immune system
• DSS-treated mice exhibit increased weight loss, inflammation and colon length shortening compared with wild-type mice
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• in bronchoalveolar lavage fluid of mice treated with ovalbumin and alum to induce asthma
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• upon ovalbumin restimulation in mice treated with ovalbumin and alum to induce asthma
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• increased CCL2 in the colon tissue of DDS-treated mice compared with wild-type mice
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• increased IL22 in colon tissue of C. rodentium-infected mice
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• in the colon tissue of DDS-treated mice
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• in bronchoalveolar lavage fluid of mice treated with ovalbumin and alum to induce asthma
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• in bronchoalveolar lavage fluid of mice treated with ovalbumin and alum to induce asthma
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• in bronchoalveolar lavage fluid of mice treated with ovalbumin and alum to induce asthma
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• in the colon tissue of DDS-treated mice
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• in the colon tissue of DDS-treated mice
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• Citrobacter rodentium-infected mice exhibit mild weight loss and increased fecal bacterial burden and bacterial load in the liver and spleen compared with wild-type mice
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digestive/alimentary system
• DSS-treated mice exhibit increased weight loss, inflammation and colon length shortening compared with wild-type mice
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growth/size/body
• in DSS-treated mice
• Citrobacter rodentium-infected mice exhibit mild weight loss compared with wild-type mice
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hematopoietic system
• in bronchoalveolar lavage fluid of mice treated with ovalbumin and alum to induce asthma
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• upon ovalbumin restimulation in mice treated with ovalbumin and alum to induce asthma
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