ライフサイエンスコーパス: pituitary hormone

1 tructures or the inappropriate expression of pituitary hormones.

2 denomas that stained positively for anterior pituitary hormones.

3 tructures or the inappropriate expression of pituitary hormones.

4 mice, we assayed for changes in thyroid and pituitary hormones.

5 CART peptide on food intake and circulating pituitary hormones.

6 in binding sulfated glycoproteins including pituitary hormones.

7 R) binds to sulfated glycoproteins including pituitary hormones.

8 ) and one or more of the other five anterior pituitary hormones.

9 mpromised production of one or more anterior pituitary hormones.

10 nous ligands alters plasma levels of several pituitary hormones.

11 n rates and elimination kinetics of selected pituitary hormones (ACTH, LH and GH).

12 The pituitary hormones adrenocorticotropic hormone (ACTH), b

13 nt studies, MIF has been found to be a novel pituitary hormone and the first protein identified to be

14 The capacity of these proteins to activate pituitary hormone and transcription factor gene promoter

15 mulation of brain AT(1) receptors, regulates pituitary hormones and autonomic activity.

16 aracterized by the deficiency of one or more pituitary hormones and can present alone or in associati

17 t of ICV injection of CART peptide on plasma pituitary hormones and finally to examine the effect of

18 nduced changes in activity, vital signs, and pituitary hormones are modulated by the orexinergic syst

19 Anterior pituitary hormones are required for development and func

20 This process is tightly controlled by the pituitary hormone arginine vasopressin and defective tra

21 , interferon gamma, calcium, phosphorus, and pituitary hormones as well as the secosteroid hormone 1,

22 the cDNA coding for eel somatolactin (SL), a pituitary hormone belonging to the growth hormone (GH)/p

23 , suggesting that the cells not only control pituitary hormones but also may modulate nearby neurons.

24 GSU-Cre, loxP mice had normal levels of most pituitary hormones, but had markedly decreased expressio

25 ACAP) stimulates release of several anterior pituitary hormones by interacting with PACAP receptors o

26 Hypophysectomy and the attendent loss of pituitary hormones, by contrast, decreased MIF protein c

27 The results indicate that pituitary hormones can adapt the mechanics of adrenal ca

28 ave insufficient levels of multiple anterior pituitary hormones causing short stature, metabolic dise

29 Sox2 mutations are associated with pituitary hormone deficiencies and the protein is requir

30 The pituitary hormone deficiencies cause secondary endocrine

31 Congenital pituitary hormone deficiencies have been reported in app

32 ne deficiency, either alone or with multiple pituitary hormone deficiencies, as identified by clinica

33 Pituitary hormone deficiencies, with Growth Hormone defi

34 fied in several human families with multiple pituitary hormone deficiencies.

35 2 regions have been associated with combined pituitary hormone deficiency (CPHD) diseases, suggesting

36 Children with combined pituitary hormone deficiency (CPHD) have insufficient le

37 Combined pituitary hormone deficiency (CPHD) in man denotes impai

38 n patients with retarded growth and combined pituitary hormone deficiency and also abnormal neck and

39 To study the contribution by combined pituitary hormone deficiency and by the local SMPD3 defi

40 complex diseases featuring combined anterior pituitary hormone deficiency and, in specific cases, los

41 x transcription factors LHX4 and PROP1 cause pituitary hormone deficiency in both humans and mice.

42 ons in the gene are associated with combined pituitary hormone deficiency in human patients and anima

43 e show here that this novel form of combined pituitary hormone deficiency is characterized by the per

44 are the predominant cause of MPHD (multiple pituitary hormone deficiency) in humans.

45 isolated growth hormone deficiency, combined pituitary hormone deficiency, and syndromes such as sept

46 ation in human PIT1(R271W), causing combined pituitary hormone deficiency, results in loss of Pit1 as

47 th fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, seizures, severe visual im

48 growth pathogenesis associated with combined pituitary hormone deficiency.

49 ses, giving rise to the syndrome of combined pituitary hormone deficiency.

50 LHX3 gene that is associated with a combined pituitary hormone disorder.

51 dwarf (dw/dw) mice are deficient in anterior pituitary hormones due to a mutation in the gene encodin

52 ntibody that targets the beta-subunit of the pituitary hormone follicle-stimulating hormone (Fsh) inc

53 statin on pituitary hormone secretion and on pituitary hormone (follicle-stimulating hormone and prol

54 chorionic gonadotropin (CG) and the anterior pituitary hormones follitropin, lutropin, and thyrotropi

55 We have shown that the pituitary hormone FSH, the levels of which are high duri

56 minal oligosaccharide sequences for anterior pituitary hormone function.

57 quences located within the promoters of some pituitary hormone genes.

58 by ERalpha appeared to be mediated through a pituitary hormone (i.e., growth hormone).

59 adenosine controls the secretion of anterior pituitary hormones in vitro, adenosine was incubated wit

60 reover, the pituitary content of a subset of pituitary hormones, including growth hormone, prolactin

61 Levels of selected pituitary hormones increased 24 hours post-cecal ligatio

62 ed that incomplete glycosylation of anterior pituitary hormones leads to the creation of hormone anta

63 CG together with the pituitary hormones lutropin (LH), follitropin, and thyro

64 a1,4GlcNAcbeta1,2Manalpha are present on the pituitary hormones lutropin (LH), thyrotropin, and pro-o

65 the pituitary, with consequent reduction in pituitary hormone output and alterations in sexual and o

66 ediates signaling induced by the polypeptide pituitary hormone prolactin (PRL) has been shown to lead

67 The pituitary hormone prolactin (PRL) is involved in regulat

68 We found that the estrogen-responsive pituitary hormone prolactin (PRL), signaling through hep

69 The anterior pituitary hormone prolactin exerts important physiologic

70 issue in the lactotrophic axis, in which the pituitary hormone prolactin is tonically inhibited by tu

71 udy extended these findings by examining the pituitary hormone prolactin, and its response to stress,

72 mmary gland ductal development, and abnormal pituitary hormone regulation in NOER mice.

73 ry glands, bone, brain, fat differentiation, pituitary hormone regulation, and metabolic effects in m

74 role of the gp130-related cytokines in human pituitary hormone regulation, we tested expression of gp

75 lement-derived cytokine, stimulates anterior pituitary hormone release and activates the hypothalamic

76 c emptying, inhibits feeding, and stimulates pituitary hormone release in rats and primates.

77 anges in hypothalamic regulation of anterior pituitary hormone release, including the decline in medi

78 inflammation and in the control of anterior pituitary hormone release.

79 I (Ang II) system plays an important role in pituitary hormone release.

80 bernation, and metabolism, are controlled by pituitary hormones released in response to annual enviro

81 median eminence (ME) to control long-lasting pituitary hormone rhythms essential for homeostasis.

82 We show that C3a receptors are expressed in pituitary hormone secreting and non-hormone secreting (f

83 formation and specification of the anterior pituitary hormone-secreting cell types.

84 icular nucleus (PVN) differentially regulate pituitary hormone secretion and autonomic output.

85 The effects of pancreastatin on pituitary hormone secretion and on pituitary hormone (fo

86 All the men had otherwise normal anterior pituitary hormone secretion and sellar anatomy.

87 amp analyses and are associated with reduced pituitary hormone secretion from AtT-20 cells.

88 projection to the median eminence to control pituitary hormone secretion possesses a spike initiation

89 n (10(-7) mol/L) treatment did not stimulate pituitary hormone secretion significantly.

90 idism, and the role of IGSF1 as regulator of pituitary hormone secretion.

91 crine cells, and are thus likely to regulate pituitary hormone secretion.

92 the median eminence for controlling anterior pituitary hormone secretion.

93 importantly to viscerosensory modulation of pituitary hormone secretion.

94 hrough its sex-dependent temporal pattern of pituitary hormone secretion.

95 ainstem unrelated to the control of anterior pituitary hormone secretion.

96 additional important functions in regulating pituitary hormone secretion.

97 tary neoplasms and that TGF-beta 1 regulates pituitary hormone secretion.

98 urons is a principal inhibitory regulator of pituitary hormone secretion.

99 nhibited the expression/secretion of several pituitary hormones (specially GH/PRL), which was accompa

100 We show that the distribution of pituitary hormones such as prolactin (PRL), growth hormo

101 n the mammalian ovary occur independently of pituitary hormone support, the factors controlling these

102 In this context, the pituitary hormone that controls thyroid hormone producti

103 reased levels of luteinizing hormone (LH), a pituitary hormone that regulates sex steroid synthesis i

104 We have shown that the anterior pituitary hormone, thyroid-stimulating hormone (TSH), ca

105 ction (including serum concentrations of the pituitary hormone thyrotropin and the thyroid hormones t

106 in adenohypophyseal cells and LIF regulates pituitary hormone transcription and cell replication in

107 The presence of most of the pituitary hormones was confirmed by using MS/MS and pseu

108 ted (15-31%, P < 0.05), while other anterior pituitary hormones were not altered by these cytokines.

109 cterized by an increased release of anterior pituitary hormones, whereas altered target-organ sensiti

110 hesis is activated in steroidogenic cells by pituitary hormones, which concomitantly induce transcrip

111 In primates, placental lactogen (PL) is a pituitary hormone with fundamental roles during pregnanc