Stereoscope Imaging
Stereoscope Imaging - Related Videos
08:04
Measuring Sensitivity to Viewpoint Change with and without Stereoscopic Cues
0 Views •
Cited by 1 •
2013
We discuss a novel method forviewpoint-rotation of visual stimuli, and demonstrate using a mirror stereoscopethe three-dimensional percept of rotation-in-depth. The technique can be used to investigate the role of stereoscopic cues in encoding viewpoint-rotated figures.
13:45
Hybrid µCT-FMT imaging and image analysis
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Cited by 34 •
2015
We describe a protocol for hybrid imaging, combining fluorescence-mediated tomography (FMT) with micro computed tomography (µCT). After fusion and reconstruction, we perform interactive organ segmentation to extract quantitative measurements of the fluorescence distribution.
10:39
Contrast Imaging in Mouse Embryos Using High-frequency Ultrasound
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Cited by 4 •
2015
Here, we present a protocol to inject ultrasound microbubble contrast agents into living, isolated late-gestation stage murine embryos. This method enables the study of perfusion parameters and of vascular molecular markers within the embryo using contrast-enhanced high-frequency ultrasound imaging.
09:08
Multiple-mouse Neuroanatomical Magnetic Resonance Imaging
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Cited by 59 •
2011
Magnetic resonance imaging (MRI) has become an increasingly popular tool for examining the phenotype of genetically altered mice. This article illustrates the methods necessary to achieve high-throughput phenotyping of genetically altered mice using multiple-mouse MRI.
06:46
Non-invasive In Vivo Fluorescence Optical Imaging of Inflammatory MMP Activity Using an Activatable Fluorescent Imaging Agent
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Cited by 4 •
2017
This paper explains the application of fluorescent imaging using an activatable optical imaging probe to visualize the in vivo activity of key matrix metalloproteinases in two different experimental models of inflammation.
FAQs
Depth perception depends on binocular disparity, the small difference between the left- and right-eye views. In Stereoscope Imaging, paired optical paths preserve these distinct perspectives so the visual system can infer surface relief and relative position. This makes depth information available for interpreting how parts of an intact specimen are arranged, rather than viewing structure as a flat image.
Distinct angles provide the visual difference needed for depth estimation. The brain uses the mismatch between corresponding features in the two views as a cue to identify surface relief and spatial relationships. The paired perspectives are valuable because they encode organization across depth, helping distinguish how structures are positioned relative to one another within a specimen.
The method prioritizes depth perception and access to spatial organization over maximal magnification. That tradeoff makes it well suited to samples whose three-dimensional arrangement is important, even when the central goal is not to enlarge the smallest possible feature. In biology, this emphasis supports interpretation of form across an intact sample.
Its strongest biological value appears when a sample can be examined as an organized whole or when relationships among structures matter. Intact organisms, tissues, dissections, and developmental specimens can all benefit because their spatial arrangement remains visible in relief. The approach is therefore useful when preserving context provides more information than isolated high-magnification details.
A biological examination begins by viewing the specimen through paired optical paths and using the resulting relief to locate structures at different spatial positions. Because the sample remains accessible during viewing, the observer can manipulate it while monitoring how its parts relate in depth. This combines three-dimensional observation with direct handling of the specimen.
Applications include examining intact organisms, tissues, dissections, and developmental specimens. In each case, the technique is most informative when researchers need to understand how structures occupy space or connect within the sample. It supports biological research and teaching by making relief, depth, and three-dimensional organization available during direct visual examination.
The resulting view can reveal surface relief, relative depth, and spatial relationships among specimen structures. These observations help investigators describe organization in three dimensions and determine how parts are arranged within an intact or dissected sample. The approach is especially relevant when biological interpretation depends on structure-in-space rather than magnification alone.