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. 2022 May 10;1(1):kyac002. doi: 10.1093/discim/kyac002

Figure 2:

Figure 2:

NKG2D expression drives disease severity. (a) Kaplan–Meier survival analysis of Apcmin/+;Klrk1+/+ (n = 40) and Apcmin/+;Klrk1−/− (n = 35) mice. (b) Correlation between number of small intestinal (SI) tumors and survival in Apcmin/+;Klrk1+/+ (top, red) and Apcmin/+;Klrk1−/− (bottom, blue) mice. (c) Number of tumors in the colon of Apcmin/+;Klrk1+/+ (n = 40) and Apcmin/+;Klrk1−/− mice (n = 35) at disease endpoint. (d) Hematocrit (HCT) measures from the blood of healthy Klrk1+/+ control mice (n = 8), Apcmin/+;Klrk1+/+ (n = 18) and Apcmin/+;Klrk1−/− (n = 15) mice at disease endpoint. Data points represent individual mice. SI: small intestine; HCT: hematocrit. Significance was determined using log-rank (Mantel–Cox) test (a), linear regression (b), Mann–Whitney U or unpaired t-test following Shapiro–Wilk normality test (c) and one-way analysis of variance (ANOVA) and Tukey’s multiple comparison test (d). *P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, and ****P ≤ 0.0001.