Hand pose recovery with a single video camera

Author(s):  
K. Kwon ◽  
H. Zhang ◽  
F. Dornaika
Keyword(s):  
2018 ◽  
Vol 142 ◽  
pp. 223-230 ◽  
Author(s):  
Chaoqun Hong ◽  
Zhiqiang Zeng ◽  
Rongsheng Xie ◽  
Weiwei Zhuang ◽  
Xiaodong Wang

Author(s):  
Meysam Madadi ◽  
Sergio Escalera ◽  
Alex Carruesco ◽  
Carlos Andujar ◽  
Xavier Baro ◽  
...  
Keyword(s):  

Author(s):  
Iasonas Oikonomidis ◽  
Nikolaos Kyriazis ◽  
Antonis A. Argyros
Keyword(s):  

Author(s):  
Farid Abedan Kondori ◽  
Shahrouz Yousefit ◽  
Ahmad Ostovar ◽  
Li Liu ◽  
Haibo Li

2018 ◽  
Vol 79 ◽  
pp. 63-75 ◽  
Author(s):  
Meysam Madadi ◽  
Sergio Escalera ◽  
Alex Carruesco ◽  
Carlos Andujar ◽  
Xavier Baró ◽  
...  

Author(s):  
Stephen R. Bolsover

The field of intracellular ion concentration measurement expanded greatly in the 1980's due primarily to the development by Roger Tsien of ratiometric fluorescence dyes. These dyes have many applications, and in particular they make possible to image ion concentrations: to produce maps of the ion concentration within living cells. Ion imagers comprise a fluorescence microscope, an imaging light detector such as a video camera, and a computer system to process the fluorescence signal and display the map of ion concentration.Ion imaging can be used for two distinct purposes. In the first, the imager looks at a field of cells, measuring the mean ion concentration in each cell of the many in the field of view. One can then, for instance, challenge the cells with an agonist and examine the response of each individual cell. Ion imagers are not necessary for this sort of experiment: one can instead use a system that measures the mean ion concentration in a just one cell at any one time. However, they are very much more convenient.


Author(s):  
Rudolf Oldenbourg

The recent renaissance of the light microsope is fueled in part by technological advances in components on the periphery of the microscope, such as the laser as illumination source, electronic image recording (video), computer assisted image analysis and the biochemistry of fluorescent dyes for labeling specimens. After great progress in these peripheral parts, it seems timely to examine the optics itself and ask how progress in the periphery facilitates the use of new optical components and of new optical designs inside the microscope. Some results of this fruitful reflection are presented in this symposium.We have considered the polarized light microscope, and developed a design that replaces the traditional compensator, typically a birefringent crystal plate, with a precision universal compensator made of two liquid crystal variable retarders. A video camera and digital image processing system provide fast measurements of specimen anisotropy (retardance magnitude and azimuth) at ALL POINTS of the image forming the field of view. The images document fine structural and molecular organization within a thin optical section of the specimen.


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