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Ultraviolet (UV) microscopy was developed in the early 20th century by the German scientists August Köhler and Moritz von Rohr.
Orthogonal-plane fluorescence optical sectioning (OPFOS) microscopy was developed for the purpose of making quantitative measurements of the intact mammalian cochlea and to facilitate 3D reconstructions of complex features.
A new method for measuring the size of parasites and other objects using optical microscopy was developed using a specifically designed movable computer ruler (MCR) derived from digital images of a stage micrometer.
A unified theoretical framework for the recovery of second-order nonlinear susceptibility tensors and sample orientations from polarization-dependent second harmonic generation and sum frequency generation microscopy was developed.
Intravital microscopy was developed to study cochlear microvessels in guinea pigs in vivo [ 14, 15], and various animal models were established to assess cochlear blood flow.
Fluorescence microscopy was developed with the same device provided with an epifluorescence source and connected to a CANON Power Shot S50 camera linked to the CANON Remote Capture software.
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A method of ultraviolet-visible absorption microscopy is developed and applied to measure the concentration of Mitomycin C in preserved mouse tumor tissue, as well as in gelatin samples.
Bifocal 4D-microscopy was developed by Dr. Ralf Schnabel (Technical University, Braunschweig) in cooperation with Zeiss.
In this work a correlative optical and scanning electron microscopy technique was developed to locate and observe multi-modal gold core nanoparticle accumulation in brain tumor models.
To efficiently and accurately quantify the interactions of bacteria with mammalian cells, a reliable fluorescence microscopy assay was developed.
A new technique using the high spatial resolution of atomic force microscopy (AFM) was developed to measure the near-tip stress field.
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