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정웅규

Jung, Woonggyu
Translational Biophotonics Lab.
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dc.citation.conferencePlace CH -
dc.citation.conferencePlace NTUH (National Taiwan University Hospital) -
dc.citation.title Focus On Microscopy (FOM) 2016 -
dc.contributor.author Min, Eunjung -
dc.contributor.author Kandell, Mikhail E. -
dc.contributor.author Lee, Junwon -
dc.contributor.author Cho, Nam Hyun -
dc.contributor.author Best-popescu, Catherine -
dc.contributor.author Popesu, Gabriel -
dc.contributor.author Jung, Woonggyu -
dc.date.accessioned 2023-12-19T21:07:51Z -
dc.date.available 2023-12-19T21:07:51Z -
dc.date.created 2016-03-31 -
dc.date.issued 2016-03-21 -
dc.description.abstract We introduce white light spatial light interference microscopy (SLIM) for ex-vivo mouse brain imaging. SLIM is label-free and non-invasive imaging technique [1,2], capable of visualizing nanoscale cytoarchitecture in the brain. By using two-dimensional scanning and mosaic algorithm, wide-field image of brain was obtained. Figure 1 shows schematic of SLIM (a) and wide-field SLIM image obtained by phase modulation technique (b). To further enhance the image contrast of anatomical structure in wide-field, light scattering property was calculated using phase image, which differentiates between myelinated axon and cell bodies. The system provides axial and transverse resolution of 1 µm and 0.4 µm, respectively. The imaging speed was 30 frames/sec. -
dc.identifier.bibliographicCitation Focus On Microscopy (FOM) 2016 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/41515 -
dc.identifier.url http://www.focusonmicroscopy.org/ -
dc.language 영어 -
dc.publisher Focus On Microscopy (FOM) 2016 -
dc.title Spatial Light Interference Microscopy for Visualization of Wide-field Ex Vivo Mouse Brain Imaging -
dc.type Conference Paper -
dc.date.conferenceDate 2016-03-20 -

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