mortality/aging
|
• with earlier onset of disease than in heterozygous mice
|
immune system
|
• at 4 months
|
|
• in the bone marrow and spleen
|
|
• in the bone marrow and spleen
|
|
• in the bone marrow and spleen
|
|
• progression through the cell cycle (G0 to G1 and S to G2/M) in B cells is delayed compared to in wild-type cells
• B cells exhibit increased viability compared with wild-type cells
|
neoplasm
|
• with earlier onset of disease than in heterozygous mice
|
hematopoietic system
|
• at 4 months
|
|
• in the bone marrow and spleen
|
|
• in the bone marrow and spleen
|
|
• in the bone marrow and spleen
|
|
• progression through the cell cycle (G0 to G1 and S to G2/M) in B cells is delayed compared to in wild-type cells
• B cells exhibit increased viability compared with wild-type cells
|
growth/size/body
|
• at 4 months
|


Analysis Tools