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Moreover, we shed some light to evaluate the saturation throughput behavior with respect to the tradeoff factor.
Like NIRS, DCS also uses the biological window to penetrate in deep tissue but DCS uses intensity correlation of the scattered light to evaluate the motion of the scatterers, i.e. in this case red blood cells [ 22].
We predicted that choosy individuals should develop either higher acuity or greater sensitivity to light to evaluate the small dorsal eyespot centers, i.e. WS females and DS males should have more facets and/or larger facets than their non-choosy DS and WS same-sex forms.
In particular, we have developed a portable optical instrument using visible-near-infrared light to evaluate the local microcirculation of periodontal tissues by measuring tissue hemoglobin concentrations and oxygen saturation in a non-invasive and real-time manner [ 13, 16, 17, 23].
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Colorimetric measurements were performed with a Konica Minolta CM600D VIS light spectrometer to evaluate the aesthetic effect of treatments.
Sections of S. stipitis beads from t 0 and t F were analyzed in light microscopy to evaluate the cells distribution and the effect of bdHSSL inside the calcium alginate matrix.
Sections were stained with hematoxylin-eosin (H&E) and examined under light microscopy to evaluate and liver damage.
Morphology of untreated and treated SH-SY5Y cells was observed under light microscope, to evaluate apoptotic features of the cells.
The sections were stained with hematoxylin and eosin, periodic acid Schiff, silver methenamine, and masson trichrome stains for light microscopy to evaluate the glomerular, interstitial, and vascular changes.
Sections (2 μm thick) were stained with haematoxylin and eosin (H & E) before examination under light microscopy to evaluate the degenerative changes of myelinated nerve fibres.
Collectively, this ex vivo characterization helped identify a subset of implanted NIR light sources to evaluate in an in vivo context.
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