An oligonucleotide microarray to detect pathogens causing a sexually transmitted disease
DC Field | Value | Language |
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dc.contributor.author | Yoon, Hyun Kyu | - |
dc.contributor.author | Kim, Jun Sub | - |
dc.contributor.author | Chung, In Hyuk | - |
dc.contributor.author | Lee, Seung Yong | - |
dc.contributor.author | Han, JaeRyul | - |
dc.contributor.author | Park, Chansoo | - |
dc.contributor.author | Hwang, Seung Yong | - |
dc.date.accessioned | 2021-06-23T13:04:15Z | - |
dc.date.available | 2021-06-23T13:04:15Z | - |
dc.date.issued | 2010-06 | - |
dc.identifier.issn | 1976-0280 | - |
dc.identifier.issn | 2092-7843 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/39710 | - |
dc.description.abstract | A sexually transmitted disease (STD) is a common infection caused by various pathogens. Many other bacteria and viruses are associated with STDs. Infection of bacterial STD agents is sometimes not accompanied by symptoms. If an infected person who has no symptoms is not tested, infection control of an STD agent will fail and the infection may then be transmitted to a new person through sexual contact. Therefore, development of proper detection methods is important in control of STDs. In this study, we developed a microarray to detect infection of bacterial STD agents. We designed specific primers and probes for each STD pathogen and then hybridized with specific target amplified DNA. In conclusion, a DNA microarray-based detection method is ideal for detection of STDs because it offers simultaneous multi-targeting as well as fast and high-throughput detection. | - |
dc.format.extent | 5 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | 한국바이오칩학회 | - |
dc.title | An oligonucleotide microarray to detect pathogens causing a sexually transmitted disease | - |
dc.type | Article | - |
dc.publisher.location | 대한민국 | - |
dc.identifier.doi | 10.1007/s13206-010-4203-z | - |
dc.identifier.scopusid | 2-s2.0-79959255057 | - |
dc.identifier.wosid | 000279007800003 | - |
dc.identifier.bibliographicCitation | BioChip Journal, v.4, no.2, pp 105 - 109 | - |
dc.citation.title | BioChip Journal | - |
dc.citation.volume | 4 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 105 | - |
dc.citation.endPage | 109 | - |
dc.type.docType | Article | - |
dc.identifier.kciid | ART001451554 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kciCandi | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
dc.subject.keywordPlus | POLYMERASE-CHAIN-REACTION | - |
dc.subject.keywordPlus | REAL-TIME PCR | - |
dc.subject.keywordPlus | NEISSERIA-GONORRHOEAE | - |
dc.subject.keywordPlus | MYCOPLASMA-GENITALIUM | - |
dc.subject.keywordPlus | CHLAMYDIA-TRACHOMATIS | - |
dc.subject.keywordPlus | DIAGNOSIS | - |
dc.subject.keywordAuthor | STD | - |
dc.subject.keywordAuthor | Trichomonas vaginalis | - |
dc.subject.keywordAuthor | Neisseria gonorrhoeae | - |
dc.subject.keywordAuthor | Haemophilus ducreyi | - |
dc.subject.keywordAuthor | Mycroplasma hominis | - |
dc.subject.keywordAuthor | Mycoplasm genitalium | - |
dc.subject.keywordAuthor | Candida albicans | - |
dc.subject.keywordAuthor | Microarray | - |
dc.subject.keywordAuthor | DNA chip | - |
dc.identifier.url | https://link.springer.com/article/10.1007/s13206-010-4203-z | - |
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