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Exact(10)
TMA blocks were sectioned to produce 4-µm sections.
Tissue blocks were sectioned to 7 μm increments.
The embedded blocks were sectioned to 5 μm perpendicular to the calcification layer.
Paraffin blocks were sectioned to 4 μm thickness and placed on positively charged glass slides.
Tissue blocks were sectioned to 5 μm, transferred to glass slides, and stained with hematoxylin/eosin.
The blocks were sectioned to obtain 400-nm-thick samples using a Diatome diamond knife.
Similar(50)
Tissue blocks were sectioned at thicknesses of 5 to 7 microns using a rotary microtome and mounted on glass slides.
Blocks were sectioned at 1 µm thickness up to the optic nerve for plastic sections and the same blocks were further sectioned at 70 nm thickness and stained with uranyl acetate and lead citrate for transmission electron microscopy, which was performed using a JEOL 1230 microscope.
To determine cell proliferation, tissue blocks were sectioned at 5 μm and placed on glass slides.
Blocks were sectioned at 5 microns.
After standard dehydration in ethanol series, paraffin embedded PG blocks were sectioned at a 4μm thickness.
More suggestions(15)
blocks were delivered to
blocks were reused to
blocks were allocated to
blocks were attributed to
blocks were added to
blocks were dried to
blocks were copied to
blocks were manufactured to
blocks were transferred to
blocks were installed to
blocks were exposed to
blocks were used to
blocks were subjected to
blocks were needed to
blocks were anchored to
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