dc.citation.conferencePlace |
CH |
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dc.citation.conferencePlace |
NTUH (National Taiwan University Hospital) |
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dc.citation.title |
Focus On Microscopy (FOM) 2016 |
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dc.contributor.author |
Min, Eunjung |
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dc.contributor.author |
Kandell, Mikhail E. |
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dc.contributor.author |
Lee, Junwon |
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dc.contributor.author |
Cho, Nam Hyun |
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dc.contributor.author |
Best-popescu, Catherine |
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dc.contributor.author |
Popesu, Gabriel |
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dc.contributor.author |
Jung, Woonggyu |
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dc.date.accessioned |
2023-12-19T21:07:51Z |
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dc.date.available |
2023-12-19T21:07:51Z |
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dc.date.created |
2016-03-31 |
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dc.date.issued |
2016-03-21 |
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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. |
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dc.identifier.bibliographicCitation |
Focus On Microscopy (FOM) 2016 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/41515 |
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dc.identifier.url |
http://www.focusonmicroscopy.org/ |
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dc.language |
영어 |
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dc.publisher |
Focus On Microscopy (FOM) 2016 |
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dc.title |
Spatial Light Interference Microscopy for Visualization of Wide-field Ex Vivo Mouse Brain Imaging |
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dc.type |
Conference Paper |
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dc.date.conferenceDate |
2016-03-20 |
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