mortality/aging
|
• mice die significantly earlier than wildtype in response to anti-FAS antibodies
|
immune system
|
• more susceptible to activation induced cell death
|
|
• enhanced susceptibility to FAS-induced apoptosis
|
|
• more rapid progression of acute fulminant hepatitis in response to anti-FAS antibodies
|
hematopoietic system
|
• more susceptible to activation induced cell death
|
|
• enhanced susceptibility to FAS-induced apoptosis
|
liver/biliary system
|
• within 2.5 hours after treatment with anti-FAS antibodies
|
|
• in response to anti-FAS antibodies
|
|
• more rapid progression of acute fulminant hepatitis in response to anti-FAS antibodies
|
|
• more rapid liver failure in response to anti-FAS antibodies
|
homeostasis/metabolism
|
• significant increase in the level of alanine aminotransferase in response to anti-FAS antibodies
|
|
• mice die significantly earlier than wildtype in response to anti-FAS antibodies
|
cardiovascular system
|
• within 2.5 hours after treatment with anti-FAS antibodies
|
cellular
|
• more susceptible to activation induced cell death
|
|
• enhanced susceptibility to FAS-induced apoptosis
|
|
• in response to anti-FAS antibodies
|
endocrine/exocrine glands
|
• enhanced susceptibility to FAS-induced apoptosis
|


Analysis Tools