Cited 6 times in
Identifying a combined biomarker for bisphosphonate-related osteonecrosis of the jaw
DC Field | Value | Language |
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dc.contributor.author | 김기열 | - |
dc.contributor.author | 장향란 | - |
dc.contributor.author | 차인호 | - |
dc.date.accessioned | 2018-08-28T17:03:27Z | - |
dc.date.available | 2018-08-28T17:03:27Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1523-0899 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/162211 | - |
dc.description.abstract | BACKGROUND: For this study, the aim was to identify combined biomarkers associated with bisphosphonate-related osteonecrosis of the jaw (BRONJ). MATERIALS AND METHODS: Microarray data for GSE7116 were downloaded from the Gene Expression Omnibus database, which contains 26 samples, including without ONJ, and 5 healthy volunteers. The combined biomarkers were identified using principal component analysis, and the pathway enrichment analyses were performed using the DAVID online tool. RESULTS: Two hundred differently expressed genes between groups were detected according to the significances. From functional annotation, Y-box binding protein 1 and heterogeneous nuclear ribonucleoprotein C were found to be included in the most significant 10 pathways. Ten combined gene sets were identified that were effective in classifying multiple myeloma (MM) with ONJ and MM without ONJ. CONCLUSION: Identifying combined gene expression profiles is expected to contribute to more personalized management of BRONJ and to improve existing therapies, and it will be helpful in finding new therapies by identifying more predictive biomarkers. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | John Wiley & Sons, Inc | - |
dc.relation.isPartOf | CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Identifying a combined biomarker for bisphosphonate-related osteonecrosis of the jaw | - |
dc.type | Article | - |
dc.contributor.college | College of Dentistry | - |
dc.contributor.department | Others | - |
dc.contributor.googleauthor | Ki-Yeol Kim | - |
dc.contributor.googleauthor | Xianglan Zhang | - |
dc.contributor.googleauthor | In-Ho Cha | - |
dc.identifier.doi | 10.1111/cid.12569 | - |
dc.contributor.localId | A00337 | - |
dc.contributor.localId | A03489 | - |
dc.contributor.localId | A04002 | - |
dc.relation.journalcode | J00580 | - |
dc.identifier.eissn | 1708-8208 | - |
dc.identifier.pmid | 29266738 | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/abs/10.1111/cid.12569 | - |
dc.subject.keyword | bisphosphonate-related osteonecrosis of the jaw | - |
dc.subject.keyword | combined biomarker | - |
dc.subject.keyword | gene expression | - |
dc.contributor.alternativeName | Kim, Ki Yeol | - |
dc.contributor.alternativeName | Zhang, Xiang Lan | - |
dc.contributor.alternativeName | Cha, In Ho | - |
dc.contributor.affiliatedAuthor | Kim, Ki Yeol | - |
dc.contributor.affiliatedAuthor | Zhang, Xiang Lan | - |
dc.contributor.affiliatedAuthor | Cha, In Ho | - |
dc.citation.volume | 20 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 191 | - |
dc.citation.endPage | 198 | - |
dc.identifier.bibliographicCitation | CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH, Vol.20(2) : 191-198, 2018 | - |
dc.identifier.rimsid | 59797 | - |
dc.type.rims | ART | - |
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