Results 101 to 110 of about 12,794 (224)
Scrapie is an infective ovine neurodegenerative disease; the only identified component of the infectious agent being an aberrant isoform (PrPSc) of the cellular prion protein (PrPC). So far, no means for ante-mortem diagnosis are available for Scrapie as
Claudia Abete +9 more
core
BackgroundMost previous analyses of scrapie outbreaks have focused on flocks run by research institutes, which may not reflect the field situation. Within this study, we attempt to rectify this deficit by describing the epidemiological characteristics of
K Marie McIntyre +4 more
doaj +1 more source
The 37kDa/67kDa laminin receptor as a therapeutic target in prion diseases: potency of antisense LRP RNA, siRNAs specific for LRP mRNA and a LRP decoy mutant [PDF]
Prion diseases are a group of rare, fatal neurodegenerative diseases, also known as transmissible spongiform encephalopathies (TSEs), that affect both animals and humans and include bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep ...
Vana, Karen
core
The factors influencing the microstructure of fresh cheese, particularly the particle size, and its reduction by mechanical post-processing, were studied.
Saunders, Ginny +41 more
core +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
Changes of Microglial Cells in the Progression of Neurodegeneration in Natural Prion Disease
Background: In recent years, neuroglia has become a therapeutic target for neurodegenerative diseases. Despite the recognition of a variety of microglial morphologies associated with the neuroinflammatory process that involve diverse ...
Marta Monzón +6 more
doaj +1 more source
Scrapie-infected brain homogenate causes PrPC-dependent loss of dendritic spines.
Primary hippocampal neurons from wild-type (WT) mice (A-F) or PrP knockout (Prn-p0/0) mice (G-J) were treated for 24 hr with brain homogenate (0.16% [w/v] final concentration) prepared from either normal mice (NBH) (A-C, G, I) or from terminally ill ...
David A. Harris (330039) +4 more
core +1 more source
MRI assessment of the blood-brain barrier in a hamster model of scrapie
Magnetic resonance (MR) imaging in combination with gadolinium-diethylenetriaminepenta-acetic acid (Gd-DTPA) enhancement was used to investigate the integrity of the blood-brain barrier in a hamster model of scrapie (263K) during the clinical phase of ...
Williams, S.C.R. +6 more
core +1 more source
Proteins as markers of TSE infection in sheep blood
Transmissible spongiform encephalopathies (TSEs) are a group of fatal infectious neurodegenerative diseases affecting both humans and agricultural animals. TSE transmission via blood transfusion has been demonstrated experimentally in rodent, primate and
Martin, Joanne
core
Different types of transmissible spongiform encephalopathies (TSEs) affect sheep and goats. In addition to the classical form of scrapie, both species are susceptible to experimental infections with the bovine spongiform encephalopathy (BSE) agent, and ...
Seuberlich, Torsten +21 more
core +1 more source

