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dc.contributor.authorWang, Nanen_US
dc.contributor.authorMiyazaki, Junen_US
dc.contributor.authorHe, Jinpingen_US
dc.contributor.authorSeto, Keisukeen_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2015-07-21T08:29:21Z-
dc.date.available2015-07-21T08:29:21Z-
dc.date.issued2015-05-15en_US
dc.identifier.issn0030-4018en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.optcom.2014.12.072en_US
dc.identifier.urihttp://hdl.handle.net/11536/124442-
dc.description.abstractPixel-by-pixel processed fluorescence difference microscopy is experimentally demonstrated by multiplexing excitation laser beams with Gaussian and donut spot shapes and then demultiplexing the fluorescent signals using lock-in amplifiers. With this scheme, a fixed sample of fluorescent spheres and a slice of mouse brain tissue are imaged with resolutions that exceed the diffraction limit. Compared to previously reported subtraction imaging techniques, this pixel-by-pixel scan can be applied to improve the resolution of a moving sample without introducing subtraction errors. The synchronized signal detection feature makes this method extendible to various applications. (C) 2014 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectConfocal microscopyen_US
dc.subjectMode multiplexingen_US
dc.subjectSuperresolutionen_US
dc.subjectImage processingen_US
dc.titleSub-diffraction-limit imaging using mode multiplexingen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.optcom.2014.12.072en_US
dc.identifier.journalOPTICS COMMUNICATIONSen_US
dc.citation.volume343en_US
dc.citation.spage28en_US
dc.citation.epage33en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000352045400005en_US
dc.citation.woscount2en_US
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