<p>A–D: Bright-field view (A), DAPI staining of the nuclei (B), and double-immunostaining for GFAP (C) and endothelia cells (Endoth) with A10-33/1 (D) of a serial section of the eye shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0116171#pone.0116171.g002" target="_blank">Fig. 2</a> (2-month-old P<sub>RPE65</sub>-ngn3 mouse). E–G: High (2.5X) magnification of the boxed region in B–D, respectively. Arrow points to a piece of retinal tissue with increased GFAP expression. Short arrows point to the scantily present endothelial cells. Scale bars (100 μm) in A also applies to B–D and that in E also applies to F, G.</p
<p>Scale bars represent (A, C) 200 m or (B, D) 100 m. A, C: The frontal cortex of 6-week-old male mi...
<p>Retinas from P21 and P42 Wild-type (WT) and Bcl-2<sup>EC</sup> mice were prepared by trypsin dige...
<p>Following OIR, mice were perfused with RCA-1-FITC to detect perfused vessels immediately prior to...
<p>A–D: Bright-field view (A), DAPI staining of the nuclei (B), and double-immunostaining for Müller...
<p><b>A.</b> Fluorescence microscopy pictures of anti-GFAP- (green) and isolectin-B4- (ILB4, red) la...
<p>Co-immunostaining was performed on retinal frozen sections of 3-week-old LRP5 littermates with en...
<p>Compared with the contralateral retinae of NTg and Hm TET-1 mice, GFAP signal was up-regulated in...
<p>A–D: Bright-field view (A), DAPI staining of the nuclei (B), and double-immunostaining for Müller...
<p>All scale bars represent 10 μm. (A–C) 6-μm paraffin sections and (D–I) 10-μm frozen sections. A: ...
<p>Astrocyte development was examined by anti-GFAP IF staining. A and B. Anti-GFAP staining at P0. I...
<p>A: WT. B–C: “super p53”. In WT and “super p53” eyes, astrocytes had a rounded body from which num...
<p>A–C: Low magnification images to show the relative positions of the retinae in a cross-section of...
<p>GFAP immunofluorescence. A: negative control for GFAP immunostaining, B: WT. C: “super p53”. In b...
<p>(A, B) Normal appearance of endothelial cells (green, arrowheads) and delineated astrocytes (red,...
<p>12 µm sections from young (A and B) and one year (C and D) wild-type and <i>Cfh</i><sup>−/−</sup>...
<p>Scale bars represent (A, C) 200 m or (B, D) 100 m. A, C: The frontal cortex of 6-week-old male mi...
<p>Retinas from P21 and P42 Wild-type (WT) and Bcl-2<sup>EC</sup> mice were prepared by trypsin dige...
<p>Following OIR, mice were perfused with RCA-1-FITC to detect perfused vessels immediately prior to...
<p>A–D: Bright-field view (A), DAPI staining of the nuclei (B), and double-immunostaining for Müller...
<p><b>A.</b> Fluorescence microscopy pictures of anti-GFAP- (green) and isolectin-B4- (ILB4, red) la...
<p>Co-immunostaining was performed on retinal frozen sections of 3-week-old LRP5 littermates with en...
<p>Compared with the contralateral retinae of NTg and Hm TET-1 mice, GFAP signal was up-regulated in...
<p>A–D: Bright-field view (A), DAPI staining of the nuclei (B), and double-immunostaining for Müller...
<p>All scale bars represent 10 μm. (A–C) 6-μm paraffin sections and (D–I) 10-μm frozen sections. A: ...
<p>Astrocyte development was examined by anti-GFAP IF staining. A and B. Anti-GFAP staining at P0. I...
<p>A: WT. B–C: “super p53”. In WT and “super p53” eyes, astrocytes had a rounded body from which num...
<p>A–C: Low magnification images to show the relative positions of the retinae in a cross-section of...
<p>GFAP immunofluorescence. A: negative control for GFAP immunostaining, B: WT. C: “super p53”. In b...
<p>(A, B) Normal appearance of endothelial cells (green, arrowheads) and delineated astrocytes (red,...
<p>12 µm sections from young (A and B) and one year (C and D) wild-type and <i>Cfh</i><sup>−/−</sup>...
<p>Scale bars represent (A, C) 200 m or (B, D) 100 m. A, C: The frontal cortex of 6-week-old male mi...
<p>Retinas from P21 and P42 Wild-type (WT) and Bcl-2<sup>EC</sup> mice were prepared by trypsin dige...
<p>Following OIR, mice were perfused with RCA-1-FITC to detect perfused vessels immediately prior to...