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For example, a standard practice in microscopy images is to apply a Fast Fourier Transform FFTT).
The ultimate lateral resolution of the scanning Auger microscopy images is determined by this value.
A diagnostic method for protein conformational diseases (PCD) from microscopy images is proposed when such conformational conflicts involve muscular intranuclear inclusions (INIs) indicative of oculopharyngeal muscular dystrophy (OPMD), one variety of PCD.
Heterogeneous illumination of the field of view in light microscopy images is inversely related to objective magnification.
An example framework for spatio-temporal modelling and simulation based on the automatic detection and analysis of biochemical species in microscopy images is described in [ 64].
Although the features formed by PCN are clearly visible in Figure 3, the contrast between modified and virgin regions in the lateral force microscopy images is not strong.
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Confocal microscopy images were obtained using a fluorescence imaging system with laser excitation at 405 nm.
Microscopy images were recorded using an Olympus Cell^R imaging station with DIC setup.
Confocal microscopy images were acquired using an LSM 510 Meta microscope and imaging software (Zeiss).
Fluorescence images, together with transmission microscopy images were captured.
Fluorescence microscopy images are presented in Figure 3.
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