digestive/alimentary system
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• fewer mature goblet cells in the colon with prevalent pregoblet cells
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• increased proliferation of cells in the colon
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• mice develop increased tumors in the large intestine, including the cecum and one third of the colons, compared with Apcmin heterozygotes
• mice develop sessile and pedunculated forms of colonic adenomas unlike Apcmin heterozygotes
• while tumor progression is stimulated to a greater extent than in Apcmin heterozygotes, tumor initiation is the same
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• noninvasive
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neoplasm
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• mice develop increased tumors in the large intestine, including the cecum and one third of the colons, compared with Apcmin heterozygotes
• mice develop sessile and pedunculated forms of colonic adenomas unlike Apcmin heterozygotes
• while tumor progression is stimulated to a greater extent than in Apcmin heterozygotes, tumor initiation is the same
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• noninvasive
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immune system
cellular
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• fewer mature goblet cells in the colon with prevalent pregoblet cells
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• increased proliferation of cells in the colon
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endocrine/exocrine glands
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• fewer mature goblet cells in the colon with prevalent pregoblet cells
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Analysis Tools