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. Author manuscript; available in PMC: 2012 Apr 1.

Published in final edited form as: Gend Med. 2011 Apr;8(2):126–138. doi: 10.1016/j.genm.2010.11.014

A. Telemetered systolic blood pressure (SBP) was significantly elevated after Sry3 (solid squares, n=6) delivery to the kidney as compared to control vector (open circles, n=6) (means, +/−s.e.m., (two-way ANOVA with repeated measures, treatment: F=20.6, p<0.001, time: n.s., interaction of treatment and time: F=3.9,p<0.05); B. Telemetered mean arterial pressure )MAP) was significantly elevated after Sry3 (solid squares) delivery to the kidney as compared to control vector (open circles, means, +/−s.e.m., two-way ANOVA with repeated measures, treatment: F=18.6, ***=p<0.001, time: n.s., interaction not significant; C. Telemetered heart rate was not significantly different after Sry3 (solid squares) delivery to the kidney as compared to control vector (open circles, means, +/−s.e.m).

A. Telemetered systolic blood pressure (SBP) was significantly elevated after Sry3 (solid squares, n=6) delivery to the kidney as compared to control vector (open circles, n=6) (means, +/−s.e.m., (two-way ANOVA with repeated measures, treatment: F=20.6, p<0.001, time: n.s., interaction of treatment and time: F=3.9,p<0.05); B. Telemetered mean arterial pressure )MAP) was significantly elevated after Sry3 (solid squares) delivery to the kidney as compared to control vector (open circles, means, +/−s.e.m., two-way ANOVA with repeated measures, treatment: F=18.6, ***=p<0.001, time: n.s., interaction not significant; C. Telemetered heart rate was not significantly different after Sry3 (solid squares) delivery to the kidney as compared to control vector (open circles, means, +/−s.e.m).