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Modeling signaling pathways in articular cartilage

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dc.contributor.author Melas, IN en
dc.contributor.author Chairakaki, AD en
dc.contributor.author Mitsos, A en
dc.contributor.author Dailiana, Z en
dc.contributor.author Provatidis, CG en
dc.contributor.author Alexopoulos, LG en
dc.date.accessioned 2014-03-01T02:47:25Z
dc.date.available 2014-03-01T02:47:25Z
dc.date.issued 2011 en
dc.identifier.issn 1557170X en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/33129
dc.subject.other Articular cartilages en
dc.subject.other Cartilage extracellular matrixes en
dc.subject.other Cell types en
dc.subject.other Chondrocytes en
dc.subject.other High throughput en
dc.subject.other Joint disease en
dc.subject.other Optimization algorithms en
dc.subject.other Predictive models en
dc.subject.other Shedding light en
dc.subject.other Signaling networks en
dc.subject.other Signaling pathways en
dc.subject.other Signaling transduction en
dc.subject.other State of the art en
dc.subject.other Algorithms en
dc.subject.other Arts computing en
dc.subject.other Body fluids en
dc.subject.other Signaling en
dc.subject.other Cartilage en
dc.title Modeling signaling pathways in articular cartilage en
heal.type conferenceItem en
heal.identifier.primary 10.1109/IEMBS.2011.6090630 en
heal.identifier.secondary http://dx.doi.org/10.1109/IEMBS.2011.6090630 en
heal.identifier.secondary 6090630 en
heal.publicationDate 2011 en
heal.abstract Chondrocytes, the only cell type in articular cartilage, are responsible for maintaining the composition of cartilage extracellular matrix (ECM) through a complex interplay of anabolic and catabolic stimuli. Although understanding the way chondrocytes respond to stimuli is of utmost importance for shedding light into the etiology of joint diseases, an integrative approach to studying their signaling transduction mechanisms is yet to be introduced. Herein, we propose an approach that combines high throughput proteomic measurements and state of the art optimization algorithms to construct a predictive model of chondrocyte signaling network, downstream of 78 receptors of interest. © 2011 IEEE. en
heal.journalName Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBS en
dc.identifier.doi 10.1109/IEMBS.2011.6090630 en
dc.identifier.volume 2011 en
dc.identifier.spage 3712 en
dc.identifier.epage 3715 en


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