Full metadata record
DC FieldValueLanguage
dc.contributor.authorWang, Hsiuyingen_US
dc.date.accessioned2019-12-13T01:12:17Z-
dc.date.available2019-12-13T01:12:17Z-
dc.date.issued2019-10-01en_US
dc.identifier.urihttp://dx.doi.org/10.3390/biom9100572en_US
dc.identifier.urihttp://hdl.handle.net/11536/153159-
dc.description.abstractMicroRNA (miRNA) is a small non-coding RNA that functions in the epigenetics control of gene expression, which can be used as a useful biomarker for diseases. Anti-NMDA receptor (anti-NMDAR) encephalitis is an acute autoimmune disorder. Some patients have been found to have tumors, specifically teratomas. This disease occurs more often in females than in males. Most of them have a significant recovery after tumor resection, which shows that the tumor may induce anti-NMDAR encephalitis. In this study, I review microRNA (miRNA) biomarkers that are associated with anti-NMDAR encephalitis and related tumors, respectively. To the best of my knowledge, there has not been any research in the literature investigating the relationship between anti-NMDAR encephalitis and tumors through their miRNA biomarkers. I adopt a phylogenetic analysis to plot the phylogenetic trees of their miRNA biomarkers. From the analyzed results, it may be concluded that (i) there is a relationship between these tumors and anti-NMDAR encephalitis, and (ii) this disease occurs more often in females than in males. This sheds light on this issue through miRNA intervention.en_US
dc.language.isoen_USen_US
dc.subjectanti-NMDA receptor encephalitisen_US
dc.subjectbiomarkeren_US
dc.subjectmicroRNAen_US
dc.subjecttumoren_US
dc.subjectteratomaen_US
dc.titlePhylogenetic Analysis to Explore the Association Between Anti-NMDA Receptor Encephalitis and Tumors Based on microRNA Biomarkersen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/biom9100572en_US
dc.identifier.journalBIOMOLECULESen_US
dc.citation.volume9en_US
dc.citation.issue10en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department統計學研究所zh_TW
dc.contributor.departmentInstitute of Statisticsen_US
dc.identifier.wosnumberWOS:000497726800064en_US
dc.citation.woscount0en_US
Appears in Collections:Articles