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1 ndothelium with the exception of perhaps the corpus luteum.
2 pha induction of the 20alpha-HSD gene in the corpus luteum.
3 tenance of pregnancy in the rat requires the corpus luteum.
4 d to prolong the functional life span of the corpus luteum.
5 t that CG and LH have similar actions on the corpus luteum.
6 rtion of the uterine horn ipsilateral to the corpus luteum.
7 he FP(B) isoform was identified in the ovine corpus luteum.
8 ntiate into steroidogenic cells, forming the corpus luteum.
9 he role of the short form, especially in the corpus luteum.
10 ulating progesterone synthesis in the bovine corpus luteum.
11 al roles in ovulation and maintenance of the corpus luteum.
12 HV-1 replicates efficiently in the ovary and corpus luteum.
13 tablished that the secretory activity of the corpus luteum absolutely depends on the presence of pitu
14 to previously reported expression limited to corpus luteum and highly angiogenic tissues such as tumo
15 the endometrium to prevent regression of the corpus luteum and prepare for establishment of pregnancy
16 n is a 6 kDa protein hormone produced by the corpus luteum and secreted into the blood during pregnan
17 ed to support progesterone production by the corpus luteum and when relaxin expression is initiated,
18 , smaller ovaries with a decreased number of corpus luteum, and an increased number of cystic/atretic
19  which is regulated by progesterone from the corpus luteum, and evaluate how it is altered by the sup
20 he brain, muscle fibers, thecal cells of the corpus luteum, and Leydig and sperm cells of the testis.
21 ice showed multiple hemorrhagic cysts and no corpus luteum, and the mammary gland development in both
22 tor (VEGF) is a key mediator of the cyclical corpus luteum angiogenesis.
23 ulating progesterone synthesis in the bovine corpus luteum, as supported by its dynamic expression pa
24 er prolonged the functional life span of the corpus luteum beyond its normal duration.
25  another tissue that undergoes angiogenesis, corpus luteum, blood vessels also expressed APN, but APN
26 opment and endocrine function of the ovarian corpus luteum (CL) are dependent on the growth of new ca
27 u (IFNT), serves as a signal to maintain the corpus luteum (CL) during early pregnancy in domestic ru
28 fect in female Dicer(d/d) mice was caused by corpus luteum (CL) insufficiency and resulted, at least
29 lpha (PGF2alpha) is an important mediator of corpus luteum (CL) regression, although the cellular sig
30 eroidogenic cells and to induce apoptosis of corpus luteum (CL)-derived endothelial cells in vitro.
31 XT on endometrium, myometrium, pituitary and corpus luteum (CL).
32 lower density of blood vessels in the mature corpus luteum compared with Galpha(13)(+/+) mice.
33 ter in transient transfection experiments in corpus luteum-derived cells (GG-CL).
34 e-endothelial cell interactions underpinning corpus luteum development contributes to infertility in
35 ily in active angiogenesis processes such as corpus luteum development.
36 hesis and luteal cell hypertrophy of the rat corpus luteum during pregnancy.
37 ute to the luteotropic effects of PRL on the corpus luteum during pregnancy.
38 niferous tubules in the testis and perturbed corpus luteum formation in the ovary.
39  of the follicle and its sequela, ovulation, corpus luteum formation, and ovulatory wound repair.
40 al vessels associated with wound healing and corpus luteum formation.
41 of follicle size at the time of ovulation on corpus luteum function and establishment and maintenance
42 gh a common intermediate, EGR 1, to regulate corpus luteum function of buffalo.
43 er of the IGF family that is secreted by the corpus luteum in humans and rodents.
44                                          The corpus luteum in the female, the testis in the male, and
45 solated LH-hypogonadotropic hypogonadism and corpus luteum insufficiency in humans.
46  the extensive vascular network required for corpus luteum integrity and production of progesterone e
47                                          The corpus luteum is a transient endocrine gland that synthe
48                                          The corpus luteum is an endocrine gland that synthesizes and
49 PKC delta in corpora lutea obtained when the corpus luteum is exposed to chronically high concentrati
50 (LH), it is unknown why the life span of the corpus luteum is extended during early pregnancy by the
51 ction in the periovulatory window and in the corpus luteum is unknown.
52 een cloned from a mid-cycle ovine large cell corpus luteum library.
53  mammals is the mechanism of maintaining the corpus luteum of pregnancy.
54 the PRL receptor have been identified in the corpus luteum of pregnant rat.
55  from impaired progesterone synthesis by the corpus luteum of the ovary, an endocrine defect in turn
56 e insulin superfamily, is synthesized by the corpus luteum of the rat ovary.
57                      GPI is expressed by the corpus luteum on days 6-9 of pregnancy, the time at whic
58 016, P = 0.029, P = 0.016), while increasing corpus luteum (P = 0.002, P = 0.02, P = 0.02).
59 which are secreted by conceptuses to prevent corpus luteum regression, nonpregnant pigs were treated
60 de of pericyte recruitment in the angiogenic corpus luteum, resulting in prominent hemorrhage, thus d
61 se-cell engulfment, egg-shell formation, and corpus luteum signaling.
62  first time, that PGF(2)alpha induces in the corpus luteum the expression of the nuclear orphan recep
63              To compare the responses of the corpus luteum to LH and human CG (hCG), cynomolgus monke
64 reduction in the responsiveness of the aging corpus luteum to LH, which can be overcome by elevated c
65 (2)alpha) binding to its receptor on the rat corpus luteum triggers various signal transduction pathw
66                 Total and viable fetuses per corpus luteum were reduced (P <= 0.05) in HS dams.
67 d stimulates progesterone synthesis from the corpus luteum, which is essential for early development