Increased c-Jun N-terminal kinase activation in human endometriotic endothelial cells
Increased JNK phosphorylation in human endometriotic endothelial cells, observed both in vivo and in vitro, is linked to peritoneal fluid cytokines and may contribute to endometriosis pathogenesis.
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References (43)
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Cited by (9)
- The role of mitogen‐activated protein kinase signaling pathway in endometriosis 2021
- Endometrial biomarkers for the non-invasive diagnosis of endometriosis 2016
- The role of decidual cells in uterine hemostasis, menstruation, inflammation, adverse pregnancy outcomes and abnormal uterine bleeding 2016
- Non‐hormonal targets underlying endometriosis: A focus on molecular mechanisms 2015
- Bentamapimod (JNK Inhibitor AS602801) Induces Regression of Endometriotic Lesions in Animal Models 2015
- Towards an understanding of the molecular mechanism of endometriosis: unbalancing epithelial-stromal genetic conflict 2013
- Pathogenesis of endometriosis: The role of initial infection and subsequent sterile inflammation (Review) 2013
- Progesterone Resistance and Targeting the Progesterone Receptors: A Therapeutic Approach to Endometriosis 2012
- ALTERAÇÕES GENÔMICAS NA ENDOMETRIOSE 2011
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