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1 ted within the ventrolateral division of the medial forebrain bundle.
2 = 6) or saline solution (n = 4) in the right medial forebrain bundle.
3 d unilateral 6-hydroxydopamine lesion of the medial forebrain bundle.
4 stration of 9 microg of 6-OHDA into the left medial forebrain bundle.
5 al 6-hydroxydopamine (6-OHDA) lesions in the medial forebrain bundle.
6 on and lateral dendrites directed toward the medial forebrain bundle.
7 ward sites activated further caudally in the medial forebrain bundle.
8 6-hydroxydopamine had been injected into the medial forebrain bundle.
9 ved throughout the lateral preoptic area and medial forebrain bundle.
10 onal bundles such as the cingulum bundle and medial forebrain bundle.
11 d by bilateral electrical stimulation of the medial forebrain bundle.
12 a and substantia nigra or transection of the medial forebrain bundle.
13  administered into the lateral ventricles or medial forebrain bundle.
14 ats were injected with 6-OHDA into the right medial forebrain bundle.
15 m, insular cortex, orbitofrontal cortex, and medial forebrain bundle.
16 ilateral projection that courses through the medial forebrain bundle and innervates the olfactostriat
17 ateral infusions of 6-hydroxydopamine to the medial forebrain bundle and peripheral administration of
18 e fed selenium-deficient diet, except in the medial forebrain bundle and somatosensory cortex where t
19 fferents, this formation was centered on the medial forebrain bundle and the fasciculus retroflexus.
20 oamine transporter-2 (VMAT) in the striatum, medial forebrain bundle and the ventral midbrain dopamin
21 ding impact of electrical stimulation of the medial forebrain bundle, as reflected by intracranial se
22  dopamine input to striatum by lesioning the medial forebrain bundle attenuated motor dysfunction.
23                Electrical stimulation of the medial forebrain bundle can reward arbitrary acts or mot
24 containing glutamatergic fibers, but not the medial forebrain bundle containing dopaminergic fibers,
25 ioned with 6-hydroxydopamine (6-OHDA) in the medial forebrain bundle display significantly elevated 8
26                                          The medial forebrain bundle electrodes supported intense ele
27 thetised rats, electrical stimulation of the medial forebrain bundle evoked antidromic spikes in both
28                Similarly, transection of the medial forebrain bundle failed to significantly deplete
29 these sites, including descending inhibitory medial forebrain bundle fibers, induces both feeding and
30 were implanted with electrodes targeting the medial forebrain bundle (for behavior studies of intracr
31 to a key structure of the reward system, the medial forebrain bundle, has yielded promising results w
32 mulation to the supero-lateral branch of the medial forebrain bundle in seven patients with highly re
33 n the brainstem and mainly ascend within the medial forebrain bundle in the forebrain.
34 otection from toxicity induced by unilateral medial forebrain bundle injection of 6-hydroxydopamine (
35 mulation of the supero-lateral branch of the medial forebrain bundle may significantly reduce symptom
36 ge appeared thick, smooth, and unbranched in medial forebrain bundle, medial lemniscus and cortex whi
37 Four monkeys received crossed lesions of the medial forebrain bundle (MFB) and inferior temporal cort
38 m this work are briefly noted: 1) DBS of the medial forebrain bundle (MFB) in humans, 2) reduction of
39                Rats with an electrode in the medial forebrain bundle (MFB) in or near the ventral teg
40 CS with stimulating electrodes placed in the medial forebrain bundle (MFB) is particularly robust.
41                          Transections of the medial forebrain bundle (mfb) likewise failed to produce
42 xytryptamine (5,7-DHT), is injected into the medial forebrain bundle (mfb) on the day of birth.
43  inhibited dopamine release evoked by either medial forebrain bundle (MFB) or pedunculopontine tegmen
44 we will describe in this protocol the use of medial forebrain bundle (MFB) stimulation together with
45 elds (RRF) decreases the rewarding effect of medial forebrain bundle (MFB) stimulation, although thes
46 n macrostructure to the rewarding effects of medial forebrain bundle (MFB) stimulation.
47 mentum (LDTg) on the reward effectiveness of medial forebrain bundle (MFB) stimulation.
48  The neurotoxin 6-OHDA was injected into the medial forebrain bundle (MFB) unilaterally to produce a
49 , which we recently described, in the murine medial forebrain bundle (mfb), which specifically expres
50 -hydroxydopamine (6-OHDA) in the ipsilateral medial forebrain bundle (MFB).
51 rtical arousal, increases before ICSS of the medial forebrain bundle (MFB).
52 m were destroyed by unilaterally cutting the medial forebrain bundle (MFB).
53 mine (6-OHDA; 8 mug/2 muL) injected into the medial forebrain bundle (MFB, full nigral lesion) as an
54 owing a unilateral 6-OHDA injection into the medial forebrain bundle of adult rats.
55 ssively lesioned by 6-OHDA injected into the medial forebrain bundle or ST, respectively.
56 6-hydroxydopamine (6-OHDA) infusion into the medial forebrain bundle, rats were classified as having
57 nsonian by a 6-hydroxydopamine lesion of the medial forebrain bundle, received either levodopa alone
58 ice unilaterally lesioned with 6-OHDA in the medial forebrain bundle resulted in more pronounced rota
59                               Lesions in the medial forebrain bundle rostral to a stimulating electro
60  PV-negative neurons and coarse axons of the medial forebrain bundle, some of which are PV-positive.
61 ting that it reduced the rewarding impact of medial forebrain bundle stimulation.
62 n the reward value for cocaine, sucrose, and medial forebrain bundle stimulation.
63 ction of 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle to deplete striatal dopamine (DA
64 tions: instead of following the route of the medial forebrain bundle ventrally, most of the SN-VTA pr
65 al 6-OHDA administration (10 microg into the medial forebrain bundle) was tested.
66 ens, evoked by electrical stimulation of the medial forebrain bundle, was monitored in the anesthetiz
67 ts working for electrical stimulation of the medial forebrain bundle, we assessed the effect of GBR-1
68  mice with a unilateral 6-OHDA lesion of the medial forebrain bundle were chosen as exemplary samples
69 actacystin (1.25 microg/side) into the mouse medial forebrain bundle were performed.
70 ction of 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle, while sham surgery rats receive
71  beforehand), unilateral pretreatment of the medial forebrain bundle with 6-OHDA (8 microg/4 microl),

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