Примери за използване на Postnatal development на Английски и техните преводи на Български
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No studies were performed regarding pre- and postnatal development.
Peri- and postnatal development has not been studied.
However, animal studies have shown adverse effects on postnatal development.
Prenatal and postnatal development, including maternal function.
Studies in animals have shown toxicity with respect to postnatal development(see section 5.3).
Bulahbel. Postnatal development and physiological maturity of sheep ovar, 1990.
Fertility, prenatal development and postnatal development were unaffected in rats.
Thus, energy reserves are accumulated for use in the initial period of postnatal development.
The postnatal development of the spiral ganglion cells in the rat was studied from birth until the adult stage.
Sunitinib(0.3, 1.0, 3.0 mg/kg/day) was evaluated in a pre-and postnatal development study in pregnant rats.
In a rat pre- and postnatal development study, the no observed effect dose was 30 mg/ kg/ day.
Animal studies with empagliflozin have shown adverse effects on postnatal development(see section 5.3).
Animal studies have demonstrated that postnatal development of the intestine occurs faster in animals fed their mother's milk.
Animal studies do not indicate direct harmful effects with respect to pregnancy,parturition or postnatal development.
The effects of ipilimumab on prenatal and postnatal development were investigated in a study in cynomolgus monkeys.
Animal studies have not provided any evidencefor effects on fertility, or perinatal and postnatal development.
The potential effects of plerixafor on male fertility and postnatal development have not been evaluated in non-clinical studies.
In a postnatal study in rats,maternal exposure to sodium zirconium cyclosilicate had no effect on postnatal development.
No specific studies on fertility,early embryonic and postnatal development, or carcinogenicity studies were conducted(see section 5.3).
Animal studies are insufficient with respect to effects on pregnancy, embryonal/foetal development, parturition or postnatal development(see section 5.3).
An enhanced pre and postnatal development(ePPND) toxicity study in pregnant cynomolgus monkeys showed no evidence of teratogenic effects.
Controlled studies of the effects of exposure to eptotermin alfa on pre and postnatal development were performed in rabbit models.
In a pre- and postnatal development study, decreased pup weights and decreased postnatal survival were observed at exposures 4 and 21 times, respectively, the human exposure.
Studies in animals do not indicate direct harmful effects with respect to fertility, pregnancy, embryonic/foetal development, parturition, or postnatal development.
In the pre- and postnatal development study in rats, one dam died at parturition at 1000 mg/kg/day, and poor nursing, suppression of body weight gain and decrease in food consumption were noted at 30 and 1000 mg/kg/day.
However, animal studies do not indicate any direct or indirect negative effects on pregnancy, embryo-foetal development, parturition or postnatal development.
Animal studies do not indicate harmful effects with respect to pregnancy, embryonal/ foetal development, parturition or postnatal development(see section 5.3 Preclinical safety data).
Administration of azacitidine to male mice prior to mating with untreated female mice resultedin decreased fertility and loss of offspring during subsequent embryonic and postnatal development.
Animal studies do not indicate harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development(see section 5.3 Preclinical safety data).
The reproductive and developmental toxicity studies conducted in rats and rabbits with AF03 did not show any effects on female fertility, pregnancy,embryofetal development or early postnatal development.