mortality/aging
N |
• pIpC-treated mice have a normal lifespan
|
• mice treated with pIpC and Moloney murine leukemia virus (MMLV) exhibit increased morbidity and mortality with all mice dying by 6 months of age unlike with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
|
hematopoietic system
N |
• pIpC-treated mice exhibit no abnormalities in peripheral blood
|
• pIpC-treated mice exhibit an increase in B cell precursors in the bone marrow compared with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
|
• pIpC-treated mice exhibit an increase in B cell precursors in the bone marrow compared with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
|
neoplasm
• mice treated with pIpC and Moloney murine leukemia virus (MMLV) exhibit increased morbidity and mortality with all mice dying by 6 months of age unlike with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
• mice treated with pIpC and MMLV develop only acute B-progenitor and lineage marker negative leukemias as early as 2.6 months compared with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes that develop T cell leukemias at 4 to 6 months
|
homeostasis/metabolism
• pIpC-treated and Moloney murine leukemia virus (MMLV)-exposed mice develop microthrombi
|
immune system
• pIpC-treated mice exhibit an increase in B cell precursors in the bone marrow compared with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
|
• pIpC-treated mice exhibit an increase in B cell precursors in the bone marrow compared with similarly treated Tcf3tm1(TCF3/HLF)Homy heterozygotes
|