| scholarly article | Q13442814 |
| P50 | author | José Antonio Del Río | Q38319564 |
| P2093 | author name string | Franc Llorens | |
| P2860 | cites work | Metabotropic glutamate receptors transduce signals for neurite outgrowth after binding of the prion protein to laminin γ1 chain. | Q51035911 |
| Developmental expression of the prion protein gene in glial cells | Q52209886 | ||
| Accumulation of cellular prion protein within dystrophic neurites of amyloid plaques in the Alzheimer's disease brain. | Q53314398 | ||
| Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob disease. | Q53664270 | ||
| Truncated Prion Protein and Doppel Are Myelinotoxic in the Absence of Oligodendrocytic PrPC | Q57083651 | ||
| Altered circadian activity rhythms and sleep in mice devoid of prion protein | Q59071240 | ||
| Generalized convulsive status epilepticus in Creutzfeldt–Jakob disease | Q59416825 | ||
| Increased Sensitivity to Seizures in Mice Lacking Cellular Prion Protein | Q59683939 | ||
| Cross-Linking Cellular Prion Protein Triggers Neuronal Apoptosis in Vivo | Q61463936 | ||
| Periodic lateralized epileptiform complexes (PLEDs) in Creutzfeldt-Jakob disease | Q72137438 | ||
| Epilepsia partialis continua in Creutzfeldt-Jakob disease | Q73317185 | ||
| Is loss of function of the prion protein the cause of prion disorders? | Q73580418 | ||
| Expression of Prnp mRNA (prion protein gene) in mouse spermatogenic cells | Q80930975 | ||
| Threshold for epileptiform activity is elevated in prion knockout mice | Q83322867 | ||
| Cellular prion protein mediates impairment of synaptic plasticity by amyloid-beta oligomers | Q22251089 | ||
| Selective interaction of JNK protein kinase isoforms with transcription factors | Q24317346 | ||
| 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 | ||
| Prions | Q24633319 | ||
| Insoluble cellular prion protein and its association with prion and Alzheimer diseases | Q27012706 | ||
| Regulation of GABA(A) and glutamate receptor expression, synaptic facilitation and long-term potentiation in the hippocampus of prion mutant mice | Q27337373 | ||
| Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation | Q28138890 | ||
| Mice devoid of prion protein have cognitive deficits that are rescued by reconstitution of PrP in neurons | Q28245704 | ||
| Physiology of the prion protein | Q28275220 | ||
| Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones | Q28476253 | ||
| Absence of excitotoxicity-induced apoptosis in the hippocampus of mice lacking the Jnk3 gene | Q28507982 | ||
| Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice | Q28586796 | ||
| PrPC directly interacts with proteins involved in signaling pathways | Q28592791 | ||
| Memory impairment in transgenic Alzheimer mice requires cellular prion protein | Q30032301 | ||
| Activation of c-Jun NH2-terminal kinase 3 is mediated by the GluR6.PSD-95.MLK3 signaling module following cerebral ischemia in rat hippocampus | Q30160089 | ||
| Prion protein attenuates excitotoxicity by inhibiting NMDA receptors | Q30481829 | ||
| Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein | Q32035009 | ||
| Molecular cloning of a candidate chicken prion protein | Q33191659 | ||
| Gene expression alterations in brains of mice infected with three strains of scrapie | Q33243428 | ||
| In vitro and in vivo neurotoxicity of prion protein oligomers. | Q33296885 | ||
| Comprehensive transcriptional profiling of prion infection in mouse models reveals networks of responsive genes | Q33322227 | ||
| The comprehensive native interactome of a fully functional tagged prion protein | Q33408170 | ||
| Functionally relevant domains of the prion protein identified in vivo | Q33501189 | ||
| Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring | Q33539797 | ||
| Context dependent neuroprotective properties of prion protein (PrP). | Q33595425 | ||
| Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy | Q33769602 | ||
| Proteomics approach to identify the interacting partners of cellular prion protein and characterization of Rab7a interaction in neuronal cells | Q33908948 | ||
| Copper binding extrinsic to the octarepeat region in the prion protein | Q33999707 | ||
| Prion protein interaction with stress-inducible protein 1 enhances neuronal protein synthesis via mTOR | Q34059200 | ||
| Axonal prion protein is required for peripheral myelin maintenance | Q34094490 | ||
| Prion protein and Abeta-related synaptic toxicity impairment | Q34233877 | ||
| Role of alpha7 nicotinic acetylcholine receptor in calcium signaling induced by prion protein interaction with stress-inducible protein 1. | Q34299079 | ||
| Hippocampal synaptic plasticity in mice devoid of cellular prion protein | Q34365739 | ||
| Lack of neuroprotection against experimental glaucoma in c-Jun N-terminal kinase 3 knockout mice | Q34699394 | ||
| Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain | Q34868772 | ||
| Alzheimer's and prion diseases: distinct pathologies, common proteolytic denominators. | Q35006483 | ||
| Cellular prion protein: implications in seizures and epilepsy | Q35018699 | ||
| Prion protein accumulation and neuroprotection in hypoxic brain damage | Q35102832 | ||
| Cellular prion protein function in copper homeostasis and redox signalling at the synapse | Q35177466 | ||
| The role of c-Jun N-terminal kinase (JNK) in Parkinson's disease. | Q35184662 | ||
| Unaltered prion protein expression in Alzheimer disease patients | Q35194930 | ||
| Prion disease induced alterations in gene expression in spleen and brain prior to clinical symptoms. | Q35205306 | ||
| Towards cellular receptors for prions | Q35588133 | ||
| Targeting the JNK signaling pathway for stroke and Parkinson's diseases therapy | Q36050610 | ||
| Prions and exosomes: from PrPc trafficking to PrPsc propagation | Q36229154 | ||
| Increased excitatory amino acid transport into murine prion protein knockout astrocytes cultured in vitro | Q36282990 | ||
| Prion protein recruits its neuronal receptor NCAM to lipid rafts to activate p59fyn and to enhance neurite outgrowth. | Q36321586 | ||
| The prion protein and lipid rafts | Q36447789 | ||
| Cellular prion protein signaling in serotonergic neuronal cells | Q36779221 | ||
| Cellular prion protein electron microscopy: attempts/limits and clues to a synaptic trait. Implications in neurodegeneration process | Q37072501 | ||
| The prion protein knockout mouse: a phenotype under challenge | Q37080450 | ||
| NADPH oxidase and extracellular regulated kinases 1/2 are targets of prion protein signaling in neuronal and nonneuronal cells. | Q37088888 | ||
| New insights into cellular prion protein (PrPc) functions: the "ying and yang" of a relevant protein. | Q37518038 | ||
| Prion protein: orchestrating neurotrophic activities. | Q37600568 | ||
| Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus | Q37693769 | ||
| Sporadic Creutzfeldt-Jakob disease presenting as nonconvulsive status epilepticus case report and review of the literature | Q37739628 | ||
| JNK: A Stress-Activated Protein Kinase Therapeutic Strategies and Involvement in Alzheimer’s and Various Neurodegenerative Abnormalities | Q37793978 | ||
| The role of lipid rafts in prion protein biology | Q37825134 | ||
| Genetics of prion disease | Q37870102 | ||
| Neuroprotective role of PrPC against kainate-induced epileptic seizures and cell death depends on the modulation of JNK3 activation by GluR6/7-PSD-95 binding | Q38274565 | ||
| Cellular prion protein transduces neuroprotective signals | Q39644937 | ||
| CREB-dependent gene regulation by prion protein: impact on MMP-9 and beta-dystroglycan. | Q39948509 | ||
| Dose-dependent, prion protein (PrP)-mediated facilitation of excitatory synaptic transmission in the mouse hippocampus | Q40797634 | ||
| Signal transduction through prion protein | Q40855079 | ||
| Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene | Q41982232 | ||
| Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease | Q42050382 | ||
| All quiet on the neuronal front: NMDA receptor inhibition by prion protein | Q42091975 | ||
| Coactivation of GABA receptors inhibits the JNK3 apoptotic pathway via disassembly of GluR6-PSD-95-MLK3 signaling module in KA-induced seizure | Q43289017 | ||
| Mild cognitive deficits associated to neocortical microgyria in mice with genetic deletion of cellular prion protein. | Q43516326 | ||
| Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein | Q43522858 | ||
| Developmental influence of the cellular prion protein on the gene expression profile in mouse hippocampus | Q43798516 | ||
| Lack of prion protein expression results in a neuronal phenotype sensitive to stress | Q43849051 | ||
| Depressive-like behaviour of mice lacking cellular prion protein | Q44190777 | ||
| Prion protein as trans-interacting partner for neurons is involved in neurite outgrowth and neuronal survival | Q44391055 | ||
| Specific pathophysiological functions of JNK isoforms in the brain | Q45240068 | ||
| Amyloid-beta oligomers increase the localization of prion protein at the cell surface | Q45827724 | ||
| Asynchronous kidney allograft loss after simultaneous pancreas-kidney transplantation: impact on pancreas allograft outcome at a single center. | Q45958472 | ||
| Autophagy and cell death of Purkinje cells overexpressing Doppel in Ngsk Prnp-deficient mice | Q46214671 | ||
| Co-activation of GABA receptors inhibits the JNK3 apoptotic pathway via the disassembly of the GluR6-PSD95-MLK3 signaling module in cerebral ischemic-reperfusion | Q46727662 | ||
| Prion protein potentiates acetylcholine release at the neuromuscular junction | Q46779822 | ||
| 129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal | Q47562788 | ||
| Prion protein (PrPc) immunocytochemistry and expression of the green fluorescent protein reporter gene under control of the bovine PrP gene promoter in the mouse brain | Q47723535 | ||
| Microglial expression of the prion protein | Q47959261 | ||
| Prion protein is necessary for normal synaptic function | Q48087355 | ||
| Prions prevent neuronal cell-line death. | Q48152328 | ||
| Expression of proteins linked to exocytosis and neurotransmission in patients with Creutzfeldt-Jakob disease | Q48200986 | ||
| Enhanced susceptibility of Prnp-deficient mice to kainate-induced seizures, neuronal apoptosis, and death: Role of AMPA/kainate receptors | Q48270909 | ||
| Age-dependent loss of PTP and LTP in the hippocampus of PrP-null mice | Q48305162 | ||
| Tissue-specific expression pattern of bovine prion gene: quantification using real-time RT-PCR. | Q48368484 | ||
| Role of cellular prion protein on LTP expression in aged mice. | Q48520160 | ||
| Selective expression of prion protein in peripheral tissues of the adult mouse | Q48544898 | ||
| Characterization of prion protein-enriched domains, isolated from rat cerebellar granule cells in culture | Q48588068 | ||
| Abnormal synaptic protein expression and cell death in murine scrapie. | Q48605040 | ||
| Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies. | Q48933812 | ||
| Unaltered SNARE complex formation in an in vivo model of prion disease | Q48965098 | ||
| P433 | issue | 3 | |
| P921 | main subject | excitotoxicity | Q901117 |
| P304 | page(s) | 245-251 | |
| P577 | publication date | 2012-07-01 | |
| P1433 | published in | Prion | Q26842757 |
| P1476 | title | Unraveling the neuroprotective mechanisms of PrP (C) in excitotoxicity | |
| P478 | volume | 6 |
| Q24317448 | Anchorless 23-230 PrPC interactomics for elucidation of PrPC protective role |
| Q33565752 | Expression of Reactive Oxygen Species-Related Transcripts in Egyptian Children With Autism |
| Q28597985 | Functions of the cellular prion protein, the end of Moore's law, and Ockham's razor theory |
| Q38129313 | Gene expression resulting from PrPC ablation and PrPC overexpression in murine and cellular models |
| Q39431937 | Implications of peptide assemblies in amyloid diseases |
| Q27308826 | Involvement of PrP(C) in kainate-induced excitotoxicity in several mouse strains |
| Q36912263 | Lack of influence of prion protein gene expression on kainate-induced seizures in mice: studies using congenic, coisogenic and transgenic strains. |
| Q28071519 | NCAM1 Polysialylation: The Prion Protein's Elusive Reason for Being? |
| Q39157220 | PrP(C) regulates epidermal growth factor receptor function and cell shape dynamics in Neuro2a cells. |
| Q43230803 | RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome |
| Q90047524 | The Quest for Cellular Prion Protein Functions in the Aged and Neurodegenerating Brain |
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