The Indian cleverness was using its traditional knowledge, however, scientifically validating it and making that journey from men to mice to men, not molecule to mice to men, you know.

Some people have a terror of mice.

It's a species close to human, with several advantages over mice

As long as he is alive.

The results of long term carcinogenicity studies in rats and mice did not show any carcinogenic potential relevant for humans.

The relevance of this mouse data to humans is unknown.

In general, however, nonsteroidal triphenylethylene derivatives are predominantly anti estrogenic in rats and man and estrogenic in mice.

It is produced in mice and purified so that it can be used in humans.

The results of long term carcinogenicity studies with lamivudine in rats and mice did not shown any carcinogenic potential.

The results of long term carcinogenicity studies with lamivudine in rats and mice did not shown any carcinogenic potential.

But what we found was that we couldn't reproduce in man the data we had shown in mice.

Carcinogenicity studies showed an increased incidence of hepatic and pulmonary tumours in female mice, but not in male mice.

119 Carcinogenicity studies showed an increased incidence of hepatic and pulmonary tumours in female mice, but not in male mice.

Rotigotine did not influence male fertility in rats, but clearly reduced female fertility in rats and mice, because of the effects on prolactin levels which are particularly significant in rodents.

In mice and human beings that lack CCR5 receptors through genetic deletion, no significant adverse consequences have been reported.

Mice, rabbits, guinea pigs...

Let's have it.

In embryo foetal development studies in mice and rats, reductions in maternal body weight were found only in mice.

In mice, no increased incidence of tumours was found at exposures

The related razoxane has been demonstrated to be embryotoxic in mice, rats and rabbits and teratogenic in rats and mice.

Carcinogenicity studies have not been conducted with temsirolimus however, sirolimus, the major metabolite of temsirolimus in humans, was carcinogenic in mice and rats.

Busulfan is teratogen in rats, mice and rabbits.

The vaccine was immunogenic in mice and rabbits.

This has all moved very quickly, and the mouse experiments of hibernating mice happened in 2005 the first human studies were done in 2008, and we should know in a couple of years whether it works or not.

The increase in liver tumours with prasugrel administration in mice is not considered a relevant human risk.

In carcinogenicity studies, nevirapine induces hepatic tumours in rats and mice.

This was not seen in monkeys, dogs or mice.

And the answer, of course, lies with mice.

And also in mice and mice are mammals like us.

And I think if you compare the natural history of flies and mice, it's really comparable.

Carcinogenicity studies using efavirenz showed an increased incidence of hepatic and pulmonary tumours in female mice, but not in male mice.

Fixing permission problems on Logitech mice

Sitagliptin was not carcinogenic in mice.

Immunomodulatory effects have been observed in mice.

Etoricoxib was not carcinogenic in mice.

Yes. You know your mice well.

How about a hundred bucks?

The increased incidence of these tumours in mice is considered not to represent a significant risk to humans based on the lack of genotoxicity of vildagliptin and its principal metabolite, the occurrence of tumours only in one species, and the high systemic exposure ratios at which tumours were observed.

We would see a greater range of defects than we do in animals like mice because it is easier to analyze human behavior and physiology.

Carcinogenicity studies in male mice, male and female rats were negative.

There was also more payment for the extermination of mice, hamsters and wasps.

Single dose toxicity studies were carried out in rats and mice.

Decreased platelet counts were noted in the mouse and rat studies.

Laboratory studies in mice and rats have shown evidence of embryotoxic effects.

Laboratory animal studies in mice and rats have shown evidence of embryotoxic effects.