High-throughput optical image crossbar switch that uses a point light source array

1993 ◽  
Vol 18 (5) ◽  
pp. 376 ◽  
Author(s):  
Masaki Fukui ◽  
Ken-ichi Kitayama
2009 ◽  
Author(s):  
Young-Tae Lim ◽  
Jae-Hyeung Park ◽  
Nam Kim ◽  
Ki-Chul Kwon

2001 ◽  
Vol 40 (Part 1, No. 8) ◽  
pp. 4913-4915 ◽  
Author(s):  
Sung-Sik Kim ◽  
Kwang-Hoon Sohn ◽  
Vladimir Savaljev ◽  
Eugene F. Pen ◽  
Jung-Young Son ◽  
...  

2018 ◽  
Vol 89 (6) ◽  
pp. 063108
Author(s):  
Wenze Xia ◽  
Yayun Ma ◽  
Shaokun Han ◽  
Yulin Wang ◽  
Fei Liu ◽  
...  

2017 ◽  
Vol 403 ◽  
pp. 110-114 ◽  
Author(s):  
Zi Wang ◽  
Anting Wang ◽  
Xiaohui Ma ◽  
Fenghua Ma ◽  
Hai Ming

2018 ◽  
Vol 2018 (4) ◽  
pp. 247-1-247-5 ◽  
Author(s):  
Hayato Watanabe ◽  
Masahiro Kawakita ◽  
Naoto Okaichi ◽  
Hisayuki Sasaki ◽  
Tomoyuki Mishina

Author(s):  
P.M. Houpt ◽  
A. Draaijer

In confocal microscopy, the object is scanned by the coinciding focal points (confocal) of a point light source and a point detector both focused on a certain plane in the object. Only light coming from the focal point is detected and, even more important, out-of-focus light is rejected.This makes it possible to slice up optically the ‘volume of interest’ in the object by moving it axially while scanning the focused point light source (X-Y) laterally. The successive confocal sections can be stored in a computer and used to reconstruct the object in a 3D image display.The instrument described is able to scan the object laterally with an Ar ion laser (488 nm) at video rates. The image of one confocal section of an object can be displayed within 40 milliseconds (1000 х 1000 pixels). The time to record the total information within the ‘volume of interest’ normally depends on the number of slices needed to cover it, but rarely exceeds a few seconds.


2020 ◽  
Vol 128 (7) ◽  
pp. 1889-1912
Author(s):  
Hiroaki Santo ◽  
Michael Waechter ◽  
Wen-Yan Lin ◽  
Yusuke Sugano ◽  
Yasuyuki Matsushita

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