Paper
4 March 2014 Enhancing imaging depth by multi-angle imaging of embryonic structures
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Abstract
Because of the ease in generating transgenic/gene knock out models and accessibility to early stages of embryogenesis, mouse and rat models have become invaluable to studying the mechanisms that underlie human birth defects. To study precisely how structural birth defects arise, Ultrasound, MRI, microCT, Optical Projection Tomography (OPT), Optical Coherence Tomography (OCT) and histological methods have all been used for imaging mouse/rat embryos. However, of these methods, only OCT enables live, functional imaging with high spatial and temporal resolution. However, one of the major limitations of conventional OCT imaging is the light depth penetration, which limits acquisition of structural information from the whole embryo. Here we introduce new imaging scheme by OCT imaging from different sides of the embryos that extend the depth penetration of OCT to permit high-resolution imaging of 3D and 4D volumes.
© (2014) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Narendran Sudheendran, Chen Wu, Mary E. Dickinson, Irina V. Larina, and Kirill V. Larin "Enhancing imaging depth by multi-angle imaging of embryonic structures", Proc. SPIE 8953, Optical Methods in Developmental Biology II, 895306 (4 March 2014); https://doi.org/10.1117/12.2045529
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Cited by 3 scholarly publications.
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KEYWORDS
Optical coherence tomography

Imaging systems

3D image processing

Glasses

3D acquisition

Image resolution

Stereoscopy

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