<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(15)</volume><submitter>Zeng D</submitter><pubmed_abstract>N&lt;sup>1&lt;/sup>-methyladenosine (m&lt;sup>1&lt;/sup>A) is an essential chemical modification of RNA. Dysregulation of RNA m&lt;sup>1&lt;/sup>A modification and m&lt;sup>1&lt;/sup>A-related regulators is detected in several adult tumors. Whether aberrant RNA m&lt;sup>1&lt;/sup>A modification is involved in hepatoblast carcinogenesis has not been reported. tRNA methyltransferase 61B (TRMT61B) is responsible for mitochondrial RNA m&lt;sup>1&lt;/sup>A modification. Some evidence has shown that genetic variants of &lt;i>TRMT61B&lt;/i> might contribute to cancer susceptibility; however, its roles in hepatoblastoma are unknown. This study attempted to discover novel hepatoblastoma susceptibility loci. With the TaqMan method, we examined genotypes of the &lt;i>TRMT61B&lt;/i> rs4563180 G>C polymorphism among germline DNA samples from 313 cas</pubmed_abstract><journal>Aging</journal><pagination>7583-7592</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10457066</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>TRMT61B&lt;/i> rs4563180 G>C variant reduces hepatoblastoma risk: a case-control study of seven medical centers.</pubmed_title><pmcid>PMC10457066</pmcid><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Liao F</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Zeng D</pubmed_authors><pubmed_authors>Cheng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>TRMT61B&lt;/i> rs4563180 G>C variant reduces hepatoblastoma risk: a case-control study of seven medical centers.</name><description>N&lt;sup>1&lt;/sup>-methyladenosine (m&lt;sup>1&lt;/sup>A) is an essential chemical modification of RNA. Dysregulation of RNA m&lt;sup>1&lt;/sup>A modification and m&lt;sup>1&lt;/sup>A-related regulators is detected in several adult tumors. Whether aberrant RNA m&lt;sup>1&lt;/sup>A modification is involved in hepatoblast carcinogenesis has not been reported. tRNA methyltransferase 61B (TRMT61B) is responsible for mitochondrial RNA m&lt;sup>1&lt;/sup>A modification. Some evidence has shown that genetic variants of &lt;i>TRMT61B&lt;/i> might contribute to cancer susceptibility; however, its roles in hepatoblastoma are unknown. This study attempted to discover novel hepatoblastoma susceptibility loci. With the TaqMan method, we examined genotypes of the &lt;i>TRMT61B&lt;/i> rs4563180 G>C polymorphism among germline DNA samples from 313 cas</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-05-28T12:17:10.028Z</modification><creation>2025-04-07T10:22:22.255Z</creation></dates><accession>S-EPMC10457066</accession><cross_references><pubmed>37531210</pubmed><doi>10.18632/aging.204926</doi></cross_references></HashMap>