ライフサイエンスコーパス: median eminence

1 erior hypothalamus, and infundibular nucleus/median eminence.

2 anum vasculosum of the lamina terminalis and median eminence.

3 in may be involved in trafficking PRL in the median eminence.

4 ic part of the supraoptic nucleus and in the median eminence.

5 , arcuate and dorsomedial nuclei, and in the median eminence.

6 e of their maintaining axon terminals in the median eminence.

7 tive (AADC +) cells were also counted in the median eminence.

8 immunoreactivity was very sparse within the median eminence.

9 -oligos were infused directly into the stalk-median eminence.

10 nscriptome present in the choroid plexus and median eminence.

11 rons inhibit GH release by projecting to the median eminence.

12 and olfactory epithelium and project to the median eminence.

13 ptical activation of GnRH projections in the median eminence.

14 ity at the cell body and DA secretion at the median eminence.

15 rvade the internal and external zones of the median eminence.

16 g changes in spontaneous GnRH release in the median eminence.

17 cts to NK3R-expressing GnRH terminals in the median eminence.

18 normally to the dorsal vagal complex and the median eminence.

19 secretory vesicles in nerve terminals in the median eminence.

20 drive the release of GnRH from fibers in the median eminence.

21 ic neurons with extensive projections to the median eminence.

22 to the GnRH terminal microenvironment in the median eminence.

23 CVS does not enhance CRH storage within the median eminence.

24 velopment and extension of GnRH axons to the median eminence.

25 hrough the internal and external zone of the median eminence.

26 ed through the tuberal hypothalamus into the median eminence.

27 e network of nerve fibers was present in the median eminence.

28 the proximity of CRH neuronal fibers in the median eminence.

29 e projections to the exterior portion of the median eminence.

30 both in the inner and the outer zones of the median eminence.

31 other astrocytes in different layers of the median eminence.

32 the processes of tanycytes projecting to the median eminence.

33 ed a dose-dependent increase in DOPAC in the median eminence and a decrease in DOPAC in the nucleus a

34 ity in the axons of the internal zone of the median eminence and a marked reduction in IL-6-like mate

35 lamus, IPe, arcuate nucleus of hypothalamus, median eminence and dorsal hypothalamic area in the dien

36 found double-labeled neurons surrounding the median eminence and in the RCA, Arc, VMH, DMH, and PMV.

37 DOPAC)) in terminals of these neurons in the median eminence and nucleus accumbens, respectively.

38 The lack of RFRP-3 fibers in the median eminence and of Fluoro-Gold uptake from the perip

39 in the rodent anterior pituitary and in the median eminence and paraventricular nucleus of the hypot

40 ecretory nuclei and in cell processes of the median eminence and pituitary stalk.

41 ons where the DA neurons that project to the median eminence and posterior pituitary are located.

42 rt photoperiod (SD) results in a decrease in median eminence and posterior pituitary dopamine (DA) co

43 r, and periventricular nuclei as well as the median eminence and the arcuate nucleus.

44 vocellular and/or magnocellular axons in the median eminence and the posterior pituitary.

45 4-dihydroxyphenylacetic acid (DOPAC), in the median eminence and the three pituitary lobes of lactati

46 within the arcuate nucleus extending to the median eminence and throughout the periventricular zone

47 entricular organs such as subfornical organ, median eminence, and area postrema.

48 including choroid plexus, subfornical organ, median eminence, and area postrema.

49 vity was present in the septum, infundibulum/median eminence, and dorsal medial hypothalamus.

50 onal sprouting into the external zone of the median eminence, and formation of subependymal perivascu

51 1(ARH)) neurons releases kisspeptin into the median eminence, and neurokinin B (NKB) and dynorphin on

52 ing was present in the retrochiasmatic area, median eminence, and posterior periventricular nucleus o

53 the arcuate nucleus of the hypothalamus, the median eminence, and the adrenal medulla.

54 was expressed in the subfornical organ, the median eminence, and the area postrema.

55 also present within the arcuate nucleus, the median eminence, and the tuberal nucleus, and light immu

56 two hypothalamic areas: the arcuate nucleus-median eminence (ARC-ME) and the paraventricular nucleus

57 nt increase in NGFI-B expression in the PVN, median eminence, arcuate nucleus, medial amygdala, CA2 a

58 Incubation with leptin of median eminence-arcuate nuclear explants from the same a

59 edial nucleus, lateral hypothalamic area and median eminence-arcuate nucleus decreased, with the earl

60 labeled CVOs include the subfornical organ, median eminence, area postrema and choroid plexus, and a

61 d that the cytoarchitectural features of the median eminence became disorganized with aging.

62 c nerve fibers were found to project via the median eminence both onto the surface and into the neuro

63 by an increase in the GnRH-ir fibers in the median eminence, but no surge in luteinizing hormone.

64 s prevented the effect of quinelorane in the median eminence, but not the nucleus accumbens.

65 e can act directly on the glial cells in the median eminence by binding to the GluR7 subunit which ma

66 ing brain, reducing innervation of the adult median eminence by GnRH-positive neurites.

67 Innervation of the hypothalamic median eminence by Gonadotropin-Releasing Hormone (GnRH)

68 The hypothalamic arcuate-median eminence complex (Arc-ME) controls energy balance

69 After median eminence compression to produce axonal injury, un

70 ird ventricle and many astrocytes within the median eminence contain the GluR7 receptor subunit mRNA

71 The external/palisade zone of the median eminence contained rich plexuses of small CARTir

72 ry hormone release, including the decline in median eminence DA concentrations.

73 molecular and cellular mechanisms underlying median eminence development and pubertal timing are inco

74 appa opioid receptors with NOR-BNI increased median eminence DOPA, and prevented the stimulatory effe

75 Administration of prolactin also increased median eminence DOPA, but did not alter the ability of q

76 but blocked quinelorane-induced increases in median eminence DOPA.

77 caused a delayed (at 6 and 12 h) increase in median eminence DOPAC concentrations in these animals wh

78 fect of systemic administration of PRL-AB on median eminence DOPAC concentrations suggesting that the

79 B-induced hypoprolactinemia) failed to alter median eminence DOPAC concentrations unless prolactin ex

80 Very few fibers were observed in the median eminence, especially in the external zone.

81 lular neuroendocrine with projections to the median eminence for controlling anterior pituitary hormo

82 showed colocalization in the arcuate nucleus/median eminence/glia limitans region.

83 In the median eminence, immunolabeled processes were restricted

84 CVS did not alter CRH median eminence immunoreactivity, indicating that CVS do

85 r GABAergic (TIGA) neurons projecting to the median eminence in both males and females.

86 rain and midbrain, the optic chiasm, and the median eminence in the forebrain.

87 aining neurons and normal innervation of the median eminence in the hypothalamus, as well as decrease

88 mmunoreactive fibers and varicosities in the median eminence in the pig.

89 ses that ramified in the arcuate nucleus and median eminence, in close association with blood vessels

90 ic nuclei, neural structures adjacent to the median eminence (including the retrochiasmatic area, arc

91 the pineal gland, medial mammillary nucleus, median eminence, infundibular stem, periaqueductal gray,

92 released into the portal circulation at the median eminence, is known to prime downstream hormone re

93 i, suprachiasmatic nucleus, arcuate nucleus, median eminence, lateral hypothalamic area, thalamus, hi

94 aminergic (DAergic) neuronal activity in the median eminence-long portal vessels (ME-LPV) and/or the

95 st some tanycytes are stem cells and, in the median eminence, may be stimulated by diet to generate n

96 The median eminence (ME) and the AL, intermediate (IL) and n

97 ricular nucleus (PVN), arcuate nucleus (AN), median eminence (ME) and the medial preoptic area (MPA)

98 to fasted animals restored PC1 levels in the median eminence (ME) and the PVN to approximately the le

99 ,4-dihydroxyphenylacetic acid (DOPAC) in the median eminence (ME) and various regions of the pituitar

100 Hypothalamic tanycytes in median eminence (ME) are emerging as a crucial cell popu

101 Placement of CFMEs in the median eminence (ME) near GnRH terminals allowed detecti

102 release their neuroendocrine signals at the median eminence (ME) to control long-lasting pituitary h

103 rons whose axons project to the hypothalamic median eminence (ME) where they release gonadotropin-rel

104 inal fluid (CSF) barrier at the level of the median eminence (ME), a circumventricular organ (CVO) lo

105 Despite its juxtaposition to the median eminence (ME), a circumventricular organ lacking

106 nteroventral periventricular nucleus (AVPv), median eminence (ME), and dorsomedial portion of the ven

107 st abundantly expressed in astrocytes of the median eminence (ME), and its enzymatic activity increas

108 ventromedial (VMH) and arcuate (ARC) nuclei, median eminence (ME), and medial habenular nucleus (MHb)

109 ,4-dihydroxyphenylacetic acid (DOPAC) in the median eminence (ME), as well as the anterior (AL), inte

110 The concentration of DA was increased in the median eminence (ME), decreased in the outer zone of the

111 ar dopamine (TIDA) neurons projecting to the median eminence (ME).

112 aining terminals in the external zone of the median eminence (ME).

113 In the median eminence, NPY/PHA-L double-labeled fibers were fo

114 hR2)-bearing adeno-associated virus into the median eminence of adult GnRH-Cre mice resulted in the s

115 nced decrease in DOPAC concentrations in the median eminence of females, but not males.

116 vessels and resembled structures seen in the median eminence of rats.

117 mber of AADC + cells was also reduced in the median eminence of SD-exposed animals.

118 ency of GnRH release detected by FSCV in the median eminence of slices from adults with previous repo

119 ytochemistry in the brain, restricted to the median eminence of the hypothalamus.

120 attenuated by infusion of letrozole into the median eminence of the hypothalamus.

121 nits GluR6 and GluR7 mRNA and protein in the median eminence of the rat.

122 nd their surrounding microenvironment in the median eminence of young (4-5 months) and old (22-24 mon

123 spatial transcriptomics to compare the mouse median eminence, one of the circumventricular organs tha

124 eurons of the lateral septum, but not in the median eminence or in the arcuate nucleus, even though b

125 No fibers with urocortin-ir were seen in the median eminence or the posterior pituitary.

126 sal hypothalamic area (MBA), arcuate nucleus/median eminence, paraventricular nuclei and piriform cor

127 rd, and most hypothalamic nuclei such as the median eminence, periventricular, suprachiasmatic, supra

128 we examine whether hypocretin modulates the median eminence-projecting proopiomelanocortin (POMC) ne

129 RH) from the medial basal hypothalamus (MBH)/median eminence region (S-ME) is essential for normal re

130 tanycytes, an ependymoglial cell type of the median eminence, regulate LHRH release during the estrou

131 that Semaphorin-6A is strongly expressed by median eminence-resident oligodendrocytes positioned adj

132 aining for PrRP in the external layer of the median eminence seems to rule out this peptide as a clas

133 on not only in the subfornical organ and the median eminence, situated outside the blood brain barrie

134 ocrine GABA neurons identified by antidromic median eminence stimulation.

135 duction, in GABAergic nerve terminals in the median eminence suggested that rather than a functional

136 roxylase in GABAergic nerve terminals in the median eminence suggests that only the non-GABAergic dop

137 Using genetic fate mapping, we found that median eminence tanycytes generate newborn neurons.

138 nycytes within the infundibular stalk/caudal median eminence, termed here gamma tanycytes, and a subs

139 corticotropin-releasing factor (CRF) in the median eminence, this observation suggests that extra-PV

140 m, inferior hypo. n., infundibular hypo. n., median eminence, three layers within the stratum griseum

141 Median eminence tissues were freeze-plunge embedded and

142 show that the GnRH neuron projection to the median eminence to control pituitary hormone secretion p

143 nucleus where they merge before entering the median eminence to release GnRH into the portal vasculat

144 se into the brain, where they project to the median eminence to release GnRH.

145 t was transported in varicose fibres via the median eminence to the posterior pituitary gland.

146 How circulating signals enter the median eminence to trigger homeostatic hypothalamic resp

147 ulating GnRH neuron patterning by tuning the median eminence vascular barrier and thereby controlling

148 ia its receptor Plexin-A2, in the control of median eminence vascular permeability to maintain neuroe

149 strous cycle in the medial preoptic nucleus, median eminence, ventromedial nucleus, suprachiasmatic n

150 e release in target brain regions and in the median eminence via a direct inhibition of vGluT2-GnRH n

151 a dense plexus of axons and terminals in the median eminence was partially depleted of growth hormone

152 RL-induced secretion of dopamine (DA) at the median eminence was strongly blunted during lactation, a

153 ition, those that project their axons to the median eminence, were robustly activated by hypocretin i

154 ,4-dihydroxyphenylacetic acid (DOPAC) in the median eminence which contains terminals of these neuron