<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>63(4)</volume><submitter>Zhang X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The progression and recurrence of pterygium mainly occur due to the abnormal proliferation and migration of stromal pterygium fibroblasts. This research explores the aberrant expression of small nucleolar RNA U3 (U3 snoRNA) in pterygium and elucidates the molecular mechanisms of U3 snoRNA in pterygium development.&lt;h4>Methods&lt;/h4>Primary human conjunctival fibroblasts (HCFs) and human pterygium fibroblasts (HPFs) were separated and cultured from fresh conjunctiva grafts and pterygium tissues. The PLKO.1 lentiviral system and CRISPR/Cas9 recombinant construct were, respectively, used to overexpress and silence U3 snoRNA in HPFs and HCFs for further specific phenotype analysis. RNA-seq and TMT-labeled quantitative protein mass spectrometry were utilized to evaluate the effe</pubmed_abstract><journal>Investigative ophthalmology &amp; visual science</journal><pagination>17</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9055567</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Atypical U3 snoRNA Suppresses the Process of Pterygium Through Modulating 18S Ribosomal RNA Synthesis.</pubmed_title><pmcid>PMC9055567</pmcid><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Xu M</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>An W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atypical U3 snoRNA Suppresses the Process of Pterygium Through Modulating 18S Ribosomal RNA Synthesis.</name><description>&lt;h4>Background&lt;/h4>The progression and recurrence of pterygium mainly occur due to the abnormal proliferation and migration of stromal pterygium fibroblasts. This research explores the aberrant expression of small nucleolar RNA U3 (U3 snoRNA) in pterygium and elucidates the molecular mechanisms of U3 snoRNA in pterygium development.&lt;h4>Methods&lt;/h4>Primary human conjunctival fibroblasts (HCFs) and human pterygium fibroblasts (HPFs) were separated and cultured from fresh conjunctiva grafts and pterygium tissues. The PLKO.1 lentiviral system and CRISPR/Cas9 recombinant construct were, respectively, used to overexpress and silence U3 snoRNA in HPFs and HCFs for further specific phenotype analysis. RNA-seq and TMT-labeled quantitative protein mass spectrometry were utilized to evaluate the effe</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-05-31T14:01:01.597Z</modification><creation>2024-11-19T21:18:25.486Z</creation></dates><accession>S-EPMC9055567</accession><cross_references><pubmed>35472218</pubmed><doi>10.1167/iovs.63.4.17</doi></cross_references></HashMap>