ライフサイエンスコーパス: luteinizing hormone

1 ailure (low/normal testosterone and elevated luteinizing hormone).

2 and lower levels of endogenous estradiol and luteinizing hormone.

3 gesterone, follicle-stimulating hormone, and luteinizing hormone.

4 iosynthesis before the preovulatory surge of luteinizing hormone.

5 d all had abnormal secretion of GnRH-induced luteinizing hormone.

6 in a significant decrease in serum levels of luteinizing hormone.

7 ted by the downstream pulsatile secretion of luteinizing hormone.

8 e, thereby inhibiting the proestrus surge in luteinizing hormone.

9 Ratios of follicle stimulating hormone to luteinizing hormone, a sexual maturity indicator, in all

10 r GalNAc to N-linked oligosaccharides on the luteinizing hormone alpha subunit and CA6 but not to tho

11 We measured follicle-stimulating hormone and luteinizing hormone and added information on menstrual p

12 oproteins including the glycoprotein hormone luteinizing hormone and carbonic anhydrase-6 (CA6).

13 A limited number of glycoproteins including luteinizing hormone and carbonic anhydrase-VI (CA6) bear

14 yp2j5 (-/-) mice, but their plasma levels of luteinizing hormone and follicle stimulating hormone wer

15 The pituitary glycoprotein hormones, luteinizing hormone and follicle-stimulating hormone (FS

16 d equally well to the stimulatory actions of luteinizing hormone and follicle-stimulating hormone and

17 ce also have decreased circulating levels of luteinizing hormone and follicle-stimulating hormone but

18 The corresponding serum luteinizing hormone and follicle-stimulating hormone fel

19 Pituitary (luteinizing hormone and follicle-stimulating hormone) an

20 pulsatile release of gonadotropin hormones (luteinizing hormone and follicle-stimulating hormone) fr

21 gent induced high levels of the gonadotropin luteinizing hormone and increased the serum concentratio

22 e time course or the plasma concentration of luteinizing hormone and its physiological effects on the

23 -releasing hormone (GnRH) induces a surge of luteinizing hormone and ovulation in a variety of specie

24 Blood luteinizing hormone and prolactin (as a positive control

25 r that is efficacious for the suppression of luteinizing hormone and testosterone in primates.

26 axis and, thus, normalizes hormone levels of luteinizing hormone and testosterone.

27 restores gonadotrophin secretion, as well as luteinizing hormone and thyroid-stimulating hormone puls

28 Serum levels of LH (luteinizing hormone) and testosterone were measured by r

29 sisting of an alpha subunit, also present in luteinizing hormone, and a unique beta subunit, which is

30 ormones: human chorionic gonadotropin, human luteinizing hormone, and follicle stimulating hormone by

31 Estradiol, progesterone, luteinizing hormone, and follicle-stimulating hormone we

32 erum levels of CRP, estradiol, progesterone, luteinizing hormone, and follicle-stimulating hormone we

33 droepiandrosterone (DHEAS), androstenedione, luteinizing hormone, and follicle-stimulating hormone.

34 d levels of follicle-stimulating hormone and luteinizing hormone, and increased variability of estrad

35 owth factor 1, follicle-stimulating hormone, luteinizing hormone, and testosterone levels).

36 for zonulin and antibodies against GnRH and luteinizing hormone, and their receptors.

37 l follicles, independently of an increase in luteinizing hormone, and this phenotype can be reversed

38 nadotropins follicle-stimulating hormone and luteinizing hormone are heterodimeric glycoproteins expr

39 estradiol, follicle-stimulating hormone, and luteinizing hormone around the woman's own mean levels w

40 e required for gonadotrope specification and luteinizing hormone beta (LH beta) gene expression.

41 hether MIP-2A can transcriptionally regulate luteinizing hormone beta (LHbeta), a pituitary-specific

42 riptional activation of both the FSHbeta and luteinizing hormone beta subunit (LHbeta) gene promoters

43 arche by regulating the transcription of the luteinizing hormone beta subunit.

44 utant mouse, whereas proopiomelanocortin and luteinizing hormone beta-subunit expression were normal

45 Tight regulation of luteinizing hormone-beta subunit (LHbeta) expression is

46 2 binding to the active but unphosphorylated luteinizing hormone/choriogonadotropin receptor (LH/CG R

47 hat agonist-dependent desensitization of the luteinizing hormone/choriogonadotropin receptor (LH/CG R

48 ine 3 (Org 41841), a partial agonist for the luteinizing hormone/choriogonadotropin receptor (LHCGR)

49 Signaling by the luteinizing hormone/choriogonadotropin receptor (LHR) is

50 We tested here, using hypogonadal luteinizing hormone/choriongonadotropin receptor (LHCGR)

51 The luteinizing hormone chorionic gonadotropin receptor (LHC

52 identified previously as an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHC

53 mical analysis colocalized expression of the luteinizing hormone/chorionic gonadotropin receptor, PRO

54 , and lower follicle-stimulating hormone and luteinizing hormone (each P < .01).

55 energy, vitamin E intake, physical activity, luteinizing hormone, follicle-stimulating hormone, and p

56 nophore-induced acrosome reaction as well as luteinizing hormone, follicle-stimulating hormone, and t

57 Estradiol, progesterone, luteinizing hormone, follicle-stimulating hormone, sex h

58 ycle arrested at prophase of meiosis I until luteinizing hormone from the pituitary acts on the folli

59 onding with an increase in expression of the luteinizing hormone gene, Lhb We demonstrate that poorly

60 Human luteinizing hormone (hLH) and human chorionic gonadotrop

61 Activation of the luteinizing hormone/human chorionic gonadotropin (LH/hCG

62 third transmembrane alpha-helix (TM3) of the luteinizing hormone/human chorionic gonadotropin recepto

63 The luteinizing hormone/human chorionic gonadotropin recepto

64 adrenocorticotropic hormone, prolactin, and luteinizing hormone hyperplasia.

65 Oral administration of 10b suppressed luteinizing hormone in castrated macaques.

66 es the interictal and postictal secretion of luteinizing hormone in mesial temporal lobe epilepsy.

67 ony between follicle-stimulating hormone and luteinizing hormone in the luteal phase.

68 hCGbeta evolved from the beta subunit of luteinizing hormone in two phases.

69 one administration results in suppression of luteinizing hormone in wild-type male mice, but paradoxi

70 ed puberty associated with low or apulsatile luteinizing hormone) in both humans and in the mouse mod

71 arcuate nucleus, and a reduced compensatory luteinizing hormone increase compared with control anima

72 er (13.4+/-3.2 nmol per liter, P<0.001), the luteinizing hormone level increased from 2.7+/-2.0 to 8.

73 one, follicle-stimulating hormone level, and luteinizing hormone level were measured and testicular h

74 had higher follicle-stimulating hormone and luteinizing hormone levels and lower estradiol levels at

75 e mean (SE) follicle-stimulating hormone and luteinizing hormone levels decreased to 8.6 (0.4) mIU/mL

76 , E1, E1S, follicle-stimulating hormone, and luteinizing hormone levels in all patients and the propo

77 ale mice, but paradoxically stimulates serum luteinizing hormone levels in GPRC6A(-/-) null mice.

78 estrous cycles and elevated testosterone and luteinizing hormone levels, suggesting altered hypothala

79 strongly associates with PCOS diagnosis and luteinizing hormone levels.

80 varies lacking corpora lutea and increase in luteinizing hormone levels.

81 he number of days from the midcycle surge in luteinizing hormone (LH) (P=.008).

82 s thought to be indirectly controlled by the luteinizing hormone (LH) acting through the LH/choriogon

83 Meiosis in mammalian oocytes is paused until luteinizing hormone (LH) activates receptors in the mura

84 Luteinizing hormone (LH) acts on ovarian follicles to re

85 The signaling pathway by which luteinizing hormone (LH) acts on the somatic cells of ve

86 with consequent diminished levels of plasma luteinizing hormone (LH) and correspondingly attenuated

87 esis and secretion of gonadotropic hormones, luteinizing hormone (LH) and follicle stimulating hormon

88 osynthesis and release of the gonadotropins, luteinizing hormone (LH) and follicle stimulating hormon

89 ith gonadotropic endocrine cells [expressing luteinizing hormone (LH) and follicle-stimulating hormon

90 Luteinizing hormone (LH) and follicle-stimulating hormon

91 close to follicle-stimulating hormone (FSH), luteinizing hormone (LH) and growth hormone (GH) cells.

92 ssociation between serum levels of wild-type luteinizing hormone (LH) and ovarian cancer risk.

93 In GnRH-CREB KO mice, basal levels of luteinizing hormone (LH) and the postovariectomy increme

94 of gonadotropin releasing hormone (GnRH) and luteinizing hormone (LH) are pivotal events in female re

95 FSH and luteinizing hormone (LH) are secreted constitutively or

96 oma cells were treated with the gonadotropin luteinizing hormone (LH) at concentrations equivalent to

97 The half-life for luteinizing hormone (LH) clearance increases in Mrc1(-/-

98 serum follicle-stimulating hormone (FSH) and luteinizing hormone (LH) clearly separated hypogonadotro

99 validate AutoDecon for application to serum luteinizing hormone (LH) concentration time series using

100 A surge of luteinizing hormone (LH) from the pituitary gland trigge

101 (GNRH)-stimulated synthesis and secretion of luteinizing hormone (LH) from the pituitary gonadotroph.

102 ating follicle-stimulating hormone (FSH) and luteinizing hormone (LH) gene expression in the pituitar

103 inhibited the kisspeptin-induced release of luteinizing hormone (LH) in rats and mice and blocked th

104 or tissue remodeling process is triggered by luteinizing hormone (LH) in the ovarian follicle.

105 and then augments (positive feedback) serum luteinizing hormone (LH) increased Kiss1 mRNA density an

106 Luteinizing hormone (LH) induces maturational processes

107 The pulsatile release of luteinizing hormone (LH) is critical for mammalian ferti

108 Synthesis of luteinizing hormone (LH) is tightly controlled by a comp

109 c mouse strain that has chronically elevated luteinizing hormone (LH) levels (LH-CTP).

110 along with minimal repression of circulating luteinizing hormone (LH) levels and no change in the lip

111 The mean luteinizing hormone (LH) levels in ovariectomized rats w

112 Follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels were measured in a subse

113 etion of GnRH is also reduced as basal serum luteinizing hormone (LH) levels were significantly lower

114 he fabrication of a nanosensor for detecting luteinizing hormone (LH) of sheep using a gold nanoparti

115 To determine whether the action of luteinizing hormone (LH) on the mouse ovarian follicle c

116 Luteinizing hormone (LH) pulsatility, body weight, ovari

117 Adult obesity is associated with blunted luteinizing hormone (LH) pulse amplitude that is partial

118 fertility, is associated with an increase in luteinizing hormone (LH) pulse frequency, implicating ab

119 from adults with previous reports of in vivo luteinizing hormone (LH) pulse frequency.

120 eavage, we sought to convert the noncleaving luteinizing hormone (LH) receptor (LHR) into a cleaved,

121 r cells in that they were 3betaHSD-negative, luteinizing hormone (LH) receptor (LHR)-negative, and pl

122 Recent studies suggest that luteinizing hormone (LH) receptor activation leads to tr

123 licular development, including expression of luteinizing hormone (LH) receptor by the granulosa cells

124 , an intracellular messenger formed when the luteinizing hormone (LH) receptor is activated.

125 l mechanisms play a major role in regulating luteinizing hormone (LH) receptor mRNA expression in the

126 Luteinizing hormone (LH) receptor mRNA is post-transcrip

127 eral motions of individual FLAG-tagged human luteinizing hormone (LH) receptors expressed on CHO cell

128 ave examined their ability to stimulate GnRH/luteinizing hormone (LH) release after peripheral or cen

129 atography was identified as OIF by eliciting luteinizing hormone (LH) release and ovulation in llamas

130 r the female-typical cyclic surge pattern of luteinizing hormone (LH) release.

131 provides the drive necessary for tonic GnRH/luteinizing hormone (LH) release.

132 acy and duration of action) of inhibition of luteinizing hormone (LH) release.

133 easing hormone (GnRH) neurons and subsequent luteinizing hormone (LH) release.

134 there is no information on the regulation of luteinizing hormone (LH) secretion by NKB or its recepto

135 positive and negative feedback control over luteinizing hormone (LH) secretion during the ovulatory

136 Locomotor activity and luteinizing hormone (LH) secretion in golden hamsters sh

137 istration of senktide (NK3R agonist) induced luteinizing hormone (LH) secretion in prepubertal and pe

138 the mRNA expression of pituitary LH-RH-R and luteinizing hormone (LH) secretion in three experimental

139 on of these neurons would generate pulsatile luteinizing hormone (LH) secretion in vivo.

140 s characterized by the pattern of endogenous luteinizing hormone (LH) secretion on the basis of frequ

141 Changes in luteinizing hormone (LH) secretion that are observed in

142 (GnRH) neurons, which in turn supports basal luteinizing hormone (LH) secretion.

143 c area (POA) to elicit a biphasic profile of luteinizing hormone (LH) secretion.

144 s of activation required to evoke a pulse of luteinizing hormone (LH) secretion.

145 g and follicle-stimulating hormone (FSH) and luteinizing hormone (LH) secretion.

146 Luteinizing hormone (LH) stimulates steroidogenesis larg

147 Although mammalian oocytes ovulated after luteinizing hormone (LH) stimulation can be fertilized a

148 riggers germinal vesicle breakdown after the luteinizing hormone (LH) surge and reentry into the meio

149 have demonstrated that IL-1beta inhibits the luteinizing hormone (LH) surge during the afternoon of p

150 e in the generation of the preovulatory GnRH/luteinizing hormone (LH) surge in the female rodent.

151 linked to the induction of the preovulatory luteinizing hormone (LH) surge in the rat.

152 ntained in prophase meiotic arrest until the luteinizing hormone (LH) surge induces reentry into the

153 ut not males, to display an estrogen-induced luteinizing hormone (LH) surge is consistent with the hi

154 provides for the timing of the preovulatory luteinizing hormone (LH) surge necessary for ovulation i

155 irregular estrous cycles, lack a coordinated luteinizing hormone (LH) surge on the day of proestrus,

156 to escalating levels of estrogen, express a luteinizing hormone (LH) surge that is prompted by a sur

157 GnRH) surge is a prerequisite signal for the luteinizing hormone (LH) surge that triggers ovulation.

158 The midcycle luteinizing hormone (LH) surge triggers several tightly

159 the DM, up to the stage of the preovulatory luteinizing hormone (LH) surge, is impaired.

160 induction of maturation by the preovulatory luteinizing hormone (LH) surge.

161 event underlying generation of the ovulatory luteinizing hormone (LH) surge.

162 tion is induced by the preovulatory surge of luteinizing hormone (LH) that acts on the ovary and trig

163 fully grown follicles, prior to the surge of luteinizing hormone (LH) that triggers meiotic resumptio

164 at clearance rates for glycoproteins such as luteinizing hormone (LH) that undergo regulated release

165 Serum luteinizing hormone (LH) was likewise suppressed within

166 n-deficient mice exhibit increased levels of luteinizing hormone (LH), a pituitary hormone that regul

167 d concentrations of estradiol, progesterone, luteinizing hormone (LH), and follicle-stimulating hormo

168 mones follicle-stimulating hormone (FSH) and luteinizing hormone (LH), and that ovarian steroids exer

169 pin's follicle-stimulating hormone (FSH) and luteinizing hormone (LH), both of which are heterodimers

170 In response to luteinizing hormone (LH), cGMP in the granulosa cells de

171 BG), dehydroepiandrosterone sulfate (DHEAS), luteinizing hormone (LH), follicle-stimulating hormone (

172 The gonadotropins, luteinizing hormone (LH), follicle-stimulating hormone (

173 Estradiol, estrone, testosterone, luteinizing hormone (LH), follicle-stimulating hormone (

174 Luteinizing hormone (LH), produced in the anterior lobe

175 pins, follicle-stimulating hormone (FSH) and luteinizing hormone (LH), under the control of pulsatile

176 ine, beta-endorphin, and enkephalin) inhibit luteinizing hormone (LH), vasopressin (VP), and oxytocin

177 In response to luteinizing hormone (LH), which binds to receptors on th

178 Dendrimer 3 showed similar luteinizing hormone (LH)-release activity to triptorelin

179 n by mature Leydig cells in vivo, we treated luteinizing hormone (LH)-stimulated adult male rats and

180 t measured urinary estrone-3-glucuronide and luteinizing hormone (LH).

181 tes under the pulsatile control of pituitary luteinizing hormone (LH).

182 in calcium oscillations and the secretion of luteinizing hormone (LH).

183 or Ink4c and Ink4d produces normal levels of luteinizing hormone (LH).

184 tory follicles resume meiosis in response to luteinizing hormone (LH).

185 ensatory elevation in levels of gonadotropin luteinizing hormone (LH).

186 ins, follicle-stimulating hormone (FSH), and luteinizing hormone (LH).

187 se hamster ovary cells expressing either the luteinizing hormone (LH)/chorionic gonadotropin (CG) or

188 ose demonstrating the presence of functional luteinizing hormone (LH)/hCG receptors in human breast c

189 to the pituitary and the resulting surge of luteinizing hormone (LH); however, the neural circuits t

190 ol <184 pmol/l (50 pg/ml), FSH <10 IU/l, and luteinizing hormone <10 IU/l, was significantly more pre

191 t explained by any deficits in testosterone, luteinizing hormone, or follicle-stimulating hormone con

192 e generated by breeding MMTV-Neu mice with a luteinizing hormone-overexpressing mouse model of ovaria

193 /23), mainly in follicle-stimulating hormone/luteinizing hormone-producing (38%) and null cell (57%)

194 the fasting-associated decrease in overnight luteinizing hormone pulse frequency but had no effect on

195 onic epilepsy was associated with changes in luteinizing hormone pulse frequency, amplitude, and mass

196 high free testosterone, and fewer numbers of luteinizing hormone pulses, but not polycystic-appearing

197 creases in testosterone and the testosterone/luteinizing hormone ratio were detected in men watching

198 t study investigated regulation of the human luteinizing hormone receptor (hLHR) gene by histone deac

199 The luteinizing hormone receptor (LHR) and beta2-adrenergic

200 n hormones to their cognate human receptors (luteinizing hormone receptor (LHR) and thyroid-stimulati

201 n A (TSA), induces derepression of the human luteinizing hormone receptor (LHR) gene by de-recruitmen

202 Transcription of luteinizing hormone receptor (LHR) gene is activated by

203 ously demonstrated that transcription of the luteinizing hormone receptor (LHR) gene is subject to re

204 We have demonstrated that silencing of luteinizing hormone receptor (LHR) gene transcription is

205 the past decade, however, the expression of luteinizing hormone receptor (LHR) has also been reporte

206 Our previous studies have identified a luteinizing hormone receptor (LHR) mRNA-binding protein

207 utant can inhibit signaling to G(s) from the luteinizing hormone receptor by 97% and from the calcito

208 Luteinizing hormone receptor is a G protein-coupled rece

209 s in the HinRs and the interhelical loops of luteinizing hormone receptor/follicle stimulating hormon

210 erize with its closely related receptor, the luteinizing hormone receptor; this association may have

211 ollicular differentiation markers, including luteinizing-hormone receptor (LHR), inhibin-alpha, micro

212 PD-PALM of two functionally defined mutant luteinizing hormone receptors (LHRs), a ligand-binding d

213 as well as human chorionic gonadotropin and luteinizing hormone receptors on male breast tissue, may

214 Increased luteinizing hormone relative to follicle-stimulating hor

215 2) priming completely blocks hormone-induced luteinizing hormone release and partially inhibits hormo

216 series induced a much prolonged increase of luteinizing hormone release compared to KP10 and increas

217 , and screened for duration of inhibition of luteinizing hormone release in a castrated male rat assa

218 Inhibition of luteinizing hormone release over time was measured in th

219 ive degradation in the orderliness of serial luteinizing hormone release.

220 Luteinizing hormone releasing hormone (LHRH) gene transc

221 n of prostaglandin E2, which then stimulates luteinizing hormone releasing hormone (LHRH) neurons to

222 dy single-chain variable fragment (scFv) and luteinizing hormone releasing hormone (LHRH) peptide, re

223 Cytotoxic analogue of luteinizing hormone releasing hormone (LHRH), AN-207, bi

224 Irradiation of luteinizing hormone releasing hormone (LHRH), growth hor

225 n releasing hormone-1 [GnRH-1, also known as luteinizing hormone releasing hormone (LHRH)] neurons ca

226 Bilateral orchiectomy or luteinizing hormone releasing hormone agonists are the r

227 Luteinizing hormone releasing hormone analog (LHRHa, des

228 ombesin (AN-215), somatostatin (AN-238), and luteinizing hormone-releasing hormone (AN-207) consisted

229 Treatment with antagonists of luteinizing hormone-releasing hormone (LH-RH) leads to d

230 Previously, we have shown that two types of luteinizing hormone-releasing hormone (LHRH) -like neuro

231 The effects of depot formulations of the luteinizing hormone-releasing hormone (LHRH) agonist Dec

232 Treatment with a luteinizing hormone-releasing hormone (LHRH) agonist inc

233 orticotropic hormone (ACTH) and hypothalamic luteinizing hormone-releasing hormone (LHRH) agonist, [D

234 Ovarian suppression with luteinizing hormone-releasing hormone (LHRH) agonists is

235 the recent developments on BPH therapy with luteinizing hormone-releasing hormone (LHRH) antagonist

236 tance and (5) a modified synthetic analog of luteinizing hormone-releasing hormone (LHRH) as a target

237 Luteinizing hormone-releasing hormone (LHRH) neurons mig

238 Functionalized with luteinizing hormone-releasing hormone (LHRH) peptide via

239 Importantly, SSA induced by luteinizing hormone-releasing hormone (LHRH) receptor an

240 estigate the mechanism by which Mn2+ induces luteinizing hormone-releasing hormone (LHRH) secretion f

241 s by which the neuroendocrine brain controls luteinizing hormone-releasing hormone (LHRH) secretion.

242 Luteinizing hormone-releasing hormone (LHRH) was used as

243 large doses of Cetrorelix, an antagonist of luteinizing hormone-releasing hormone (LHRH), reduces le

244 naling pathway that prompts the secretion of luteinizing hormone-releasing hormone (LHRH), the neurop

245 ne (LH) surge that is prompted by a surge in luteinizing hormone-releasing hormone (LHRH).

246 othalamic neurons secreting the neuropeptide luteinizing hormone-releasing hormone (LHRH).

247 ng afferent pathways to neurons synthesizing luteinizing hormone-releasing hormone (LHRH, also known

248 coexpressed in neurons containing mammalian luteinizing hormone-releasing hormone (m-LHRH).

249 itive tumors also received letrozole (plus a luteinizing hormone-releasing hormone [LHRH] agonist if

250 diation plus immediate androgen suppression (luteinizing hormone-releasing hormone [LHRH] agonist), w

251 steroid ablation using leuprolide acetate, a luteinizing hormone-releasing hormone agonist (LHRHa), i

252 Luteinizing hormone-releasing hormone agonist (LHRHa; le

253 AST, which was defined as 6 months of both a luteinizing hormone-releasing hormone agonist and an ant

254 ts receiving combined androgen blockade with luteinizing hormone-releasing hormone agonist and bicalu

255 les, followed by total androgen suppression (luteinizing hormone-releasing hormone agonist plus bical

256 tients were randomized soon after initiating luteinizing hormone-releasing hormone agonist with antia

257 n deprivation (AD) to cixutumumab added to a luteinizing hormone-releasing hormone agonist with bical

258 S; two injections of every-3-months depot of luteinizing hormone-releasing hormone agonist) to primar

259 Patients were randomly assigned 2:1 to a luteinizing hormone-releasing hormone agonist, bicalutam

260 Bilateral orchiectomy or luteinizing hormone-releasing hormone agonists are recom

261 ; and three, when chemical suppression using luteinizing hormone-releasing hormone agonists is the ch

262 of 5 ng per milliliter or higher received a luteinizing hormone-releasing hormone analogue and an an

263 Whether the administration of luteinizing hormone-releasing hormone analogues (LHRHa)

264 s monotherapy or with adjuvant castration or luteinizing hormone-releasing hormone superagonists to b

265 For luteinizing hormone-releasing hormone, all but two expec

266 k suggests that cytotoxic peptide analogs of luteinizing hormone-releasing hormone, somatostatin, and

267 ne and metabolic variables were measured and luteinizing hormone sampled over 8 hours on days 2 to 5

268 hormone-secreting (GH-secreting) GH3 cells, luteinizing hormone-secreting (LH-secreting) LbetaT2 cel

269 for estradiol-mediated suppression of tonic luteinizing hormone secretion (an indirect measure of Gn

270 crucial role in the regulation of pituitary luteinizing hormone secretion and reproduction.

271 Pulsatile luteinizing hormone secretion and spermatogenesis were d

272 We characterized luteinizing hormone secretion in patients with mesial te

273 Deconvolution analysis defined luteinizing hormone secretion in terms of interpulse int

274 rs in GnIH-ir nuclei, and GnIH inhibition of luteinizing hormone secretion indicate the discovery of

275 stent with a role in regulating preovulatory luteinizing hormone secretion, rostral projections from

276 cute seizures induced timing irregularity in luteinizing hormone secretion, whereas chronic epilepsy

277 ted a robust GnRH discharge, as reflected by luteinizing hormone secretion, which was abolished by pr

278 In vivo GnIH administration rapidly inhibits luteinizing hormone secretion.

279 lels between MSP signaling in C. elegans and luteinizing hormone signaling in mammals.

280 g, n = 24; 12.8 nmol/kg, n = 24) to induce a luteinizing hormone surge and egg maturation.

281 otein increased >10-fold after the ovulatory luteinizing hormone surge in wild-type but not PRKO mice

282 t in the ovary for extended periods before a luteinizing hormone surge induces entry into the first m

283 eleasing hormone (GnRH) release triggers the luteinizing hormone surge that induces ovulation.

284 losa cells of periovulatory follicles by the luteinizing hormone surge through a progesterone recepto

285 han during the luteal phase (6-10 days after luteinizing hormone surge).

286 ein alters the amplitude of the preovulatory luteinizing hormone surge, likely by perturbing GnRH rel

287 n several hours after the ovulation-inducing luteinizing hormone surge, whereas they undergo differen

288 kisspeptin is involved in generation of the luteinizing hormone surge, which is required for ovulati

289 d by the puberty-triggering and preovulatory luteinizing hormone surge-mediating peptide, kisspeptin.

290 expected time of the proestrous preovulatory luteinizing hormone surge.

291 d for regulation of a full preovulatory-like luteinizing hormone surge.

292 rsting activity associated with the GnRH/LH (luteinizing hormone) surge.

293 n brain slices from a model exhibiting daily luteinizing hormone surges.

294 ens, disrupted reproductive cycles, and high luteinizing hormone, the latter reflecting increased gon

295 Luteinizing hormone then acts on receptors in outer gran

296 nts with abnormal levels of testosterone and luteinizing hormone was less pronounced-57% and 21%, res

297 estradiol, total and free testosterone, and luteinizing hormone were higher by 5.26% (95% CI: 1.27%,

298 ic antigen, thyroid stimulating hormone, and luteinizing hormone) were printed in an array format ont

299 tes pituitary synthesis of a large amount of luteinizing hormone, which is required for ovulation.

300 We used transgenic mice that overexpress luteinizing hormone with subsequent ovarian hyperstimula