Exact(3)
Details of the sheets are shown at high magnification below the main panels.
White boxes mark the axon initial segment, which is shown at a higher magnification below each image (scale bars, 10 µm).
(A, B ) Scanning electron microscopy (SEM) of inner (A ) and outer (B ) hair cells from Myo15 ΔN/ΔN, normal hearing Myo15 +/ΔN littermates and Myo15 sh2/sh2 cochleae at P4. Highlighted regions of IHC bundles (white boxes) are shown at higher magnification below.
Similar(56)
Below: Magnification X 25 (Masson-Goldner staining).
Higher magnification images (below) highlight the size difference between the small VGlut1 (green arrowheads) and large VGlut2 (red arrowheads) Nanogold particles.
The squares in the overview indicate locations of magnifications shown below for each group.
Below are high magnification images from areas marked with red boxes (1 4) in top panels.
This automated method is described below: Constant magnification in volume reconstruction is achieved to facilitate the forthcoming processing.
Orange squares mark the area of 40× magnification for the respective images below.
Confocal laser endomicroscopy (CLE) enables surface and subsurface imaging of living cells in vivo at ×1000 magnification and up to 250 μm below the tissue surface.
The stacked waveforms of the X phase are magnified relative to the stacked P wave, and the magnification factor for each trace is shown below the event name.
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