Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/7534
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorWang, F-
dc.creatorChan, LWC-
dc.creatorTsui, NBY-
dc.creatorWong, SCC-
dc.creatorSiu, PM-
dc.creatorYip, SP-
dc.creatorYung, BYM-
dc.date.accessioned2015-10-13T08:26:19Z-
dc.date.available2015-10-13T08:26:19Z-
dc.identifier.issn2314-6133en_US
dc.identifier.urihttp://hdl.handle.net/10397/7534-
dc.language.isoenen_US
dc.publisherHindawi Publishing Corporationen_US
dc.rightsCopyright © 2015 Fengfeng Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following article: Wang, F., Chan, L. W., Tsui, N. B., Wong, S. C., Siu, P. M., Yip, S. P., & Yung, B. Y. (2015). Coexpression pattern analysis of NPM1-associated genes in chronic myelogenous leukemia. BioMed research international, 2015, is available at https//doi.org/10.1155/2015/610595en_US
dc.titleCoexpression pattern analysis of NPM1-associated genes in chronic myelogenous leukemiaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume2015en_US
dc.identifier.doi10.1155/2015/610595en_US
dcterms.abstractBackground. Nucleophosmin 1 (NPM1) plays an important role in ribosomal synthesis and malignancies, but NPM1 mutations occur rarely in the blast-crisis and chronic-phase chronic myelogenous leukemia (CML) patients. The NPM1-associated gene set (GCM-NPM1), in total 116 genes including NPM1, was chosen as the candidate gene set for the coexpression analysis. We wonder if NPM1-associated genes can affect the ribosomal synthesis and translation process in CML. Results. We presented a distribution-based approach for gene pair classification by identifying a disease-specific cutoff point that classified the coexpressed gene pairs into strong and weak coexpression structures. The differences in the coexpression patterns between the normal and the CML groups were reflected from the overall structure by performing two-sample Kolmogorov-Smirnov test. Our developed method effectively identified the coexpression pattern differences from the overall structure: P value=1.71×10-22<0.05 for the maximum deviation D=0.109. Moreover, we found that genes involved in the ribosomal synthesis and translation process tended to be coexpressed in the CML group. Conclusion. Our developed method can identify the coexpression difference between two different groups. Dysregulation of ribosomal synthesis and translation process may be related to the CML disease. Our significant findings may provide useful information for the novel CML mechanism exploration and cancer treatment.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBioMed research international, 2015, v. 2015, 610595-
dcterms.isPartOfBioMed research international-
dcterms.issued2015-
dc.identifier.scopus2-s2.0-84928803667-
dc.identifier.pmid25961029-
dc.identifier.eissn2314-6141en_US
dc.identifier.rosgroupid2014001172-
dc.description.ros2014-2015 > Academic research: refereed > Publication in refereed journalen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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