Примери за използване на Dogs and monkeys на Английски и техните преводи на Български
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Cows, dogs and monkeys found asylum in the Asrama.
An increase in heart rate was observed in rats,rabbits, dogs and monkeys.
Cows, dogs and monkeys found asylum in his Ashrama.
Mainly reversible increases in cholesterol levels were seen in rats, dogs and monkeys.
People, camels, lots of cars, dogs and monkeys were everywhere around us.
The preclinical safety profile of fingolimod was assessed in mice,rats, dogs and monkeys.
Rats, dogs and monkeys tolerated daily doses of 2, 2.5 and 8 mg/ kg/ d respectively without harmful effects.
Now, another study has looked into whether that applies to animals,such as dogs and monkeys.
Investigation of QTc in dogs and monkeys showed no prolongation after administration of cilostazol or its metabolites.
The preclinical safety profile of fingolimod was assessed in mice, rats, dogs and monkeys.
Preclinical studies of tenofovir disoproxil fumarate conducted in rats, dogs and monkeys revealed effects on boneand a decrease in serum phosphate concentration.
Toxicology assessment of trifluridine/tipiracil hydrochloride was performed in rats, dogs and monkeys.
In mice, rats,rabbits, dogs and monkeys, pegaptanib distributes primarily into plasma volumeand is not extensively distributed to peripheral tissues after intravenous administration.
Non-clinical studies have been conducted in animal species including mice, rats,rabbits, dogs and monkeys.
Preclinical studies of tenofovir disoproxil fumarate conducted in rats, dogs and monkeys revealed target organ effects in gastrointestinal tract, kidney, bone and a decrease in serum phosphate concentration.
However, testicular and ovarian toxicity has been observed in rats, dogs, and monkeys(see section 5.3).
In repeated dose toxicity studies in rats, dogs and monkeys, lymphoid depletion/atrophy of lymph nodes, spleen and thymus, decreased erythrocytes, reticulocytes, leukocytes, and platelets(dog and monkey), in association with bone marrow hypocellularity, and adverse gastrointestinal effects(dog and monkey) were observed with eravacycline.
The toxicological profile of tasonermin has been investigated in preclinical studies using mice, rats,rabbits, dogs and monkeys.
In the repeat-dose studies, target organs for toxicity were the gastrointestinal tract(emesis in dogs and monkeys, diarrhoea and mucosal alteration), testes(decreased spermatogenesis), bone marrow(hypocellularity) and lymphoid organs(depletion/atrophy).
Elevated transaminase levels asociated with signs of hepatotoxicity,were also observed in rats, dogs and monkeys.
Being flightless, it nested on the ground, leaving its eggs and chicks tragically easy prey for pigs, dogs, and monkeys brought to the island by outsiders.
Preclinical toxicity studies have demonstrated the most commonly observed effects include bone marrow depression in rats, dogs and monkeys.
There is evidence from animal studies that high doses of ceftriaxone calcium salt led to formation of concrements and precipitates in the gallbladder of dogs and monkeys, which proved to be reversible.
The absolute bioavailability of pegaptanib after intravitreal administration has not been assessed in humans, butis approximately 70-100% in rabbits, dogs and monkeys.
Embryotoxicity manifesting as decreased foetal viability, reduced live litter sizes, and developmental delays has been reported in species including mice, hamsters,cats, dogs, and monkeys at doses comparable to human doses.
Acute toxicity studies were performed in rats, rabbits and monkeys Subacute toxicity studies were performed in rats, dogs and monkeys.
In preclinical safety studies candesartan had effects on the kidneys and on red cell parameters at high doses in mice,rats, dogs and monkeys.
Major findings in repeat-dose toxicity studies of lurasidone were centrally-mediated endocrine changes resulting from serum prolactin elevations in rats, dogs and monkeys.
In toxicology studies, plasma volume expansion with haemodilution, anaemia, and reversible eccentric cardiac hypertrophy was consistently apparent after repeated dosing of mice,rats, dogs, and monkeys.
The haematopoietic and lymphoid systems were the primary organs affected in toxicology studies conducted with mycophenolate mofetil in the rat,mouse, dog and monkey.