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Mouse feeding and exploratory behaviors were analyzed using a food-search-compulsion-apparatus (FSCA), which was designed to distinguish between the two behaviors under standard living conditions.
Mouse feeding and exploratory behaviors were analyzed using a food search compulsion apparatus, which was designed to distinguish between the two behaviors under standard living conditions.
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Mice were housed in filter-top micro isolator cages and provided with commercial mouse feed and water ad libitum.
For in vivo studies Swiss albino mice were taken, which were housed in well-ventilated cages and fed with standard mouse feed and water ad libitum.
Nonfasting, randomly sampled glucose and insulin levels were obtained from mice fed ad libitum as an appropriate and acceptable method based on mouse feeding habits and the stress caused by fasting [ 11].
Non-fasting, randomly sampled glucose and insulin levels were obtained from mice fed ad libitum, as an appropriate and acceptable method based on mouse feeding habits and the stress caused by fasting [ 23].
SPF mice fed the same autoclaved chow did not develop increased IgE, and germ-free mice fed and raised on an antigen-free elemental diet also developed high IgE levels.
First, we analyzed carotenoid levels in the mice feed and liver extracts from low-fat and high-fat-fed mice to verify that β-Carotene from the algal powder accumulated in tissues following its absorption.
A total of 117 genes are differentially expressed both between mice fed human and chimpanzee diets and between humans and chimpanzees in liver (Table S5).
Mesenteric arteries from Apoe−/− and Apoe−/−/IL-R1−/− mice fed Western and WHC diets did not differ in their sensitivity to phenylephrine (PE) (table S3).
The caecal and colonic contents of mice fed chokeberry and bilberry had a dark purple to black colour suggesting high concentration of anthocyanins in the gut.
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