In vivo confocal and multiphoton microendoscopy

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dc.contributor.authorKim, Pilhanko
dc.contributor.authorPuoris'haag, Mko
dc.contributor.authorCote, Dko
dc.contributor.authorLin, CPko
dc.contributor.authorYun, SHko
dc.date.accessioned2013-03-06T20:21:08Z-
dc.date.available2013-03-06T20:21:08Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2008-
dc.identifier.citationJOURNAL OF BIOMEDICAL OPTICS, v.13, no.1-
dc.identifier.issn1083-3668-
dc.identifier.urihttp://hdl.handle.net/10203/88335-
dc.description.abstractThe ability to conduct high-resolution fluorescence imaging in internal organs of small animal models in situ and over time can make a significant impact in biomedical research. Toward this goal, we developed a real-time confocal and multiphoton endoscopic imaging system. Using 1-mm-diameter endoscopes based on gradient index lenses, we demonstrate video-rate multicolor multimodal imaging with cellular resolution in live mice. (C) 2008 Society of Photo-Optical Instrumentation Engineers.-
dc.languageEnglish-
dc.publisherSPIE-SOC PHOTOPTICAL INSTRUMENTATION ENGINEERS-
dc.subjectENDOSCOPY-
dc.subjectMICROSCOPY-
dc.titleIn vivo confocal and multiphoton microendoscopy-
dc.typeArticle-
dc.identifier.wosid000254632300001-
dc.identifier.scopusid2-s2.0-44649125728-
dc.type.rimsART-
dc.citation.volume13-
dc.citation.issue1-
dc.citation.publicationnameJOURNAL OF BIOMEDICAL OPTICS-
dc.identifier.doi10.1117/1.2839043-
dc.contributor.localauthorKim, Pilhan-
dc.contributor.nonIdAuthorPuoris'haag, M-
dc.contributor.nonIdAuthorCote, D-
dc.contributor.nonIdAuthorLin, CP-
dc.contributor.nonIdAuthorYun, SH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorendoscopy-
dc.subject.keywordAuthorimaging-
dc.subject.keywordAuthorfluorescence-
dc.subject.keywordAuthormicroscopy-
dc.subject.keywordAuthorconfocal optics-
dc.subject.keywordAuthormultiphoton processes-
dc.subject.keywordPlusENDOSCOPY-
dc.subject.keywordPlusMICROSCOPY-
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