1 lated and cultivated with five species of mould, and sample images were captured.

2  images were captured centered on the fovea, and additional images were captured after steering the field of view inferio

3                                                             Images were captured and the measurements of retinal morpholo

4                                                             Images were captured as 12-bit tiff files and postprocessed t

5             To verify DEP response, fluorescence microscope images were captured before and after the electric excitation

6                                                        CIMT images were captured by a single ultrasonographer at 1 center

7                                                     The FAF images were captured centered on the fovea, and additional im

8                                           Light microscopic images were captured in 32 regions of each optic nerve.

9                                                             Images were captured on Bioptigen SD-OCT, Zeiss Cirrus HD-OCT

10 e 200 degrees pseudocolor and fundus autofluorescence (FAF) images were captured on the Optos 200 Tx Ultrawide-field devi

11 Rotational image sequences consisting of 40 two-dimensional images were captured using an optically corrected digital ima

12                                                  The SD-OCT images were captured using Macular Cube (200x200 or 512x128)

13                                              Cell migration images were captured with a camera attached to the microscope

14 ow-passage human SC cells using calcein AM fluorescent dye; images were captured with a confocal microscope, and data wer

15            Specimens were examined by light microscopy, and images were captured with a digital camera.

16            Specimens were examined by light microscopy, and images were captured with a digital camera.