cellular
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• frequent anaphase bridging in the intestinal crypt cells in late generation homozygous mice
|
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• successive generational intercrosses yielded mice with progressively shorter telomeres
• the third/fourth generation showed classic cytogenetic and constitutional signs of telomere dysfunction
|
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• frequent apoptosis and p53 induction in the intestinal crypt cells in late generation homozygous mice
|
liver/biliary system
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• marked reduction in the incidence of early neoplastic lesions of hepatocellular carcinoma initiation
|
reproductive system
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• in late generation homozygous mice
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• in late generation homozygous mice
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• in late generation homozygous mice
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neoplasm
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• reduced incidence of induced hepatocellular carcinoma after CCl4 treatment in late generation (G3/4) homozygous mice compared to early generation (G0) mice
|
|
• marked reduction in the incidence of early neoplastic lesions of hepatocellular carcinoma initiation
|
homeostasis/metabolism
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• reduced incidence of induced hepatocellular carcinoma after CCl4 treatment in late generation (G3/4) homozygous mice compared to early generation (G0) mice
|
endocrine/exocrine glands
|
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• in late generation homozygous mice
|


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