Pages that link to "Item:Q166888"
The following pages link to Prion Diseases: Causes and Molecular Basis (Q166888):
Displayed 50 items.
- A dynamic spatio-temporal model for spatial data (Q240131) (← links)
- Aaron M. Foley (Q241394) (← links)
- Dennis M. Heisey (Q241897) (← links)
- Kenneth H. Johnson (Q243142) (← links)
- Jay R. Schneider (Q243181) (← links)
- Low copper and high manganese levels in prion protein plaques (Q243200) (← links)
- In vitro prion protein conversion suggests risk of bighorn sheep (Ovis canadensis) to transmissible spongiform encephalopathies (Q243497) (← links)
- Michael R. Ebinger (Q243637) (← links)
- Michael D. Samuel (Q243761) (← links)
- Paul Slota (Q243948) (← links)
- Is exposure to cyanobacteria an environmental risk factor for amyotrophic lateral sclerosis and other neurodegenerative diseases? (Q244135) (← links)
- Red-backed vole brain promotes highly efficient in vitro amplification of abnormal prion protein from macaque and human brains infected with variant Creutzfeldt-Jakob disease agent. (Q244686) (← links)
- Association mapping of genetic risk factors for chronic wasting disease in wild deer (Q244782) (← links)
- Using landscape epidemiological models to understand the distribution of chronic wasting disease in the Midwestern USA (Q244868) (← links)
- Emerging prion disease drives host selection in a wildlife population (Q245952) (← links)
- Highly efficient amplification of chronic wasting disease agent by protein misfolding cyclical amplification with beads (PMCAb) (Q245974) (← links)
- The role of genetics in chronic wasting disease of North American cervids (Q246044) (← links)
- Mapping brucellosis increases relative to elk density using hierarchical Bayesian models (Q247863) (← links)
- Linking process to pattern: estimating spatiotemporal dynamics of a wildlife epidemic from cross‐sectional data (Q248125) (← links)
- Bison PRNP genotyping and potential association with Brucella spp. seroprevalence (Q249293) (← links)
- Modeling routes of chronic wasting disease transmission: Environmental prion persistence promotes deer population decline and extinction (Q250960) (← links)
- Diversity and distribution of white-tailed deer mtDNA lineages in chronic wasting disease (CWD) outbreak areas in southern Wisconsin, USA (Q251491) (← links)
- Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmission (Q251544) (← links)
- Soil clay content underlies prion infection odds (Q251661) (← links)
- Homogenization of large-scale movement models in ecology (Q251672) (← links)
- Persistence of pathogenic prion protein during simulated wastewater treatment processes (Q252047) (← links)
- Landscape genetics and the spatial distribution of chronic wasting disease (Q252391) (← links)
- Pathogenic prion protein is degraded by a manganese oxide mineral found in soils (Q259525) (← links)
- Cognitive and behavioral coping in response to wildlife disease: The case of hunters and chronic wasting disease (Q266907) (← links)
- Applying a Bayesian weighted surveillance approach to detect chronic wasting disease in white‐tailed deer (Q268013) (← links)
- Prion seeding activity in plant tissues detected by RT-QuIC (Q269364) (← links)
- Plants as vectors for environmental prion transmission (Q269481) (← links)
- Chronic wasting disease: State of the science (Q276403) (← links)
- Susceptibility of beavers to chronic wasting disease (Q277354) (← links)
- Deer carcass decomposition and potential scavenger exposure to chronic wasting disease (Q285687) (← links)
- Landscape features fail to explain spatial genetic structure in white-tailed deer across Ohio, USA (Q285788) (← links)
- The ecology of chronic wasting disease in wildlife (Q286176) (← links)
- On the origin of brucellosis in bison of Yellowstone National Park: a review (Q286241) (← links)
- Institutional trust, beliefs, and evaluation of regulations, and management of chronic wasting disease (CWD) (Q288859) (← links)
- Genetic susceptibility to chronic wasting disease in free-ranging white-tailed deer: complement component C1q and Prnp polymorphisms (Q289997) (← links)
- Spatial heterogeneity of prion gene polymorphisms in an area recently infected by chronic wasting disease (Q293357) (← links)
- Surveillance for transmissible spongiform encephalopathy in scavengers of white-tailed deer carcasses in the chronic wasting disease area of wisconsin (Q294088) (← links)
- Increased attack rates and decreased incubation periods in raccoons with chronic wasting disease passaged through meadow voles (Q296008) (← links)
- Chronic wasting disease alters the movement behavior and habitat use of mule deer during clinical stages of infection (Q297358) (← links)
- Epidemiological differences between sexes affect management efficacy in simulated chronic wasting disease systems (Q300816) (← links)
- Examination of the interaction between age-specific predation and chronic disease in the Greater Yellowstone Ecosystem (Q301715) (← links)
- Spatial and temporal patterns of chronic wasting disease: Fine-scale mapping of a wildlife epidemic in Wisconsin (Q301793) (← links)
- Ultraviolet-ozone treatment reduces levels of disease-associated prion protein and prion infectivity (Q307694) (← links)
- Department for Environment Food and Rural Affairs (Q331695) (← links)
- National Wildlife Health Center (Q331853) (← links)