Normal human bronchial epithelial HBE was used as normal control.
Experiment was designed as normal Control, 20% ethanol, 10% DF and 10% DF + 20% ethanol groups.
The fourth group comprised of age-matched rats that served as normal control.
In addition, 9 anonymized samples of histopathological verified reactive lymph node hyperplasia (RLH) were included as normal control.
Three groups were subjected to chronic mild stress and the fourth group served as normal control group.
Male rats were allocated into five groups of which one group received saline and served as normal control.
Animals were divided into different groups as normal control (untreated), glucose primed control, reference group (glucose primed + glibenclamide), test groups (glucose primed + test extract).
Furthermore, the human skin fibroblast strain AG01523 (Coriell Institute for Medical Research, Camden, NJ, USA) was also used as normal control.
The antitumor effects of these compounds were studied against two different MM cell lines (A375 and CN-mel) and a fibroblast cell line (BJ) as normal control.
Animals were divided into five different groups as normal control (NC), diabetic control (DC), reference group (RG), test group-1 (BR-1) (250 mg/kg), test group-2 (BR-2) (500 mg/kg) each group containing six animals.
Nephrectomized kidneys served as normal control kidneys.
