コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 AHP currents in oxytocin (OT) neurons of the supraoptic nucleus.
2 ate of identified oxytocin neurones from the supraoptic nucleus.
3 cin (OT)- and (VP)-containing neurons of the supraoptic nucleus.
4 n the lateral hypothalamic are dorsal to the supraoptic nucleus.
5 and the parallel-projecting dendrites of the supraoptic nucleus.
6 t naloxone was effective when given into the supraoptic nucleus.
7 n-1) onto the exposed ventral surface of the supraoptic nucleus.
8 s along the ventral lamina terminalis to the supraoptic nucleus.
9 en glial coverage of synapses and LTP in the supraoptic nucleus.
10 and somata of magnocellular neurones in the supraoptic nucleus.
11 gest in neostriatum, olfactory tubercle, and supraoptic nucleus.
12 on the properties of neurons in the OVLT and supraoptic nucleus.
13 localized in the paraventricular nucleus and supraoptic nucleus.
14 ventricular nucleus of the hypothalamus, and supraoptic nucleus.
15 d with 5-min sampling frequency from the rat supraoptic nucleus.
16 cleus, paraventricular hypothalamic nucleus, supraoptic nucleus, accessory neurosecretory nuclei, per
17 ry tract, the ventrolateral medulla, and the supraoptic nucleus, all showed increases in cFos-IR in t
18 e in the number of Fos-positive cells in the supraoptic nucleus and a 3.4-fold increase in the latera
19 expression of tenascin by astrocytes in the supraoptic nucleus and associated ventral glial limitans
22 ediated glutamate excitatory function in the supraoptic nucleus and paraventricular nucleus of hypert
24 lamic regions outside the SCN, including the supraoptic nucleus and the subparaventricular region.
25 Targets included the lateral nucleus, peri-supraoptic nucleus, and subparaventricular zone of the h
26 regulate hemodynamic processes including the supraoptic nucleus, and the magnocellular division of hy
27 e, piriform cortex, paraventricular nucleus, supraoptic nucleus, arcuate nucleus, and hippocampal CA
28 aventricular nucleus of the hypothalamus and supraoptic nucleus, as well as in the cortex, septal nuc
29 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 and 4 weeks after MI compared wi
30 e neurons in the paraventricular nucleus and supraoptic nucleus at 2 weeks after MI compared with mic
31 ures, including the paraventricular nucleus, supraoptic nucleus, bed nucleus of the stria terminalis
32 microscopic level, labeled fibers within the supraoptic nucleus branched frequently, were punctuated
33 s induced oxytocin release from the isolated supraoptic nucleus, but only allopregnanolone induced si
34 urosteroids induce oxytocin release from the supraoptic nucleus by a mechanism that partly depends on
36 ged in most nuclei, but had increased in the supraoptic nucleus by the end of pregnancy and remained
37 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central amygdala, nucleus tractus so
38 paraventricular nucleus of the hypothalamus, supraoptic nucleus, central nucleus of amygdala, lateral
39 ncreased bilaterally in the piriform cortex, supraoptic nucleus, central nucleus of the amygdala, and
40 t on to directly measure GABA release in the supraoptic nucleus during hypertonic infusion, confirmin
41 )) to VP and OT neurones of the hypothalamic supraoptic nucleus elicited by repetitive extracellular
42 , most vasopressin cells of the hypothalamic supraoptic nucleus fire action potentials in a 'phasic'
43 agonists of GluK1-containing KARs in the rat supraoptic nucleus has an opposite action on glutamaterg
44 ocellular neurosecretory cells (MNCs) of the supraoptic nucleus has been attributed mainly to synapti
45 A1, CA2, and CA3 regions, the dentate gyrus, supraoptic nucleus, hypothalamus, and cortical layers II
46 burst firing in oxytocin (OT) neurons in the supraoptic nucleus in brain slices from lactating rats.
48 cordings from magnocellular cells of the rat supraoptic nucleus in vivo and in vitro and between oxyt
50 and the total number of GABA synapses in the supraoptic nucleus is substantially higher in lactating
51 opioid agonists primarily occurs within the supraoptic nucleus itself, since the antagonist naloxone
52 he highest levels of immunostaining were the supraoptic nucleus, magnocellular PVH, ARH, and suprachi
53 ime points, but not at 6 hours, included the supraoptic nucleus, magnocellular regions of the paraven
54 Here we analysed the discharge patterning of supraoptic nucleus neurones in vivo, to infer the charac
56 t both oxytocin and vasopressin cells in the supraoptic nucleus of normal rats respond to intravenous
57 ecretory cells (MNCs) were isolated from the supraoptic nucleus of rat hypothalamus, and properties o
58 (0.1-10.0 micrograms microliter-1) onto the supraoptic nucleus of rats made dependent by intracerebr
59 osecretory cells (MNCs) dissociated from the supraoptic nucleus of the adult guinea-pig were identifi
60 cation of N-methyl-D-aspartate (NMDA) to the supraoptic nucleus of the hypothalamus (SON) generates c
61 sopressin from magnocellular neurones in the supraoptic nucleus of the hypothalamus has important aut
66 ole-cell patch clamp recordings were made in supraoptic nucleus OT neurons in brain slices from male
71 c area, bed nucleus of the stria terminalis, supraoptic nucleus, paraventricular nucleus, zona incert
72 organum vasculosum of the lamina terminalis, supraoptic nucleus, periaqueductal gray, and medial nucl
73 in select groups of nuclei (e.g., habenula, supraoptic nucleus, pontine nucleus) contained pronounce
74 measurements of SK channel subunits mRNA in supraoptic nucleus punches revealed a diminished express
76 benoxathian directly onto the surface of the supraoptic nucleus reduced the activity of oxytocin neur
77 The central nucleus of the amygdala and the supraoptic nucleus, regions that are involved in autonom
78 ular regions of the paraventricular nucleus, supraoptic nucleus, septohypothalamic nucleus, medial se
79 s, medial septum, and cortex, but not in the supraoptic nucleus, septohypothalamic nucleus, or organu
80 eurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON) and accessory neurosecretory nu
81 d Fos-like immunoreactivity (Fos-LIR) in the supraoptic nucleus (SON) and paraventricular nucleus (PV
82 late AVP steady-state gene expression in the supraoptic nucleus (SON) and PVN, and/or CRF mRNA in the
83 logical functions of PRR were studied in the supraoptic nucleus (SON) because this brain region showe
85 (VP)-secreting magnocellular neurons of the supraoptic nucleus (SON) display calcium-dependent after
86 sured expression of the oxytocin gene in the supraoptic nucleus (SON) during pregnancy, parturition a
88 ministration of hypertonic saline to the rat supraoptic nucleus (SON) increases the expression of sev
89 recordings were obtained from sixty-five rat supraoptic nucleus (SON) neurones in brain slices to inv
90 ole-cell patch recordings were obtained from supraoptic nucleus (SON) neurones in horizontal brain sl
92 ergic and excitatory glutamatergic inputs to supraoptic nucleus (SON) neurons can influence the relea
93 e appearance of Fos and Jun in the nuclei of supraoptic nucleus (SON) neurons following intraperitone
94 g direct olfactory (glutamatergic) inputs to supraoptic nucleus (SON) neurons increases interneuronal
96 nd adenosine receptors (AR) are expressed in supraoptic nucleus (SON) neurons, we postulated that con
98 ower subparaventricular zone, LSPV), and the supraoptic nucleus (SON) of grass rats (Arvicanthis nilo
99 in the paraventricular nucleus (PVN) and the supraoptic nucleus (SON) of the hypothalamus are activat
103 rom the suprachiasmatic nucleus (SCN) to the supraoptic nucleus (SON) of the hypothalamus were charac
104 was used to assess the relative responses of supraoptic nucleus (SON) oxytocin- (OX) and vasopressin-
105 the hypothalamic paraventricular nucleus and supraoptic nucleus (SON) respond to glucocorticoids by r
106 nvestigated in magnocellular neurones of rat supraoptic nucleus (SON) using whole-cell patch recordin
107 ion in the paraventricular nucleus (PVN) and supraoptic nucleus (SON) was evaluated by real time RT-P
108 nohistochemically identified neurones in the supraoptic nucleus (SON) was investigated in the hypotha
109 nearby forebrain cholinergic neurons to the supraoptic nucleus (SON) were used to study synaptic pot
110 lateral amygdaloid nucleus, 1.2-times in the supraoptic nucleus (SON), 1.6-times in the magnocellular
111 in areas receiving input from the SFO is the supraoptic nucleus (SON), a source of vasopressin synthe
112 f neurosecretory neurons in the hypothalamic supraoptic nucleus (SON), a well studied model of struct
113 ensin (Ang)-(1-7)-IR cells were found in the supraoptic nucleus (SON), and in the anterior (ap-), med
114 in 3 receptors (NK3-Rs) are expressed in the supraoptic nucleus (SON), and SON is innervated by subst
115 ral superfusion of 3 microM TTX into the rat supraoptic nucleus (SON), delivered with the use of a mi
116 ocellular neurosecretory system (MNS) of the supraoptic nucleus (SON), in which dendritic release of
117 duces structural changes in the hypothalamic supraoptic nucleus (SON), including increased glutamate
118 urons were particularly abundant in the PVN, supraoptic nucleus (SON), infundibular nucleus, and prem
119 rtion of the paraventricular nucleus (PVNp), supraoptic nucleus (SON), magnocellular PVN and suprachi
120 organum vasculosum lamina terminalis (OVLT), supraoptic nucleus (SON), magnocellular region of the pa
121 e measured in paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic area (MePO), s
122 served in the paraventricular nucleus (PVN), supraoptic nucleus (SON), median preoptic nucleus (MnPO)
123 ular nucleus (PVN), subfornical organ (SFO), supraoptic nucleus (SON), nucleus accumbens (NAc) shell
124 hypothalamus, suprachiasmatic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN),
125 significant Fos expression in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN),
127 in the rat paraventricular nucleus (PVN) and supraoptic nucleus (SON), regions which lack ERalpha.
128 that VRACs are absent in neurons of the rat supraoptic nucleus (SON), suggesting that glial cells ar
129 ch as the paraventricular nucleus (PVH), the supraoptic nucleus (SON), the lateral hypothalamic area
140 nuates that of neurosecretory neurons in the supraoptic nucleus (SON; which secrete oxytocin and vaso
141 gly stained, whereas in the hypothalamus the supraoptic nucleus stood out with strong immunoreactivit
142 ior paraventricular nucleus of the thalamus, supraoptic nucleus, subfornical organ, and paraventricul
143 eceptors (MC4Rs) are highly expressed in the supraoptic nucleus, suggesting that alpha-MSH and oxytoc
144 um, diagonal band, pallidum, preoptic areas, supraoptic nucleus, suprachiasmatic nucleus, paraventric
145 e prominently localized to astrocytes in the supraoptic nucleus, the neurons of which contain only sm
146 e anorectic TB rats, most prominently in the supraoptic nucleus, the parvocellular portion of the par
147 nterior and retrochiasmatic divisions of the supraoptic nucleus, the suprachiasmatic nucleus, the ven
148 lular neurosecretory cells (MNCs) in the rat supraoptic nucleus to different osmotic milieus by salt-
149 teral hypothalamus, paraventricular nucleus, supraoptic nucleus, ventromedial hypothalamus) and two h
151 that alpha-MSH induces Fos expression in the supraoptic nucleus when injected centrally and demonstra
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。