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dc.contributor.authorDe Rossi, Gen_US
dc.contributor.authorWhiteford, JRen_US
dc.date.accessioned2016-08-17T13:21:21Z
dc.date.available2013-12-09en_US
dc.date.issued2013en_US
dc.date.submitted2016-08-10T13:21:41.089Z
dc.identifier.issn2046-1402en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/14730
dc.description.abstractSyndecan-3 is one of the four members of the syndecan family of heparan sulphate proteoglycans and has been shown to interact with numerous growth factors via its heparan sulphate chains. The extracellular core proteins of syndecan-1,-2 and -4 all possess adhesion regulatory motifs and we hypothesized that syndecan-3 may also possess such characteristics. Here we show that a bacterially expressed GST fusion protein consisting of the entire mature syndecan-3 ectodomain has anti-angiogenic properties and acts via modulating endothelial cell migration. This work identifies syndecan-3 as a possible therapeutic target for anti-angiogenic therapy.en_US
dc.description.sponsorshipThis work was funded by Arthritis Research-UK (Grant No. 19207) and funds from the William Harvey Research Foundation both to JRW.en_US
dc.format.extent270 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofF1000Resen_US
dc.titleA novel role for syndecan-3 in angiogenesis.en_US
dc.typeArticle
dc.rights.holder© 2013 De Rossi G and Whiteford JR.
dc.rights.holderThis is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).
dc.identifier.doi10.12688/f1000research.2-270.v1en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/24555114en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume2en_US
dcterms.dateAccepted2013-12-09en_US


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