Примери за използване на Mice and monkeys на Английски и техните преводи на Български
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Flora is pathogenic for white mice and monkeys.
When tested on mice and monkeys, it proved 100 percent effective.
So the polio vaccine--developed using mice and monkeys.
Early tests on mice and monkeys proved to be 100 percent successful.
Chromosomal aberrations have also been detected in in vivo studies in mice and monkeys.
Studies in adult mice and monkeys have not demonstrated similar findings.
However, testicular effects were observed in mice and monkeys(see section 5.3).
These fared well in mice and monkeys, but when they were eventually tested in human clinical trials, they didn't work.
In the studies involving RAD140, also known as Testolone,testing was carried out mostly on mice and monkeys.
This can be successful with mice and monkeys, as their brains are stable.
Effects on fertility and Sertoli cells have been observed in rats but not in mice and monkeys.
Further tests in mice and monkeys suggest that IONIS-HTTRx is well tolerated, with no dose-limiting side effects.
The CRISPR technology has already been used to change the DNA in the cells of mice and monkeys, other organisms as well.
This technique was used in mice and monkeys, and it will be the first time to be used in humans.
In labs across the world, scientists have found ways of extending the lives of a range of organisms- from microscopic worms and flies to mice and monkeys.
The technique has been demonstrated in mice and monkeys, but this would be the first time it's been used in humans.
A drug that could target the cause of Huntington's disease has been safely and effectively tested in mice and monkeys, and human trials will follow.
Evidence in mice and monkeys suggests it is important for storing important immune cellsand may even make them more effective at fighting infection.
Although cladribine may have a potential for genotoxicity,long-term data in mice and monkeys did not provide any evidence of a relevant increased carcinogenicity risk in humans.
The increase of spontaneous abortion and/or resorption in animals with restricted PD-L1 expression(knock-out or anti-PD1/ PD-L1 monoclonal antibodies)has been shown in both mice and monkeys.
Testicular toxicity was not observed in mice and monkeys at the highest doses tested at exposures up to 4-foldand 2-fold, respectively, the exposures in humans at the RHD.
The primary target organs identified in the repeat-dose toxicology studies by parenteral routes(intravenous orsubcutaneous) up to 1-year duration in mice and monkeys were the lymphoid and haematopoietic system.
Everolimus appeared to spontaneously exacerbate background diseases(chronic myocarditis in rats, coxsackie virus infection of plasma and heart in monkeys, coccidian infestation of the gastrointestinal tract in minipigs,skin lesions in mice and monkeys).
Self-administration studies in rats, mice and monkeys have produced conflicting results, whereas tolerance to GHB as well as cross-tolerance to alcohol have been clearly demonstrated in rodents.
Effects of apremilast on pregnancy included embryofoetal loss in mice and monkeys, and reduced foetal weightsand delayed ossification in mice at doses higher than the currently recommended highest human dose.
Reproduction toxicology studies(rats, mice, rabbits and monkeys) showed no sign of embryotoxicity or teratogenicity.
The mean lethal doses in rats, mice, and cynomolgus monkeys were higher than 2000 mg/kg body weight.
Decreased platelet counts were observed in chronic toxicity studies in mice, rats and monkeys at 1.4 to 2-fold the human AUC at the recommended therapeutic inotersen dose.
Single and repeat-dose toxicity studies in mice, rats and monkeys showed the adverse responses that could be expected from an exaggerated pharmacodynamic impact of lepirudin.