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No significant difference in albumin extravasation was detected between any of the groups at the light microscope level using the albumin marker.
Through this step chromatin acquires the appearance of a net with mesh size of 50 200 nm roughly corresponding to the average displacement of the chromatin domains observed at light microscope level.
At the light microscope level, we compared the intranuclear distribution of H2B-GFP-tagged H2B-GFP-tagged H2B-GFP-taggedf replichromatinbeled chromandn domains in the same individual cells in vivo, after fixation with 4% positionsldehyde, and after 3D-FISH.
However, our control experiments (Fig. S1) did not find any evidence for mistargeting of the GFP-APEX2-tagged S1R, at least at the confocal light microscope level.
In contrast, pyramidal neuron ultrastructure appeared normal in gerbils that exhibited complete area CA1b neuroprotection (defined at the light microscope level) by diazepam when studied two, seven or 30 days after ischemia.
Where DNA-barcoding proved inconclusive, algae were subjected to morphological examination at the light microscope level and images compared to online culture collections (e.g. the Culture Collection of Autotrophic Organisms (CCALA)).
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Analysis at both the light and electron microscope levels reveals a fully differentiated cornified layer in TCDD-treated organotypic cultures at earlier time points than observed in vehicle (dimethyl sulfoxide -treated controlsulfoxide -treated
These days with the help of various new techniques and increased computing power, the meso- and microscale (electron microscope) levels come into focus.
These are fluorescent nanocrystals with an electron-dense core, directly visible in the electron microscope, and well-suited for multiprotein labeling at both the light microscope and electron microscope levels (see below).
We see no apparent structural differences in those ELS that are Congo red birefringence-positive and those that are birefringence-negative, at either the light or electron microscope levels.
Examination of postmortem lungs among cases clinically diagnosed as ARDS identified a cohort that showed a consistent morphology at the light and electron microscope levels, and featured pathognomonic structures which we termed elastin-staining laminar structures (ELS).
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