Exact(22)
Cryopreserved tumour samples were standard HE stained.
Histology of all other organs was examined on Haematoxylin/Eosin (HE) stained sections.
Deparaffinized sections (3 5 μm) were Haematoxylin Eosin (HE) stained using a standard protocol.
Areas of necrosis, determined using Hematoxylin and Eosin (HE) stained consecutive tumor sections, were excluded from analysis.
Sections were HE stained, using standard protocol (Htx 4 min, Eosin 30 s) for orientation and examination of tissue conditions.
The resected pathological specimens were hematoxylin-eosin (HE) stained.
Similar(38)
Due to less reliable NeuN staining in post-mortem tissue, neurons of autopsy controls were counted on HE-stained sections.
Histopathological analysis was performed by scoring of the tissue damage observed in HE-stained kidney sections from euthanized mice.
HE-stained sections served to assess any morphological alterations.
Histopathology was investigated in paraffin-embedded HE-stained tissue sections.
Then, images of the corresponding HE-stained fields were captured.
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