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1 nd a promoter selective to noradrenergic and adrenergic neurons.
2  of the central nervous system (CNS) rich in adrenergic neurons.
3  (SNA) after the depletion of bulbospinal C1 adrenergic neurones.
4 at consisting of noncatecholaminergic and C1 adrenergic neurons (3:2 ratio).
5 n amounts as low as 50 ng results in loss of adrenergic neurons and apoptosis after 18 h.
6 a (RVLM) region that contains bulbospinal C1 adrenergic neurons and is involved in blood pressure con
7 s expressed selectively in noradrenergic and adrenergic neurons and neuroendocrine cells in the nervo
8 s selectively expressed in noradrenergic and adrenergic neurons and neuroendocrine cells.
9 ship between relay visceral sensory and (nor)adrenergic neurons, and suggest that it may be a common
10  cardioprotection: NHE inhibition in cardiac adrenergic neurons as a means to prevent ischemic arrhyt
11 that the fate and innervation pattern of the adrenergic neurons, as well as the development of the ce
12   In a separate group, pretreatment with the adrenergic neuron blocker, guanethidine (20 mg/kg), also
13 radrenaline-depleting drug reserpine and the adrenergic neuron-blocking agent guanethidine.
14 ological properties of the rostral medullary adrenergic neurons (C(1)) that express neuropeptide Y (N
15   In summary, the loss of 84% of bulbospinal adrenergic neurones does not alter the ability of RVLM t
16 ars normal, but the integrity of sympathetic adrenergic neurons has not been tested.
17                                  The central adrenergic neurons have been suggested to play a role in
18  both adrenergic (auto-alpha(2a)ARs) and non-adrenergic neurons (hetero-alpha(2a)ARs) for the first t
19 , and respiration that may be mediated by C1 adrenergic neurons in the rostral ventrolateral medulla
20 ng the sympathoexcitatory and wake-promoting adrenergic neurons in the rostral ventrolateral medulla
21 ected 3,4-dihydroxyphenylglycolaldehyde onto adrenergic neurons in the rostral ventrolateral medulla.
22 either region were equally likely to contact adrenergic neurons in the RVL (21% for NTS, 25% for CVL)
23 with immunocytochemical identification of C1 adrenergic neurons in the RVL to compare the morphology
24  [dopaminergic (DA), noradrenergic (NA), and adrenergic] neurons in the zebrafish, Danio rerio.
25 ity of GBy subunits for the SNARE complex in adrenergic neurons, in which auto-a(2a)ARs respond to ep
26 laminergic (dopaminergic, noradrenergic, and adrenergic) neurons, in relationship to each other and t
27 ed by tyrosine hydroxylase (TH) antibody, or adrenergic neurons labeled by phenylethanolamine-N-methy
28 stral ventrolateral medulla (including to C1 adrenergic neurons), locus coeruleus, A5 cell group, par
29 Nurr1 expression was also excluded from (nor)adrenergic neurons of the brainstem.
30 DNPI/VGLUT2 mRNA was detected in most of the adrenergic neurons of the C1, C2, and C3 groups (75-80%
31 tion-evoked norepinephrine (NE) release from adrenergic neurons of the CNS from naive rats.
32                      Here we report that the adrenergic neurons of these mutant mice are present in n
33          Brainstem visceral sensory and (nor)adrenergic neurons play crucial roles in modulating card
34 luding the rostral ventrolateral medulla (C1 adrenergic neurons), rostral ventromedial medulla, cauda
35   Intestinal injury induces the outgrowth of adrenergic neurons that stimulate a proregenerative path
36 ne acetyltransferase positive) and intrinsic adrenergic neurons (tyrosine hydroxylase positive) follo
37                                              Adrenergic neurons were identified by their content of t
38                                Large, mainly adrenergic neurons, were surrounded by preganglionic cho
39 a mode of endogenous AR cross-talk in native adrenergic neurons whereby canonical betaAR-mediated sig
40 t neuronal firing rate change in a subset of adrenergic neurons with an EC(50)=2.7 microM, a dose wel