digestive/alimentary system
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• decreased adenoma and microadenoma compared with ApcMin heterozygotes without a change in intestinal crypt apoptosis and proliferation rates
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mortality/aging
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• mice survive longer than ApcMin heterozygotes
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neoplasm
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• decreased adenoma and microadenoma compared with ApcMin heterozygotes without a change in intestinal crypt apoptosis and proliferation rates
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Analysis Tools