Integrated Bioinformatics Analysis Reveals Function and Regulatory Network of miR‐200b‐3p in Endometriosis
This bioinformatics study identified 110 target genes of miR-200b-3p associated with MAPK signaling and vasculogenesis, and four interacting lncRNAs, providing insights into miR-200b-3p's role in endometriosis.
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References (47)
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Cited by (13)
- Characteristics of menstrual blood-derived stem cells from women with endometriosis: A systematic review 2026
- Mechanisms of KLF10 in Regulating Proliferation of Endometriotic Stromal Cells in Endometriosis 2025
- Medicina traslacional en el manejo de la endometriosis: Nuevos esquemas terapéuticos 2024
- Machine learning algorithms for a novel cuproptosis-related gene signature of diagnostic and immune infiltration in endometriosis 2023
- Resveratrol protected against the development of endometriosis by promoting ferroptosis through miR-21-3p/p53/SLC7A11 signaling pathway 2023
- MiR-518c-3p alleviates endometriosis by inhibiting ectopic endometrial migration and epithelial–mesenchymal transition via targeting ZNF608 2022
- MicroRNA Variants miR-27a rs895819 and miR-423 rs6505162, but not miR-124-1 rs531564, are Linked to Endometriosis and its Severity 2022
- MicroRNAs Dysregulation as Potential Biomarkers for Early Diagnosis of Endometriosis 2022
- Bioinformatical analysis of the key differentially expressed genes and associations with immune cell infiltration in development of endometriosis 2022
- Overexpression of miR-200b-3p in Menstrual Blood-Derived Mesenchymal Stem Cells from Endometriosis Women 2022
- Expression of lncRNA NEAT1 in endometriosis and its biological functions in ectopic endometrial cells as mediated via miR-124-3p 2022
- Screening differentially expressed genes between endometriosis and ovarian cancer to find new biomarkers for endometriosis 2021
- New Therapeutics in Endometriosis: A Review of Hormonal, Non-Hormonal, and Non-Coding RNA Treatments 2021
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- europepmc
- last seen: 2026-06-16T06:07:01.518242+00:00
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- last seen: 2026-06-10T17:14:06.276822+00:00
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