戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 s were neither type I SGNs nor olivocochlear efferents.
2 n the MVe and most brain areas receiving MVe efferents.
3 hRs localized exclusively in corticothalamic efferents.
4 ions were the result of damage to entorhinal efferents.
5 within the zone of termination of cerebellar efferents.
6  unilateral ventral rhizotomies to eliminate efferents.
7  oxide synthase may be found in some retinal efferents.
8  also synaptic targets of lateral geniculate efferents.
9 , somatosensory, and motor telencephalofugal efferents.
10 e convergence of afferents and divergence of efferents.
11  pallidal- versus nigral-projecting striatal efferents.
12  with feedback loops, modulatory inputs, and efferents.
13 ely operated by static and dynamic fusimotor efferents.
14 ine central gray are major recipients of LHb efferents.
15 tion of BST regions that receive hippocampal efferents.
16 nto the left NA to anterogradely label vagal efferents.
17 recruitment of the autonomic and somatomotor efferents.
18 propriate activation of selected sympathetic efferents.
19 pression in lateral and medial olivocochlear efferents.
20 nt activation of somatomotor and sympathetic efferents.
21 comitant activation of motor and sympathetic efferents.
22  Broca (MS) is a site at which noradrenergic efferents act to influence EEG state via actions at beta
23 nts in their peripherally located parts, and efferents also innervate muscle fibers.
24  the nucleus accumbens, but some hippocampal efferents also originated in the parasubiculum, the pros
25 vian mSCN and vSCN collectively express more efferents and afferents than does the mammalian SCN.
26  of the brain owing to interruption of their efferents and afferents.
27 B in the mSCN and vSCN were used to identify efferents and afferents.
28                Schwann cells of degenerating efferents and endoneurial cells also incorporated label.
29            Morphological differences between efferents and interneurons are discussed in light of a h
30 inputs were found primarily on the autonomic efferents and interneurons in the medial and intermediat
31  the connectivity between lateral geniculate efferents and neurons of the hypothalamus, including tho
32 ings suggest that the interaction between OC efferents and OHCs early in development may be critical
33 ption, given that they innervate sympathetic efferents and project at best very lightly to the VRC.
34 eased densities of NGF-sensitive sympathetic efferents and sensory afferents.
35 PGi is by means of preganglionic and somatic efferents and spinal interneurons closely associated wit
36  reticulata (SNr), a main target of striatal efferents and the primary output nucleus of the basal ga
37                   Thus, medial olivocochlear efferents and type II afferents, which both contact oute
38 esult in death of cortical neurons and their efferents and ultimately in death or damage of thalamoco
39 e is capable of activating prey motor neuron efferents, and hence muscles.
40 ses from collaterals of medial olivocochlear efferents, and the other arises from neurons that projec
41 cleus was the major source of these amygdala efferents, and there was a crude topography as parts of
42 ack hindbrain bmn, suggesting that the motor efferents are crucial for appropriate sensory axon proje
43 w that interneurons are En-positive, whereas efferents are En-negative.
44                           Here, we show that efferents are essential for long-term maintenance of coc
45                                        These efferents are functionally inhibitory, using the same io
46 se data further suggest that all hippocampal efferents are not homogeneous, and that the hippocampus
47 us and supports the hypothesis that cortical efferents are required scaffolds to guide TCAs into cort
48                     It is also known that LC efferents are spatially organized with respect to their
49 ir cell areas suggested that outer hair cell efferents are the most important in minimizing this neur
50             To evaluate whether SCN/AH graft efferents arise from the donor SCN, we used micropunch g
51        The precise functional role of neural efferents arising from SCN/AH grafts in the restoration
52 rian degeneration of the cortical descending efferents as observed in the basilar pons.
53  the nucleus ambiguus to label vagal cardiac efferents (at 3, 6, and 9 months).
54 oordinates activation of motor and autonomic efferents before or at the onset of exercise.
55 peripheral vagal afferents and central vagal efferents but less information is available regarding th
56 both innervated and regulated by sympathetic efferents, but the distribution and identity of the cell
57  pathway to the inner ear, the olivocochlear efferents, by examining otoacoustic emissions created by
58 ern for locomotion, maturation of peripheral efferents, changes in afferent modulation of the central
59 ir cells and calyx endings, show that turtle efferents commonly contact afferent boutons terminating
60 nostaining included: 1) the medial habenula, efferents composing the fasciculus retroflexus, and the
61              In these sites, intergeniculate efferents contacted populations of neurons that were ret
62            These findings suggest that vagal efferents continue to maintain homeostatic control over
63  to the medial prefrontal cortex, that these efferents contribute to fear memory behavior, and that C
64  afferents, or the temporal lobe subcortical efferents, contributed to the behavioural syndrome and t
65 agal capsaicin induces degeneration of vagal efferents controlling GI functions.
66              Two candidate sites at which LC efferents could influence ECoG and HEEG are the medial s
67 ade trans-synaptic transport of cre from NAc efferents decreased cocaine self-administration in rats.
68 SO to the cochlea, the lateral olivocochlear efferents, disrupted the normal interaural correlation i
69                  For these nerves, the motor efferents form prior to the sensory afferents, and their
70 s to each of the plexuses; (3) these cardiac efferents formed dense basket terminals around individua
71                                    Ascending efferents from all three nuclei of the torus innervate c
72                           In contrast to the efferents from area 25 previously described in the rat,
73                                     Although efferents from both regions formed both symmetric and as
74 t has been demonstrated that the subcortical efferents from CA3 and CA1 can be selectively disrupted
75                   These results suggest that efferents from different subnuclei of the secondary gust
76 opils that are distinct from those receiving efferents from divisions of the vertical lobe that repre
77 orsal expression of collapsin-1 prevents all efferents from entering the cord early and sustained ven
78 MAv are in many respects similar to those of efferents from M1.
79 escending commands mediated by corticospinal efferents from old M1 must use the integrative mechanism
80                                              Efferents from PaS and PrS show a selective laminar term
81 asolateral nucleus of the amygdala (BLA) and efferents from the BLA that run through the stria termin
82                                 In contrast, efferents from the CMAd terminate most densely in the do
83              Finally, we identified specific efferents from the CRH-containing region of the LHA to t
84                     We also hypothesize that efferents from the dorsocentral (DC) telencephalon proje
85 3% in the head of the caudate nucleus, where efferents from the dorsolateral prefrontal cortex projec
86  and piriform cortex share target areas, but efferents from the endopiriform nucleus lack the precise
87                                              Efferents from the GLv follow a descending course throug
88                         Surprisingly, though efferents from the lateral hypothalamic orexin field wer
89                                              Efferents from the left habenula terminate along the ent
90  also examined the pattern of termination of efferents from the primary motor cortex (M1).
91 re to assess more directly whether damage to efferents from the retrohippocampal region, rather than
92                                  Conversely, efferents from the right habenula adopt a more extensive
93 on may depend on specific ipsilateral neural efferents from the SCN to LH releasing hormone (LHRH)-co
94 examine the pattern of spinal termination of efferents from the supplementary motor area (SMA) and th
95 also innervated by two groups of cholinergic efferents from the ventral nucleus of the trapezoid body
96 and motor actions through striatum-targeting efferents from ventral tegmental area (VTA) and substant
97       Given a model in which these accumbens efferents gate the excitability of basal forebrain choli
98                                     Cortical efferents growing in the same environment diverge early
99 radrenergic receptors on basolateral nucleus efferents has wide-ranging implications for the numerous
100 us, the cellular associations of cholinergic efferents, identified by the low-affinity, p75 neurotrop
101 sual object) information from perforant path efferents in a unique manner that is consistent with the
102   The vagal afferents, PNs and vagal cardiac efferents in diabetic mice were compared with age-matche
103 l of sympathetic outflow to the cold defense efferents in mammals.
104            Stimulation of vagal afferents or efferents in mice 24 hours before IRI markedly attenuate
105 mine system and several of its afferents and efferents in motivational function.
106 ovide the first functional evidence for such efferents in neurologically intact hamsters by exploitin
107 hese results suggest that septal cholinergic efferents in the dentate gyrus: (1) preferentially inner
108                                           No efferents in the group were En-positive.
109 ution of intergeniculate and suprachiasmatic efferents in the hypothalamus and their similar relation
110 ith the effects of electrical stimulation of efferents in the mammalian cochlea.
111   In complementary experiments, the 20 or so efferents in the T3 DUM group, which are octopaminergic,
112 ally specific optogenetic inhibition of RMTg efferents in the ventral tegmental area.
113 proprioceptive organs that are innervated by efferents in their peripherally located parts, and effer
114 ive labeling of motoneurons and ventral root efferents-in particular, in an extremely densely labeled
115 rm potentiation in downstream targets of BLA efferents, including the hippocampus.
116 he localization of NADPH-diaphorase in these efferents indicated that they may use nitric oxide to mo
117          This extended terminal field of DMP efferents indicates that mMAN encompasses a core populat
118 ylcholine or electrical stimulation of vagal efferents, indicating that our system could detect incre
119      Electrical stimulation of cardiac vagal efferents induced a voltage-related bradycardia, the mag
120  known about the function of the cholinergic efferents innervating peripheral vestibular hair cells.
121  known about the function of the cholinergic efferents innervating peripheral vestibular hair cells.
122 jections, the topographic specificity of LHb efferents is not completely understood, and the relative
123              Rostral ventrolateral medullary efferents labeled with BDA were apposed to thoracic reti
124 by sensory afferents (but not by sympathetic efferents) leads to a further increase of terminal arbor
125 nt paradigm were abolished by lesions of LHb efferents, lesions of the RMTg, or by optogenetic inacti
126                         In the corticotectal efferents, LI-rTMS improved topography of the most abnor
127 cleus of the solitary tract (NTS), where VMH efferents make close contacts with catecholaminergic neu
128                           The sprouted motor efferents may account for some of the reorganization of
129 cystokinin, and that MC4R signaling in vagal efferents may contribute to the control of the liver and
130 3 receptor levels in limbic striatum and its efferents observed in patients with schizophrenia may be
131 reflex responses of static and dynamic gamma-efferents occurs that is dependent upon behavioural cont
132                                          The efferents of Ep2 traveled dorsolaterally to terminate in
133 present study investigated the afferents and efferents of MeA and MeP by using combined anterograde a
134 ith serial two-photon tomography, to map the efferents of the LHb on a standard coordinate system for
135                                          The efferents of the MHb homolog selectively target the inte
136 uences reach even into the inner ear via the efferents of the olivocochlear bundle, the medial branch
137 of previous studies have shown afferents and efferents of the presumptive "nucleus accumbens," detail
138                                 The visceral efferents of the superior cervical ganglia did not conta
139 sive measure of the effect of human auditory efferents on cochlear gain and compression.
140                           These neurons send efferents onto key hypothalamic circuits, including thos
141 ) to determine more specifically whether SCN efferents originated in the core or shell using neuroche
142           There has been speculation whether efferents play a necessary role in directing or achievin
143 cleus cholinergic neurons and their thalamic efferents play a role in postural control in patients wi
144 these experimental conditions, noradrenergic efferents, presumably arising from LC, modulate forebrai
145 s to TPO, whereas posterior Ep2 neurons sent efferents primarily to NIL.
146 eased expression of 5-HT1B receptors in NAcc efferents, probably in the terminals of medium spiny neu
147                                 SCN/AH graft efferents project into areas normally innervated by the
148  at an ISI of 1 ms, indicating that cortical efferents project onto a shared population of target neu
149 jections to corresponding parts of Ep, whose efferents projected to intermediate and posterior Ep2, r
150 structural remodeling of vagal afferents and efferents provides a foundation for further analysis of
151 metry extends to protein levels in habenular efferents, providing additional evidence that left and r
152 also show that approximately 68% of mPOA-VTA efferents release gamma-aminobutyric acid (GABA), over 7
153 clock function and the extent of SCN-derived efferents remain to be determined.
154  M-channels in CA3 pyramidal neurons and its efferents - Schaffer collateral, which causes the depola
155 ; however, it is not known whether these NTS efferents specifically target LC dendrites.
156 ical fear conditioning, with CA3 subcortical efferents supporting acquisition of both cued and contex
157 ntion of contextual fear and CA1 subcortical efferents supporting the encoding and retrieval of both
158 t the endopiriform nucleus; (2) endopiriform efferents target cortical rather than nuclear structures
159 d support the hypotheses that (i) cerebellar efferents target frontal lobe neurons involved in formin
160                       The terminals of these efferents target protocerebral neuropils that are distin
161                                  Hippocampal efferents terminated most densely in the medial and vent
162 , ensuring maximal remote activation of prey efferents that blocks subsequent prey movement by induci
163                                 GFP-positive efferents that co-expressed choline acetyltransferase sp
164                              All 12 are CCAP efferents that exit the central nervous system.
165 ng, suggesting that beta-2 AR regulate vBNST efferents that release CRF into the VTA, activating CRF
166 mmunohistochemistry to characterize VTA GABA efferents throughout the brain.
167  nucleus enabled the selective tracing of C3 efferents throughout the rat CNS, thus revealing the ana
168 pothalamus in neuronal populations that send efferents to areas where alpha-MSH1-13 is released from
169 here exists: 1) lateralization of hypocretin efferents to basal forebrain and brainstem arousal-relat
170 ndicate that approximately 80% of hypocretin efferents to basal forebrain regions project ipsilateral
171                                  Although PG efferents to DL are spatially organized, the projection
172 t enter the hindbrain in order for the motor efferents to exit.
173 e and shell each project through commissural efferents to homologous contralateral areas.
174     Taken together, the distribution of GnIH efferents to neural sites regulating reproductive behavi
175  These regions have major afferents from and efferents to other associative cortices.
176          Moreover, the capacity of the vagal efferents to reinnervate the GI tract under comparable c
177  demonstrate a broad spatial organization of efferents to striatum and regions surrounding RA, thus d
178 posed by the prefrontal cortex (PFC) and its efferents to the amygdala.
179                   Thus, the anterior Ec sent efferents to the anterior Ep, which in turn sent project
180 eral vs. contralateral distribution of raphe efferents to the ependymal wall of the lateral ventricle
181                           Severing habenular efferents to the IPN, or only those from the left dHb, p
182                        Thus, activity of LHb efferents to the midbrain is aversive but can also serve
183  FG and AR showed that over one-third of MPO efferents to the PAG contain receptors for either estrog
184 s of Meynert/substantia innominata; and sent efferents to the pons, superior colliculus, reticular nu
185                          Vagal preganglionic efferents to the rat stomach were labeled anterogradely
186 support the hypothesis that a portion of NTS efferents to the RVL may be involved in sympathoexcitato
187                                              Efferents to the sacculus, the main auditory end organ,
188 nse potentiates evoked GABA release from MSN efferents to the SNr and drives motor sensitization.
189 FO that were identified as neurons that send efferents to the SON.
190  of electrocommunication signals, whereas DC efferents to the tectum modulate sensory control of move
191  study, we examined the relationship of VLPO efferents to the TMN using both retrograde and anterogra
192 calize the cells in the brain giving rise to efferents to the turtle retina.
193 the origin and organization of noradrenergic efferents to these basal forebrain regions by using comb
194  quantitative investigation of preoptic area efferents to these monoaminergic groups.
195      Approximately 80-85% of locus coeruleus efferents to these regions project ipsilaterally.
196 amined: 1) lateralization of locus coeruleus efferents to these regions; 2) the topographical organiz
197 ion to subcortical sites, the majority of LC efferents to VB and POm thalamus originate in the ipsila
198 turn, directs the posterior outgrowth of dHb efferents toward the IPN and, when disrupted, results in
199                                    These VMH efferents travel caudally through the periaqueductal gra
200 of CA3 efferents via the fimbria and the CA1 efferents via the dorsal fornix for encoding and consoli
201 ent was designed to evaluate the role of CA3 efferents via the fimbria and the CA1 efferents via the
202 , the recovery of secretomotor and vasomotor efferents was determined by recording salivary flow from
203 h in emphasis from pallidal to mesencephalic efferents was not observed for dopamine-induced motor ac
204                                      Retinal efferents were evaluated in 45 subcortical structures.
205               Contacts between afferents and efferents were observed frequently in the inner spiral b
206  leucoagglutinin-labeled, lateral geniculate efferents were observed in the suprachiasmatic nucleus,
207         In anaesthetised cats, afferents and efferents were recorded in intramuscular nerve branches
208  effective subthalamic nucleus afferents and efferents were reduced by stimulation, whereas cortico-s
209                                      The bmn efferents were unaffected in these mutants.
210                                              Efferents were unaffected, and supporting cells, though
211 t the distribution patterns of SCN and vSPVZ efferents were very similar.
212 sal fibres activated by individual fusimotor efferents) were separated by a minimum conduction path o
213 es by both vagal sensory afferents and motor efferents, which allowed us to assess the sites innervat
214 y to contact adrenergic somata than were NTS efferents, which usually contacted dendrites.
215  during electrical stimulation of vestibular efferents while applying several subtype-selective nAChR
216                The shifting of afferents and efferents with cortical reduction or expansion at very e
217  that combines anterograde tracing of nigral efferents with pre-embedding choline acetyltransferase (
218 sensory miswiring, culminating in functional efferents within proximal afferent pathways.
219 xcitation of T stellate cells by cholinergic efferents would be expected to enhance the encoding of s

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。
 
Page Top