<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(2)</volume><submitter>Xiong M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Periodontitis, a chronic inflammatory disease, represents the primary cause of tooth loss in Chinese adults. Wilms tumor 1-associating protein (WTAP) is a key component of the N6-methyladenosine (m6A) methyltransferase complex, and has an unclear role in periodontitis pathogenesis, particularly concerning its regulatory functions in periodontal ligament stem cells (PDLSCs).&lt;h4>Methods&lt;/h4>The target gene was identified through the GES260558 dataset and Genecards database. Gene expression was measured using reverse transcription-quantitative PCR (RT-qPCR) and western blot. Periodontitis-derived PDLSCs (P-PDLSCs) were isolated and identified by alkaline phosphatase (ALP) staining, oil red O staining, and flow cytometry. Malondialdehyde (MDA), superoxide dismutase (SOD), an</pubmed_abstract><journal>Immunity, inflammation and disease</journal><pagination>e70335</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12873629</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>WTAP Contributes to Periodontitis Pathogenesis by Promoting PDLSC Senescence and Impairing Osteogenic Differentiation via m6A-Dependent Regulation of TP53BP1.</pubmed_title><pmcid>PMC12873629</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Xiong M</pubmed_authors><pubmed_authors>Wang T</pubmed_authors></additional><is_claimable>false</is_claimable><name>WTAP Contributes to Periodontitis Pathogenesis by Promoting PDLSC Senescence and Impairing Osteogenic Differentiation via m6A-Dependent Regulation of TP53BP1.</name><description>&lt;h4>Background&lt;/h4>Periodontitis, a chronic inflammatory disease, represents the primary cause of tooth loss in Chinese adults. Wilms tumor 1-associating protein (WTAP) is a key component of the N6-methyladenosine (m6A) methyltransferase complex, and has an unclear role in periodontitis pathogenesis, particularly concerning its regulatory functions in periodontal ligament stem cells (PDLSCs).&lt;h4>Methods&lt;/h4>The target gene was identified through the GES260558 dataset and Genecards database. Gene expression was measured using reverse transcription-quantitative PCR (RT-qPCR) and western blot. Periodontitis-derived PDLSCs (P-PDLSCs) were isolated and identified by alkaline phosphatase (ALP) staining, oil red O staining, and flow cytometry. Malondialdehyde (MDA), superoxide dismutase (SOD), an</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-05T03:08:57.414Z</modification><creation>2026-07-05T03:08:02.377Z</creation></dates><accession>S-EPMC12873629</accession><cross_references><pubmed>41641517</pubmed><doi>10.1002/iid3.70335</doi></cross_references></HashMap>