Analysis of key candidate genes and pathways of endometriosis pathophysiology by a genomics-bioinformatics approach
This study integrated gene expression datasets to identify 94 differentially expressed genes and 18 central node genes, primarily involved in the angiotensin system, smooth muscle contraction, cell junction organization, and lipoxin pathways, offering insights into endometriosis pathophysiology.
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Cited by (10)
- Angiotensin II – AT1 receptor signalling regulates the plasminogen-plasmin system in human stromal endometrial cells increasing extracellular matrix degradation, cell migration and inducing a proinflammatory profile 2024
- The Biological Characteristics of Eutopic and Ectopic EndometrialProgenitor Cells in Endometriosis 2023
- Identification of potential diagnostic biomarkers and therapeutic targets for endometriosis based on bioinformatics and machine learning analysis 2023
- The role of genetic factors in developing endometrioid lesions 2023
- Integrated bioinformatic analysis of dysregulated <scp>microRNA‐mRNA</scp> co‐expression network in ovarian endometriosis 2022
- Multi‐omics analysis reveals the interaction between the complement system and the coagulation cascade in the development of endometriosis 2021
- Clinical examples of the rational applying of the «gold standard» of hormonal therapy for endometriosis 2021
- Guidelines for biomarker discovery in endometrium: correcting for menstrual cycle bias reveals new genes associated with uterine disorders 2021
- Involvement of angiotensin II receptor type 1/NF‑κB signaling in the development of endometriosis 2020
- Bioinformatic analysis reveals the importance of epithelial-mesenchymal transition in the development of endometriosis 2020
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