ライフサイエンスコーパス: sex steroid hormone

1 ke outcomes seen during life stages with low sex steroid hormones.

2 ence that likely results from the effects of sex steroid hormones.

3 ted with differences in circulating SHBG and sex steroid hormones.

4 cancer cells, particularly that mediated by sex steroid hormones.

5 rogenase responsible for the inactivation of sex steroid hormones.

6 he rate-limiting step in the biosynthesis of sex-steroid hormones.

7 The female sex steroid hormones 17beta-estradiol and progesterone m

8 In order to better understand where sex steroid hormones act to regulate social behavior in

9 e data reveal mechanisms not only for female sex steroid hormone action but also in the regulation of

10 the physiology and pathophysiology of female sex steroid hormone actions in target organs.

11 We discuss the important role of sex steroid hormones and of neurotrophins in creating a

12 suggest a heritable component to circulating sex steroid hormones and sex hormone-binding globulin (S

13 sequent nuclear translocation in response to sex steroid hormones and stress stimuli.

14 use, it is becoming increasingly clear that sex steroid hormones, and in particular the principle fe

15 tions in endogenous postmenopausal levels of sex steroid hormones are not substantially related to th

16 sheep but not in monkeys or humans, although sex steroid hormones are still secreted.

17 Several endocrine factors, including sex-steroid hormones are known to influence adiponectin

18 e ERalpha in the human eye suggests that the sex steroid hormone axis may play a role in the pathogen

19 Vocal plasticity is linked to the actions of sex steroid hormones, but the precise mechanisms are unc

20 in male 3xTg-AD mice depleted of endogenous sex steroid hormones by gonadectomy (GDX).

21 receptor- and progesterone receptor-mRNA in sex steroid hormone-concentrating brain areas of the par

22 t correlations between urinary BPA and serum sex steroid hormone concentrations in adults.

23 e assessed pubertal staging, measured plasma sex steroid hormone concentrations, and analysed semen q

24 Sex-steroid hormone concentrations were assayed by using

25 Sex steroid hormones contribute significantly to sex-bas

26 act symptoms (LUTS), and it is not clear how sex steroid hormones contribute to the rates of change i

27 ine epinephrine output (but not cortisol and sex steroid hormones) correlated inversely with proinfla

28 The phenotype depends on sex-steroid hormones: dihydrotestosterone treatment of g

29 oculture system was used to demonstrate that sex steroid hormones direct development of a sexually di

30 may be mediated by organizational actions of sex steroid hormones during development.

31 ns and songbirds is linked to the actions of sex steroid hormones during ontogeny but also in adultho

32 evaluated how the organizational effects of sex steroid hormones during postnatal development may af

33 brain regions develop under the influence of sex steroid hormones during the perinatal period, but ho

34 cent studies have shown that progesterone, a sex steroid hormone, enhances the sexual transmission of

35 The sex-steroid hormone estradiol (E2) enhances the psychoac

36 The female sex steroid hormones, estrogens and progesterone, are pr

37 Sex steroid hormones exert a profound influence on the s

38 Sex steroid hormones exert opposite effects on lung matu

39 ing and estradiol in the mechanisms by which sex-steroid hormone fluctuations provoke depressive symp

40 Sex steroid hormones have been shown to affect the expre

41 Altered concentrations of sex steroid hormones, impaired reproductive performance,

42 rain neurons are differentially regulated by sex steroid hormones in a dose-dependent manner.

43 sities of neurons that express receptors for sex steroid hormones in a pattern that is remarkably sim

44 Ovariectomy-induced depletion of sex steroid hormones in adult female 3xTg-AD mice signif

45 and clinical observations suggest a role of sex steroid hormones in the occurrence of meningioma.

46 and their relation to circulating levels of sex steroid hormones in women and to risk of endometrial

47 Together, sex steroid hormone-induced activation of WOX1 and WOX2

48 Sex steroid hormones influence the development of sex di

49 al. show that resistance (insensitivity) to sex steroid hormones is encountered in animals lacking m

50 These results suggest that both absolute sex steroid hormone levels and the rates at which the le

51 We measured plasma sex steroid hormones levels in plasma collected in 1989

52 sical function, frailty, renal function, and sex-steroid hormone levels and seemed to be partially me

53 different between men and women, and female sex steroid hormones likely have a role in this regulati

54 in the interrelationship between endogenous sex-steroid hormone metabolism, risk factors and disease

55 lar and biochemical mechanisms through which sex-steroid hormones modulate memory, and a specific hyp

56 was an important mediator of the effects of sex steroid hormones on T47D cell proliferation.

57 Despite the well-known influence of sex steroid hormones on the incidence of cardiovascular

58 recent decades has demonstrated that ovarian sex-steroid hormones, particularly 17beta-estradiol (E2)

59 Genetic variation in genes in the sex steroid hormone pathway is associated with differenc

60 rtium, 874 SNPs in 37 candidate genes in the sex steroid hormone pathway were examined in relation to

61 P<5 x 10(-8)), implicating genes involved in sex steroid hormone pathways (FN1, CCDC170, ESR1, SYNE1

62 stem provides a model for the important role sex steroid hormones play in mediating adult neural plas

63 Although age, genetics, and sex steroid hormones play prominent roles in the cause o

64 The sex steroid hormone progesterone (Pg) is critically invo

65 idization experiments showed that the female sex steroid hormone, progesterone, decreases steady stat

66 rmones, local growth factors and circulating sex steroid hormones promote pituitary tumor growth and

67 response of the uterine epithelium to female sex steroid hormones provides an excellent model to stud

68 Sex steroid hormone receptors are expressed in the colon

69 in and support the important role of nuclear sex steroid hormone receptors in modulating social behav

70 leotide polymorphisms (SNP) in genes for the sex-steroid hormone receptors are not strongly associate

71 hemicals (EDCs) due to their ability to bind sex-steroid hormone receptors.

72 Sex steroid hormones regulate various neural functions t

73 Sex steroid hormones released from the gonads play an im

74 nse to infection were related to circulating sex steroid hormones, sex steroid concentrations were ma

75 near specific genes with important roles in sex steroid hormone signalling and function, and offer u

76 rtility, with low levels of gonadotropic and sex steroid hormones, small testes or ovaries, impaired

77 Sex steroid hormones such as estrogen and testosterone h

78 ed endogenous concentrations of estradiol, a sex steroid hormone that is known to influence UL risk.

79 07, to examine associations between baseline sex steroid hormones, the rate of change in these hormon

80 Here, we used the cross-sex steroid hormone treatment of transsexuals seeking se

81 tional analyses of caregiving and endogenous sex steroid hormones were also conducted.

82 asonal fluctuations in circulating levels of sex-steroid hormones, which are known to be potent neuro