Please use this identifier to cite or link to this item: https://doi.org/10.1002/pmic.200800051
DC FieldValue
dc.titlePhosphoproteomics, oncogenic signaling and cancer research
dc.contributor.authorChong, P.-K.
dc.contributor.authorLee, H.
dc.contributor.authorKong, J.W.-F.
dc.contributor.authorLoh, M.C.-S.
dc.contributor.authorWong, C.-H.
dc.contributor.authorLim, Y.-P.
dc.date.accessioned2014-11-25T09:48:56Z
dc.date.available2014-11-25T09:48:56Z
dc.date.issued2008-11
dc.identifier.citationChong, P.-K., Lee, H., Kong, J.W.-F., Loh, M.C.-S., Wong, C.-H., Lim, Y.-P. (2008-11). Phosphoproteomics, oncogenic signaling and cancer research. Proteomics 8 (21) : 4370-4382. ScholarBank@NUS Repository. https://doi.org/10.1002/pmic.200800051
dc.identifier.issn16159853
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/108677
dc.description.abstractThe past 5 years have seen an explosion of phosphoproteomics methods development. In this review, using epidermal growth-factor signaling as a model, we will discuss how phosphoproteomics, along with bioinformatics and computational modeling, have impacted key aspects of oncogenic signaling such as in the temporal fine mapping of phosphorylation events, and the identification of novel tyrosine kinase substrates and phosphorylation sites. We submit that the next decade will see considerable exploitation of phosphoproteomics in cancer research. Such a phenomenon is already happening as exemplified by its use in promoting the understanding of the molecular etiology of cancer and target-directed therapeutics. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/pmic.200800051
dc.sourceScopus
dc.subjectCancer
dc.subjectEpidermal growth factor receptor
dc.subjectPhosphoproteomics
dc.subjectPhosphorylation
dc.subjectTyrosine kinase
dc.typeReview
dc.contributor.departmentNATIONAL UNIVERSITY MEDICAL INSTITUTES
dc.description.doi10.1002/pmic.200800051
dc.description.sourcetitleProteomics
dc.description.volume8
dc.description.issue21
dc.description.page4370-4382
dc.description.codenPROTC
dc.identifier.isiut000261003800002
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