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Expression of the above mentioned markers was characterized using a Gallios flow cytometer (Beckman Coultier, Mississauga, Canada).
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Unfortunately, the immunohistochemistry analysis of above mentioned markers were not performed in K9TCC 4Molly due to an insufficient size of biopsy sample obtained during the cystoscopy.Primary K9TCC 5Lilly cell line was established from biopsy sample of urinary bladder of a 13-year-old female mixed-breed dog.
A combination of the above-mentioned markers was used to characterize both cell types in more detail.
All the above mentioned markers and technologies are a matter of controversy, each having their advantages and drawbacks.
We believe that the methods of detection of the above mentioned virulence markers are reasonably easy and screening them in a clinical microbiology laboratory is a worthwhile exercise.
Morphology, phenotypic expression of above mentioned markers, and the ultrastructure of myofibroblastic cells were evaluated.
Furthermore, no association was detected between interdialytic weight gain and the mentioned markers (data not shown).
These findings could be partially explained by opposite correlations of mentioned markers with hsCRP and total cholesterol levels.
Briefly, we also want to mention markers that have been investigated on biopsies but did not show additional value.
It is noteworthy to mention that CA markers were specific for C. albicans [ 44, 66].
However, the co-occurrence of histone markers was not considered in all these methods mentioned above.
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