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There was no effect of CPS on the basal, minimum or maximum core body temperature of offspring in 12L:12D or during constant darkness.
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To our knowledge, there has not yet been any reported evaluation by ultrasonography of the effect of CP on distal femoral cartilage.
The co-administration of CP with DPPD or l-cysteine significantly reduced the elevation in LPO, however the co-administration of CP with Vit C, DPPD or l-cysteine reduced the effect of CP on superoxide anion and antioxidant enzymes and also on the antioxidants contents.
Data presented in Table 1 and Fig. 4 showed the genotoxic effect of CP on hepatocytes and the protective role of ABG.
The effect of CP on survival after primary-tumour excision on Day 10 was observed.
Lastly, we examined an in vivo effect of CP on innate immune response in arthritis using K/BxN serum transfer arthritis model and found that CP treatment significantly inhibited inflammation and joint swelling.
Based on recent results, cultures of primary rat hepatocytes and pneumocytes have been selected as key cellular models in the investigation of possible adverse effects of CPs on the DNA level and thus their genotoxicity [ 28– 30].
In order to illustrate the behavioral regulation of the rare minnow in CP stress, the current study was therefore performed to assess the effects of CPs on the aquatic environment by examining the behavioral effects of arprocarb, carbofuran, and oxamyl with an online monitoring system and Self-Organizing Map analysis.
They investigated the effects of CP on the length of hospital stay, complications, hospital cost, and functional outcomes.
The present experiment was conducted to examine the effects of CP on white matter and hippocampal damage induced by chronic cerebral hypoperfusion.
The present studies in mice and cancer-bearing patients, treated with C. parvum (CP) immunotherapy, were to determine the effects of CP on the production of immune complexes (IC) and associated disease.
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