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1 ate the trafficking itinerary of NET in live noradrenergic neurons.
2 BA on a subpopulation of spinally-projecting noradrenergic neurons.
3 sed norepinephrine in central and peripheral noradrenergic neurons.
4 hat are known to contain spinally projecting noradrenergic neurons.
5 group to inactivate the spinally-projecting noradrenergic neurons.
6 k synaptic activation of spinally-projecting noradrenergic neurons.
7 t is mediated in part by spinally-projecting noradrenergic neurons.
8 of biogenic amines and is expressed in brain noradrenergic neurons.
9 adrenergic receptors residing on targets of noradrenergic neurons.
10 All groups contained both dopaminergic and noradrenergic neurons.
11 to the development of central and peripheral noradrenergic neurons.
12 in the locus coeruleus, a brain area rich in noradrenergic neurons.
13 rmine whether nNOS is expressed by A1 and A2 noradrenergic neurons.
14 utamate receptor subtype with respect to the noradrenergic neurons.
15 kinase in Ang II-mediated neuromodulation in noradrenergic neurons.
16 instem GABAergic interneurons that innervate noradrenergic neurons.
17 se the firing of both peripheral and central noradrenergic neurons.
18 known about how MeCP2 regulates function of noradrenergic neurons.
19 n the NST may preferentially affect putative noradrenergic neurons.
20 lamine biosynthesis that defines sympathetic noradrenergic neurons.
21 rtant for the cell autonomous development of noradrenergic neurons.
22 is a significant loss of locus ceruleus (LC) noradrenergic neurons.
23 m secretory vesicles in chromaffin cells and noradrenergic neurons.
24 may provide interneuronal integration for LC noradrenergic neurons.
25 ent there and in the large majority of other noradrenergic neurons.
26 ti-DH-SAP also eliminated the majority of A5 noradrenergic neurones.
27 ndent rats is a consequence of excitation of noradrenergic neurones.
28 sed c-fos expression in pontine A7 and other noradrenergic neurones.
29 hydroxylase [TH]-positive [i.e., presumably noradrenergic neurons].
31 ase (DBH), could selectively destroy central noradrenergic neurons after intraventricular administrat
32 Transgenic mice overexpressing galanin in noradrenergic neurons also showed decreased morphine wit
34 stimulation of C1 neurons activates pontine noradrenergic neurons and sympathetic nerve discharge, p
36 6-Hydroxydopamine (6-OHDA) lesions of brain noradrenergic neurons and terminals were made in rats to
37 rin, a treatment that destroys a majority of noradrenergic neurons and their projections, validated t
39 cranial sensory, sympathetic, and hindbrain noradrenergic neurons, and is available to these cells i
40 neurons contact locus coeruleus, A1, and A2 noradrenergic neurons, and ultrastructural evidence that
41 dicate that sub-populations of the A1 and A2 noradrenergic neurons are capable of generating nitric o
43 om recording studies in animals reveals that noradrenergic neurons are excited mainly by any change i
44 everal lines of evidence indicate that these noradrenergic neurons are located in the pontine A7 cate
45 ugh the specification and differentiation of noradrenergic neurons are the focus, I have tried to int
47 ndrites of DRN serotoninergic neurons and LC noradrenergic neurons but were not apposed to cholinergi
48 least in part, due to activation of pontine noradrenergic neurones, but is not mediated by ORX type
49 pendent on the proper functioning of central noradrenergic neurons, but do not involve increased NE r
50 o few (tof)--that develops hindbrain 5HT and noradrenergic neurons, but does not develop hypothalamic
51 e is compensation occurring in the remaining noradrenergic neurons, but there does appear to be a los
52 lays a critical role in the specification of noradrenergic neurons by inducing the expression of dopa
54 ted, in part, by its uptake into presynaptic noradrenergic neurons by the plasma-membrane NE transpor
55 or work, we reported that, during cataplexy, noradrenergic neurons cease discharge, and serotonergic
57 system (CNS)- and neural crest (NC)-derived noradrenergic neuron differentiation, coordinates cell c
58 he LC may be equally important in modulating noradrenergic neurons during chronic opiate exposure.
59 brain stem nucleus containing cell bodies of noradrenergic neurons, dynamically tracks the level of u
60 hese experiments demonstrate that loss of LC noradrenergic neurons exacerbates multiple phenotypes ca
61 pses between mitral and granule cells (GCs), noradrenergic neurons extending from the brainstem provi
63 from the substantia nigra pars compacta and noradrenergic neurons from the locus coeruleus in monkey
66 nerve ablation, we show that elimination of noradrenergic neurons improves survival during Klebsiell
67 also expressed high levels of Kir6.2, while noradrenergic neurons in A5 and A2 areas expressed lower
69 s study was to determine if the surviving LC noradrenergic neurons in PD demonstrate compensatory cha
71 s in the ventromedial medulla project to the noradrenergic neurons in the A7 catecholamine cell group
75 us of the solitary tract (NTS), including A2 noradrenergic neurons in the caudal half of the NTS.
76 eus, pre-locus coeruleus region, NTS, and A1 noradrenergic neurons in the caudal ventrolateral medull
77 are presynaptic autoinhibitory receptors of noradrenergic neurons in the central and peripheral symp
78 release in the frontal cortex by activating noradrenergic neurons in the coeruleo-frontal cortex pat
80 to determine whether compensation occurs in noradrenergic neurons in the LC and hippocampus of subje
81 tudy, we test directly whether activation of noradrenergic neurons in the LC influences brainstem par
83 amino acid, glutamate, may locally modulate noradrenergic neurons in the LC through kainate-type rec
84 hrine may elicit concerted actions on common noradrenergic neurons in the LC via separate sets of aff
86 the laterodorsal tegmental nucleus; lateral noradrenergic neurons in the LC; medial GABAergic neuron
88 mice we measured a doubling in the number of noradrenergic neurons in the locus coeruleus (LC) and a
89 ectivity between Hcrt neurons and downstream noradrenergic neurons in the locus coeruleus (LC) during
90 disease (PD), there is a significant loss of noradrenergic neurons in the locus coeruleus (LC) in add
92 the dopaminergic nigrostriatal system and of noradrenergic neurons in the locus coeruleus are importa
94 substantia nigra pars compacta (SNpc) and of noradrenergic neurons in the locus coeruleus is accompan
95 ject to, synapse on, and positively regulate noradrenergic neurons in the locus coeruleus, a brain ce
96 on gastric vago-vagal reflexes suggest that noradrenergic neurons in the NST are particularly import
97 previously, anti-DBH-SAP selectively killed noradrenergic neurons in the NTS while SAP conjugated to
98 t axonal projections from the neighboring A2 noradrenergic neurons in the NTS, and from the same pont
99 on to rostral C2 adrenergic and mid-level A2 noradrenergic neurons in the NTS, many C1 and A1 neurons
100 ervate the medial pericoerulear dendrites of noradrenergic neurons in the nucleus locus coeruleus (LC
101 may serve as a neurotransmitter to activate noradrenergic neurons in the nucleus locus coeruleus (LC
103 the A7 catecholamine cell group, a group of noradrenergic neurons in the pons known to effect antino
104 In the current study, the distribution of noradrenergic neurons in the pontine tegmentum that proj
107 re and supernumerary pontine cholinergic and noradrenergic neurons indicate that the control of unihe
110 hich is expressed on the plasma membranes of noradrenergic neurons, is important in terminating neuro
111 mined the effect of C1 activation on pontine noradrenergic neurons (LC and A5) using a more selective
112 omical evidence indicates that the remaining noradrenergic neurons may be compensating for the loss.
114 ate the locus coeruleus as well as A1 and A2 noradrenergic neurons monosynaptically by releasing glut
115 jection protected neostriatal and cerebellar noradrenergic neurons NE levels (110-122% of the control
116 , these data suggest that NO and CO activate noradrenergic neurons of LC via a cGMP-dependent protein
117 ous input) changed the effect of morphine on noradrenergic neurons of the A7 and A5 cell groups, and
120 s, including midbrain dopamine (DA) neurons, noradrenergic neurons of the locus ceruleus, and retinal
121 l biochemical changes have been described in noradrenergic neurons of the locus coeruleus (LC) after
123 R) agonists potently inhibit the activity of noradrenergic neurons of the locus coeruleus (LC), an ef
124 l and Cresyl violet staining showed that the noradrenergic neurons of the locus coeruleus are destroy
127 ory amino acid receptors with respect to the noradrenergic neurons of the nucleus locus coeruleus (LC
128 te of the evidence that at least some of the noradrenergic neurons of the primate hindbrain express t
130 o determine whether there is also loss of LC noradrenergic neurons or evidence of degenerative change
131 cp2 from either TH-positive dopaminergic and noradrenergic neurons or PET1-positive serotonergic neur
132 results suggest that DR serotonergic and LC noradrenergic neurons play differential roles in orexin
133 promoter (AVV-PRS) to retrogradely label the noradrenergic neurons projecting to the lumbar (L4-L5) d
134 ese results suggest that rimcazole activates noradrenergic neurons projecting to the PVN via a mechan
137 UT2(flox/flox) mice, into the caudal VLM (A1 noradrenergic neuron-rich region) of DbetaH(Cre/0) mice
139 ctively, retrogradely target the pontospinal noradrenergic neurons that are likely to be involved in
140 in neurons, as well as two populations of A7 noradrenergic neurons that exert a bidirectional effect
141 antinociception that is mediated in part by noradrenergic neurons that innervate the spinal cord dor
142 axon terminal profiles were identified near noradrenergic neurons that were visualized by processing
145 particular vulnerability of dopaminergic and noradrenergic neurons to neurodegeneration in PARK7-rela
146 We hypothesized that the responsiveness of noradrenergic neurons to ovarian steroids is altered dur
147 el previously inaccessible subpopulations of noradrenergic neurons to reveal details of their three-d
148 concluded that the altered responsiveness of noradrenergic neurons to steroid priming in middle-aged
149 bjects, the loss of dendrites from surviving noradrenergic neurons was also apparent with TH-immunore
152 [(18)F]dopa is taken up by serotonergic and noradrenergic neurons which also degenerate in advanced
153 ventrolateral pons contains the A5 group of noradrenergic neurons which regulate the circulation and
154 activated by sodium depletion, and by the A2 noradrenergic neurons, which are activated by visceral a
156 ound very few examples of WGA-immunoreactive noradrenergic neurons, which suggests that there is cons
158 In the present study we investigated whether noradrenergic neurons within the locus coeruleus (LC), t
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