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

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

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

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

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

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

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

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

8 posterior magnocellular subdivisions of the hypothalamic paraventricular nucleus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 The hypothalamic paraventricular nucleus (PVN) coordinates m

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

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

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

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

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

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

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

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

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

68 The hypothalamic paraventricular nucleus (PVN) integrates pr

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

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

71 The hypothalamic paraventricular nucleus (PVN) is an importa

72 The hypothalamic paraventricular nucleus (PVN) is an importa

73 The hypothalamic paraventricular nucleus (PVN) is critically

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

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

76 The hypothalamic paraventricular nucleus (PVN) is responsive

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

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

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

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

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

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

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

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

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

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

87 The hypothalamic paraventricular nucleus (PVN) regulates num

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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