasting disease inoculum pool |
Q37523060 | Could avian scavengers translocate infectious prions to disease-free areas initiating new foci of chronic wasting disease? |
Q90597989 | Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases |
Q47313313 | Detection of Prions in Blood of Cervids at the Asymptomatic Stage of Chronic Wasting Disease |
Q35077622 | Detection of chronic wasting disease prions in salivary, urinary, and intestinal tissues of deer: potential mechanisms of prion shedding and transmission |
Q33576063 | Detection of protease-resistant cervid prion protein in water from a CWD-endemic area |
Q30946000 | Detection of sub-clinical CWD infection in conventional test-negative deer long after oral exposure to urine and feces from CWD+ deer |
Q51394138 | Diversity and distribution of white-tailed deer mtDNA lineages in chronic wasting disease (CWD) outbreak areas in southern Wisconsin, USA. |
Q47866649 | Efficient prion disease transmission through common environmental materials |
Q42184885 | Environmental sources of scrapie prions |
Q34618920 | Estimating prion adsorption capacity of soil by BioAssay of Subtracted Infectivity from Complex Solutions (BASICS). |
Q91604185 | Estimating relative CWD susceptibility and disease progression in farmed white-tailed deer with rare PRNP alleles |
Q42165503 | Evidence for distinct chronic wasting disease (CWD) strains in experimental CWD in ferrets |
Q40125310 | Experimental Transmission of the Chronic Wasting Disease Agent to Swine after Oral or Intracranial Inoculation. |
Q38189236 | Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches. |
Q26783714 | Genetics of Prion Disease in Cattle |
Q34476650 | Grass plants bind, retain, uptake, and transport infectious prions |
Q37535837 | Horizontal Transmission of Chronic Wasting Disease in Reindeer |
Q90590729 | Hypermobile human predators |
Q90399308 | Immunotherapy against Prion Disease |
Q39431937 | Implications of peptide assemblies in amyloid diseases |
Q92320578 | In Vitro detection of Chronic Wasting Disease (CWD) prions in semen and reproductive tissues of white tailed deer bucks (Odocoileus virginianus) |
Q35041621 | In vitro detection of prionemia in TSE-infected cervids and hamsters |
Q36148348 | Inactivation of Prions and Amyloid Seeds with Hypochlorous Acid |
Q34519527 | Infectious Disease and Grouping Patterns in Mule Deer |
Q30145567 | Infectious Prions in the Pregnancy Microenvironment of Chronic Wasting Disease-Infected Reeves' Muntjac Deer |
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 |
Q26829499 | Lichens: unexpected anti-prion agents? |
Q35973527 | Longitudinal Detection of Prion Shedding in Saliva and Urine by Chronic Wasting Disease-Infected Deer by Real-Time Quaking-Induced Conversion. |
Q92605438 | Modeling current and potential distributions of mammal species using presence-only data: A case study on British deer |
Q33908554 | Modeling routes of chronic wasting disease transmission: environmental prion persistence promotes deer population decline and extinction |
Q33777544 | Molecular genealogy tools for white-tailed deer with chronic wasting disease. |
Q34972484 | Mother to offspring transmission of chronic wasting disease in reeves' muntjac deer |
Q36340013 | Mule deer spatial association patterns and potential implications for transmission of an epizootic disease |
Q34257676 | Occurrence, transmission, and zoonotic potential of chronic wasting disease |
Q37270298 | Pathogen persistence in the environment and insect-baculovirus interactions: disease-density thresholds, epidemic burnout, and insect outbreaks |
Q38934923 | Pathways of Prion Spread during Early Chronic Wasting Disease in Deer |
Q84582194 | PrP(Sc) is associated with B cells in the blood of scrapie-infected sheep |
Q33556021 | Prion amplification and hierarchical Bayesian modeling refine detection of prion infection |
Q37800332 | Prion transmission: prion excretion and occurrence in the environment |
Q31144537 | Prion-seeding activity in cerebrospinal fluid of deer with chronic wasting disease |
Q37675385 | Procedures for identifying infectious prions after passage through the digestive system of an avian species |
Q34989982 | Rapid antemortem detection of CWD prions in deer saliva |
Q34982680 | Replication efficiency of soil-bound prions varies with soil type |
Q38061481 | Review: membrane-associated misfolded protein propagation in natural transmissible spongiform encephalopathies (TSEs), synthetic prion diseases and Alzheimer's disease |
Q35918937 | Salivary prions in sheep and deer |
Q97070651 | Scientific opinion on chronic wasting disease (II) |
Q36523240 | Sensitivity of protein misfolding cyclic amplification versus immunohistochemistry in ante-mortem detection of chronic wasting disease |
Q89997527 | Shedding and stability of CWD prion seeding activity in cervid feces |
Q91686279 | Spatial heterogeneity of prion gene polymorphisms in an area recently infected by chronic wasting disease |
Q37224841 | Specificity, Size, and Frequency of Spaces That Characterize the Mechanism of Bulk Transepithelial Transport of Prions in the Nasal Cavities of Hamsters and Mice |
Q52737115 | Spiroplasma spp. biofilm formation is instrumental for their role in the pathogenesis of plant, insect and animal diseases. |
Q36607404 | Susceptibility of domestic cats to chronic wasting disease |
Q42241160 | Temperature influences the interaction of ruminant PrP (TSE) with soil |
Q37272257 | Temporal-spatial heterogeneity in animal-environment contact: implications for the exposure and transmission of pathogens |
Q39342335 | The Ecology of Prions |
Q38178407 | The case for involvement of spiroplasma in the pathogenesis of transmissible spongiform encephalopathies |
Q89616664 | The ecology of chronic wasting disease in wildlife |
Q35666089 | The oral secretion of infectious scrapie prions occurs in preclinical sheep with a range of PRNP genotypes. |
Q34776566 | Transport of the pathogenic prion protein through soils |
Q51767259 | Uptake dynamics of scrapie agent in the intestinal villous epithelium of suckling and weanling Syrian hamsters. |
Q40127635 | Using White-tailed Deer (Odocoileus virginianus) in Infectious Disease Research |
Q34453109 | Variant CJD. 18 years of research and surveillance |