about
Oral transmissibility of prion disease is enhanced by binding to soil particlesMitochondrial biogenesis drives a vicious cycle of metabolic insufficiency and mitochondrial DNA deletion mutation accumulation in aged rat skeletal muscle fibersMolecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys.Ultraviolet-ozone treatment reduces levels of disease-associated prion protein and prion infectivity.Prion strain mutation determined by prion protein conformational compatibility and primary structure.Highly efficient amplification of chronic wasting disease agent by protein misfolding cyclic amplification with beads (PMCAb).Mitochondrial DNA deletion mutations: a causal role in sarcopenia.Prion protein polymorphisms affect chronic wasting disease progressionTransport of the pathogenic prion protein through soils.Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmissionEstablishment and characterization of Prnp knockdown neuroblastoma cells using dual microRNA-mediated RNA interferenceTranscriptomic responses to prion disease in ratsBile Acids Reduce Prion Conversion, Reduce Neuronal Loss, and Prolong Male Survival in Models of Prion Disease.Deposition pattern and subcellular distribution of disease-associated prion protein in cerebellar organotypic slice cultures infected with scrapie.Prion Infectivity Plateaus and Conversion to Symptomatic Disease Originate from Falling Precursor Levels and Increased Levels of Oligomeric PrPSc Species.Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains.Apoptosis and necrosis mediate skeletal muscle fiber loss in age-induced mitochondrial enzymatic abnormalities.Low copper and high manganese levels in prion protein plaques.Infectious prions accumulate to high levels in non proliferative C2C12 myotubes.Latent mitochondrial DNA deletion mutations drive muscle fiber loss at old age.Transport of the pathogenic prion protein through landfill materials.Prion disease tempo determined by host-dependent substrate reduction.Replication of prions in differentiated muscle cellsPotential role of soil properties in the spread of CWD in western Canada.The standard scrapie cell assay: development, utility and prospects.Digital PCR Quantitation of Muscle Mitochondrial DNA: Age, Fiber Type, and Mutation-Induced Changes.Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy.Emerging prion disease drives host selection in a wildlife population.Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion.Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiency.Dual MicroRNA to Cellular Prion Protein Inhibits Propagation of Pathogenic Prion Protein in Cultured Cells.Toll-like receptor-mediated immune response inhibits prion propagation.Persistence of pathogenic prion protein during simulated wastewater treatment processes.Strain-specific propagation of PrP(Sc) properties into baculovirus-expressed hamster PrP(C).Mitochondrial abnormalities are more frequent in muscles undergoing sarcopenia.Identification of a putative calcium-binding protein as a dioxin-responsive gene in zebrafish and rainbow trout.The host range of chronic wasting disease is altered on passage in ferrets.Reversibility of scrapie inactivation is enhanced by copper.Long term rapamycin treatment improves mitochondrial DNA quality in aging mice.Labeling of the scrapie-associated prion protein in vitro and in vivo.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Debbie McKenzie
@ast
Debbie McKenzie
@en
Debbie McKenzie
@es
Debbie McKenzie
@nl
Debbie McKenzie
@sl
type
label
Debbie McKenzie
@ast
Debbie McKenzie
@en
Debbie McKenzie
@es
Debbie McKenzie
@nl
Debbie McKenzie
@sl
altLabel
McKenzie D
@en
McKenzie DI
@en
prefLabel
Debbie McKenzie
@ast
Debbie McKenzie
@en
Debbie McKenzie
@es
Debbie McKenzie
@nl
Debbie McKenzie
@sl
P1053
G-4459-2015
P106
P1153
7202305081
P21
P31
P496
0000-0002-9291-6977