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Current image analysis of SR microscopy data rely mostly on complex analytical tools and MatLab (www.mathworks.com) based routines.
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Secondly, the data rely on hospital coding.
The data relied on self-report.
A model accounting for the spatial variation of nanotube alignment relies on electron microscopy data and is consistent with the strong thickness dependence of the modulus data.
The fluorescent microscopy results were in accordance with our electron microscopy data.
Furthermore, there was a strong correlation between the TMP confocal microscopy data and results obtained using epifluorescence microscopy.
This was confirmed by confocal microscopy (data not shown).
Comparisons were made based on the patients with microscopy data.
SPSS was used to compute statistics for electron microscopy data.
Our scanning confocal microscopy data show differential localization of hornerin.
LD and EST acquired and analyzed the microscopy data.
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