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1 nous ligands alters plasma levels of several pituitary hormones.
2 mice, we assayed for changes in thyroid and pituitary hormones.
3 tructures or the inappropriate expression of pituitary hormones.
4 denomas that stained positively for anterior pituitary hormones.
5 tructures or the inappropriate expression of pituitary hormones.
6 CART peptide on food intake and circulating pituitary hormones.
7 in binding sulfated glycoproteins including pituitary hormones.
8 R) binds to sulfated glycoproteins including pituitary hormones.
9 ) and one or more of the other five anterior pituitary hormones.
10 mpromised production of one or more anterior pituitary hormones.
14 ting the reciprocal relationship with tropic pituitary hormone and effector hormone have unraveled an
15 nt studies, MIF has been found to be a novel pituitary hormone and the first protein identified to be
16 The capacity of these proteins to activate pituitary hormone and transcription factor gene promoter
18 aracterized by the deficiency of one or more pituitary hormones and can present alone or in associati
19 popituitarism is a deficiency in one or more pituitary hormones and encompasses a spectrum of clinica
20 t of ICV injection of CART peptide on plasma pituitary hormones and finally to examine the effect of
24 nduced changes in activity, vital signs, and pituitary hormones are modulated by the orexinergic syst
26 This process is tightly controlled by the pituitary hormone arginine vasopressin and defective tra
27 , interferon gamma, calcium, phosphorus, and pituitary hormones as well as the secosteroid hormone 1,
28 the cDNA coding for eel somatolactin (SL), a pituitary hormone belonging to the growth hormone (GH)/p
29 lassical neurotransmitters, hypothalamic and pituitary hormones, biogenic amines, melatonin, and gluc
30 , suggesting that the cells not only control pituitary hormones but also may modulate nearby neurons.
31 GSU-Cre, loxP mice had normal levels of most pituitary hormones, but had markedly decreased expressio
32 the evidence of local production of certain pituitary hormones by bone marrow-derived cells displays
33 ACAP) stimulates release of several anterior pituitary hormones by interacting with PACAP receptors o
34 Hypophysectomy and the attendent loss of pituitary hormones, by contrast, decreased MIF protein c
36 ave insufficient levels of multiple anterior pituitary hormones causing short stature, metabolic dise
37 secretion, plasma osmolality, haematocrit or pituitary hormone content, and reviewed them in light of
41 ne deficiency, either alone or with multiple pituitary hormone deficiencies, as identified by clinica
44 2 regions have been associated with combined pituitary hormone deficiency (CPHD) diseases, suggesting
48 n patients with retarded growth and combined pituitary hormone deficiency and also abnormal neck and
50 complex diseases featuring combined anterior pituitary hormone deficiency and, in specific cases, los
51 x transcription factors LHX4 and PROP1 cause pituitary hormone deficiency in both humans and mice.
52 ons in the gene are associated with combined pituitary hormone deficiency in human patients and anima
53 e show here that this novel form of combined pituitary hormone deficiency is characterized by the per
56 isolated growth hormone deficiency, combined pituitary hormone deficiency, and syndromes such as sept
57 ation in human PIT1(R271W), causing combined pituitary hormone deficiency, results in loss of Pit1 as
58 th fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, seizures, severe visual im
64 dwarf (dw/dw) mice are deficient in anterior pituitary hormones due to a mutation in the gene encodin
65 ntibody that targets the beta-subunit of the pituitary hormone follicle-stimulating hormone (Fsh) inc
66 statin on pituitary hormone secretion and on pituitary hormone (follicle-stimulating hormone and prol
67 chorionic gonadotropin (CG) and the anterior pituitary hormones follitropin, lutropin, and thyrotropi
75 ormone have unraveled an independent role of pituitary hormone in skeletal remodeling beyond the role
76 adenosine controls the secretion of anterior pituitary hormones in vitro, adenosine was incubated wit
77 reover, the pituitary content of a subset of pituitary hormones, including growth hormone, prolactin
80 ed that incomplete glycosylation of anterior pituitary hormones leads to the creation of hormone anta
84 correctly predicts the mean daily levels of pituitary hormones LH and FSH, and ovarian hormones E2,
86 a1,4GlcNAcbeta1,2Manalpha are present on the pituitary hormones lutropin (LH), thyrotropin, and pro-o
88 the pituitary, with consequent reduction in pituitary hormone output and alterations in sexual and o
89 g, whereas most of their upstream regulating pituitary hormones peak only months later, in summer.
91 n self-renew and differentiate into multiple pituitary hormone-producing cell types as organoids.
92 complete deficiency of anterior or posterior pituitary hormone production leads to central hypoadrena
93 ific mRNA binding proteins in the control of pituitary hormone production, pituitary responses to hyp
94 ediates signaling induced by the polypeptide pituitary hormone prolactin (PRL) has been shown to lead
99 issue in the lactotrophic axis, in which the pituitary hormone prolactin is tonically inhibited by tu
100 udy extended these findings by examining the pituitary hormone prolactin, and its response to stress,
102 e (TIDA) neurons that control release of the pituitary hormone, prolactin, which triggers key materna
105 ry glands, bone, brain, fat differentiation, pituitary hormone regulation, and metabolic effects in m
106 role of the gp130-related cytokines in human pituitary hormone regulation, we tested expression of gp
107 lement-derived cytokine, stimulates anterior pituitary hormone release and activates the hypothalamic
110 anges in hypothalamic regulation of anterior pituitary hormone release, including the decline in medi
114 bernation, and metabolism, are controlled by pituitary hormones released in response to annual enviro
116 median eminence (ME) to control long-lasting pituitary hormone rhythms essential for homeostasis.
117 We show that C3a receptors are expressed in pituitary hormone secreting and non-hormone secreting (f
123 projection to the median eminence to control pituitary hormone secretion possesses a spike initiation
125 genesis, clinical presentation of disordered pituitary hormone secretion, assessment of hyperprolacti
135 nhibited the expression/secretion of several pituitary hormones (specially GH/PRL), which was accompa
137 n the mammalian ovary occur independently of pituitary hormone support, the factors controlling these
138 y consultation, dedicated pituitary imaging, pituitary hormone testing and visual assessment are warr
140 reased levels of luteinizing hormone (LH), a pituitary hormone that regulates sex steroid synthesis i
142 ction (including serum concentrations of the pituitary hormone thyrotropin and the thyroid hormones t
144 in adenohypophyseal cells and LIF regulates pituitary hormone transcription and cell replication in
147 ted (15-31%, P < 0.05), while other anterior pituitary hormones were not altered by these cytokines.
148 cterized by an increased release of anterior pituitary hormones, whereas altered target-organ sensiti
149 hesis is activated in steroidogenic cells by pituitary hormones, which concomitantly induce transcrip
150 In primates, placental lactogen (PL) is a pituitary hormone with fundamental roles during pregnanc