Results 41 to 50 of about 20,782 (249)

The Role of Unfolded Protein Response and Mitogen-Activated Protein Kinase Signaling in Neurodegenerative Diseases with Special Focus on Prion Diseases

open access: yesFrontiers in Aging Neuroscience, 2017
Prion diseases are neurodegenerative pathologies characterized by the accumulation of a protease-resistant form of the cellular prion protein named prion protein scrapie (PrPSc) in the brain. PrPSc accumulation in the endoplasmic reticulum (ER) result in
Lifeng Yang   +3 more
doaj   +1 more source

Pathogenetical significance of porencephalic lesions associated with intracerebral inoculation of sheep with the bovine spongiform encephalopathy (BSE) agent [PDF]

open access: yes, 2009
Decreased rates of transmission of transmissible spongiform encephalopathies (TSEs) to sheep have been attributed to some polymorphisms of the prion protein (PrP) and to a ‘species barrier’ on interspecies experiments.
Card   +21 more
core   +1 more source

The Central Role of IFI204 in IFN-β Release and Autophagy Activation during Mycobacterium bovis Infection

open access: yesFrontiers in Cellular and Infection Microbiology, 2017
Mycobacterium bovis (M. bovis) is the pathogen of animals and humans that can replicate in the phagosomes of myeloid cells. Cytosolic detection of bacterial products plays a crucial role in initiating the innate immune response, including autophagy ...
Liu Chunfa   +6 more
doaj   +1 more source

Methods for differentiating prion types in food-producing animals [PDF]

open access: yes, 2015
Prions are an enigma amongst infectious disease agents as they lack a genome yet confer specific pathologies thought to be dictated mainly, if not solely, by the conformation of the disease form of the prion protein (PrPSc).
Gough, Kevin C.   +3 more
core   +2 more sources

Molecular Dynamics Studies on the Buffalo Prion Protein [PDF]

open access: yes, 2015
It was reported that buffalo is a low susceptibility species resisting to prion diseases, which are invariably fatal and highly infectious neurodegenerative diseases that affect a wide variety of species.
Chatterjee, Subhojyoti   +2 more
core   +3 more sources

Neuropathological and molecular comparison between clinical and asymptomatic bovine spongiform encephalopathy cases [PDF]

open access: yes, 2018
Interest in the proper neuropathological and molecular characterization of bovine spongiform encephalopathy (BSE) has increased since asymptomatic and atypical cases were detected in the cattle population by active disease surveillance.
Sisó, Silvia   +6 more
core   +2 more sources

Advanced survival models for risk-factor analysis in scrapie [PDF]

open access: yes, 2007
Because of the confounding effects of long incubation duration and flock management, accurate epidemiological studies of scrapie outbreaks are difficult to carry out.
Andréoletti, Olivier   +6 more
core   +4 more sources

The Molecular Pathology of Prion Diseases [PDF]

open access: yes, 2004
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are a group of invariably fatal neurodegenerative disorders. Uniquely, they may present as sporadic, inherited, or infectious forms, all of which involve conversion of the normal ...
Herms, Jochen   +2 more
core  

Coping with uncertainty in public health: the use of heuristics [PDF]

open access: yes, 2014
The observation that experts and lay people use cognitive shortcuts or heuristics to arrive at judgements about complex problems is certainly not new.
Bond   +7 more
core   +1 more source

Harvest increase and culling as tools for managing chronic wasting disease in white‐tailed deer

open access: yesThe Journal of Wildlife Management, EarlyView.
We used an agent‐based model to simulate the effect of CWD management on a white‐tailed deer population in northwest Indiana and northeast Illinois. Our results suggest that wildlife managers should reconsider how and if they should manage CWD. Abstract Chronic wasting disease (CWD), a transmissible spongiform encephalopathy that affects white‐tailed ...
Jonathan D. Brooks   +3 more
wiley   +1 more source

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