Altered expression of 3´paralogus HOX A-D clusters in endometriosis disease: A case-control study
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This study investigated HOXA, HOXB, HOXC, and HOXD gene expression in endometriosis tissues and found significant differences in ectopic tissues compared to controls.
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Abstract
BACKGROUND: clusters are subdivided into 13 paralogous groups). OBJECTIVE: genes (A, B, C, and D) in ectopic and eutopic tissues of women with endometriosis compared to the normal endometrium. MATERIALS AND METHODS: genes was investigated by quantitative real-time polymerase chain reaction technique. RESULTS: in ectopic tissues versus control. CONCLUSION: ) in ectopic and eutopic tissues compare to control group. Therefore, it is possible that change of expression level of these genes in endometrium plays a role in the pathogenesis of endometriosis.
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Cited by (9)
- An update on epigenetic mechanisms in endometriosis 2024
- Evidence of shared genetic factors in the etiology of gastrointestinal disorders and endometriosis and clinical implications for disease management 2023
- Evidence of shared genetic factors in the aetiology of gastrointestinal disorders and endometriosis and clinical implications for disease management 2022
- HOX cluster and their cofactors showed an altered expression pattern in eutopic and ectopic endometriosis tissues 2021
- Additional file 1 of HOX cluster and their cofactors showed an altered expression pattern in eutopic and ectopic endometriosis tissues 2021
- Insight into epigenetics of human endometriosis organoids: DNA methylation analysis of HOX genes and their cofactors 2020
- Analysis of Proteomic Differences between Eutopic Endometrium and Ectopic Endometrium in Patients with Endometriosis 2020
- Network-based bioinformatics analysis of HOX genes and their related genes in endometriosis 2020
- Network-based bioinformatics analysis of HOX genes and their related genes in endometriosis 2020
Source provenance
- europepmc
- last seen: 2026-06-04T01:30:01.192114+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-05-13T22:23:01.605684+00:00
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