<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kalesnykas G</submitter><funding>NEI NIH HHS</funding><pagination>3847-57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3630905</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53(7)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To study sequential changes in retinal ganglion cell (RGC) morphology in mice after optic nerve crush and after induction of experimental glaucoma.&lt;h4>Methods&lt;/h4>Nerve crush or experimental glaucoma was induced in mice that selectively express yellow fluorescent protein (YFP) in RGCs. Mice were euthanized 1, 4, and 9 days after crush and 1, 3, and 6 weeks after induction of glaucoma by bead injection. All YFP-RGCs were identified in retinal whole mounts. Then confocal images of randomly selected RGCs were quantified for somal fluorescence brightness, soma size, neurite outgrowth, and dendritic complexity (Sholl analysis).&lt;h4>Results&lt;/h4>By 9 days after crush, 98% of RGC axons died and YFP-RGCs decreased by 64%. After 6 weeks of glaucoma, 31% of axons died, but there was no</pubmed_abstract><journal>Investigative ophthalmology &amp; visual science</journal><pubmed_title>Retinal ganglion cell morphology after optic nerve crush and experimental glaucoma.</pubmed_title><pmcid>PMC3630905</pmcid><funding_grant_id>R56 EY002120</funding_grant_id><funding_grant_id>EY-02120</funding_grant_id><funding_grant_id>P30 EY001765</funding_grant_id><funding_grant_id>R01 EY002120</funding_grant_id><funding_grant_id>EY-01765</funding_grant_id><pubmed_authors>Oglesby EN</pubmed_authors><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Pease ME</pubmed_authors><pubmed_authors>Quigley HA</pubmed_authors><pubmed_authors>Kalesnykas G</pubmed_authors><pubmed_authors>Cone FE</pubmed_authors><pubmed_authors>Zack DJ</pubmed_authors><pubmed_authors>Steinhart MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Retinal ganglion cell morphology after optic nerve crush and experimental glaucoma.</name><description>&lt;h4>Purpose&lt;/h4>To study sequential changes in retinal ganglion cell (RGC) morphology in mice after optic nerve crush and after induction of experimental glaucoma.&lt;h4>Methods&lt;/h4>Nerve crush or experimental glaucoma was induced in mice that selectively express yellow fluorescent protein (YFP) in RGCs. Mice were euthanized 1, 4, and 9 days after crush and 1, 3, and 6 weeks after induction of glaucoma by bead injection. All YFP-RGCs were identified in retinal whole mounts. Then confocal images of randomly selected RGCs were quantified for somal fluorescence brightness, soma size, neurite outgrowth, and dendritic complexity (Sholl analysis).&lt;h4>Results&lt;/h4>By 9 days after crush, 98% of RGC axons died and YFP-RGCs decreased by 64%. After 6 weeks of glaucoma, 31% of axons died, but there was no</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jun</publication><modification>2025-04-25T22:10:46.201Z</modification><creation>2019-03-27T01:07:39Z</creation></dates><accession>S-EPMC3630905</accession><cross_references><pubmed>22589442</pubmed><doi>10.1167/iovs.12-9712</doi></cross_references></HashMap>