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Development of Non-Erythropoietic Erythropoietin Variants for Neuroprotection

Development of Non-Erythropoietic Erythropoietin Variants for Neuroprotection

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TORUP, Lars, Marcel LEIST, 2006. Development of Non-Erythropoietic Erythropoietin Variants for Neuroprotection. In: HÖKE, Ahmet, ed.. Erythropoietin and the Nervous System. Berlin:Springer, pp. 1-9

@incollection{Torup2006Devel-7441, title={Development of Non-Erythropoietic Erythropoietin Variants for Neuroprotection}, year={2006}, address={Berlin}, publisher={Springer}, booktitle={Erythropoietin and the Nervous System}, pages={1--9}, editor={Höke, Ahmet}, author={Torup, Lars and Leist, Marcel} }

<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/7441"> <dc:creator>Leist, Marcel</dc:creator> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> <dc:creator>Torup, Lars</dc:creator> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:34:27Z</dc:date> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <dc:contributor>Torup, Lars</dc:contributor> <dcterms:bibliographicCitation>First publ. in: Erythropoietin and the Nervous System / Ahmet Höke (ed.). Berlin: Springer, 2006, pp. 1-9</dcterms:bibliographicCitation> <dcterms:issued>2006</dcterms:issued> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:abstract xml:lang="eng">Erythropoietin is well known to possess erythropoietic activity, but also tissue protection. Here, we present examples on how to separate these two activities. One possibility is to generate a short-lived variant by removal of EPO s sialic acid residues. Although asialo-EPO has a high affinity for the classical EPO-R, it lacks hematopoetic activity in vivo upon bolus injection, because of its short plasma half-life. Another approach we followed was to generate carbamylated EPO (CEPO), which has no affinity for the EPO receptor, but the same neuroprotective potency as EPO. Our data suggest that the cytoprotective signal transduction of EPO is distinct from the hematopoietic signaling machinery.</dcterms:abstract> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dc:language>eng</dc:language> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/7441/1/Hoke_Chapter_13_final.pdf"/> <dcterms:title>Development of Non-Erythropoietic Erythropoietin Variants for Neuroprotection</dcterms:title> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:34:27Z</dcterms:available> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/7441"/> <dc:contributor>Leist, Marcel</dc:contributor> <dc:rights>terms-of-use</dc:rights> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/7441/1/Hoke_Chapter_13_final.pdf"/> <dc:format>application/pdf</dc:format> </rdf:Description> </rdf:RDF>

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