Figure 5
From: A mutation in Ampd2 is associated with nephrotic syndrome and hypercholesterolemia in mice
Temporal hypercholesterolemia and proteinuria in Ampd2m/mmice in mixed B6/C3 and pure B6 genetic background. A and D) Plasma cholesterol level time course in Ampd2+/+ and Ampd2m/m mice. B and E) Proteinuria level time course in Ampd2+/+ and Ampd2m/m mice. C and F) Plasma albumin levels time course in Ampd2+/+ and Ampd2m/m mice on a mixed B6/C3 background and pure B6 background (n = 4-6). Statistical analyses were carried out by unpaired two-tailed t-tests; * p <0.05; ** p <0.01; *** p <0.001; **** p <0.0001 vs. Ampd2+/+.