mortality/aging
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• 16% of heterozygotes die within 1 year, due to lymphomas
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immune system
|
• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
• tumor cells are found outside the capsule
|
|
• majority of moribund mice have a huge thymus
|
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• cellularity is reduced to ~60% of wild-type level
|
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• most tumor cells are CD4+CD8+ with varying contribution by CD8 single positive cells
|
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• under non-competitive conditions, pro-B cell compartment is increased 2-fold relative to wild-type mice
• B cell numbers normalize at later developmental stages
|
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• T-cell development is partially blocked at the earliest pro-T cell stage
|
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• absolute numbers are significantly lower than in wild-type
|
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• absolute numbers are significantly lower than in wild-type
|
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• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
|
|
• all diseased mice show splenomegaly
|
|
• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
• tumor cells are found outside the capsule
|
|
• all diseased mice show lymphadenopathy
|
hematopoietic system
|
• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
• tumor cells are found outside the capsule
|
|
• majority of moribund mice have a huge thymus
|
|
• cellularity is reduced to ~60% of wild-type level
|
|
• most tumor cells are CD4+CD8+ with varying contribution by CD8 single positive cells
|
|
• under non-competitive conditions, pro-B cell compartment is increased 2-fold relative to wild-type mice
• B cell numbers normalize at later developmental stages
|
|
• T-cell development is partially blocked at the earliest pro-T cell stage
|
|
• absolute numbers are significantly lower than in wild-type
|
|
• absolute numbers are significantly lower than in wild-type
|
|
• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
|
|
• all diseased mice show splenomegaly
|
neoplasm
|
• mice develop lymphoma with a longer latency and at lower incidence than homozygotes
|
|
• most tumor cells are CD4+CD8+ with varying contribution by CD8 single positive cells
|
cardiovascular system
|
• extensive tumor infiltrates are found in the heart in moribund mice
|
digestive/alimentary system
|
• extensive tumor infiltrates are seen in salivary glands in moribund mice
|
endocrine/exocrine glands
|
• extensive tumor infiltrates are seen in salivary glands in moribund mice
|
|
• complete disruption of normal architecture by monomorphic population of medium-sized lymphoid cells
• tumor cells are found outside the capsule
|
|
• majority of moribund mice have a huge thymus
|
|
• cellularity is reduced to ~60% of wild-type level
|
|
• most tumor cells are CD4+CD8+ with varying contribution by CD8 single positive cells
|
liver/biliary system
|
• extensive tumor infiltrates are found in the liver in moribund mice
|
renal/urinary system
|
• extensive tumor infiltrates are found in kidneys of moribund mice
|
respiratory system
|
• extensive tumor infiltrates are found in lungs in moribund mice
|
growth/size/body
|
• all diseased mice show splenomegaly
|


Analysis Tools