1. It was safe to draw a conclusion that eutopic endometrium was more similar to ectopic endometrium other than normal endometrium in the expression of these chemokines receptors.

2. The expression of VEGF in eutopic endometria in secretory stage was significantly higher than that in eutopic endometria in proliferative stage.

3. Conclusion:CCR5 and CXCR4 in endometriotic foci and eutopic endometrium were significantly higher than those in normal endometrium.

4. Conclusions:The expression of MMP-2, MMP-7 and TIMP-1 was irrespective of the phase of the menstrual cycle in the ectopic and eutopic endometrium of adenomyosis group .

5. Ultrastucture of EOS from modeling group is different from eutopic EM, Three weeks' treatment with Danazol can make organelle altered and cell necrotized.

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6. Objectives To investigate the expression of substance P(SP)and calcitonin gene-related peptide(CGRP)in adenomyosis tissues and in eutopic endometrium.

7. Conclusion:The persistently exaggerated expression of VEGF in ectopic endometrium and eutopic endometrium in patients with EM may be related to the pathogenesis of EM.

8. Conclusion:(1)There is no significant difference in the number of NK cells between ectopic and eutopic endometrium in patients with EM.

9. Methods Using immunohistochemistry SP method, the expression of COX-2 and VEGF was examined in ectopic endometrium and eutopic endometrium, compared with normal endometrium.

10. That the expression of HLA-G in glandular cells in ectopic endometrium was higher than that in glandular cells in eutopic endometrium makes ectopic endometrium more resistive.

11. OBJECTIVE:The purpose of this study was to evaluate endometrial biopsy and curettage in detecting small nerve fibers in eutopic endometrium for diagnosis of endometriosis.