mortality/aging
• 6 months after tamoxifen treatment, mice develop intestinal disease and eventually die or are sacrificed
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digestive/alimentary system
• tamoxifen-treated mice exhibit partial or complete fibrosis of the small intestine and cecum unlike in wild-type mice with increased submucosal connective tissue and proportional increase in fibroblast-like cells and collagenous matrix
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• tamoxifen-treated mice exhibit partial or complete fibrosis of the small intestine and cecum unlike in wild-type mice with increased submucosal connective tissue and proportional increase in fibroblast-like cells and collagenous matrix
|
• tamoxifen-treated mice exhibit partial or complete fibrosis of the small intestine and cecum unlike in wild-type mice with increased submucosal connective tissue and proportional increase in fibroblast-like cells and collagenous matrix
|
• in tamoxifen-treated mice
|
cardiovascular system
• in tamoxifen-treated mice
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renal/urinary system
• sclerotic glomeruli in tamoxifen-treated mice
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• in tamoxifen-treated mice
|
• enlarged glomeruli in tamoxifen-treated mice
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• in tamoxifen-treated mice
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neoplasm
• at between 44 and 76 weeks of age, 5 of 29 tamoxifen-treated mice develop sarcomas arising from dermis or muscle connective tissue
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muscle
• in tamoxifen-treated mice
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respiratory system
• around the bronchioles in tamoxifen-treated mice
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integument
tight skin
(
J:146617
)
• in tamoxifen-treated mice
|