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The time of morbidity was recorded.
After 20 days, mice were challenged i.p. with 2.5×105 cells CMT.TAP1,2/Kb cells and the time of morbidity was recorded.
For detection of tumorigenicity, C57BL/6 mice or nude mice (each group, n = 10) were injected i.p. with 5×104 tumor cells (in 500 µl PBS), and the time of morbidity was recorded.
For tumor challenge experiments, C57BL/6 mice (each group, n = 10) were immunized i.p. with γ-irradiated tumor cells, and after a 20-day immunization the mice were challenged i.p. with live CMT.64 tumor cells (2.5×105 cells/mouse), and the time of morbidity was recorded.
Surgical morbidity was recorded in 126 (38%) patients.
Case-mix adjustment was applied and morbidity was recorded using a validated outcome measure.
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Toxicity and therapy-induced morbidity were recorded according to WHO criteria.
For these participants compliance and morbidity were recorded by weekly mobile phone calls; this is reflected in the different completion rates for morbidity and anthropometric measurements.
However, despite effective VEGF inactivation no increase in perioperative morbidity is recorded suggesting that VEGF activity is not essential in the immediate postoperative recovery period.
Speed of insertion and success rates, leak pressures (LP) at different cuff pressures, dynamic airway compliance, and signs of postoperative airway morbidity were recorded.
Since examination of clinical signs plays major role in toxicological testing [ 21], mortality and morbidity were recorded twice a day throughout the study.
More suggestions(15)
rate was recorded
morbidity was noted
morbidity was performed
morbidity were recorded
morbidity was associated
morbidity was influenced
morbidity was detected
morbidity was decreased
morbidity was studied
morbidity was limited
morbidity was observed
morbidity was measured
morbidity was found
morbidity was obtained
morbidity was related
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