Figure 2.
Cumulative incidence of leukemia is delayed in the p50−/−;TCL1 mice. All experiments were carried out under protocols approved by The Ohio State University Institutional Animal Care and Use Committee. (A) A competing risks model was used to assess the occurrence of B-cell leukemia. The p50−/−;TCL1 mice had a significantly lower incidence of leukemia compared with p50+/+;TCL1 mice (subdistribution hazard ratio [SHR] for p50+/+ vs p50−/− = 3.53; 95% CI, 1.28, 9.72; P = .015). (B) The overall log-rank P value among the 3 genotypes was calculated and Kaplan-Meier estimates of the survival function are presented.

Cumulative incidence of leukemia is delayed in the p50/;TCL1 mice. All experiments were carried out under protocols approved by The Ohio State University Institutional Animal Care and Use Committee. (A) A competing risks model was used to assess the occurrence of B-cell leukemia. The p50/;TCL1 mice had a significantly lower incidence of leukemia compared with p50+/+;TCL1 mice (subdistribution hazard ratio [SHR] for p50+/+ vs p50/ = 3.53; 95% CI, 1.28, 9.72; P = .015). (B) The overall log-rank P value among the 3 genotypes was calculated and Kaplan-Meier estimates of the survival function are presented.

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