https://embryology.med.unsw.edu.au/embryology/index.php?action=history&feed=atom&title=File%3AJNK1.png 2026-10-20T08:59:09Z Revision history for this page on the wiki MediaWiki 1.39.10 https://embryology.med.unsw.edu.au/embryology/index.php?title=File:JNK1.png&diff=105075&oldid=prev 2012-10-02T17:31:27Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en-GB"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 04:31, 3 October 2012</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1">Line 1:</td> <td colspan="2" class="diff-lineno">Line 1:</td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Figure:  JNK is phosphorylated during mitosis of retinal progenitor cells.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Figure:  <ins style="font-weight: bold; text-decoration: none;">'''&quot;</ins>JNK is phosphorylated during mitosis of retinal progenitor cells.<ins style="font-weight: bold; text-decoration: none;">&quot;'''</ins></div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>(A, B) Representative confocal photomicrographs of immunohistochemistry for phospho-JNK (red) and phospho-histone-H3 (green) in sections of retinal tissue maintained for 3 hours in vitro either in absence (A - CTR) or presence of taxol (B - TAX) showing the NBL. The sections were counterstained with DAPI (blue). Arrows indicate examples of cells double stained for phospho-JNK and phospho-histone-H3. Scale bar: 20 µm. (C) Higher magnification of mitotic cell showing the subcellular localization of phospho-JNK (red), phospho-histone-H3 (green), and DAPI (blue). Scale bar: 10 µm. (D) Numbers of phospho-JNK or phospho-histone-H3 stained cells per 100 µm of linear extent parallel to the retinal surface, along the mitotic stratum of retinal explants maintained in vitro for 3 hours, either in the absence (CTR) or presence of taxol (TAX). (E) Percentage of cells stained for phospho-JNK among all cells immunolabeled for phospho-histone-H3 in the mitotic stratum. Data are means±S.E.M. from three independent experiments. CTR - control; TAX - taxol; NBL - neuroblastic layer; *** P&lt;0.001 versus CTR.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div> </div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">&quot;</ins>(A, B) Representative confocal photomicrographs of immunohistochemistry for phospho-JNK (red) and phospho-histone-H3 (green) in sections of retinal tissue maintained for 3 hours in vitro either in absence (A - CTR) or presence of taxol (B - TAX) showing the NBL. The sections were counterstained with DAPI (blue). Arrows indicate examples of cells double stained for phospho-JNK and phospho-histone-H3. Scale bar: 20 µm. (C) Higher magnification of mitotic cell showing the subcellular localization of phospho-JNK (red), phospho-histone-H3 (green), and DAPI (blue). Scale bar: 10 µm. (D) Numbers of phospho-JNK or phospho-histone-H3 stained cells per 100 µm of linear extent parallel to the retinal surface, along the mitotic stratum of retinal explants maintained in vitro for 3 hours, either in the absence (CTR) or presence of taxol (TAX). (E) Percentage of cells stained for phospho-JNK among all cells immunolabeled for phospho-histone-H3 in the mitotic stratum. Data are means±S.E.M. from three independent experiments. CTR - control; TAX - taxol; NBL - neuroblastic layer; *** P&lt;0.001 versus CTR. <ins style="font-weight: bold; text-decoration: none;">&quot;</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>doi:10.1371/journal.pone.0034483.g001</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>doi:10.1371/journal.pone.0034483.g001</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br/></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Citation: <del style="font-weight: bold; text-decoration: none;">Ribas VT, Gonçalves BS, Linden R, Chiarini LB (2012) Activation of c-Jun N-Terminal Kinase (JNK) during Mitosis in Retinal Progenitor Cells. PLoS ONE 7(4): e34483. doi:10.1371</del>/<del style="font-weight: bold; text-decoration: none;">journal.pone.0034483</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Citation: <ins style="font-weight: bold; text-decoration: none;">&lt;pubmed&gt;22496813&lt;</ins>/<ins style="font-weight: bold; text-decoration: none;">pubmed&gt;</ins></div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div> </div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Copyright: © 2012 Ribas et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Copyright: © 2012 Ribas et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">{{Template:Student Image}}</ins></div></td></tr> <!-- diff cache key embryology:diff::1.12:old-102721:rev-105075 --> </table>

Z3370664 https://embryology.med.unsw.edu.au/embryology/index.php?title=File:JNK1.png&diff=102721&oldid=prev 2012-09-19T01:31:38Z

<p>Figure: JNK is phosphorylated during mitosis of retinal progenitor cells. (A, B) Representative confocal photomicrographs of immunohistochemistry for phospho-JNK (red) and phospho-histone-H3 (green) in sections of retinal tissue maintained for 3 hours in</p> <p><b>New page</b></p><div>Figure: JNK is phosphorylated during mitosis of retinal progenitor cells.<br /> (A, B) Representative confocal photomicrographs of immunohistochemistry for phospho-JNK (red) and phospho-histone-H3 (green) in sections of retinal tissue maintained for 3 hours in vitro either in absence (A - CTR) or presence of taxol (B - TAX) showing the NBL. The sections were counterstained with DAPI (blue). Arrows indicate examples of cells double stained for phospho-JNK and phospho-histone-H3. Scale bar: 20 µm. (C) Higher magnification of mitotic cell showing the subcellular localization of phospho-JNK (red), phospho-histone-H3 (green), and DAPI (blue). Scale bar: 10 µm. (D) Numbers of phospho-JNK or phospho-histone-H3 stained cells per 100 µm of linear extent parallel to the retinal surface, along the mitotic stratum of retinal explants maintained in vitro for 3 hours, either in the absence (CTR) or presence of taxol (TAX). (E) Percentage of cells stained for phospho-JNK among all cells immunolabeled for phospho-histone-H3 in the mitotic stratum. Data are means±S.E.M. from three independent experiments. CTR - control; TAX - taxol; NBL - neuroblastic layer; *** P&lt;0.001 versus CTR.<br /> doi:10.1371/journal.pone.0034483.g001<br /> <br /> Citation: Ribas VT, Gonçalves BS, Linden R, Chiarini LB (2012) Activation of c-Jun N-Terminal Kinase (JNK) during Mitosis in Retinal Progenitor Cells. PLoS ONE 7(4): e34483. doi:10.1371/journal.pone.0034483<br /> Copyright: © 2012 Ribas et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</div>

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