<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE267nnn/GSE267409/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Homo sapiens</species><gds_type>Methylation profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE267409</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>TET2 affects keratinocytes and psoriatic dermatitis by regulating MECOM and NTRK1 hydroxymethylation</name><description>The ten-eleven translocation (TET) family dioxygenases TET2 oxidize 5-methylcytosine (5-mC) to 5-hmC in DNA. DNA hydroxymethylation is the most crucial epigenetic modifications in the occurrence and development of a variety of skin diseases. The goal is to determine the targets of TET2 knockdown including DNA hydroxymethylation in keratinocytes. We profiled a number of important signaling pathways and key factors that may be associated with psoriasis hydroxymethylation and may be potential biomarkers for psoriasis.</description><dates><publication>2026/06/01</publication></dates><accession>GSE267409</accession><cross_references><GSM>GSM8265313</GSM><GSM>GSM8265312</GSM><GSM>GSM8265315</GSM><GSM>GSM8265314</GSM><GPL>13497</GPL><GSE>267409</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>