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Cited 57 time in webofscience Cited 60 time in scopus
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dc.contributor.authorYun, Seong-Wook-
dc.contributor.authorLeong, Cheryl-
dc.contributor.authorZhai, Duanting-
dc.contributor.authorTan, Yee Ling-
dc.contributor.authorLim, Linda-
dc.contributor.authorBi, Xuezhi-
dc.contributor.authorLee, Jae-Jung-
dc.contributor.authorKim, Han Jo-
dc.contributor.authorKang, Nam-Young-
dc.contributor.authorNg, Shin Hui-
dc.contributor.authorStanton, Lawrence W.-
dc.contributor.authorChang, Young-Tae-
dc.date.accessioned2018-06-15T05:18:35Z-
dc.date.available2018-06-15T05:18:35Z-
dc.date.created2017-09-08-
dc.date.issued2012-06-
dc.identifier.issn0027-8424-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/50334-
dc.description.abstractFluorescent small molecules have become indispensable tools for biomedical research along with the rapidly developing optical imaging technology. We report here a neural stem cell specific boron-dipyrromethane (BODIPY) derivative compound of designation red 3 (CDr3), developed through a high throughput/content screening of in-house generated diversity oriented fluorescence library in stem cells at different developmental stages. This novel compound specifically detects living neural stem cells of both human and mouse origin. Furthermore, we identified its binding target by proteomic analysis as fatty acid binding protein 7 (FABP7), also known as brain lipid binding protein) which is highly expressed in neural stem cells and localized in the cytoplasm. CDr3 will be a valuable chemical tool in the study and applications of neural stem cells.-
dc.languageEnglish-
dc.publisherNATL ACAD SCIENCES-
dc.relation.isPartOfPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.subjectRADIAL GLIAL-CELLS-
dc.subjectNEURONAL LINEAGE-
dc.subjectDIFFERENTIATION-
dc.subjectNEUROGENESIS-
dc.subjectPROTEINS-
dc.subjectGENE-
dc.titleNeural stem cell specific fluorescent chemical probe binding to FABP7-
dc.typeArticle-
dc.identifier.doi10.1073/pnas.1200817109-
dc.type.rimsART-
dc.identifier.bibliographicCitationPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.109, no.26, pp.10214 - 10217-
dc.identifier.wosid000306291400032-
dc.date.tcdate2019-02-01-
dc.citation.endPage10217-
dc.citation.number26-
dc.citation.startPage10214-
dc.citation.titlePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.citation.volume109-
dc.contributor.affiliatedAuthorChang, Young-Tae-
dc.identifier.scopusid2-s2.0-84863004107-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc35-
dc.type.docTypeArticle-
dc.subject.keywordPlusRADIAL GLIAL-CELLS-
dc.subject.keywordPlusNEURONAL LINEAGE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusNEUROGENESIS-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusGENE-
dc.subject.keywordAuthorBLBP-
dc.subject.keywordAuthorDOFL-
dc.subject.keywordAuthorhigh throughput screening-
dc.subject.keywordAuthormass spectrometry-
dc.subject.keywordAuthorradial glia-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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