| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/SJ.MP.4001400 |
| P953 | full work available at URL | https://www.nature.com/articles/4001400 |
| https://www.nature.com/articles/4001400.pdf | ||
| P698 | PubMed publication ID | 14515136 |
| P5875 | ResearchGate publication ID | 9075814 |
| P2093 | author name string | J. P. Huidobro-Toro | |
| N. C. Inestrosa | |||
| M. A. Chacón | |||
| M. I. Barría | |||
| R. Lorca | |||
| P2860 | cites work | Neurobiology of Aging | Q7002141 |
| Molecular features of the copper binding sites in the octarepeat domain of the prion protein | Q24292484 | ||
| Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection | Q24534939 | ||
| Copper stimulates endocytosis of the prion protein | Q28589040 | ||
| Expression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper delivery | Q28592762 | ||
| Developments of a water-maze procedure for studying spatial learning in the rat | Q29617561 | ||
| Copper binding to the prion protein: structural implications of four identical cooperative binding sites | Q30558995 | ||
| Copper and prion disease | Q34317924 | ||
| The cellular prion protein binds copper in vivo | Q34450742 | ||
| Normal prion protein has an activity like that of superoxide dismutase. | Q34505606 | ||
| Location and properties of metal-binding sites on the human prion protein. | Q37104327 | ||
| Attenuation of focal cerebral ischemic injury in transgenic mice overexpressing CuZn superoxide dismutase | Q37642165 | ||
| Kinky hair disease: twenty five years later. | Q39228340 | ||
| Cellular prion protein transduces neuroprotective signals | Q39644937 | ||
| Role of oxidants in ischemic brain damage | Q40998721 | ||
| Deficiency of copper can cause neuronal degeneration | Q41125466 | ||
| Ablation of the metal ion-induced endocytosis of the prion protein by disease-associated mutation of the octarepeat region | Q43645286 | ||
| Copper binding to the octarepeats of the prion protein. Affinity, specificity, folding, and cooperativity: insights from circular dichroism | Q44231104 | ||
| Tethering the N-terminus of the prion protein compromises the cellular response to oxidative stress | Q44297149 | ||
| Copper reduction by copper binding proteins and its relation to neurodegenerative diseases | Q44305645 | ||
| The human prion octarepeat fragment prevents and reverses the inhibitory action of copper in the P2X4 receptor without modifying the zinc action | Q44402839 | ||
| Prion protein selectively binds copper(II) ions | Q46492410 | ||
| Reduction of CuZn-superoxide dismutase activity exacerbates neuronal cell injury and edema formation after transient focal cerebral ischemia | Q46827301 | ||
| Prion protein is necessary for normal synaptic function | Q48087355 | ||
| A comparison of the biochemical changes induced in mouse brain by cuprizone toxicity and by scrapie infection | Q48564755 | ||
| Clinical and Histological Observations on Cuprizonc Toxicity and Scrapie in Mice | Q48810387 | ||
| The cellular prion protein binds copper in vivo | Q56058857 | ||
| Altered circadian activity rhythms and sleep in mice devoid of prion protein | Q59071240 | ||
| Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical study | Q72736191 | ||
| Sleep and sleep regulation in normal and prion protein-deficient mice | Q73067776 | ||
| The N-terminal tandem repeat region of human prion protein reduces copper: role of tryptophan residues | Q73525251 | ||
| Prion protein binds copper within the physiological concentration range | Q73692926 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurotoxicity | Q3338704 |
| prion protein family | Q24724413 | ||
| P304 | page(s) | 853-62, 835 | |
| P577 | publication date | 2003-10-01 | |
| P1433 | published in | Molecular Psychiatry | Q6895973 |
| P1476 | title | A human prion protein peptide (PrP(59-91)) protects against copper neurotoxicity | |
| A human prion protein peptide (PrP59–91) protects against copper neurotoxicity | |||
| P478 | volume | 8 |
| Q36006619 | Cellular prion protein neuroprotective function: implications in prion diseases |
| Q33501189 | Functionally relevant domains of the prion protein identified in vivo |
| Q28584119 | Induction of cellular prion protein gene expression by copper in neurons |
| Q34582715 | Involvement of ryanodine receptors in neurotrophin-induced hippocampal synaptic plasticity and spatial memory formation |
| Q28475611 | Prion protein paralog doppel protein interacts with alpha-2-macroglobulin: a plausible mechanism for doppel-mediated neurodegeneration |
| Q36895918 | Prion proteins: a biological role beyond prion diseases |
| Q33830151 | Redox control of prion and disease pathogenesis |
| Q28538070 | Solvent microenvironments and copper binding alters the conformation and toxicity of a prion fragment |
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