Примери за използване на Juvenile rats на Английски и техните преводи на Български
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In juvenile rats the types of toxicity do not differ qualitatively from those observed in adult rats. .
Reduced acoustic startle response was observed in juvenile rats 1-2 weeks after exposure at>
Studies in juvenile rats reveal transient effects on neurobehaviour,
In juvenile rats, brivaracetam exposure levels 6- to 15-fold the clinical AUC exposure at the maximum recommended dose induced developmental adverse effects(i.e. mortality,
The main effects reported after repeated administration of propranolol in adult and juvenile rats were a transient decrease in body weight
Treatment of juvenile rats from postnatal Day 4 to Day 114 caused reduced body weight gain leading to secondary effects on development(slight delay of descensus testis,
In juvenile rats, the changes consisted of thickening of trabecular bone
Most adverse effects observed in the juvenile rats were similar to those seen in the repeated-dose toxicity studies of zonisamide in adult rats,
Findings of cataracts were observed in juvenile rats dosed with ivacaftor at 0.32 times the maximum recommended human dose based on systemic exposure of ivacaftor
Most adverse effects observed in the juvenile rats were similar to those seen in the repeated-dose toxicity studies of zonisamide in adult rats,
In a repeat dose toxicity study in juvenile rats, cobimetinib systemic exposures were 2 to11 fold higher on post natal day 10 than on post natal day 38 when exposures were similar to those in adult rats. .
definitive studies in juvenile rats were similar to those observed in adult mice,
Findings of cataracts were observed in juvenile rats dosed from postnatal Day 7 through 35 with dose levels of 10 mg/kg/day
In juvenile rats, cobimetinib administration resulted in similar changes as seen in the pivotal toxicity studies in adults,
high acute toxicity in juvenile rats are caused by immature MDR1,
Dapagliflozin: Direct administration of dapagliflozin to weanling juvenile rats and indirect exposure during late pregnancy(corresponding to the second and third trimesters of
pelvic dilation in juvenile rats was seen only at 100 mg/kg/day,
the exposure at the NOAEL(no observed adverse effect level) in juvenile rats treated as early as postnatal day 7 was 0.3-fold that of adult patients at 25 mg twice daily,
Larotrectinib was administered to juvenile rats from postnatal day(PND)
For the surviving juvenile rats, no effects on behavioural or reproductive performance were observed.