Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XXV 2018
DOI: 10.1117/12.2289336
|View full text |Cite
|
Sign up to set email alerts
|

Volumetric bioimaging based on light field microscopy with temporal focusing illumination

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 44 publications
0
1
0
Order By: Relevance
“…Compared with computational approaches, optical sectioning achieved by physical means not only rejects background, but also removes its inherent shot noise. Yang combined holographic multi-spot two-photon excitation in 3D with light field imaging [ 28 ], and Hsu and colleagues achieved localized two-photon excitation in a plane 6.8 μm thick using temporal focusing in the light field [ 29 ]. These demonstrations have solved the background issue nicely, but the imaging speeds are limited by the low fluorescence excitation efficiency of two-photon microscopy.…”
Section: Considerations In Optimizing Light Field Microscopymentioning
confidence: 99%
“…Compared with computational approaches, optical sectioning achieved by physical means not only rejects background, but also removes its inherent shot noise. Yang combined holographic multi-spot two-photon excitation in 3D with light field imaging [ 28 ], and Hsu and colleagues achieved localized two-photon excitation in a plane 6.8 μm thick using temporal focusing in the light field [ 29 ]. These demonstrations have solved the background issue nicely, but the imaging speeds are limited by the low fluorescence excitation efficiency of two-photon microscopy.…”
Section: Considerations In Optimizing Light Field Microscopymentioning
confidence: 99%