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. Author manuscript; available in PMC: 2011 May 3.
Published in final edited form as: AIDS. 2010 Sep 10;24(14):2161–2170. doi: 10.1097/QAD.0b013e32833dbc31

Table 1.

Comparison of immunohistochemistry staining from the glomeruli of normal and HIV-transgenic rats.

Normal rats HIV-1 Tg rats P
PCNA 25.1 ± 9.77 40.59 ± 13.7 <0.0001**
Ki67 ND 3.26 ± 2.56 <0.0001**
p27 50.8 ± 14.2 35.0 ± 10.1 <0.0001**
WT1 16.18 ± 4.3 13.52 ± 5.2   0.017*
Synaptopodin 50.0 ± 6.8 26.26 ± 13.5 <0.0001**
Desmin ND 14.8 ± 19.2 <0.0001**
Notch1 IC 0.15 ± 0.87 2.5 ± 3.3 <0.0001**
Notch2 IC 51.4 ± 13.4 49.3 ± 14.4   0.28
Notch3 IC 40.9 ± 11.7 44.5 ± 14.6   0.15
Notch4 IC 24.00 ± 9.5 47.0 ± 12.4 <0.0001**
Hes1 54.27 ± 12.22 59.8 ± 11.8   0.04*
Cux1 20.33 ± 7.2 42.0 ± 15.9 <0.0001**
TLE4 8.9 ± 5.14 33.33 ± 9.7 <0.0001**

Cells showing positive staining were counted manually in the first 30 random glomeruli from the three wild-type and HIV-Tg slides each. Synaptopodin staining was measured by image J program from NIH and presented as percentage area of the glomeruli positive for the staining. Values are represented as mean ± SD. Cux1, cut-like homeobox; Hes, hairy enhancer of split; HIV-Tg, HIV-1 transgenic sections; IC, intracellular; ND, not detected; NIH, National Institute for Health; normal, wild-type kidney sections; PCNA, proliferating cell nuclear antigen; TLE, transducin-like enhancer of split; WT1, Wilms tumor 1.

*

P < 0.05 was considered as statistically significant.

**

P < 0.001 was considered highly statistically significant.