Results 61 to 70 of about 2,730 (186)
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt–Jakob Disease MV1 Subtype
We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Satish K. Nemani +6 more
wiley +1 more source
Hunter perceptions toward chronic wasting disease: Implications for harvest and management
Previous human dimension research has reported negative perceptions among hunters toward Chronic Wasting Disease (CWD) and disease‐related regulations that may limit hunter participation, reduce harvest, and generally complicate management.
Jacob M. Haus +3 more
doaj +1 more source
Risk behaviors in a rural community with a known point-source exposure to chronic wasting disease
Background The emergence and continuing spread of Chronic Wasting Disease (CWD) in cervids has now reached 14 U.S. states, two Canadian provinces, and South Korea, producing a potential for transmission of CWD prions to humans and other animals globally.
Weeks Jennifer +12 more
doaj +1 more source
Biocontrol for Shrimp Disease: Comprehensive Review and a Bacterial Disease Biocontrol Practice
ABSTRACT Biocontrol is a key strategy for disease control, as it is environmentally friendly and widely applicable. This review elaborates on biocontrol in aquaculture, particularly in shrimp culture. Biocontrol in shrimp culture mainly relies on four strategies: (i) direct kill pathogen by Bdellovibrio or bacteriophages; (ii) suppression of intestinal
Xinyi He +11 more
wiley +1 more source
Characterization of the prion protein in relation to normal cellular function and in disease [PDF]
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of rare and fatal neurodegenerative disorders that can affect both human and animals.
Wik, Lotta
core
Objective Quaking‐induced conversion (QuIC) tests, which detect prion‐seeding activity in cerebrospinal fluid (CSF), have markedly advanced the antemortem diagnosis of prion diseases such as Creutzfeldt‐Jakob disease (CJD). These tests provide high diagnostic accuracy and enable timely differentiation from other rapidly progressive neurodegenerative ...
Jennifer Myskiw +13 more
wiley +1 more source
Prospective fecal microbiomic biomarkers for chronic wasting disease
Chronic wasting disease (CWD) is a naturally occurring prion disease in cervids that has been rapidly proliferating in the United States. Here, we investigated a potential link between CWD infection and gut microbiome by analyzing 50 fecal samples ...
Adam Didier +12 more
doaj +1 more source
We opportunistically characterize a 2.5 km white‐tailed deer movement along a beach in a suburban coastal environment, providing a natural history account of deer behavior amidst intersectional factors. We also describe multiple notable behaviors performed by the deer that could be caused by a variety of factors, including disorientation, illness, or ...
David J. Kurz +6 more
wiley +1 more source
Chronic Wasting Disease Questions and Answers (FAQs)
This document contains information about white-tailed deer and Chronic Wasting Disease (CWD) and addresses some of the more common questions related to this issue. The questions include: What is CWD?, Isn't CJD (Creutzfeldt-Jakob disease) the same as mad
core +1 more source
Chronic wasting disease as a model for human prion therapy
Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), are fatal neurodegenerative disorders that result from abnormally folded prion proteins. These disorders can be sporadic, acquired, or genetic.
Michael Bordonaro
doaj +1 more source

