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1 ies of the functional endometrium during the secretory phase.
2 degeneration shortly after completion of the secretory phase.
3 tosis that led to an enhancement of the slow secretory phase.
5 synthesized by endometrial cells in the late secretory phase and early pregnancy under hormonal regul
7 ated degradation of p27 compared with normal secretory-phase endometrial tissue (SE) such that 4% and
14 ta is expressed during the proliferative and secretory phases of the cycle and is restricted to the l
19 expression of Dr ligands occurred during the secretory phase, whereas receptors were expressed in the
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