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1 bles tissue dendritic cells, in the theca of antral follicles.
2 cells than in mural granulosa cells of mouse antral follicles.
3 ral follicles, but is not expressed in large antral follicles.
4 /hCG) in the granulosa layer of preovulatory antral follicles.
5 d small, nongrowing oocytes in secondary and antral follicles.
6 anulosa complexes (OCGCs) derived from early antral follicles (0.5-1 mm) to in vitro growth (IVG) cul
7 like lesions grew no larger than the size of antral follicles and contained very few proliferating ce
9 r2-Edn2KO ovaries had a higher percentage of antral follicles and fewer corpora lutea; follicles prog
10 primary, secondary, small antral, and large antral follicles and used Expression Analysis Systematic
12 s and theca interna of small to medium-sized antral follicles, but is not expressed in large antral f
15 tropin secretion resulted in reduced ovarian antral follicle count and ovarian volume, but levels of
16 d maternal factors including anovulation and antral follicle counting, the corresponding ORs were 1.1
17 EVs change in their levels and makeup during antral follicle development and point to the potential f
19 microinjected fluorescent tracers into live antral follicle-enclosed mouse oocytes, and we demonstra
20 ells in immunocompromised mice and recovered antral follicles for purification and downstream single-
23 n, classic polycystic ovaries, reduced large antral follicle health, and several metabolic traits inc
24 rom Gpr3 knockout mice resume meiosis within antral follicles, independently of an increase in lutein
27 cyst formation, and a progressive decline in antral follicle numbers, however, the few surviving larg
31 developmental competence of oocytes in early antral follicles through GSH depletion, which can induce
37 ling in DHT-induced ovarian steroidogenesis, antral follicles were isolated from wild type and CMKLR1