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All mice were monitored for body weight change and survival rate.
Cows were monitored for body condition score, milk yield, dry matter intake, and energy balance from calving to week 8 postpartum, and blood was sampled weekly from 95 cows from calving to week 8 postpartum.
After treatment, animals were monitored for body weight and blood glucose.
Some mice were humanely killed so their lungs could be harvested; others were monitored for body weight and death.
For carcinogenesis experiments, treatments were continued up to 8 months of age, and during this time animals were monitored for body weight and possible rectal bleeding.
During each visit, patients were monitored for body weight, blood pressure, serum creatinine levels, fasting plasma glucose levels, lipid profile, calcium, phosphorus, hemoglobin (Hb), and other parameters.
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Both groups of animals had also been monitored for daily body weight gain (gd-1), feed conversion ratio and final body weight at slaughter (kg).
Moreover, using small juvenile C. concholepas of ca. 20 mm of peristomal length, collected in the field, we monitored for the body size and live weight traits in laboratory and field rearing conditions.
The ferrets were monitored for changes in body temperature and weight and the presence of the following clinical symptoms: sneezing, lethargy, anorexia, nasal or ocular discharge, dyspnea, diarrhea, and neurological dysfunction.
In two separate experiments, 9 reconstituted and 6 non-reconstituted Rag2−/−/γc−/− mice were injected i.v. with K562 cells and were monitored for loss of body weight and tumor formation.
Ferrets were monitored for changes in body temperature and weight, and the presence of the following clinical signs: sneezing, lethargy, anorexia, nasal or ocular discharge, dyspnea, diarrhea, neurological dysfunction [33].
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