On the public citation graph
Physiology of the Prion Protein
0 signed · 1183 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archinte.165.14.1663-bopenalex-snapshot
Dilated Cardiomyopathy and Creutzfeldt-Jakob Disease: Evidence for a Role of Cellular Prion Protein in the Heart?
inferredcites →https://doi.org/10.1001/archinte.165.3.338openalex-snapshot
Prion-Associated Dilated Cardiomyopathy
inferredcites →https://doi.org/10.1002/(sici)1097-4547(19990115)55:2<261::aid-jnr14>3.0.co;2-iopenalex-snapshot
Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junction
inferredcites →https://doi.org/10.1002/(sici)1097-4695(199812)37:4<502::aid-neu2>3.0.co;2-sopenalex-snapshot
Identification of Reggie-1 and Reggie-2 as plasmamembrane-associated proteins which cocluster with activated GPI-anchored cell adhesion molecules in non-caveolar micropatches in neurons
inferredcites →https://doi.org/10.1002/(sici)1098-1136(19990201)25:3<282::aid-glia8>3.0.co;2-nopenalex-snapshot
Astrocytic glutamate uptake and prion protein expression
inferredcites →https://doi.org/10.1002/(sici)1098-2744(200005)28:1<5::aid-mc2>3.0.co;2-gopenalex-snapshot
Eyes wide shut: Protein kinase C isozymes are not the only receptors for the phorbol ester tumor promoters
inferredcites →https://doi.org/10.1002/1097-0029(20000701)50:1<58::aid-jemt9>3.0.co;2-5openalex-snapshot
Immunolocalization of the cellular prion protein in normal brain
inferredcites →https://doi.org/10.1002/1097-0029(20000701)50:1<66::aid-jemt10>3.0.co;2-3openalex-snapshot
Synaptic prion protein immuno-reactivity in the rodent cerebellum
inferredcites →https://doi.org/10.1002/1097-0029(20000701)50:1<76::aid-jemt11>3.0.co;2-#openalex-snapshot
Ultrastructural localization of prion proteins: Physiological and pathological implications
inferredcites →https://doi.org/10.1002/1615-9861(200108)1:8<1010::aid-prot1010>3.0.co;2-lopenalex-snapshot
Mass spectrometric characterization of proteins extracted from Jurkat T cell detergent-resistant membrane domains
inferredcites →https://doi.org/10.1002/1615-9861(200108)1:8<1010::aid-prot1010>3.3.co;2-copenalex-snapshot
Mass spectrometric characterization of proteins extracted from Jurkat T cell detergent-resistant membrane domains
inferredcites →https://doi.org/10.1002/ana.10507openalex-snapshot
PRNP Val129 homozygosity increases risk for early‐onset Alzheimer's disease
inferredcites →https://doi.org/10.1002/ana.10658openalex-snapshot
Early cognitive decline is associated with prion protein codon 129 polymorphism
inferredcites →https://doi.org/10.1002/ana.10748openalex-snapshot
Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan
inferredcites →https://doi.org/10.1002/ana.410310308openalex-snapshot
Creutzfeldt‐Jakob disease cosegregates with the codon 178AsnPRNP mutation in families of European origin
inferredcites →https://doi.org/10.1002/bies.20107openalex-snapshot
Hop: more than an Hsp70/Hsp90 adaptor protein
inferredcites →https://doi.org/10.1002/dneu.20330openalex-snapshot
Transgene expression of prion protein induces crinophagy in intermediate pituitary cells
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00467.xopenalex-snapshot
Prion protein (PrP) with amino‐proximal deletions restoring susceptibility of PrP knockout mice to scrapie.
inferredcites →https://doi.org/10.1002/jcp.20682openalex-snapshot
Bovine prion (PrP) and Doppel (Dpl) proteins expression after in vitro leukocyte activation or Dpl/PrP blocking
inferredcites →https://doi.org/10.1002/jmr.545openalex-snapshot
The hidden code in genomics: a tool for gene discovery
inferredcites →https://doi.org/10.1002/jnr.10118openalex-snapshot
Lack of prion protein expression results in a neuronal phenotype sensitive to stress
inferredcites →https://doi.org/10.1002/jnr.10556openalex-snapshot
Glutamate regulates caveolin expression in rat hippocampal neurons
inferredcites →https://doi.org/10.1002/jnr.20509openalex-snapshot
Hypoglycemia enhances the expression of prion protein and heat-shock protein 70 in a mouse neuroblastoma cell line
inferredcites →https://doi.org/10.1002/mrd.20807openalex-snapshot
Association of the prion protein and its expression with ovarian follicle development in cattle
inferredcites →https://doi.org/10.1002/neu.10323openalex-snapshot
Signaling endosome hypothesis: A cellular mechanism for long distance communication
inferredcites →https://doi.org/10.1002/path.1633openalex-snapshot
The prion protein in human neuromuscular diseases
inferredcites →https://doi.org/10.1002/pmic.200500066openalex-snapshot
Identification of prion protein binding proteins by combined use of far‐Western immunoblotting, two dimensional gel electrophoresis and mass spectrometry
inferredcites →https://doi.org/10.1002/prot.1077openalex-snapshot
Cryptic epitopes in N‐terminally truncated prion protein are exposed in the full‐length molecule: Dependence of conformation on pH
inferredcites →https://doi.org/10.1002/rmv.408openalex-snapshot
Towards cellular receptors for prions
inferredcites →https://doi.org/10.1006/bbrc.1994.1835openalex-snapshot
Tight Hormonal Control of PRP Gene Expression in Endocrine Pancreatic Cells
inferredcites →https://doi.org/10.1006/bbrc.1995.1233openalex-snapshot
Copper Binding to the N-Terminal Tandem Repeat Regions of Mammalian and Avian Prion Protein
inferredcites →https://doi.org/10.1006/bbrc.1995.2384openalex-snapshot
Copper Binding to the N-Terminal Tandem Repeat Region of Mammalian and Avian Prion Protein: Structural Studies Using Synthetic Peptides
inferredcites →https://doi.org/10.1006/bbrc.1996.0179openalex-snapshot
Identification of a Promoter Region in the Rat Prion Protein Gene
inferredcites →https://doi.org/10.1006/bbrc.1997.6575openalex-snapshot
Expression of PrP mRNA Is Regulated by a Fragment of MRP8 in Human Fibroblasts
inferredcites →https://doi.org/10.1006/bbrc.2000.3604openalex-snapshot
Copper Refolding of Prion Protein
inferredcites →https://doi.org/10.1006/bbrc.2001.4538openalex-snapshot
Distribution of Cellular Isoform of Prion Protein in T Lymphocytes and Bone Marrow, Analyzed by Wild-Type and Prion Protein Gene-Deficient Mice
inferredcites →https://doi.org/10.1006/bbrc.2002.6460openalex-snapshot
Ablation of Cellular Prion Protein Expression Affects Mitochondrial Numbers and Morphology
inferredcites →https://doi.org/10.1006/cimm.1995.1213openalex-snapshot
Signaling by a New Anti-Thy 1 Monoclonal Antibody Inhibits T Cell Proliferation and Interferes with T-Cell-Mediated Induction of Costimulatory Molecule B7-2
inferredcites →https://doi.org/10.1006/cimm.2000.1751openalex-snapshot
The Expression and Potential Function of Cellular Prion Protein in Human Lymphocytes
inferredcites →https://doi.org/10.1006/excr.2001.5151openalex-snapshot
Transcriptional Activation of Prion Protein Gene in Growth-Arrested and Differentiated Mouse Erythroleukemia and Human Neoplastic Cells
inferredcites →https://doi.org/10.1006/exnr.1994.1220openalex-snapshot
Prion Protein Gene Expression in Cultured Astrocytes Treated by Recombinant Growth Hormone and Insulin-like Growth Factor
inferredcites →https://doi.org/10.1006/exnr.1997.6505openalex-snapshot
Prion Protein-Deficient Cells Show Altered Response to Oxidative Stress Due to Decreased SOD-1 Activity
inferredcites →https://doi.org/10.1006/jmbi.1999.3108openalex-snapshot
Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel
inferredcites →https://doi.org/10.1006/jmbi.2000.5183openalex-snapshot
Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein
inferredcites →https://doi.org/10.1006/mcne.1996.0023openalex-snapshot
Clonal Cell Lines Produced by Infection of Neocortical Neuroblasts Using Multiple Oncogenes Transduced by Retroviruses
inferredcites →https://doi.org/10.1006/mcne.2001.1060openalex-snapshot
Isolation and Characterization of Detergent-Resistant Microdomains Responsive to NCAM-Mediated Signaling from Growth Cones
inferredcites →https://doi.org/10.1006/nbdi.1997.0130openalex-snapshot
Identification of Candidate Proteins Binding to Prion Protein
inferredcites →https://doi.org/10.1006/nbdi.2000.0290openalex-snapshot
Evidence for Oxidative Stress in Experimental Prion Disease
inferredcites →https://doi.org/10.1006/nbdi.2000.0369openalex-snapshot
Prion Protein Affects Ca2+-Activated K+ Currents in Cerebellar Purkinje Cells
inferredcites →https://doi.org/10.1006/nbdi.2001.0400openalex-snapshot
Primary Myopathy and Accumulation of PrPSc-Like Molecules in Peripheral Tissues of Transgenic Mice Expressing a Prion Protein Insertional Mutation
inferredcites →https://doi.org/10.1006/nbdi.2002.0477openalex-snapshot
Oxidative Damage to Nucleic Acids in Human Prion Disease
inferredcites →https://doi.org/10.1006/nbdi.2002.0496openalex-snapshot
Increased Lipid Peroxidation in Cerebrospinal Fluid and Plasma from Patients with Creutzfeldt–Jakob Disease
inferredcites →https://doi.org/10.1006/smim.2000.0300openalex-snapshot
Raft membrane domains: from a liquid-ordered membrane phase to a site of pathogen attack
inferredcites →https://doi.org/10.1007/978-1-4757-5806-1openalex-snapshot
Membrane Dynamics and Domains
inferredcites →https://doi.org/10.1007/978-1-4757-5806-1_2openalex-snapshot
Rafts, Little Caves and Large Potholes: How Lipid Structure Interacts with Membrane Proteins to Create Functionally Diverse Membrane Environments
inferredcites →https://doi.org/10.1007/978-3-7091-0651-8_64openalex-snapshot
Prions prevent brain damage after experimental brain injury: a preliminary report
inferredcites →https://doi.org/10.1007/bf00294214openalex-snapshot
The mRNA encoding the scrapie agent protein is present in a variety of non-neuronal cells
inferredcites →https://doi.org/10.1007/bf00369996openalex-snapshot
Three-exon structure of the gene encoding the rat prion protein and its expression in tissues
inferredcites →https://doi.org/10.1007/bf01941177openalex-snapshot
Use of aggregating cell cultures for toxicological studies
inferredcites →https://doi.org/10.1007/bf02780662openalex-snapshot
129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal
inferredcites →https://doi.org/10.1007/s00018-004-4318-2openalex-snapshot
Modulation of signal transduction through the cellular prion protein is linked to its incorporation in lipid rafts
inferredcites →https://doi.org/10.1007/s00018-005-4511-yopenalex-snapshot
Phagocytosis of apoptotic cells: a matter of balance
inferredcites →https://doi.org/10.1007/s00018-007-6370-1openalex-snapshot
Scavenger, transducer, RNA chaperone? What ligands of the prion protein teach us about its function
inferredcites →https://doi.org/10.1007/s00401-003-0700-7openalex-snapshot
Polymorphism of the codon 129 of the prion protein (PrP) gene and neuropathology of cerebral ageing
inferredcites →https://doi.org/10.1007/s004010000271openalex-snapshot
Prion protein expression in senile plaques in Alzheimer's disease
inferredcites →https://doi.org/10.1007/s004010100405openalex-snapshot
Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases
inferredcites →https://doi.org/10.1007/s00415-003-1057-5openalex-snapshot
The 129 codon polymorphism of the Prion Protein gene influences earlier cognitive performance in Down syndrome subjects
inferredcites →https://doi.org/10.1007/s00415-004-0457-5openalex-snapshot
Comment on ?The codon 129 polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects?
inferredcites →https://doi.org/10.1007/s004280050474openalex-snapshot
The pattern of prion-related protein expression in the gastrointestinal tract
inferredcites →https://doi.org/10.1007/s004410051036openalex-snapshot
Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues
inferredcites →https://doi.org/10.1007/s11373-005-9058-2openalex-snapshot
F-box proteins: the key to protein degradation
inferredcites →https://doi.org/10.1016/0003-9861(89)90409-8openalex-snapshot
Asparagine-linked glycosylation of the scrapie and cellular prion proteins
inferredcites →https://doi.org/10.1016/0006-8993(87)90465-3openalex-snapshot
Developmental expression and regional distribution of the scrapie-associated protein mRNA in the rat central nervous system
inferredcites →https://doi.org/10.1016/0012-1606(87)90143-6openalex-snapshot
Developmental expression of prion protein gene in brain
inferredcites →https://doi.org/10.1016/0013-4694(81)90225-xopenalex-snapshot
Sleep deprivation: Effect on sleep stages and EEG power density in man
inferredcites →https://doi.org/10.1016/0014-5793(89)81180-9openalex-snapshot
Identification of a neurite outgrowth‐promoting domain of laminin using synthetic peptides
inferredcites →https://doi.org/10.1016/0014-5793(96)00610-2openalex-snapshot
Molecular biology of transmissible spongiform encephalopathies
inferredcites →https://doi.org/10.1016/0014-5793(96)01104-0openalex-snapshot
Metal‐dependent α‐helix formation promoted by the glycine‐rich octapeptide region of prion protein
inferredcites →https://doi.org/10.1016/0042-6822(87)90072-9openalex-snapshot
Purified scrapie prions resist inactivation by procedures that hydrolyze, modify, or shear nucleic acids
inferredcites →https://doi.org/10.1016/0092-8674(84)90533-6openalex-snapshot
Purification and structural studies of a major scrapie prion protein
inferredcites →https://doi.org/10.1016/0092-8674(85)90333-2openalex-snapshot
A cellular gene encodes scrapie PrP 27-30 protein
inferredcites →https://doi.org/10.1016/0092-8674(86)90662-8openalex-snapshot
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
inferredcites →https://doi.org/10.1016/0092-8674(87)90134-6openalex-snapshot
Distinct prion proteins in short and long scrapie incubation period mice
inferredcites →https://doi.org/10.1016/0092-8674(87)90150-4openalex-snapshot
Scrapie prion protein contains a phosphatidylinositol glycolipid
inferredcites →https://doi.org/10.1016/0092-8674(90)90225-4openalex-snapshot
Cellular isoform of the scrapie agent protein participates in lymphocyte activation
inferredcites →https://doi.org/10.1016/0092-8674(94)90177-5openalex-snapshot
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
inferredcites →https://doi.org/10.1016/0092-8674(95)90236-8openalex-snapshot
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
inferredcites →https://doi.org/10.1016/0140-6736(91)91198-4openalex-snapshot
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred
inferredcites →https://doi.org/10.1016/0140-6736(91)91199-5openalex-snapshot
Seroepidemiological study of filovirus related to Ebola in the Philippines
inferredcites →https://doi.org/10.1016/0166-4328(84)90186-4openalex-snapshot
Effect of sleep deprivation on sleep and EEG power spectra in the rat
inferredcites →https://doi.org/10.1016/0166-4328(95)00025-oopenalex-snapshot
Is sleep fundamentally different between mammalian species?
inferredcites →https://doi.org/10.1016/0168-9525(87)90180-6openalex-snapshot
Glycosylation mutants and the functions of mammalian carbohydrates
inferredcites →https://doi.org/10.1016/0169-328x(91)90093-dopenalex-snapshot
Regulation of the glial fibrillary acidic protein, β actin and prion protein mRNAs during brain development in mouse
inferredcites →https://doi.org/10.1016/0169-328x(94)90055-8openalex-snapshot
Modulation of prion protein gene expression by growth factors in cultured mouse astrocytes and PC-12 cells
inferredcites →https://doi.org/10.1016/0169-328x(95)00013-iopenalex-snapshot
The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system
inferredcites →https://doi.org/10.1016/0169-328x(95)00323-kopenalex-snapshot
Analysis of interaction sites in homo- and heteromeric complexes containing Bcl-2 family members and the cellular prion protein
inferredcites →https://doi.org/10.1016/0248-4900(91)90095-5openalex-snapshot
Fluid phase endocytosis investigated by fluorescence with trimethylamino‐diphenylhexatriene in L929 cells; the influence of temperature and of cytoskeleton depolymerizing drugs
inferredcites →https://doi.org/10.1016/0304-3940(89)90565-xopenalex-snapshot
Nerve endings from rat brain tissue release copper upon depolarization. A possible role in regulating neuronal excitability
inferredcites →https://doi.org/10.1016/0304-3940(96)12596-9openalex-snapshot
Hippocampal slices from prion protein null mice: disrupted Ca2+-activated K+ currents
inferredcites →https://doi.org/10.1016/0896-6273(91)90074-aopenalex-snapshot
Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice
inferredcites →https://doi.org/10.1016/0896-6273(95)90307-0openalex-snapshot
Developmental expression of the prion protein gene in glial cells
inferredcites →https://doi.org/10.1016/0959-440x(95)80103-0openalex-snapshot
The protein kinase C and protein kinase C related gene families
inferredcites →https://doi.org/10.1016/0968-0004(89)90062-5openalex-snapshot
Glycoproteins: what are the sugar chains for?
inferredcites →https://doi.org/10.1016/j.bbamcr.2005.06.009openalex-snapshot
Secrets of caveolae- and lipid raft-mediated endocytosis revealed by mammalian viruses
inferredcites →https://doi.org/10.1016/j.bbamem.2004.04.008openalex-snapshot
Membrane order conservation in raft and non-raft regions of hepatocyte plasma membranes from thermally acclimated rainbow trout
inferredcites →https://doi.org/10.1016/j.bbr.2005.02.003openalex-snapshot
Altered behavioural response to acute stress in mice lacking cellular prion protein
inferredcites →https://doi.org/10.1016/j.bbr.2006.04.024openalex-snapshot
Neurological abnormalities in caveolin-1 knock out mice
inferredcites →https://doi.org/10.1016/j.bbrc.2004.11.092openalex-snapshot
Octapeptide repeat region and N-terminal half of hydrophobic region of prion protein (PrP) mediate PrP-dependent activation of superoxide dismutase
inferredcites →https://doi.org/10.1016/j.bbrc.2004.12.132openalex-snapshot
PrP cooperates with STI1 to regulate SOD activity in PrP-deficient neuronal cell line
inferredcites →https://doi.org/10.1016/j.bbrc.2005.04.099openalex-snapshot
Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survival
inferredcites →https://doi.org/10.1016/j.bbrc.2005.11.158openalex-snapshot
Prion protein induced signaling cascades in monocytes
inferredcites →https://doi.org/10.1016/j.bbrc.2007.04.202openalex-snapshot
Signaling induced by hop/STI-1 depends on endocytosis
inferredcites →https://doi.org/10.1016/j.bcmd.2005.06.013openalex-snapshot
Prions and exosomes: From PrPc trafficking to PrPsc propagation
inferredcites →https://doi.org/10.1016/j.brainres.2005.12.045openalex-snapshot
Synaptosomal glutamate release and uptake in mice lacking the cellular prion protein
inferredcites →https://doi.org/10.1016/j.brainres.2005.12.105openalex-snapshot
Prion protein mRNA expression in Xenopus laevis: No induction during melanotrope cell activation
inferredcites →https://doi.org/10.1016/j.brainres.2006.04.056openalex-snapshot
Role of cellular prion protein on LTP expression in aged mice
inferredcites →https://doi.org/10.1016/j.brainresbull.2005.12.005openalex-snapshot
A hypothesis on prion disorders: Are infectious, inherited, and sporadic causes so distinct?
inferredcites →https://doi.org/10.1016/j.brainresrev.2004.07.021openalex-snapshot
Chemokine receptors in the central nervous system: role in brain inflammation and neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.coi.2006.05.017openalex-snapshot
T cell–dendritic cell immunological synapses
inferredcites →https://doi.org/10.1016/j.conb.2005.01.010openalex-snapshot
Long-distance retrograde neurotrophic signaling
inferredcites →https://doi.org/10.1016/j.crvi.2005.05.001openalex-snapshot
Local environmental effects on the structure of the prion protein
inferredcites →https://doi.org/10.1016/j.febslet.2004.08.076openalex-snapshot
Clustering of cellular prion protein induces ERK1/2 and stathmin phosphorylation in GT1‐7 neuronal cells
inferredcites →https://doi.org/10.1016/j.febslet.2005.08.065openalex-snapshot
Bovine PrPC directly interacts with αB‐crystalline
inferredcites →https://doi.org/10.1016/j.febslet.2006.01.008openalex-snapshot
Heterogeneous PrPC metabolism in skeletal muscle cells
inferredcites →https://doi.org/10.1016/j.febslet.2006.07.053openalex-snapshot
Traffic of prion protein between different compartments on the neuronal surface, and the propagation of prion disease
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.09.019openalex-snapshot
Prion protein does not redox-silence Cu2+, but is a sacrificial quencher of hydroxyl radicals
inferredcites →https://doi.org/10.1016/j.gene.2004.11.049openalex-snapshot
The prion protein gene: Identifying regulatory signals using marsupial sequence
inferredcites →https://doi.org/10.1016/j.ijdevneu.2004.07.017openalex-snapshot
Role of cytokines and chemokines in prion infections of the central nervous system
inferredcites →https://doi.org/10.1016/j.imlet.2004.08.006openalex-snapshot
The normal cellular form of prion protein modulates T cell responses
inferredcites →https://doi.org/10.1016/j.it.2004.11.016openalex-snapshot
Merging complexes: properties of membrane raft assembly during lymphocyte signaling
inferredcites →https://doi.org/10.1016/j.jmb.2006.07.045openalex-snapshot
Molecular Details of cAMP Generation in Mammalian Cells: A Tale of Two Systems
inferredcites →https://doi.org/10.1016/j.mam.2005.07.011openalex-snapshot
Is there a role for copper in neurodegenerative diseases?
inferredcites →https://doi.org/10.1016/j.mcn.2005.07.003openalex-snapshot
Proper axonal distribution of PrPC depends on cholesterol–sphingomyelin-enriched membrane domains and is developmentally regulated in hippocampal neurons
inferredcites →https://doi.org/10.1016/j.metabol.2006.07.006openalex-snapshot
Genetics of the sleep-wake cycle and its disorders
inferredcites →https://doi.org/10.1016/j.micinf.2003.11.002openalex-snapshot
Interaction between Brucella abortus and cellular prion protein in lipid raft microdomains
inferredcites →https://doi.org/10.1016/j.molbrainres.2004.02.005openalex-snapshot
The cellular prion protein (PrPC) prevents apoptotic neuronal cell death and mitochondrial dysfunction induced by serum deprivation
inferredcites →https://doi.org/10.1016/j.molbrainres.2004.08.004openalex-snapshot
Hippocampal synaptic plasticity in mice devoid of cellular prion protein
inferredcites →https://doi.org/10.1016/j.nbd.2005.01.001openalex-snapshot
Mice devoid of prion protein have cognitive deficits that are rescued by reconstitution of PrP in neurons
inferredcites →https://doi.org/10.1016/j.nbd.2005.04.002openalex-snapshot
Aggravation of ischemic brain injury by prion protein deficiency: Role of ERK-1/-2 and STAT-1
inferredcites →https://doi.org/10.1016/j.nbd.2007.01.005openalex-snapshot
Short-term memory formation and long-term memory consolidation are enhanced by cellular prion association to stress-inducible protein 1
inferredcites →https://doi.org/10.1016/j.neulet.2004.01.049openalex-snapshot
Pathogenic human prion protein rescues PrP null phenotype in transgenic mice
inferredcites →https://doi.org/10.1016/j.neulet.2004.09.030openalex-snapshot
Upregulation of cellular prion protein (PrPc) after focal cerebral ischemia and influence of lesion severity
inferredcites →https://doi.org/10.1016/j.neulet.2004.11.012openalex-snapshot
Normal brain mitochondrial respiration in adult mice lacking cellular prion protein
inferredcites →https://doi.org/10.1016/j.neulet.2005.05.067openalex-snapshot
Genetic influences on oxidative stress and their association with normal cognitive ageing
inferredcites →https://doi.org/10.1016/j.neulet.2005.06.033openalex-snapshot
Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein
inferredcites →https://doi.org/10.1016/j.neulet.2006.02.021openalex-snapshot
Regulation of PrPC expression: Nerve growth factor (NGF) activates the prion gene promoter through the MEK1 pathway in PC12 cells
inferredcites →https://doi.org/10.1016/j.neuro.2006.06.004openalex-snapshot
Interaction of metals with prion protein: Possible role of divalent cations in the pathogenesis of prion diseases
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2004.10.004openalex-snapshot
Prion protein (PrPc) promotes β-amyloid plaque formation
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2005.05.025openalex-snapshot
Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.06.095openalex-snapshot
Female-specific neuroprotection against transient brain ischemia observed in mice devoid of prion protein is abolished by ectopic expression of prion protein-like protein
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.05.037openalex-snapshot
Axotomy-induced motoneuron death is delayed in mice overexpressing PrPc
inferredcites →https://doi.org/10.1016/j.preteyeres.2004.10.001openalex-snapshot
Control of programmed cell death by neurotransmitters and neuropeptides in the developing mammalian retina
inferredcites →https://doi.org/10.1016/j.smim.2004.09.004openalex-snapshot
Single-molecule tracking of membrane molecules: plasma membrane compartmentalization and dynamic assembly of raft-philic signaling molecules
inferredcites →https://doi.org/10.1016/j.tcb.2004.12.002openalex-snapshot
The highways and byways of prion protein trafficking
inferredcites →https://doi.org/10.1016/j.tibs.2005.06.004openalex-snapshot
Detergent-resistant membranes should not be identified with membrane rafts
inferredcites →https://doi.org/10.1016/j.tig.2006.08.005openalex-snapshot
Charging it up: global analysis of protein phosphorylation
inferredcites →https://doi.org/10.1016/j.tins.2006.07.005openalex-snapshot
Different molecular cascades in different sites of the brain control memory consolidation
inferredcites →https://doi.org/10.1016/j.tips.2006.06.002openalex-snapshot
Higher-order organization and regulation of adenylyl cyclases
inferredcites →https://doi.org/10.1016/j.yexcr.2004.11.022openalex-snapshot
Dynamic reorganization of chemokine receptors, cholesterol, lipid rafts, and adhesion molecules to sites of CD4 engagement
inferredcites →https://doi.org/10.1016/j.ygeno.2005.12.012openalex-snapshot
Comparative genomic organization of the human and bovine PRNP locus
inferredcites →https://doi.org/10.1016/s0002-9440(10)61192-3openalex-snapshot
Bovine Prion Is Endocytosed by Human Enterocytes via the 37 kDa/67 kDa Laminin Receptor
inferredcites →https://doi.org/10.1016/s0002-9440(10)63291-9openalex-snapshot
Prion Protein Accumulation and Neuroprotection in Hypoxic Brain Damage
inferredcites →https://doi.org/10.1016/s0002-9440(10)64517-8openalex-snapshot
Gene Expression Profile in Prion Protein-Deficient Fibroblasts in Culture
inferredcites →https://doi.org/10.1016/s0002-9440(10)65487-9openalex-snapshot
Prion Protein-Deficient Neurons Reveal Lower Glutathione Reductase Activity and Increased Susceptibility to Hydrogen Peroxide Toxicity
inferredcites →https://doi.org/10.1016/s0002-9440(10)65683-0openalex-snapshot
Expression of Cellular Prion Protein in Activated Hepatic Stellate Cells
inferredcites →https://doi.org/10.1016/s0002-9440(10)65720-3openalex-snapshot
Human Keratinocytes Express Cellular Prion-Related Proteinin Vitro and during Inflammatory Skin Diseases
inferredcites →https://doi.org/10.1016/s0006-291x(03)01239-7openalex-snapshot
Absence of superoxide dismutase activity in a soluble cellular isoform of prion protein produced by baculovirus expression system
inferredcites →https://doi.org/10.1016/s0006-291x(03)01263-4openalex-snapshot
Expression of normal cellular prion protein (PrP ) on T lymphocytes and the effect of copper ion: analysis by wild-type and prion protein gene-deficient mice
inferredcites →https://doi.org/10.1016/s0006-291x(03)01459-1openalex-snapshot
Impairment of superoxide dismutase activation by N-terminally truncated prion protein (PrP) in PrP-deficient neuronal cell line
inferredcites →https://doi.org/10.1016/s0006-3495(02)73899-xopenalex-snapshot
Exploring the Propensities of Helices in PrPC to Form β Sheet Using NMR Structures and Sequence Alignments
inferredcites →https://doi.org/10.1016/s0006-8993(99)01307-4openalex-snapshot
Activation of NMDA receptors protects against glutamate neurotoxicity in the retina: evidence for the involvement of neurotrophins
inferredcites →https://doi.org/10.1016/s0014-5793(00)02070-6openalex-snapshot
Laminin‐induced PC‐12 cell differentiation is inhibited following laser inactivation of cellular prion protein
inferredcites →https://doi.org/10.1016/s0014-5793(01)03147-7openalex-snapshot
Biochemical and structural studies of the prion protein polymorphism
inferredcites →https://doi.org/10.1016/s0014-5793(02)02291-3openalex-snapshot
Cellular prion protein: on the road for functions
inferredcites →https://doi.org/10.1016/s0014-5793(03)01463-7openalex-snapshot
Immunoseparation of Prion protein‐enriched domains from other detergent‐resistant membrane fractions, isolated from neuronal cells
inferredcites →https://doi.org/10.1016/s0014-5793(04)00029-8openalex-snapshot
Prion protein is a component of the multimolecular signaling complex involved in T cell activation
inferredcites →https://doi.org/10.1016/s0014-5793(97)00920-4openalex-snapshot
NMR characterization of the full‐length recombinant murine prion protein, mPrP(23–231)
inferredcites →https://doi.org/10.1016/s0021-9258(18)41985-0openalex-snapshot
Evidence for synthesis of scrapie prion proteins in the endocytic pathway.
inferredcites →https://doi.org/10.1016/s0021-9258(18)54480-xopenalex-snapshot
Functional analysis of T-cell mutants defective in the biosynthesis of glycosylphosphatidylinositol anchor. Relative importance of glycosylphosphatidylinositol anchor versus N-linked glycosylation in T-cell activation.
inferredcites →https://doi.org/10.1016/s0021-9258(18)54943-7openalex-snapshot
Functional domains of the 67-kDa laminin receptor precursor.
inferredcites →https://doi.org/10.1016/s0021-9258(18)55257-1openalex-snapshot
The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive.
inferredcites →https://doi.org/10.1016/s0021-9258(18)82340-7openalex-snapshot
A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells
inferredcites →https://doi.org/10.1016/s0021-9258(19)41840-1openalex-snapshot
The covalent and three-dimensional structural of concanavalin A. I. Amino acid sequence of cyanogen bromide fragments F1 and F2.
inferredcites →https://doi.org/10.1016/s0022-5193(88)80272-8openalex-snapshot
Biological implications of complementary hydropathy of amino acids
inferredcites →https://doi.org/10.1016/s0092-8674(00)80483-3openalex-snapshot
Neuronal Death in the Hippocampus Is Promoted by Plasmin-Catalyzed Degradation of Laminin
inferredcites →https://doi.org/10.1016/s0092-8674(00)80830-2openalex-snapshot
Structure of TPR Domain–Peptide Complexes
inferredcites →https://doi.org/10.1016/s0092-8674(00)81572-xopenalex-snapshot
Expression of Amino-Terminally Truncated PrP in the Mouse Leading to Ataxia and Specific Cerebellar Lesions
inferredcites →https://doi.org/10.1016/s0140-6736(03)15171-9openalex-snapshot
Transmissible spongiform encephalopathies
inferredcites →https://doi.org/10.1016/s0140-6736(05)17700-9openalex-snapshot
A prion lexicon (out of control)
inferredcites →https://doi.org/10.1016/s0165-0173(97)00036-2openalex-snapshot
Neurotrophin receptors: mediators of life and death
inferredcites →https://doi.org/10.1016/s0166-2236(00)02089-0openalex-snapshot
Small is not beautiful: antagonizing functions for the prion protein PrPC and its homologue Dpl
inferredcites →https://doi.org/10.1016/s0168-3659(02)00126-8openalex-snapshot
pH-dependent receptor/ligand dissociation as a determining factor for intracellular sorting of ligands for epidermal growth factor receptors in rat hepatocytes
inferredcites →https://doi.org/10.1016/s0169-328x(02)00163-8openalex-snapshot
Localization of adenylyl cyclase proteins in the rodent retina
inferredcites →https://doi.org/10.1016/s0169-328x(02)00526-0openalex-snapshot
Decreased hyperlocomotion induced by MK-801, but not amphetamine and caffeine in mice lacking cellular prion protein (PrPC)
inferredcites →https://doi.org/10.1016/s0169-328x(99)00193-xopenalex-snapshot
Normal inhibitory avoidance learning and anxiety, but increased locomotor activity in mice devoid of PrPC
showing the first 200 of 595 · page through all 595
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4820084openalex-extracted
Unraveling the Structural Facets of Prp127-132 Polymorphic Variants Using Combined Molecular Dynamics/Markov Modeling
inferred← citeshttps://doi.org/10.1001/archneurol.2009.224openalex-snapshot
Codistribution of Amyloid β Plaques and Spongiform Degeneration in Familial Creutzfeldt-Jakob Disease With the E200K-129M Haplotype
inferred← citeshttps://doi.org/10.1002/2211-5463.12002openalex-snapshot
A specific role for PRND in goat foetal Leydig cells is suggested by prion family gene expression during gonad development in goats and mice
inferred← citeshttps://doi.org/10.1002/9780470015902.a0000426openalex-snapshot
Prion Diseases of Humans
inferred← citeshttps://doi.org/10.1002/9781444341256.ch31openalex-snapshot
Introduction to Prion Disorders
inferred← citeshttps://doi.org/10.1002/9783527634323.ch10openalex-snapshot
Membrane Changes in BSE and Scrapie
inferred← citeshttps://doi.org/10.1002/adfm.201601621openalex-snapshot
Water‐Soluble Conjugated Polymers for the Detection and Inhibition of Protein Aggregation
inferred← citeshttps://doi.org/10.1002/biof.161openalex-snapshot
Possible role for Ca2+ in the pathophysiology of the prion protein?
inferred← citeshttps://doi.org/10.1002/chem.201405502openalex-snapshot
Cross‐Talk Between the Octarepeat Domain and the Fifth Binding Site of Prion Protein Driven by the Interaction of Copper(II) with the N‐terminus
inferred← citeshttps://doi.org/10.1002/cne.22157openalex-snapshot
Developmental expression of prion protein and its ligands stress‐inducible protein 1 and vitronectin
inferred← citeshttps://doi.org/10.1002/ece3.5724openalex-snapshot
Differential gene expression in chronic wasting disease‐positive white‐tailed deer (Odocoileus virginianus)
inferred← citeshttps://doi.org/10.1002/elps.201200384openalex-snapshot
Prion protein as a mediator of neurocardiosympathetic interactions
inferred← citeshttps://doi.org/10.1002/elps.201500244openalex-snapshot
Application of capillary immunoelectrophoresis revealed an age‐ and gender‐dependent regulated expression of PrPC in liver
inferred← citeshttps://doi.org/10.1002/glia.20861openalex-snapshot
Prion protein and its ligand stress inducible protein 1 regulate astrocyte development
inferred← citeshttps://doi.org/10.1002/ijc.24425openalex-snapshot
Prion protein ablation increases cellular aggregation and embolization contributing to mechanisms of metastasis
inferred← citeshttps://doi.org/10.1002/iub.2528openalex-snapshot
Condition‐dependent structural collapse in the intrinsically disordered N‐terminal domain of prion protein
inferred← citeshttps://doi.org/10.1002/mc.20642openalex-snapshot
Prion protein expression and the M129V polymorphism of the PRNP gene in patients with colorectal cancer
inferred← citeshttps://doi.org/10.1002/mus.22225openalex-snapshot
The octapeptide repeat PrPC region and cobalamin‐deficient polyneuropathy of the rat
inferred← citeshttps://doi.org/10.1002/mus.24708openalex-snapshot
Age-dependent neuromuscular impairment in prion protein knockout mice
inferred← citeshttps://doi.org/10.1002/psc.1293openalex-snapshot
Improved Fmoc‐based solid‐phase synthesis of homologous peptide fragments of human and mouse prion proteins
inferred← citeshttps://doi.org/10.1002/psc.3216openalex-snapshot
Prion protein—Semisynthetic prion protein (PrP) variants with posttranslational modifications
inferred← citeshttps://doi.org/10.1002/stem.1663openalex-snapshot
Functional Cross-Talk Between the Cellular Prion Protein and the Neural Cell Adhesion Molecule is Critical for Neuronal Differentiation of Neural Stem/Precursor Cells
inferred← citeshttps://doi.org/10.1002/stem.2501openalex-snapshot
The Cellular Prion Protein Controls Notch Signaling in Neural Stem/Progenitor Cells
inferred← citeshttps://doi.org/10.1002/stem.664openalex-snapshot
Enhanced Neural Progenitor/Stem Cells Self‐Renewal via the Interaction of Stress‐Inducible Protein 1 with the Prion Protein
inferred← citeshttps://doi.org/10.1002/wrna.118openalex-snapshot
The role of RNA in mammalian prion protein conversion
inferred← citeshttps://doi.org/10.1007/128_2011_158openalex-snapshot
Molecular Dynamics as an Approach to Study Prion Protein Misfolding and the Effect of Pathogenic Mutations
inferred← citeshttps://doi.org/10.1007/128_2011_160openalex-snapshot
Neuroprotective and Neurotoxic Signaling by the Prion Protein
inferred← citeshttps://doi.org/10.1007/128_2011_165openalex-snapshot
Prion Protein and Its Conformational Conversion: A Structural Perspective
inferred← citeshttps://doi.org/10.1007/978-1-4614-5305-5_5openalex-snapshot
Insoluble Cellular Prion Protein
inferred← citeshttps://doi.org/10.1007/978-1-4939-7211-1_15openalex-snapshot
The Use of Transgenic and Knockout Mice in Prion Research
inferred← citeshttps://doi.org/10.1007/978-3-031-20565-1_4openalex-snapshot
Insoluble Cellular Prion Protein and Other Neurodegeneration-Related Protein Aggregates in the Brain of Asymptomatic Individuals
inferred← citeshttps://doi.org/10.1007/978-3-031-97055-9_5openalex-snapshot
Therapeutic Trajectories in Human Prion Diseases
inferred← citeshttps://doi.org/10.1007/978-3-319-15889-1_8openalex-snapshot
Therapeutic Importance of Curcumin in Neurological Disorders Other Than Alzheimer Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-48838-7_8openalex-snapshot
Protein Assembly Disorders and Protein-Based Inheritance
inferred← citeshttps://doi.org/10.1007/978-94-007-6167-4_552-1openalex-snapshot
Genetic Engineering and Animal Welfare
inferred← citeshttps://doi.org/10.1007/978-94-024-1179-9_552openalex-snapshot
Genetic Engineering and Animal Welfare
inferred← citeshttps://doi.org/10.1007/978-981-10-5765-6_13openalex-snapshot
Prion Protein Family Contributes to Tumorigenesis via Multiple Pathways
inferred← citeshttps://doi.org/10.1007/s00018-011-0847-7openalex-snapshot
Allosteric function and dysfunction of the prion protein
inferred← citeshttps://doi.org/10.1007/s00018-011-0879-zopenalex-snapshot
Functional mechanisms of the cellular prion protein (PrPC) associated anti-HIV-1 properties
inferred← citeshttps://doi.org/10.1007/s00018-013-1328-yopenalex-snapshot
The unconventional secretion of stress-inducible protein 1 by a heterogeneous population of extracellular vesicles
inferred← citeshttps://doi.org/10.1007/s00018-022-04468-yopenalex-snapshot
Lighting up Nobel Prize-winning studies with protein intrinsic disorder
inferred← citeshttps://doi.org/10.1007/s00109-022-02245-9openalex-snapshot
The multiple functions of PrPC in physiological, cancer, and neurodegenerative contexts
inferred← citeshttps://doi.org/10.1007/s00204-010-0577-xopenalex-snapshot
Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples
inferred← citeshttps://doi.org/10.1007/s00401-010-0700-3openalex-snapshot
Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease
inferred← citeshttps://doi.org/10.1007/s00415-013-7152-3openalex-snapshot
Myelin damage due to local quantitative abnormalities in normal prion levels: evidence from subacute combined degeneration and multiple sclerosis
inferred← citeshttps://doi.org/10.1007/s00705-020-04529-2openalex-snapshot
Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy
inferred← citeshttps://doi.org/10.1007/s00775-014-1115-8openalex-snapshot
Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids
inferred← citeshttps://doi.org/10.1007/s00775-019-01700-2openalex-snapshot
Impact of pyridine-2-carboxaldehyde-derived aroylhydrazones on the copper-catalyzed oxidation of the M112A PrP103–112 mutant fragment
inferred← citeshttps://doi.org/10.1007/s10072-013-1494-6openalex-snapshot
Prnp gene and cerebellum volume in patients with refractory mesial temporal lobe epilepsy
inferred← citeshttps://doi.org/10.1007/s10495-010-0480-1openalex-snapshot
The relationship between the 20S proteasomes and prion-mediated neurodegenerations: potential therapeutic opportunities
inferred← citeshttps://doi.org/10.1007/s10571-019-00741-0openalex-snapshot
Elucidating Critical Proteinopathic Mechanisms and Potential Drug Targets in Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s10585-016-9788-8openalex-snapshot
Prion protein binding to HOP modulates the migration and invasion of colorectal cancer cells
inferred← citeshttps://doi.org/10.1007/s10719-008-9198-5openalex-snapshot
Glycosylation-related genes are variably expressed depending on the differentiation state of a bioaminergic neuronal cell line: implication for the cellular prion protein
inferred← citeshttps://doi.org/10.1007/s11010-021-04078-5openalex-snapshot
Cellular prion protein activates Caspase 3 for apoptotic defense mechanism in astrocytes
inferred← citeshttps://doi.org/10.1007/s11010-022-04631-wopenalex-snapshot
Cellular prion protein offers neuroprotection in astrocytes submitted to amyloid β oligomer toxicity
inferred← citeshttps://doi.org/10.1007/s11033-015-3865-yopenalex-snapshot
The mRNA expression of immune-related genes in crossbred and Tharparkar cattle in response to in vitro infection with Theileria annulata
inferred← citeshttps://doi.org/10.1007/s11064-016-1885-1openalex-snapshot
Expression of Tyrosine Hydroxylase is Negatively Regulated Via Prion Protein
inferred← citeshttps://doi.org/10.1007/s12031-013-9962-2openalex-snapshot
Cellular Prion Protein Participates in the Regulation of Inflammatory Response and Apoptosis in BV2 Microglia During Infection with Mycobacterium bovis
inferred← citeshttps://doi.org/10.1007/s12031-014-0319-2openalex-snapshot
Prion Protein Participates in the Protection of Mice from Lipopolysaccharide Infection by Regulating the Inflammatory Process
inferred← citeshttps://doi.org/10.1007/s12031-015-0544-3openalex-snapshot
Creutzfeldt-Jakob Disease Subtype-Specific Regional and Temporal Regulation of ADP Ribosylation Factor-1-Dependent Rho/MLC Pathway at Pre-Clinical Stage
inferred← citeshttps://doi.org/10.1007/s12031-016-0733-8openalex-snapshot
Cellular Prion Protein Promotes Neuronal Differentiation of Adipose-Derived Stem Cells by Upregulating miRNA-124
inferred← citeshttps://doi.org/10.1007/s12035-013-8529-0openalex-snapshot
Gene Expression Resulting from PrPC Ablation and PrPC Overexpression in Murine and Cellular Models
inferred← citeshttps://doi.org/10.1007/s12035-013-8616-2openalex-snapshot
Anchorless 23–230 PrPC Interactomics for Elucidation of PrPC Protective Role
inferred← citeshttps://doi.org/10.1007/s12035-015-9360-6openalex-snapshot
Domain-Specific Activation of Death-Associated Intracellular Signalling Cascades by the Cellular Prion Protein in Neuroblastoma Cells
inferred← citeshttps://doi.org/10.1007/s12035-017-0451-4openalex-snapshot
Involvement of Cellular Prion Protein in α-Synuclein Transport in Neurons
inferred← citeshttps://doi.org/10.1007/s12035-017-0506-6openalex-snapshot
iPS Cell Cultures from a Gerstmann-Sträussler-Scheinker Patient with the Y218N PRNP Mutation Recapitulate tau Pathology
inferred← citeshttps://doi.org/10.1007/s12035-019-1505-6openalex-snapshot
Prions Strongly Reduce NMDA Receptor S-Nitrosylation Levels at Pre-symptomatic and Terminal Stages of Prion Diseases
inferred← citeshttps://doi.org/10.1007/s12035-019-1510-9openalex-snapshot
Copper Binding Regulates Cellular Prion Protein Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-374105-9.00166-0openalex-snapshot
Creutzfeldt–Jacob Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-385902-0.00002-4openalex-snapshot
5-HT6 Receptor Memory and Amnesia: Behavioral Pharmacology – Learning and Memory Processes
inferred← citeshttps://doi.org/10.1016/b978-0-12-411637-5.00002-0openalex-snapshot
Anomalous Protein–DNA Interactions Behind Neurological Disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-416041-5.00026-3openalex-snapshot
Food Safety Implications of Prion Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-811304-2.00008-0openalex-snapshot
Prion-Like Propagation in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-444-63945-5.00015-5openalex-snapshot
Fatal familial insomnia and sporadic fatal insomnia
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2021.08.001openalex-snapshot
The role of membranes in function and dysfunction of intrinsically disordered amyloidogenic proteins
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.06.001openalex-snapshot
Functions of the Prion Protein
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.06.008openalex-snapshot
Gene Targeted Transgenic Mouse Models in Prion Research
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.08.008openalex-snapshot
The role of the cellular prion protein in the uptake and toxic signaling of pathological neurodegenerative aggregates
inferred← citeshttps://doi.org/10.1016/j.ajpath.2015.03.009openalex-snapshot
Multiple Mechanisms of Unfolded Protein Response–Induced Cell Death
inferred← citeshttps://doi.org/10.1016/j.bbadis.2025.168049openalex-snapshot
Unmasking the tumorigenic potential of cellular prion protein in cancer progression
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.11.027openalex-snapshot
G-quadruplex-based aptamers against protein targets in therapy and diagnostics
inferred← citeshttps://doi.org/10.1016/j.bbapap.2026.141175openalex-snapshot
Structural and energetic landscape of the human HOP-PrPC Axis: Multi-domain stabilization and peptide-mediated disruption by melittin
inferred← citeshttps://doi.org/10.1016/j.bbr.2014.03.006openalex-snapshot
Deletion of the prion gene Prnp affects offensive aggression in mice
inferred← citeshttps://doi.org/10.1016/j.bbr.2014.05.067openalex-snapshot
Cellular prion protein (PrPC) modulates ethanol-induced behavioral adaptive changes in mice
inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113386openalex-snapshot
Dissociation of genotype-dependent cognitive and motor behavior in a strain of aging mice devoid of the prion protein
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.04.202openalex-snapshot
Signaling induced by hop/STI-1 depends on endocytosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.12.026openalex-snapshot
From cell protection to death: May Ca2+ signals explain the chameleonic attributes of the mammalian prion protein?
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.12.030openalex-snapshot
Normal prion protein in Drosophila enhances the toxicity of pathogenic polyglutamine proteins and alters susceptibility to oxidative and autophagy signaling modulators
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.06.007openalex-snapshot
Mutation directional selection sheds light on prion pathogenesis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.08.049openalex-snapshot
Generation of Sprn-regulated reporter mice reveals gonadic spatial expression of the prion-like protein Shadoo in mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.11.021openalex-snapshot
Expression of the prion-like protein Shadoo in the developing mouse embryo
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.11.081openalex-snapshot
PrPC interacts with potassium channel tetramerization domain containing 1 (KCTD1) protein through the PrP51-136 region containing octapeptide repeats
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.12.098openalex-snapshot
PrPC displays an essential protective role from oxidative stress in an astrocyte cell line derived from PrPC knockout mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.172openalex-snapshot
Activation of human natural killer cells by the soluble form of cellular prion protein
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.02.122openalex-snapshot
The prion protein selectively binds to and modulates the content of purinergic receptor P2X4R
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.07.118openalex-snapshot
Almost a century of prion protein(s): From pathology to physiology, and back to pathology
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.09.016openalex-snapshot
Autocrine STIP1 signaling promotes tumor growth and is associated with disease outcome in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.10.075openalex-snapshot
A valine-to-lysine substitution at position 210 induces structural conversion of prion protein into a β-sheet rich oligomer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.02.102openalex-snapshot
Prion protein interacts with the metabotropic glutamate receptor 1 and regulates the organization of Ca2+ signaling
inferred← citeshttps://doi.org/10.1016/j.biocel.2014.09.011openalex-snapshot
Relationships between cobalamin, epidermal growth factor, and normal prions in the myelin maintenance of central nervous system
inferred← citeshttps://doi.org/10.1016/j.biochi.2013.01.002openalex-snapshot
Cobalamin and normal prions: A new horizon for cobalamin neurotrophism
inferred← citeshttps://doi.org/10.1016/j.biochi.2014.06.009openalex-snapshot
PrPC signalling in neurons: From basics to clinical challenges
inferred← citeshttps://doi.org/10.1016/j.bios.2021.113035openalex-snapshot
Electrochemical biosensors for biometal-protein interactions in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.bpc.2008.12.011openalex-snapshot
Enhanced prion protein stability coupled to DNA recognition and milieu acidification
inferred← citeshttps://doi.org/10.1016/j.bpc.2016.03.004openalex-snapshot
Use of molecular dynamics simulation to explore structural facets of human prion protein with pathogenic mutations
inferred← citeshttps://doi.org/10.1016/j.brainres.2008.08.097openalex-snapshot
Mild cognitive deficits associated to neocortical microgyria in mice with genetic deletion of cellular prion protein
inferred← citeshttps://doi.org/10.1016/j.brainres.2019.146550openalex-snapshot
Substrain-related dependence of Cu(I)-ATPase activity among prion protein-null mice
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2009.06.002openalex-snapshot
New insights into cellular prion protein (PrPc) functions: The “ying and yang” of a relevant protein
inferred← citeshttps://doi.org/10.1016/j.canlet.2009.07.009openalex-snapshot
Prion protein: From physiology to cancer biology
inferred← citeshttps://doi.org/10.1016/j.cbi.2009.07.021openalex-snapshot
Prion metal interaction: Is prion pathogenesis a cause or a consequence of metal imbalance?
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.03.008openalex-snapshot
The art of building multifunctional metal-binding agents from basic molecular scaffolds for the potential application in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.03.038openalex-snapshot
Interactions of Cu2+ with prion family peptide fragments: Considerations on affinity, speciation and coordination
inferred← citeshttps://doi.org/10.1016/j.cellsig.2016.03.010openalex-snapshot
Glycan-deficient PrP stimulates VEGFR2 signaling via glycosaminoglycan
inferred← citeshttps://doi.org/10.1016/j.ejcb.2010.11.015openalex-snapshot
Cellular prion protein localizes to the nucleus of endocrine and neuronal cells and interacts with structural chromatin components
inferred← citeshttps://doi.org/10.1016/j.expneurol.2011.11.003openalex-snapshot
Cobalamin (vitamin B12) regulation of PrPC, PrPC-mRNA and copper levels in rat central nervous system
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.12.038openalex-snapshot
Regulation of focal adhesion formation and filopodia extension by the cellular prion protein (PrPC)
inferred← citeshttps://doi.org/10.1016/j.febslet.2009.06.014openalex-snapshot
Cells and prions: A license to replicate
inferred← citeshttps://doi.org/10.1016/j.febslet.2009.09.027openalex-snapshot
The prion or the related Shadoo protein is required for early mouse embryogenesis
inferred← citeshttps://doi.org/10.1016/j.febslet.2012.11.032openalex-snapshot
High levels of Cellular Prion Protein improve astrocyte development
inferred← citeshttps://doi.org/10.1016/j.humpath.2018.05.016openalex-snapshot
Aberrant expression of stress-induced phosphoprotein 1 in colorectal cancer and its clinicopathologic significance
inferred← citeshttps://doi.org/10.1016/j.ibneur.2025.08.011openalex-snapshot
Research hotspots and trends in the interaction mechanisms of neuroinflammation and sleep disorders: A bibliometric analysis based on WOS
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101642openalex-snapshot
Cellular prion protein in human plasma–derived extracellular vesicles promotes neurite outgrowth via the NMDA receptor–LRP1 receptor system
inferred← citeshttps://doi.org/10.1016/j.jcpa.2011.08.011openalex-snapshot
Increased Immunohistochemical Labelling for Prion Protein Occurs in Diverse Neurological Disorders of Sheep: Relevance for Normal Cellular PrP Function
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2012.04.008openalex-snapshot
Copper(II) complexation to 1-octarepeat peptide from a prion protein: Insights from theoretical and experimental UV-visible studies
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.04.040openalex-snapshot
Prion Protein NMR Structure from Tammar Wallaby (Macropus eugenii) Shows that the β2–α2 Loop Is Modulated by Long-Range Sequence Effects
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.10.075openalex-snapshot
Structure of the Flexible Amino-Terminal Domain of Prion Protein Bound to a Sulfated Glycan
inferred← citeshttps://doi.org/10.1016/j.jmb.2010.09.060openalex-snapshot
Pathogenic Mutations in the Hydrophobic Core of the Human Prion Protein Can Promote Structural Instability and Misfolding
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.05.027openalex-snapshot
Interrogating the Dimerization Interface of the Prion Protein Via Site-Specific Mutations to p-Benzoyl-L-Phenylalanine
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.05.020openalex-snapshot
Both N-Terminal and C-Terminal Histidine Residues of the Prion Protein Are Essential for Copper Coordination and Neuroprotective Self-Regulation
inferred← citeshttps://doi.org/10.1016/j.jmb.2022.167925openalex-snapshot
Prion Propagation is Dependent on Key Amino Acids in Charge Cluster 2 within the Prion Protein
inferred← citeshttps://doi.org/10.1016/j.jmgm.2024.108927openalex-snapshot
Structural characterization of codon 129 polymorphism in prion peptide segments (PrP127-132) using the Markov State Models
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2014.06.021openalex-snapshot
Increased expression of stress inducible protein 1 in glioma-associated microglia/macrophages
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2015.07.002openalex-snapshot
Activation and function of murine primary microglia in the absence of the prion protein
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2019.05.006openalex-snapshot
Prevention of clinical and histological signs of MOG-induced experimental allergic encephalomyelitis by prolonged treatment with recombinant human EGF
inferred← citeshttps://doi.org/10.1016/j.jns.2015.09.365openalex-snapshot
Are PrPCs involved in some human myelin diseases? Relating experimental studies to human pathology
inferred← citeshttps://doi.org/10.1016/j.jocs.2016.03.007openalex-snapshot
Identification of common therapeutic targets for selected neurodegenerative disorders: An in silico approach
inferred← citeshttps://doi.org/10.1016/j.mad.2017.08.002openalex-snapshot
Role of Prion protein in premature senescence of human fibroblasts
inferred← citeshttps://doi.org/10.1016/j.mcn.2009.07.004openalex-snapshot
Differential solubility of prions is associated in manifold phenotypes
inferred← citeshttps://doi.org/10.1016/j.mehy.2013.12.009openalex-snapshot
Protein conformational modulation by photons: A mechanism for laser treatment effects
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2023.105246openalex-snapshot
Emerging concepts towards a translational framework in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.neuint.2018.11.010openalex-snapshot
The prion protein in neuroimmune crosstalk
inferred← citeshttps://doi.org/10.1016/j.neulet.2009.05.049openalex-snapshot
Characterization of a specific interaction between ADAM23 and cellular prion protein
inferred← citeshttps://doi.org/10.1016/j.neulet.2011.03.096openalex-snapshot
Involvement of the cellular prion protein in the migration of brain microvascular endothelial cells
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.10.032openalex-snapshot
Atorvastatin stimulates neuroblastoma cells to induce neurite outgrowth by increasing cellular prion protein expression
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.134866openalex-snapshot
Plasma exosomal prion protein levels are correlated with cognitive decline in PD patients
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2015.05.013openalex-snapshot
Cytokine profiles and the role of cellular prion protein in patients with vascular dementia and vascular encephalopathy
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2011.10.025openalex-snapshot
Microglial stress inducible protein 1 promotes proliferation and migration in human glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2012.04.034openalex-snapshot
Overexpression of cellular prion protein (PrPC) prevents cognitive dysfunction and apoptotic neuronal cell death induced by amyloid-β (Aβ1–40) administration in mice
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.04.020openalex-snapshot
Low levels of cobalamin, epidermal growth factor, and normal prions in multiple sclerosis spinal cord
inferred← citeshttps://doi.org/10.1016/j.nlm.2009.08.009openalex-snapshot
Time-course of 5-HT6 receptor mRNA expression during memory consolidation and amnesia
inferred← citeshttps://doi.org/10.1016/j.nlm.2011.08.003openalex-snapshot
The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2013.11.009openalex-snapshot
p53 in neurodegenerative diseases and brain cancers
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.109650openalex-snapshot
Context-dependent PrPᶜ signaling in cancer stemness, mesenchymal stromal cell repair, and extracellular vesicle biology
inferred← citeshttps://doi.org/10.1016/j.physbeh.2013.06.006openalex-snapshot
Altered behavioral aspects of aged mice lacking the cellular prion protein
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2014.01.002openalex-snapshot
Metabolism and functions of copper in brain
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.03.001openalex-snapshot
Role of cellular prion protein in interneuronal amyloid transmission
inferred← citeshttps://doi.org/10.1016/j.str.2016.04.017openalex-snapshot
Interaction between Prion Protein's Copper-Bound Octarepeat Domain and a Charged C-Terminal Pocket Suggests a Mechanism for N-Terminal Regulation
inferred← citeshttps://doi.org/10.1016/j.talanta.2011.12.052openalex-snapshot
Gold nanoparticles as a label-free probe for the detection of amyloidogenic protein
inferred← citeshttps://doi.org/10.1016/j.tins.2011.10.002openalex-snapshot
Prion protein at the crossroads of physiology and disease
inferred← citeshttps://doi.org/10.1016/j.virol.2008.12.005openalex-snapshot
Prion expression is activated by Adenovirus 5 infection and affects the adenoviral cycle in human cells
inferred← citeshttps://doi.org/10.1016/j.virusres.2014.10.015openalex-snapshot
Decoding the function of the N-terminal tail of the cellular prion protein to inspire novel therapeutic avenues for neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.virusres.2023.199249openalex-snapshot
Antiviral activity of prion protein against Japanese encephalitis virus infection in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.yexcr.2023.113656openalex-snapshot
Prion protein-dependent regulation of p53-MDM2 crosstalk during endoplasmic reticulum stress and doxorubicin treatments might be essential for cell fate in human breast cancer cell line, MCF-7
inferred← citeshttps://doi.org/10.1016/j.yhbeh.2016.05.002openalex-snapshot
Oxytocin and vasopressin hormone genes in children's externalizing problems: A cognitive endophenotype approach
inferred← citeshttps://doi.org/10.1016/j.ymeth.2010.12.002openalex-snapshot
Experimental approaches to the interaction of the prion protein with nucleic acids and glycosaminoglycans: Modulators of the pathogenic conversion
inferred← citeshttps://doi.org/10.1016/s1937-6448(10)80003-6openalex-snapshot
Membrane Trafficking in Protozoa
inferred← citeshttps://doi.org/10.1016/s2211-9698(24)74943-7openalex-snapshot
10.1016/s2211-9698(24)74943-7
inferred← citeshttps://doi.org/10.1021/ac101865sopenalex-snapshot
Sensitive Discrimination and Detection of Prion Disease-Associated Isoform with a Dual-Aptamer Strategy by Developing a Sandwich Structure of Magnetic Microparticles and Quantum Dots
inferred← citeshttps://doi.org/10.1021/ac202810bopenalex-snapshot
Aptamer-Mediated Nanoparticle-Based Protein Labeling Platform for Intracellular Imaging and Tracking Endocytosis Dynamics
inferred← citeshttps://doi.org/10.1021/acs.biochem.3c00129openalex-snapshot
Prion Protein Octarepeat Domain Forms Transient β-Sheet Structures upon Residue-Specific Binding to Cu(II) and Zn(II) Ions
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5b02794openalex-snapshot
Spectroscopic and Theoretical Study of CuI Binding to His111 in the Human Prion Protein Fragment 106–115
inferred← citeshttps://doi.org/10.1021/acschemneuro.6c00207openalex-snapshot
Alzheimer’s Disease: A Review of Molecular Mechanisms and Interventions Targeting Aβ-Binding Receptors
inferred← citeshttps://doi.org/10.1021/bi101449fopenalex-snapshot
Diverse Effects on the Native β-Sheet of the Human Prion Protein Due to Disease-Associated Mutations
inferred← citeshttps://doi.org/10.1021/cn300045dopenalex-snapshot
Kisspeptin Prevention of Amyloid-β Peptide Neurotoxicityin Vitro
inferred← citeshttps://doi.org/10.1021/cr9000176openalex-snapshot
Medicinal Inorganic Chemistry Approaches to Passivation and Removal of Aberrant Metal Ions in Disease
inferred← citeshttps://doi.org/10.1021/ja910964copenalex-snapshot
Direct Observation of Nucleation and Growth in Amyloid Self-Assembly
inferred← citeshttps://doi.org/10.1021/jacsau.1c00451openalex-snapshot
G-Quadruplexes in Neurobiology and Virology: Functional Roles and Potential Therapeutic Approaches
inferred← citeshttps://doi.org/10.1021/jp901030aopenalex-snapshot
Molecular Dynamics Study of the Cu2+ Binding-Induced “Structuring” of the N-Terminal Domain of Human Prion Protein
inferred← citeshttps://doi.org/10.1021/pr2001989openalex-snapshot
Proteomics Approach to Identify the Interacting Partners of Cellular Prion Protein and Characterization of Rab7a Interaction in Neuronal Cells
inferred← citeshttps://doi.org/10.1021/pr200759mopenalex-snapshot
Relative Quantification of Membrane Proteins in Wild-Type and Prion Protein (PrP)-Knockout Cerebellar Granule Neurons
inferred← citeshttps://doi.org/10.1021/pr500329wopenalex-snapshot
Proteomics Analysis of Amyloid and Nonamyloid Prion Disease Phenotypes Reveals Both Common and Divergent Mechanisms of Neuropathogenesis
inferred← citeshttps://doi.org/10.1038/aps.2017.28openalex-snapshot
Amyloid beta: structure, biology and structure-based therapeutic development
inferred← citeshttps://doi.org/10.1038/cddis.2012.195openalex-snapshot
Pathogenic prions deviate PrPC signaling in neuronal cells and impair A-beta clearance
inferred← citeshttps://doi.org/10.1038/cddis.2016.310openalex-snapshot
Hypoxia-induced expression of cellular prion protein improves the therapeutic potential of mesenchymal stem cells
inferred← citeshttps://doi.org/10.1038/cddis.2017.37openalex-snapshot
Regulation of RhoA activity by the cellular prion protein
inferred← citeshttps://doi.org/10.1038/ncomms14977openalex-snapshot
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
inferred← citeshttps://doi.org/10.1038/ncomms2135openalex-snapshot
Prion protein facilitates uptake of zinc into neuronal cells
inferred← citeshttps://doi.org/10.1038/nn.4648openalex-snapshot
α-synuclein interacts with PrPC to induce cognitive impairment through mGluR5 and NMDAR2B
inferred← citeshttps://doi.org/10.1038/nrneurol.2016.65openalex-snapshot
Advanced tests for early and accurate diagnosis of Creutzfeldt–Jakob disease
inferred← citeshttps://doi.org/10.1038/onc.2014.261openalex-snapshot
Disruption of prion protein–HOP engagement impairs glioblastoma growth and cognitive decline and improves overall survival
inferred← citeshttps://doi.org/10.1038/onc.2017.200openalex-snapshot
Cellular prion protein (PrPC) in the development of Merlin-deficient tumours
showing the first 200 of 588 · page through all 588
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.