Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication. - Wikidata - awgldk - TriplyDB

Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.

Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.

http://www.wikidata.org/entity/Q36455926

about

Selective incorporation of polyanionic molecules into hamster prions.Generating a prion with bacterially expressed recombinant prion protein.Formation of native prions from minimal components in vitro Strain-specified relative conformational stability of the scrapie prion protein The POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes.Repetitive immunization enhances the susceptibility of mice to peripherally administered prions.Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein Efficient lymphoreticular prion propagation requires PrP(c) in stromal and hematopoietic cells.Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody.Prion protein genes and prion diseases: studies in transgenic mice.Prions in skeletal muscle.Differential sorting and fate of endocytosed GPI-anchored proteins.Human HMGA2 protein overexpressed in mice induces precursor T-cell lymphoblastic leukemia PrP polymorphisms tightly control sheep prion replication in cultured cells Species-dependent differences in cofactor utilization for formation of the protease-resistant prion protein in vitro.Cultured peripheral neuroglial cells are highly permissive to sheep prion infection.The intricate mechanisms of neurodegeneration in prion diseases.Human prions and plasma lipoproteins.B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice.Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein Biological effects and use of PrPSc- and PrP-specific antibodies generated by immunization with purified full-length native mouse prions.Aerosols: an underestimated vehicle for transmission of prion diseases?Progress in prion vaccines and immunotherapies.PrPc does not mediate internalization of PrPSc but is required at an early stage for de novo prion infection of Rov cells.Prions and their lethal journey to the brain.Overexpression of lymphotoxin in T cells induces fulminant thymic involution.Prion proteins: a biological role beyond prion diseases.Olfactory behavior and physiology are disrupted in prion protein knockout mice Cells and prions: a license to replicate.Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice.Humoral immune response to native eukaryotic prion protein correlates with anti-prion protection.Analysis of the hippocampal proteome in ME7 prion disease reveals a predominant astrocytic signature and highlights the brain-restricted production of clusterin in chronic neurodegeneration.Gene expression resulting from PrPC ablation and PrPC overexpression in murine and cellular models.Prion protein (PrP) gene-knockout cell lines: insight into functions of the PrP.Role of amyloid β protein receptors in mediating synaptic plasticity.Circumventing tolerance to the prion protein (PrP): vaccination with PrP-displaying retrovirus particles induces humoral immune responses against the native form of cellular PrP.PrP-dependent association of prions with splenic but not circulating lymphocytes of scrapie-infected mice.How do PrPSc Prions Spread between Host Species, and within Hosts?Similar turnover and shedding of the cellular prion protein in primary lymphoid and neuronal cells.

P2860

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P2860

Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication.

http://www.wikidata.org/entity/Q36455926

description

1999 nî lūn-bûn

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Ectopic expression of prion pr ...... to sustain prion replication.

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Aguzzi A

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Brandner S

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Klein MA

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P2860

Structure and regulation of the human interferon regulatory factor 1 (IRF-1) and IRF-2 genes: implications for a gene network in the interferon system

Mice devoid of PrP are resistant to scrapie

Follicular dendritic cell (FDC) precursors in primary lymphoid tissues

Novel proteinaceous infectious particles cause scrapie

Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.

Structure and polymorphism of the mouse prion protein gene.

Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent.

B lymphocytes induce the formation of follicular dendritic cell clusters in a lymphotoxin alpha-dependent fashion.

The sequential role of lymphotoxin and B cells in the development of splenic follicles.

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3987-3992

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10.1073/PNAS.96.7.3987

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7

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24453329

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10097150

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Prion protein family

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22407

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