Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system. - Wikidata - wikimedia - TriplyDB

Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system.

Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system.

http://www.wikidata.org/entity/Q36688984

about

Infectivity versus Seeding in Neurodegenerative Diseases Sharing a Prion-Like Mechanism Transmission of prions Selection of ovine housekeeping genes for normalisation by real-time RT-PCR; analysis of PrP gene expression and genetic susceptibility to scrapie Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response Progress on low susceptibility mechanisms of transmissible spongiform encephalopathies Early mechanisms of pathobiology are revealed by transcriptional temporal dynamics in hippocampal CA1 neurons of prion infected mice Alzheimer's disease and prion protein Functions of the cellular prion protein, the end of Moore's law, and Ockham's razor theory Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions.Utilizing NMR and EPR spectroscopy to probe the role of copper in prion diseases.The comprehensive native interactome of a fully functional tagged prion protein Transfer of pathogenic and nonpathogenic cytosolic proteins between spinal cord motor neurons in vivo in chimeric mice Monoclonal antibody F89/160.1.5 defines a conserved epitope on the ruminant prion protein.Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases A receptor for infectious and cellular prion protein.Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel Grafting mouse brains: from neurocarcinogenesis to neurodegeneration.Generation of antisera to purified prions in lipid rafts Pathogenesis of prion diseases: a progress report.Interventional strategies against prion diseases.Comparative analysis of the Shadoo gene between cattle and buffalo reveals significant differences.The molecular pathology of CJD: old and new variants.Prion pathogenesis is faithfully reproduced in cerebellar organotypic slice cultures.Crucial role for prion protein membrane anchoring in the neuroinvasion and neural spread of prion infection White matter involvement in sporadic Creutzfeldt-Jakob disease.B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice.Recent developments in the pathogenesis, diagnosis, and therapy of prion diseases.Prion proteins and the gut: une liaison dangereuse?Lower specific infectivity of protease-resistant prion protein generated in cell-free reactions.Prions impair bioaminergic functions through serotonin- or catecholamine-derived neurotoxins in neuronal cells.Hematological shift in goat kids naturally devoid of prion protein.Antiprion immunotherapy: to suppress or to stimulate?Fatal neurological disease in scrapie-infected mice induced for experimental autoimmune encephalomyelitis Prion protein expression differences in microglia and astroglia influence scrapie-induced neurodegeneration in the retina and brain of transgenic mice Propagation of Neuronal Damage to Embryonic Grafts Transplanted in the Hippocampus of Murine Models of Alzheimer's Disease.Removing endogenous tau does not prevent tau propagation yet reduces its neurotoxicity Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis.Synthetic prions.Antiprion prophylaxis by gene transfer of a soluble prion antagonist.

P2860

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P2860

Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system.

http://www.wikidata.org/entity/Q36688984

description

1996 nî lūn-bûn

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Proceedings of the National Academy of Sciences of the United States of America

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Normal host prion protein (PrP ...... in the central nervous system.

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P2093

Aguzzi A

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Blättler T

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Brandner S

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Fischer M

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P2860

Mice devoid of PrP are resistant to scrapie

Novel proteinaceous infectious particles cause scrapie

Does the agent of scrapie replicate without nucleic acid?

Self-replication and scrapie.

Viruses as transneuronal tracers.

Mortality, neoplasia, and Creutzfeldt-Jakob disease in patients treated with human pituitary growth hormone in the United Kingdom.

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.

Regional mapping of prion proteins in brain.

Scrapie prions.

Bovine spongiform encephalopathy. Epidemiology, low dose exposure and risks.

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Prion protein family

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24061

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