ライフサイエンスコーパス: hypothalamic paraventricular nucleus

1 sponses and impaired c-fos activation in the hypothalamic paraventricular nucleus.

2 identified G(z) mRNA and G(z)-protein in the hypothalamic paraventricular nucleus.

3 ups in all the amygdaloid regions and in the hypothalamic paraventricular nucleus.

4 teral septum, ventromedial hypothalamus, and hypothalamic paraventricular nucleus.

5 straint-induced c-fos mRNA expression in the hypothalamic paraventricular nucleus.

6 he amygdala and parvocellular neurons of the hypothalamic paraventricular nucleus.

7 ctor response elicited by stimulation of the hypothalamic paraventricular nucleus.

8 ted by activation of 5-HT2A receptors in the hypothalamic paraventricular nucleus.

9 posterior magnocellular subdivisions of the hypothalamic paraventricular nucleus.

10 s are present on neuroendocrine cells in the hypothalamic paraventricular nucleus.

11 y implanted double-barreled cannula into the hypothalamic paraventricular nucleus 15 min before a per

12 firm the presence of 5-HT2A receptors in the hypothalamic paraventricular nucleus, 5-HT2A receptors w

13 r drugs (Gi-DREADD) in KORcre neurons of the hypothalamic paraventricular nucleus, a key node of the

14 are mediated by activation of neurons in the hypothalamic paraventricular nucleus and associated circ

15 d density of neurons that express ENK in the hypothalamic paraventricular nucleus and central nucleus

16 tress exacerbated neuronal activation in the hypothalamic paraventricular nucleus and medial nucleus

17 ression of MC4Rs only in SIM1 neurons in the hypothalamic paraventricular nucleus and neurons in the

18 ut to the anterior parvicellular part of the hypothalamic paraventricular nucleus and nucleus of the

19 f Y1 receptors in Arc NPY projections areas (hypothalamic paraventricular nucleus and perifornical ar

20 nd parvocellular neuroendocrine cells of the hypothalamic paraventricular nucleus and supraoptic nucl

21 ear recall, but had normal activation in the hypothalamic paraventricular nucleus and the amygdalar c

22 increased water intake, was increased in the hypothalamic paraventricular nucleus and the subfornical

23 xin receptor 1, and orexin receptor 2 in the hypothalamic paraventricular nucleus and these effects w

24 aining each of these peptides project to the hypothalamic paraventricular nucleus, and (3) each has b

25 of the solitary tract, periaqueductal gray, hypothalamic paraventricular nucleus, and medial preopti

26 a, they regulate the production of OT in the hypothalamic paraventricular nucleus, and through ER-alp

27 s exhibited higher levels of CRH mRNA in the hypothalamic paraventricular nucleus but lower basal lev

28 tein levels in carotid bodies, striatum, and hypothalamic paraventricular nucleus, but not in the nuc

29 nced the number of Fos-positive cells in the hypothalamic paraventricular nucleus by 60%, whereas lep

30 letion of Trpc5 from oxytocin neurons in the hypothalamic paraventricular nucleus caused obesity in b

31 asing factor (CRF)-expressing neurons in the hypothalamic paraventricular nucleus (CRF(PVN)) respond

32 ontrast, microinjection of muscimol into the hypothalamic paraventricular nucleus failed to reduce ch

33 Knockout of the X-linked Fgf13 in the hypothalamic paraventricular nucleus impairs sympathetic

34 vasopressin terminals, originating from the hypothalamic paraventricular nucleus, in the CA2 of mice

35 ide the blood brain barrier, but also in the hypothalamic paraventricular nucleus, located inside the

36 howed activation during the orgasms included hypothalamic paraventricular nucleus, medial amygdala, a

37 er the serotonin2A (5-HT2A) receptors in the hypothalamic paraventricular nucleus mediate the neuroen

38 ucleus (MnPO) with axonal projections to the hypothalamic paraventricular nucleus (MnPO-PVN) respond

39 in the medial parvocellular division of the hypothalamic paraventricular nucleus (mpPVN) in corticos

40 ARC TH cells project to the hypothalamic paraventricular nucleus; optogenetic stimul

41 not in vasopressin-containing neurons in the hypothalamic paraventricular nucleus or CRF cells in the

42 id antagonists microinjected into either the hypothalamic paraventricular nucleus or the nucleus accu

43 s and the medial parvocellular region of the hypothalamic paraventricular nucleus (PAmp).

44 twork (central amygdalar nucleus, descending hypothalamic paraventricular nucleus, parasubthalamic nu

45 ted extravasation of BM-derived cells to the hypothalamic paraventricular nucleus, presumably via a m

46 s, 19 were antidromically activated from the hypothalamic paraventricular nucleus (PVH) (latency: 10.

47 The Arc and its projection to the hypothalamic paraventricular nucleus (PVH) are both comp

48 cument a role for glutamatergic input to the hypothalamic paraventricular nucleus (PVH) in stress-ind

49 is a well-established orexigenic peptide and hypothalamic paraventricular nucleus (PVH) is one major

50 may involve activation of a pathway from the hypothalamic paraventricular nucleus (PVH) to the rostra

51 ventromedial preoptic nucleus (VMPO) and the hypothalamic paraventricular nucleus (PVH), although Fos

52 Several brain regions including the hypothalamic paraventricular nucleus (PVH), the anterove

53 ateral medulla (RVLM), A5 cell group and the hypothalamic paraventricular nucleus (PVH).

54 ticoid receptors are highly expressed in the hypothalamic paraventricular nucleus (PVN) and arcuate n

55 bunits of the GABA(A)receptor within the rat hypothalamic paraventricular nucleus (PVN) and hippocamp

56 Evidence indicates that the hypothalamic paraventricular nucleus (PVN) and oxytocin

57 H), produced by parvocellular neurons of the hypothalamic paraventricular nucleus (PVN) and released

58 alis (OVLT), median preoptic nucleus (MNPO), hypothalamic paraventricular nucleus (PVN) and supraopti

59 arginine vasopressin (AVP) neurons from the hypothalamic paraventricular nucleus (PVN) and supraopti

60 These prominently included the hypothalamic paraventricular nucleus (PVN) and the nucle

61 CRH mRNA and protein levels in the hypothalamic paraventricular nucleus (PVN) are increased

62 evidence that the effects of NPS within the hypothalamic paraventricular nucleus (PVN) are mediated

63 parvocellular neurosecretory neurons of the hypothalamic paraventricular nucleus (PVN) by the glucoc

64 Calcineurin activity in the hypothalamic paraventricular nucleus (PVN) constitutivel

65 resent study sought to determine whether the hypothalamic paraventricular nucleus (PVN) contributes i

66 sporter-1 (NKCC1, encoded by Slc12a2) in the hypothalamic paraventricular nucleus (PVN) contributes t

67 The hypothalamic paraventricular nucleus (PVN) contributes t

68 The hypothalamic paraventricular nucleus (PVN) controls neur

69 The hypothalamic paraventricular nucleus (PVN) coordinates m

70 nocellular and parvocellular neurones of the hypothalamic paraventricular nucleus (PVN) differentiall

71 CRH mRNA expression in hypothalamic paraventricular nucleus (PVN) diminished af

72 num vasculosum laminae terminalis (OVLT) and hypothalamic paraventricular nucleus (PVN) each contribu

73 es that ghrelin stimulates VP neurons in the hypothalamic paraventricular nucleus (PVN) in a nutritio

74 REB (PCREB) immunolabeled cell nuclei in the hypothalamic paraventricular nucleus (PVN) in fasted as

75 demonstrated that NMU microinjected into the hypothalamic paraventricular nucleus (PVN) in rats incre

76 opin-releasing factor mRNA expression in the hypothalamic paraventricular nucleus (PVN) in response t

77 ICER mRNA in the hypothalamic paraventricular nucleus (PVN) increased aft

78 HT) or cholecystokinin (CCK) injected in the hypothalamic paraventricular nucleus (PVN) inhibits feed

79 The hypothalamic paraventricular nucleus (PVN) integrates pr

80 The development of the hypothalamic paraventricular nucleus (PVN) involves seve

81 eostatic challenges such as dehydration, the hypothalamic paraventricular nucleus (PVN) is activated

82 The hypothalamic paraventricular nucleus (PVN) is an importa

83 The hypothalamic paraventricular nucleus (PVN) is critically

84 -D-aspartate (NMDA) receptor activity in the hypothalamic paraventricular nucleus (PVN) is crucial fo

85 The hypothalamic paraventricular nucleus (PVN) is essential

86 NMDAR activity in the hypothalamic paraventricular nucleus (PVN) is increased

87 trated that relaxin-3/RXFP3 signaling in the hypothalamic paraventricular nucleus (PVN) is necessary

88 The hypothalamic paraventricular nucleus (PVN) is responsive

89 The hypothalamic paraventricular nucleus (PVN) is strongly i

90 To test the hypothesis that neurons in the hypothalamic paraventricular nucleus (PVN) may be under

91 ), and dihydroxyphenylacetic acid (DOPAC) in hypothalamic paraventricular nucleus (PVN) microdialysat

92 Neurocircuit inhibition of hypothalamic paraventricular nucleus (PVN) neurons contr

93 rating NADPH oxidase (NOX) in AVP-expressing hypothalamic paraventricular nucleus (PVN) neurons in "m

94 e of glutamate effects on stress-integrative hypothalamic paraventricular nucleus (PVN) neurons remai

95 P), messenger ribonucleic acid (mRNA) in the hypothalamic paraventricular nucleus (PVN) of the rat.

96 ration of E2 by microdialysis, either in the hypothalamic paraventricular nucleus (PVN) or in the ven

97 A antagonist SB334867 microinjected into the hypothalamic paraventricular nucleus (PVN) or into the b

98 Glutamatergic synaptic input in the hypothalamic paraventricular nucleus (PVN) plays a criti

99 d-aspartate receptor (NMDAR) activity in the hypothalamic paraventricular nucleus (PVN) plays a major

100 creased sympathetic drive emanating from the hypothalamic paraventricular nucleus (PVN) plays a major

101 The hypothalamic paraventricular nucleus (PVN) regulates num

102 ting evidence supports a contribution of the hypothalamic paraventricular nucleus (PVN) to sympathoex

103 h projection extends from cell bodies in the hypothalamic paraventricular nucleus (PVN) to the nucleu

104 Indeed, a neuronal pathway from the hypothalamic paraventricular nucleus (PVN) to the spinal

105 Tmem18 expression in the murine hypothalamic paraventricular nucleus (PVN) was altered b

106 properties of pre-autonomic neurones in the hypothalamic paraventricular nucleus (PVN) were characte

107 entral nucleus of the amygdala (CeA) and the hypothalamic paraventricular nucleus (PVN) were evaluate

108 bitory synaptic inputs to neurons of the rat hypothalamic paraventricular nucleus (PVN) were studied

109 tive oxygen production in ERB neurons in the hypothalamic paraventricular nucleus (PVN), a critical n

110 ole in heightened glutamate signaling in the hypothalamic paraventricular nucleus (PVN), a key centra

111 ole in heightened glutamate signaling in the hypothalamic paraventricular nucleus (PVN), a key centra

112 uite unexpectedly, NPY concentrations in the hypothalamic paraventricular nucleus (PVN), a major site

113 eleasing factor (CRF) mRNA expression in the hypothalamic paraventricular nucleus (PVN), and plasma c

114 pothalamus (PFH), lateral hypothalamus (LH), hypothalamic paraventricular nucleus (PVN), and ventral

115 nt in the pituitary (PIT), cerebellum (CBL), hypothalamic paraventricular nucleus (PVN), and, to a le

116 hippocampus (HI), caudate putamen (CP), the hypothalamic paraventricular nucleus (PVN), arcuate nucl

117 eased immediate-early gene expression in the hypothalamic paraventricular nucleus (PVN), arcuate nucl

118 Neuronal activity in the hypothalamic paraventricular nucleus (PVN), as well as s

119 s of the stria terminalis, central amygdala, hypothalamic paraventricular nucleus (PVN), Barrington's

120 al BT administration induced c-Fos-IR in the hypothalamic paraventricular nucleus (PVN), central nucl

121 otropin-releasing hormone (CRH) cells of the hypothalamic paraventricular nucleus (PVN), in the contr

122 Oxytocin(1,2,9-15), which is released by the hypothalamic paraventricular nucleus (PVN), is a critica

123 H innervates TRH-synthesizing neurons in the hypothalamic paraventricular nucleus (PVN), we raised th

124 dietary sodium intake evoked an endogenous, hypothalamic paraventricular nucleus (PVN)-specific, dec

125 releasing hormone (CRH) neurons of the fetal hypothalamic paraventricular nucleus (PVN).

126 c nucleus, and the magnocellular division of hypothalamic paraventricular nucleus (PVN).

127 ropin-releasing hormone (CRH) within the rat hypothalamic paraventricular nucleus (PVN).

128 of galanin, neuropeptide Y or saline in the hypothalamic paraventricular nucleus (PVN).

129 circuitry and neuroendocrine neurons of the hypothalamic paraventricular nucleus (PVN).

130 ocampus or the expression of CRH mRNA in the hypothalamic paraventricular nucleus (PVN).

131 ked to augmented sympathetic output from the hypothalamic paraventricular nucleus (PVN).

132 tor (NMDAR)-mediated excitatory input to the hypothalamic paraventricular nucleus (PVN).

133 ith glutamate-dependent dysregulation of the hypothalamic paraventricular nucleus (PVN).

134 ocortin-4 receptors (MC4R) in neurons of the hypothalamic paraventricular nucleus (PVN).

135 nt hypertension mediated in part through the hypothalamic paraventricular nucleus (PVN).

136 dorphin receptor blockade in the ipsilateral hypothalamic paraventricular nucleus (PVN).

137 HR) responses elicited by the stimulation of hypothalamic paraventricular nucleus (PVN).

138 indirectly contact neurons projecting to the hypothalamic paraventricular nucleus (PVN).

139 ellular signal-regulated kinase (ERK) in the hypothalamic paraventricular nucleus (PVN).

140 have little or no direct projections to the hypothalamic paraventricular nucleus (PVN).

141 ropin releasing hormone (CRH) neurons of the hypothalamic paraventricular nucleus (PVN).

142 to identified RVLM-projecting neurons of the hypothalamic paraventricular nucleus (PVN-RVLM) contribu

143 Oxytocin neurons in the hypothalamic paraventricular nucleus respond differentia

144 were found in autonomic brain regions (i.e., hypothalamic paraventricular nucleus, rostral ventrolate

145 drive that, unexpectedly, emanates from the hypothalamic paraventricular nucleus, specifically from

146 ropin-releasing hormone (CRH) neurons in the hypothalamic paraventricular nucleus that govern neuroen

147 nal projections from oxytocin neurons in the hypothalamic paraventricular nucleus to midbrain DA regi

148 the regulation of TRH gene expression in the hypothalamic paraventricular nucleus, we examined prepro

149 icosterone level and c-fos expression in the hypothalamic paraventricular nucleus where TLR5 was expr

150 s, reduced the levels of G(z)-protein in the hypothalamic paraventricular nucleus, whereas missense o