1
All positive cases showed dot-like cytoplasmic staining; nuclear staining was not seen.
2
DNA gel electrophoresis and nuclear staining were performed for cell apoptosis assay.
3
They were positive for cytokeratin and showed nuclear staining for calretinin.
4
Immunofluorescent studies showed neutrophils to have a lobulated pattern suggestive of nuclear staining.
5
Cells in the tissue microarray showed nuclear staining for phosphorylated Stat3 in all instances.
6
Early-stage apoptotic cells were marked by crescent-shaped or granular yellow-green acridine orange nuclear staining.
7
The extent of nuclear staining of epithelial cells in the cholesteatomas studied was significantly increased.
8
After 24-h incubation, apoptosis was quantified by flow cytometry by using propidium iodide nuclear staining.
9
Most of the proteins showed nuclear staining, whereas some also showed cytoplasmic or membranous staining.
10
None of the surrounding non-tumorous tissues expressed nuclear staining.
11
Intense nuclear staining was present in tumor cells that occurred in groups or in isolated form.
12
Principal findings: DJ-1 in RPE cells under baseline conditions, displays a diffuse cytoplasmic and nuclear staining.
13
Immunohistochemistry and nuclear staining showed that nearly all rodent and human taste cells express this channel.
14
Sections were scored according to staining intensity and the proportion of epithelial cells showing nuclear staining.
15
In contrast to normal skin, keratinocytes of basal and suprabasal layers showed nuclear staining in cholesteatoma epithelium.
16
Moreover, multinucleated giant cells with deep nuclear staining and distributed in pseudovascular spaces were found within the tumor.
