mortality/aging
• median survival is 361 days compared with over 770 days for wild-type mice
|
neoplasm
• mice develop fewer hematological malignancy compared with Trp53tm1Thst homozygotes
|
• in most mice
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• in some mice
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• in some mice
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• in some mice
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immune system
N |
• mice exhibit normal thymic senescence staining and reactive oxygen species levels
|
• following gamma irradiation
• however, apoptosis response to dexamethasone is normal
|
• in most mice
|
• nonmalignant in most mice
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cellular
• mouse embryonic fibroblasts infected with retroviruses expressing E1A and HRasG12V exhibit increased tumor growth when injecgted subcutaneously in immunocompromised mice and tumors do not exhibit increased apoptosis after chemotherapy compared with when wild-type cells are used
|
• following whole body gamma irradiation, mice are resistant to apoptosis in the thymus, developing cerebellum and intestinal crypt compared with wild-type mice
|
• following gamma irradiation
• however, apoptosis response to dexamethasone is normal
|
hematopoietic system
• following gamma irradiation
• however, apoptosis response to dexamethasone is normal
|
• in most mice
|
• nonmalignant in most mice
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endocrine/exocrine glands
• following gamma irradiation
• however, apoptosis response to dexamethasone is normal
|
• in most mice
|
growth/size/body
• nonmalignant in most mice
|
muscle
• in some mice
|