| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Ina Vorberg | Q61142561 |
| P2093 | author name string | James Graham | |
| Hanna Wolf | |||
| Julia Hofmann | |||
| Andrea Grassmann | |||
| P2860 | cites work | Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform | Q48767220 |
| Identification of a protein that purifies with the scrapie prion | Q48858653 | ||
| Role of microglia and host prion protein in neurotoxicity of a prion protein fragment | Q49050987 | ||
| GFP-tagged PrP supports compromised prion replication in transgenic mice. | Q50744011 | ||
| Proteasome inhibitors promote the sequestration of PrPSc into aggresomes within the cytosol of prion-infected CAD neuronal cells. | Q51740431 | ||
| Heparin enhances the cell-protein misfolding cyclic amplification efficiency of variant Creutzfeldt-Jakob disease. | Q51768009 | ||
| A novel generation of heparan sulfate mimetics for the treatment of prion diseases. | Q51834544 | ||
| Glypican-1 mediates both prion protein lipid raft association and disease isoform formation | Q21131569 | ||
| Assigning functions to distinct regions of the N-terminus of the prion protein that are involved in its copper-stimulated, clathrin-dependent endocytosis | Q24292997 | ||
| Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection | Q24534939 | ||
| Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal | Q24541459 | ||
| Intracellular re-routing of prion protein prevents propagation of PrP(Sc) and delays onset of prion disease | Q24550300 | ||
| Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells | Q24610255 | ||
| Assignment of the human and mouse prion protein genes to homologous chromosomes | Q24629546 | ||
| α-Synuclein propagates from mouse brain to grafted dopaminergic neurons and seeds aggregation in cultured human cells | Q24633663 | ||
| Transmission and spreading of tauopathy in transgenic mouse brain | Q24651334 | ||
| Inclusion formation and neuronal cell death through neuron-to-neuron transmission of alpha-synuclein | Q24655848 | ||
| Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates | Q24657543 | ||
| Formation of native prions from minimal components in vitro | Q24676353 | ||
| Staging of brain pathology related to sporadic Parkinson's disease | Q28131702 | ||
| Protein misfolding, functional amyloid, and human disease | Q28131732 | ||
| Clathrin | Q28145011 | ||
| The low-density lipoprotein receptor gene family: a cellular Swiss army knife? | Q28205768 | ||
| The disintegrins ADAM10 and TACE contribute to the constitutive and phorbol ester-regulated normal cleavage of the cellular prion protein | Q28209519 | ||
| Internalization but not binding of thrombospondin-1 to low density lipoprotein receptor-related protein-1 requires heparan sulfate proteoglycans | Q28247513 | ||
| Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host | Q28264821 | ||
| Physiology of the prion protein | Q28275220 | ||
| Prion protein gene variation among primates | Q28306403 | ||
| Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor | Q28363055 | ||
| Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones | Q28476253 | ||
| Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein | Q28570280 | ||
| Functionally different GPI proteins are organized in different domains on the neuronal surface | Q28580230 | ||
| Copper stimulates endocytosis of the prion protein | Q28589040 | ||
| Novel proteinaceous infectious particles cause scrapie | Q29547678 | ||
| Eight prion strains have PrP(Sc) molecules with different conformations | Q29617277 | ||
| Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice | Q29620597 | ||
| Developmental expression of the prion protein gene in glial cells | Q52209886 | ||
| In vitro propagation of the scrapie agent. I. Transformation of mouse glia and neuroblastoma cells after infection with the mouse-adapted scrapie strain c-506. | Q53562199 | ||
| The prion protein has DNA strand transfer properties similar to retroviral nucleocapsid protein. | Q54014038 | ||
| Proteinase-resistant protein in human neuroblastoma cells infected with brain material from Creutzfeldt-Jakob patient. | Q54177738 | ||
| Endocytic Intermediates Involved with the Intracellular Trafficking of a Fluorescent Cellular Prion Protein | Q57372050 | ||
| LRP1 controls biosynthetic and endocytic trafficking of neuronal prion protein | Q60405515 | ||
| The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive | Q68318139 | ||
| Failure of the scrapie agent to replicate in L5178Y mouse leukaemic cells | Q68640335 | ||
| Isolation and partial characterization of high affinity laminin receptors in neural cells | Q70061816 | ||
| A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells | Q72227174 | ||
| Heparin-like molecules bind differentially to prion-proteins and change their intracellular metabolic fate | Q72656295 | ||
| The majority of cellular prion protein released from endothelial cells is soluble | Q73288199 | ||
| Diverse patterns of expression of the 67-kD laminin receptor in human small intestinal mucosa: potential binding sites for prion proteins? | Q73949292 | ||
| Scrapie produced experimentally in goats with special reference to the clinical syndrome | Q78964364 | ||
| Prion proteins with insertion mutations have altered N-terminal conformation and increased ligand binding activity and are more susceptible to oxidative attack | Q82553609 | ||
| Prion infection of differentiated neurospheres | Q83142947 | ||
| Self-propagation and transmission of misfolded mutant SOD1: prion or prion-like phenomenon? | Q83799357 | ||
| Endocytosis of prion protein is required for ERK1/2 signaling induced by stress-inducible protein 1. | Q37335792 | ||
| Synthesis and trafficking of prion proteins in cultured cells | Q37373585 | ||
| Isolation of a cDNA clone encoding the leader peptide of prion protein and expression of the homologous gene in various tissues | Q37396928 | ||
| Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics | Q37397268 | ||
| Prions can infect primary cultured neurons and astrocytes and promote neuronal cell death | Q37484906 | ||
| Cryo-immunogold electron microscopy for prions: toward identification of a conversion site | Q37484910 | ||
| Tunnelling nanotubes: a highway for prion spreading? | Q37496462 | ||
| Prion-like propagation of cytosolic protein aggregates: insights from cell culture models | Q37630197 | ||
| Protection from cytosolic prion protein toxicity by modulation of protein translocation | Q37671821 | ||
| Glypican‐1 facilitates prion conversion in lipid rafts | Q37777420 | ||
| Allosteric function and dysfunction of the prion protein | Q37943799 | ||
| Sulfated glycans stimulate endocytosis of the cellular isoform of the prion protein, PrPC, in cultured cells. | Q38287981 | ||
| DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation | Q38295713 | ||
| Structural insights into the interaction between prion protein and nucleic acid | Q38311203 | ||
| Asparagine-linked glycosylation of the scrapie and cellular prion proteins | Q38343527 | ||
| Cell-surface prion protein interacts with glycosaminoglycans | Q38363614 | ||
| Assaying prions in cell culture: the standard scrapie cell assay (SSCA) and the scrapie cell assay in end point format (SCEPA). | Q38476735 | ||
| Sulfated glycosaminoglycans in amyloid plaques of prion diseases | Q39102794 | ||
| Prion protein facilitates uptake of zinc into neuronal cells | Q39258090 | ||
| Establishment of a cell line persistently infected with chronic wasting disease prions | Q39336080 | ||
| Human prion protein binds Argonaute and promotes accumulation of microRNA effector complexes. | Q39368038 | ||
| Rapid cell-surface prion protein conversion revealed using a novel cell system | Q39556052 | ||
| Cultured cell sublines highly susceptible to prion infection | Q39590907 | ||
| The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein | Q39644598 | ||
| Conversion of raft associated prion protein to the protease-resistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes | Q39646797 | ||
| Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein | Q39673524 | ||
| PrP expression and replication by Schwann cells: implications in prion spreading | Q39682667 | ||
| BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein | Q39686522 | ||
| Clathrin-independent internalization of normal cellular prion protein in neuroblastoma cells is associated with the Arf6 pathway | Q39785389 | ||
| The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein | Q39790846 | ||
| Prion-induced activation of cholesterogenic gene expression by Srebp2 in neuronal cells | Q39800328 | ||
| alpha-cleavage of the prion protein occurs in a late compartment of the secretory pathway and is independent of lipid rafts | Q39908845 | ||
| Immunolocalisation of PrPSc in scrapie-infected N2a mouse neuroblastoma cells by light and electron microscopy | Q39932784 | ||
| Genetic heterogeneity versus molecular analysis of prion susceptibility in neuroblasma N2a sublines | Q39951583 | ||
| Proper axonal distribution of PrP(C) depends on cholesterol-sphingomyelin-enriched membrane domains and is developmentally regulated in hippocampal neurons | Q46684364 | ||
| Antiprion properties of prion protein-derived cell-penetrating peptides | Q46736477 | ||
| Characterization of the role of dendritic cells in prion transfer to primary neurons | Q48107300 | ||
| Cytosolic prion protein in neurons. | Q48232623 | ||
| The truncated 23-230 form of the prion protein localizes to the nuclei of inducible cell lines independently of its nuclear localization signals and is not cytotoxic | Q48484408 | ||
| Neural stem cell model for prion propagation | Q48513161 | ||
| Murine bone marrow stromal cell culture with features of mesenchymal stem cells susceptible to mouse-adapted human TSE agent, Fukuoka-1. | Q48515136 | ||
| In vitro replication of scrapie agent in a neuronal model: infection of PC12 cells | Q48595899 | ||
| Two Creutzfeldt-Jakob disease agents reproduce prion protein-independent identities in cell cultures | Q30597888 | ||
| Novel heparan mimetics potently inhibit the scrapie prion protein and its endocytosis | Q31028422 | ||
| Pathologic prion protein infects cells by lipid-raft dependent macropinocytosis | Q33434501 | ||
| Lipid rafts and clathrin cooperate in the internalization of PrP in epithelial FRT cells | Q33463351 | ||
| Infection of cell lines with experimental and natural ovine scrapie agents | Q33648916 | ||
| Sulfated dextrans enhance in vitro amplification of bovine spongiform encephalopathy PrP(Sc) and enable ultrasensitive detection of bovine PrP(Sc). | Q33722019 | ||
| Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein | Q33794942 | ||
| Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform | Q33847297 | ||
| A simple, versatile and sensitive cell-based assay for prions from various species | Q33926922 | ||
| Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody | Q33930771 | ||
| Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent | Q33931107 | ||
| Prions in skeletal muscle | Q34020521 | ||
| Cell-based quantification of chronic wasting disease prions | Q34046147 | ||
| Scrapie strains maintain biological phenotypes on propagation in a cell line in culture | Q34080020 | ||
| Inhibition of protease-resistant prion protein formation in a transformed deer cell line infected with chronic wasting disease | Q34301796 | ||
| Interaction of prion proteins with cell surface receptors, molecular chaperones, and other molecules | Q34304988 | ||
| Mouse-adapted scrapie infection of SN56 cells: greater efficiency with microsome-associated versus purified PrP-res | Q34434726 | ||
| Complementary hydropathy identifies a cellular prion protein receptor | Q34449035 | ||
| PrP polymorphisms tightly control sheep prion replication in cultured cells | Q34471219 | ||
| Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis | Q34480339 | ||
| Cultured peripheral neuroglial cells are highly permissive to sheep prion infection | Q34553074 | ||
| Prions hijack tunnelling nanotubes for intercellular spread | Q34938949 | ||
| Prion infection of mouse neurospheres | Q34944193 | ||
| Fukuoka-1 strain of transmissible spongiform encephalopathy agent infects murine bone marrow-derived cells with features of mesenchymal stem cells | Q35038696 | ||
| Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein | Q35053001 | ||
| Bovine prion is endocytosed by human enterocytes via the 37 kDa/67 kDa laminin receptor. | Q35085199 | ||
| Proteasomal dysfunction and endoplasmic reticulum stress enhance trafficking of prion protein aggregates through the secretory pathway and increase accumulation of pathologic prion protein | Q35311053 | ||
| High CJD infectivity remains after prion protein is destroyed | Q35449351 | ||
| Abrogation of complex glycosylation by swainsonine results in strain- and cell-specific inhibition of prion replication | Q35562607 | ||
| Microglial cell line established from prion protein-overexpressing mice is susceptible to various murine prion strains | Q35635237 | ||
| PrPc on the road: trafficking of the cellular prion protein | Q35646000 | ||
| Transmission of new bovine prion to mice | Q35792647 | ||
| Prion infection of muscle cells in vitro | Q35857376 | ||
| A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis. | Q35899061 | ||
| Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice | Q35946149 | ||
| Trans-cellular propagation of Tau aggregation by fibrillar species | Q36003836 | ||
| The highways and byways of prion protein trafficking | Q36032511 | ||
| PrPc does not mediate internalization of PrPSc but is required at an early stage for de novo prion infection of Rov cells | Q36099038 | ||
| Cell division modulates prion accumulation in cultured cells | Q36156685 | ||
| A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions | Q36161465 | ||
| Birth of a prion: spontaneous generation revisited | Q36211122 | ||
| Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells | Q36223171 | ||
| Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform | Q36235271 | ||
| Chimeric prion protein expression in cultured cells and transgenic mice | Q36277480 | ||
| Prion protein recruits its neuronal receptor NCAM to lipid rafts to activate p59fyn and to enhance neurite outgrowth. | Q36321586 | ||
| Trafficking of prion proteins through a caveolae-mediated endosomal pathway | Q36325084 | ||
| The prion protein and lipid rafts | Q36447789 | ||
| Cells release prions in association with exosomes | Q36448448 | ||
| Prion Protein Genes: Evolutionary and Functional Aspects | Q36549301 | ||
| Traffic of prion protein between different compartments on the neuronal surface, and the propagation of prion disease | Q36555039 | ||
| Searching for anti-prion compounds: cell-based high-throughput in vitro assays and animal testing strategies | Q36626116 | ||
| Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells | Q36640586 | ||
| Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis | Q36682161 | ||
| Prion strain discrimination in cell culture: the cell panel assay | Q36693359 | ||
| The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies | Q36731460 | ||
| Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells | Q36780119 | ||
| N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state | Q36828108 | ||
| Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins | Q36866642 | ||
| Acute cellular uptake of abnormal prion protein is cell type and scrapie-strain independent. | Q37039973 | ||
| The Scrapie Agent In Vitro | Q37040434 | ||
| Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains | Q37057378 | ||
| The yeast Sup35NM domain propagates as a prion in mammalian cells | Q37062021 | ||
| Cells expressing anchorless prion protein are resistant to scrapie infection | Q37157117 | ||
| Identification of an intracellular site of prion conversion | Q37170450 | ||
| Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture | Q39966821 | ||
| PrP(C) association with lipid rafts in the early secretory pathway stabilizes its cellular conformation | Q39968483 | ||
| Canine MDCK cell lines are refractory to infection with human and mouse prions | Q39990591 | ||
| Mouse neuroblastoma cells release prion infectivity associated with exosomal vesicles | Q39990786 | ||
| A cell line infectible by prion strains from different species | Q40033746 | ||
| Transcriptional stability of cultured cells upon prion infection | Q40035094 | ||
| Scrapie infection of prion protein-deficient cell line upon ectopic expression of mutant prion proteins | Q40139360 | ||
| M1 and M3 muscarinic receptors control physiological processing of cellular prion by modulating ADAM17 phosphorylation and activity. | Q40146616 | ||
| Packaging of prions into exosomes is associated with a novel pathway of PrP processing. | Q40163902 | ||
| Efficient dissemination of prions through preferential transmission to nearby cells. | Q40179305 | ||
| Copper-dependent co-internalization of the prion protein and glypican-1. | Q40241315 | ||
| The 37-kDa/67-kDa laminin receptor acts as a receptor for infectious prions and is inhibited by polysulfated glycanes | Q40245615 | ||
| Reactive oxygen species (ROS)-mediated beta-cleavage of the prion protein in the mechanism of the cellular response to oxidative stress | Q40358582 | ||
| Reciprocal interference between specific CJD and scrapie agents in neural cell cultures | Q40359630 | ||
| Skin-derived dendritic cells acquire and degrade the scrapie agent following in vitro exposure | Q40383848 | ||
| Comparison of protease-resistant prion protein inhibitors in cell cultures infected with two strains of mouse and sheep scrapie | Q40394280 | ||
| Intravesicular localization and exocytosis of alpha-synuclein and its aggregates. | Q40405368 | ||
| Uptake and neuritic transport of scrapie prion protein coincident with infection of neuronal cells. | Q40417083 | ||
| The scrapie prion protein is present in flotillin-1-positive vesicles in central- but not peripheral-derived neuronal cell lines | Q40427322 | ||
| Heparan sulfate is a cellular receptor for purified infectious prions. | Q40466338 | ||
| Acute formation of protease-resistant prion protein does not always lead to persistent scrapie infection in vitro | Q40558005 | ||
| Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin. | Q40558969 | ||
| Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents | Q40595199 | ||
| Dual mechanisms for shedding of the cellular prion protein | Q40601379 | ||
| Filipin prevents pathological prion protein accumulation by reducing endocytosis and inducing cellular PrP release | Q40734071 | ||
| Transfer of scrapie prion infectivity by cell contact in culture | Q40739845 | ||
| The prion protein has RNA binding and chaperoning properties characteristic of nucleocapsid protein NCP7 of HIV-1. | Q40817022 | ||
| Phorbol ester-regulated cleavage of normal prion protein in HEK293 human cells and murine neurons | Q40859808 | ||
| Cellular prion protein binds laminin and mediates neuritogenesis | Q40893573 | ||
| The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells | Q41077192 | ||
| Mutant and infectious prion proteins display common biochemical properties in cultured cells. | Q41237869 | ||
| Retrovirus infection strongly enhances scrapie infectivity release in cell culture | Q41445328 | ||
| Evidence for synthesis of scrapie prion proteins in the endocytic pathway | Q41608575 | ||
| Alterations in neurotransmitter-related enzyme activity in scrapie-infected PC12 cells | Q41682773 | ||
| Cellular factors implicated in prion replication | Q41853767 | ||
| Infection of a cell line of mouse L fibroblasts with scrapie agent | Q41885514 | ||
| Neuronal low-density lipoprotein receptor-related protein 1 binds and endocytoses prion fibrils via receptor cluster 4. | Q41910802 | ||
| Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene | Q41982232 | ||
| Apolipoprotein E includes a binding site which is recognized by several amyloidogenic polypeptides | Q42203052 | ||
| Increased proportions of C1 truncated prion protein protect against cellular M1000 prion infection | Q42832124 | ||
| The low-density lipoprotein receptor-related protein 1 (LRP1) mediates the endocytosis of the cellular prion protein | Q42976032 | ||
| Up-regulation of functionally impaired insulin-like growth factor-1 receptor in scrapie-infected neuroblastoma cells | Q43680929 | ||
| Identification of the heparan sulfate binding sites in the cellular prion protein | Q43908316 | ||
| Characterization of scrapie infection in mouse neuroblastoma cells | Q44079577 | ||
| Stimulation of PrP(C) retrograde transport toward the endoplasmic reticulum increases accumulation of PrP(Sc) in prion-infected cells | Q44090721 | ||
| Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain | Q44424303 | ||
| Cellular heparan sulfate participates in the metabolism of prions | Q44519369 | ||
| Multiplication of Scrapie Agent in Cell Culture | Q44726183 | ||
| PrPc capping in T cells promotes its association with the lipid raft proteins reggie-1 and reggie-2 and leads to signal transduction | Q45042655 | ||
| Purification and properties of the cellular and scrapie hamster prion proteins | Q45166038 | ||
| PrPSc incorporation to cells requires endogenous glycosaminoglycan expression | Q45236630 | ||
| Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid | Q45935884 | ||
| The low-density lipoprotein receptor-related protein-1 associates transiently with lipid rafts | Q46089677 | ||
| Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor | Q46096263 | ||
| Scrapie prions aggregate to form amyloid-like birefringent rods | Q46201693 | ||
| Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein | Q46251858 | ||
| Ultrastructural localization of scrapie prion proteins in cytoplasmic vesicles of infected cultured cells | Q46361947 | ||
| Demonstration of scrapie strain diversity in infected PC12 cells | Q46665678 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | protein biosynthesis | Q211935 |
| transmissible spongiform encephalopathy | Q703961 | ||
| prion | Q47051 | ||
| prion protein family | Q24724413 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 374-405 | |
| P577 | publication date | 2013-01-22 | |
| P1433 | published in | Viruses | Q7935305 |
| P1476 | title | Cellular aspects of prion replication in vitro | |
| P478 | volume | 5 |
| Q37252741 | A specific population of abnormal prion protein aggregates is preferentially taken up by cells and disaggregated in a strain-dependent manner |
| Q93005212 | All the Same? The Secret Life of Prion Strains within Their Target Cells |
| Q38734782 | Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells |
| Q40061707 | Cell Biology Approaches to Studying Prion Diseases |
| Q36762492 | Cell-to-cell propagation of infectious cytosolic protein aggregates |
| Q88673114 | Cellular mechanisms responsible for cell-to-cell spreading of prions |
| Q40111506 | Chronic wasting disease prion infection of differentiated neurospheres |
| Q40103519 | Correlation of cellular factors and differential scrapie prion permissiveness in ovine microglia |
| Q40267284 | Dual MicroRNA to Cellular Prion Protein Inhibits Propagation of Pathogenic Prion Protein in Cultured Cells. |
| Q89893387 | Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments |
| Q92353432 | Gene-edited murine cell lines for propagation of chronic wasting disease prions |
| Q38693596 | Generation of Infectious Prions and Detection with the Prion-Infected Cell Assay |
| Q46174770 | Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner |
| Q37415409 | Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes |
| Q38136055 | Life cycle of cytosolic prions |
| Q36080838 | Modulation of Glycosaminoglycans Affects PrPSc Metabolism but Does Not Block PrPSc Uptake. |
| Q36569559 | Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells |
| Q34423386 | Prion protein-specific antibodies-development, modes of action and therapeutics application |
| Q38650733 | Prion strains depend on different endocytic routes for productive infection. |
| Q36578308 | Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin-proteasome system |
| Q38166717 | Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins |
| Q39237605 | Prions on the run: How extracellular vesicles serve as delivery vehicles for self-templating protein aggregates |
| Q89446379 | Quantifying Nucleation In Vivo Reveals the Physical Basis of Prion-like Phase Behavior |
| Q33821808 | Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells |
| Q36147951 | Susceptibility of GT1-7 cells to mouse-passaged field scrapie isolates with a long incubation |
| Q34458035 | Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA. |
| Q39437151 | The relevance of contact-independent cell-to-cell transfer of TDP-43 and SOD1 in amyotrophic lateral sclerosis |
| Q38324712 | The standard scrapie cell assay: development, utility and prospects |
| Q92757387 | Transient multimers modulate conformer abundances of prion protein monomer through conformational selection |
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