Examples of using Embryonic development in English and their translations into Finnish
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How is the embryonic development.
This receptor is highly expressed during embryonic development.
No effects on fertility or early embryonic development were noted in animals see section 5.3.
Typically, these deviations occur in the first six weeks of embryonic development.
A later stage of embryonic development considered at a certain point in time, almost five days after fertilisation.
During this period the embryonic development.
In a fertility and early embryonic development study in rats, atazanavir altered oestrus cycling with no effects on mating or fertility.
Fertility and early embryonic development.
In a fertility and early embryonic development study in rats, pomalidomide was administered to males and females at dosages of 25, 250, and 1000 mg/kg/day.
At exposures sufficiently in excess of exposure in humans after therapeutic doses, empagliflozin had no adverse effects on fertility or early embryonic development.
In a fertility and early embryonic development study in rats, an increase in non-viable conceptuses was observed.
No studies were performed that covered fertility and early embryonic development see section 5.3.
In a non-clinical fertility and early embryonic development study in rats, atazanavir altered oestrus cycling with no effects on mating or fertility see section 5.3.
In this disease, the brain of the newborn at birth is a violation of embryonic development or genetic diseases.
In a fertility and early embryonic development study in rats, a male-mediated effect was observed at high doses(300 µg/kg/day, s.c.) and is consistent with the sedative effects of fentanyl in animal studies.
In this regard, we note that expression of exogenous,catalytically active Ago2 did not perturb embryonic development Supplemental Fig.
In rats, boceprevir induced reversible effects on fertility and early embryonic development in female rats at exposures 1.2-fold the human exposure at the recommended therapeutic dose.
At exposures sufficiently in excess of exposure in humans after therapeutic doses, empagliflozin had no adverse effects on fertility or early embryonic development.
A serious confirmation of this fact is research in the field of embryology, which studies the embryonic development of vertebrates, from the superclass of Pisces and ending with the class Mammals.
Animal studies show that empagliflozin crosses the placenta during late gestation to a very limited extent but do not indicate direct orindirect harmful effects with respect to early embryonic development.
Insufficient zinc content significantly increases the risk of spontaneous abortion, embryonic development defects, and later to premature birth, uterine inertia, low weight newborn crumbs.
The material allows you to maintain a healthy hormonal balance and increases the potency, improving blood flow to organs of male and female reproductive system,which in turn is good for the process of spermatogenesis and embryonic development.
In a fertility and early embryonic development study in rats, a male-mediated effect was observed at high doses(300 mcg/kg/day, s.c.) and is consistent with the sedative effects of fentanyl in animal studies.
Dasatinib did not affect male or female fertility in a conventional rat fertility and early embryonic development study, but induced embryolethality at dose levels approximating human clinical exposures.
In a fertility and early embryonic development study in rats, a male-mediated effect was observed at high doses(300 mcg/kg/day, s.c.) and is considered secondary to the sedative effects of fentanyl in animal studies.
Worth noting that multivitamin"Aevitum" sometimes prescribed during pregnancy for normal embryonic development, as its constituent retinol is of great importance for the development of the human body and the normal functioning of the muscular and nervous systems.
Eltrombopag did not affect female fertility,early embryonic development or embryofoetal development in rats at doses up to 20 mg/kg/day 2 times the human clinical exposure in adult or adolescent(12-17 years old) ITP patients at 75 mg/day and equivalent to the human clinical exposure in HCV patients at 100 mg/day, based on AUC.