ライフサイエンスコーパス: corpus luteum

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 he FP(B) isoform was identified in the ovine corpus luteum.

7 ntiate into steroidogenic cells, forming the corpus luteum.

8 he role of the short form, especially in the corpus luteum.

9 tablished that the secretory activity of the corpus luteum absolutely depends on the presence of pitu

10 to previously reported expression limited to corpus luteum and highly angiogenic tissues such as tumo

11 n is a 6 kDa protein hormone produced by the corpus luteum and secreted into the blood during pregnan

12 ed to support progesterone production by the corpus luteum and when relaxin expression is initiated,

13 , smaller ovaries with a decreased number of corpus luteum, and an increased number of cystic/atretic

14 he brain, muscle fibers, thecal cells of the corpus luteum, and Leydig and sperm cells of the testis.

15 ice showed multiple hemorrhagic cysts and no corpus luteum, and the mammary gland development in both

16 tor (VEGF) is a key mediator of the cyclical corpus luteum angiogenesis.

17 er prolonged the functional life span of the corpus luteum beyond its normal duration.

18 another tissue that undergoes angiogenesis, corpus luteum, blood vessels also expressed APN, but APN

19 opment and endocrine function of the ovarian corpus luteum (CL) are dependent on the growth of new ca

20 fect in female Dicer(d/d) mice was caused by corpus luteum (CL) insufficiency and resulted, at least

21 lpha (PGF2alpha) is an important mediator of corpus luteum (CL) regression, although the cellular sig

22 eroidogenic cells and to induce apoptosis of corpus luteum (CL)-derived endothelial cells in vitro.

23 lower density of blood vessels in the mature corpus luteum compared with Galpha(13)(+/+) mice.

24 ter in transient transfection experiments in corpus luteum-derived cells (GG-CL).

25 e-endothelial cell interactions underpinning corpus luteum development contributes to infertility in

26 ily in active angiogenesis processes such as corpus luteum development.

27 hesis and luteal cell hypertrophy of the rat corpus luteum during pregnancy.

28 ute to the luteotropic effects of PRL on the corpus luteum during pregnancy.

29 niferous tubules in the testis and perturbed corpus luteum formation in the ovary.

30 al vessels associated with wound healing and corpus luteum formation.

31 of follicle size at the time of ovulation on corpus luteum function and establishment and maintenance

32 er of the IGF family that is secreted by the corpus luteum in humans and rodents.

33 The corpus luteum in the female, the testis in the male, and

34 solated LH-hypogonadotropic hypogonadism and corpus luteum insufficiency in humans.

35 the extensive vascular network required for corpus luteum integrity and production of progesterone e

36 PKC delta in corpora lutea obtained when the corpus luteum is exposed to chronically high concentrati

37 (LH), it is unknown why the life span of the corpus luteum is extended during early pregnancy by the

38 een cloned from a mid-cycle ovine large cell corpus luteum library.

39 mammals is the mechanism of maintaining the corpus luteum of pregnancy.

40 the PRL receptor have been identified in the corpus luteum of pregnant rat.

41 from impaired progesterone synthesis by the corpus luteum of the ovary, an endocrine defect in turn

42 e insulin superfamily, is synthesized by the corpus luteum of the rat ovary.

43 GPI is expressed by the corpus luteum on days 6-9 of pregnancy, the time at whic

44 which are secreted by conceptuses to prevent corpus luteum regression, nonpregnant pigs were treated

45 de of pericyte recruitment in the angiogenic corpus luteum, resulting in prominent hemorrhage, thus d

46 first time, that PGF(2)alpha induces in the corpus luteum the expression of the nuclear orphan recep

47 To compare the responses of the corpus luteum to LH and human CG (hCG), cynomolgus monke

48 reduction in the responsiveness of the aging corpus luteum to LH, which can be overcome by elevated c

49 (2)alpha) binding to its receptor on the rat corpus luteum triggers various signal transduction pathw

50 d stimulates progesterone synthesis from the corpus luteum, which is essential for early development