戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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  of function from OHCs and both afferent and efferent neurons.
2 exes that relate to postsynaptic profiles of efferent neurons.
3 rons without transduction of parasympathetic efferent neurons.
4 lear hair cells are inhibited by cholinergic efferent neurons.
5 rum and gives rise to a distinctive class of efferent neurons.
6  yields many interneurons and relatively few efferent neurons.
7 es LES motor tone via GBR expressed by vagal efferent neurons.
8 ial lobes, which receive axon collaterals of efferent neurons.
9 ites and respond to transmitters released by efferent neurons.
10           We explored how stimulation of the efferent neurons affects the mechanical responsiveness o
11  is supplied by collaterals from medial lobe efferent neurons and by terminals from the central compl
12      The preponderance of similarities among efferent neurons and elicited motor activity suggests a
13 present in a subpopulation of both brainstem efferent neurons and peripheral vestibular efferent bout
14 s caused by the arrival of the olivocochlear efferent neurons and the resulting competition for synap
15 of neurotrophins in adult vagal afferent and efferent neurons and thus serve as a template to discern
16                                              Efferent neurons are believed to play essential roles in
17 abeling experiments revealed that vestibular efferent neurons are located adjacent to, but are not in
18                                              Efferent neurons are uniquely identifiable.
19         CGRP is also expressed in vestibular efferent neurons as well as a number of central vestibul
20     In vertebrate animals, motor and sensory efferent neurons carry information from the central nerv
21 In contrast to CF5 neurons, other classes of efferent neurons (CCI, CCC, CF6) were much less active d
22 In contrast to CF5 neurons, other classes of efferent neurons (CCI, CCC, CF6) were much less active d
23 (r4), of the hindbrain and a group of caudal efferent neurons (CENs) that arises in r5.
24 reover, a network of acetylcholine-releasing efferent neurons controls afferent excitability by closi
25 r, intracellular recordings of mushroom body efferent neurons demonstrate that they respond to multim
26 let a-cells supports a model for sympathetic efferent neurons directly regulating glucagon secretion.
27 romote synaptogenesis between hair cells and efferent neurons during regeneration.
28                    Stimulation of vestibular efferent neurons excites calyx and dimorphic (CD) affere
29 In addition, we find that two populations of efferent neurons from different regions of the lPBN coll
30 rly every vertebrate, cholinergic vestibular efferent neurons give rise to numerous presynaptic varic
31                A new category of "recurrent" efferent neuron has been identified that provides feedba
32 s effector Gata3 are essential for inner-ear efferent neuron (IEE) but not FBMN development.
33 nnervated by a distinct pair of afferent and efferent neurons: IHCs are contacted by type I afferents
34 ditional motif instances functional in other efferent neurons, implicating broader functions for this
35 (2) and P2X(4)R-IR in the cell soma of vagal efferent neurones in the DVN following the nerve section
36 en in females, the structure and function of efferent neurons in abdominal ganglia of both sexes were
37 eved to be critical for the function of CCAP efferent neurons in ecdysis.
38                            The activation of efferent neurons in heterozygous mice evoked biphasic po
39 data suggest a potential role for vestibular efferent neurons in modulating the dynamics of the vesti
40                   Medial olivocochlear (MOC) efferent neurons in the brainstem comprise the final sta
41 nd Pd5, the only identified cilia-activating efferent neurons in Tritonia.
42 rior crista during electrical stimulation of efferent neurons, in combination with pharmacological pr
43                                        These efferent neurons inhibit inner hair cells, raising the p
44 ATPase is uniquely expressed in afferent and efferent neurons innervating muscle spindles in the peri
45                   While stimulation of vagal efferent neurons is known to reduce maladaptive host res
46                              DUM neurons are efferent neurons, local interneurons, or intersegmental
47   A bilateral projection from the vestibular efferent neurons, located dorsal to the genu of the faci
48 Cs, and whether ACh, the neurotransmitter of efferent neurons, modulates the stiffness of the cortica
49 ocus on the development of the octavolateral efferent neurons (OENs) and their interactions with the
50 f the cochlear amplifier can be modulated by efferent neurons of the medial olivocochlear complex.
51 ities to eurydendroid neurons, the principal efferent neurons of the teleost cerebellum.
52 [125I]-labeled neurotrophins by afferent and efferent neurons of the vagus nerve was determined to pr
53 hibitory corollary discharges from hindbrain efferent neurons onto afferents during locomotion.
54 y neurons failed to activate hindbrain vagal efferent neurons or to drive catecholamine release from
55 mit crab, intrinsic neurons and one class of efferent neurons originate from neuronal somata of globu
56                            The clustering of efferent neurons precedes the formation of cholinergic f
57  topography, but they also link afferent and efferent neurons precisely enough that alterations in PC
58 nd central amygdala neurons; and sympathetic efferent neurons projected from medullary and hypothalam
59 ne the relationship of these varicosities to efferent neurons projecting to the cochlea, olivocochlea
60         Electrical stimulation of vestibular efferent neurons rapidly excites the resting discharge o
61 utput quantitative analysis unveils that BLA efferent neurons receive a diverse array of afferents wi
62                                              Efferent neurons receive bilateral input and project uni
63 edial lobe where the dendritic trees of some efferent neurons receive inputs from one calyx only.
64 n in two distinct groups: a group of rostral efferent neurons (RENs) that arises in the fourth segmen
65                                  In general, efferent neurons respond to a variety of modalities in a
66                              The majority of efferent neurons showed an increase in activity that occ
67  to the specification of BMP target genes in efferent neuron subsets.
68  dopamine release from lateral olivocochlear efferent neurons suppresses spontaneous and sound-evoked
69 lla are accompanied by terminals of a second efferent neuron T1, the dendrites of which match NMDAR1-
70                                  Medial lobe efferent neurons terminate in the lateral protocerebrum
71            LL responsiveness is modulated by efferent neurons that aid in distinguishing between exte
72                                              Efferent neurons that are active only during stimulation
73 rons that terminate locally in the cortex on efferent neurons that are equivalent to cerebellar nucle
74 ctive strata are visited by the dendrites of efferent neurons that carry information from the mushroo
75  large ganglion and large fusiform cells are efferent neurons that convey electrosensory information
76           Olivocochlear neurons are auditory efferent neurons that convey information from the brains
77 l glomeruli are each supplied by retinotopic efferent neurons that have restricted dendritic fields i
78                      We recorded from single efferent neurons that innervate the inner ear and latera
79 us of the solitary tract is relayed to vagal efferent neurons that originate from two brain stem nucl
80                                              Efferent neurons that show endogenous activity have dend
81           Cortical afferents excite striatal efferent neurons through activation of N-methyl-D-aspart
82 ared the ability of electroreceptors and ELL efferent neurons to encode the position of moving object
83 hroom bodies demonstrated the sensitivity of efferent neurons to multimodal stimuli.
84 udy, we use direct electrical stimulation of efferent neurons to probe its effects on the hair cells'
85 f olfactory (or other) stimuli is relayed by efferent neurons to the lateral protocerebrum where it i
86 se target genes across subsets of Drosophila efferent neurons, to differentiate neuropeptidergic neur
87 arget cell innervation of olivocochlear (OC) efferent neurons was investigated in the postnatal hamst
88                 Regions containing autonomic efferent neurones were predominantly devoid of labelling
89  Cranial nerve motoneurons and octavolateral efferent neurons were aligned to the reticulospinal scaf
90                                              Efferent neurons were double-labeled by the unilateral i
91 extran amine (BDA), but large percentages of efferent neurons were found to be double labeled when us
92                                              Efferent neurons were found with double retrograde trace
93                                              Efferent neurons were labeled via injections of biocytin
94 s to verify the presence of NOS in brainstem efferent neurons were performed in young chinchillas.
95                    In contrast, responses of efferent neurons were relatively unaffected by tail move
96                              Four classes of efferent neurons were studied: corticocortical (CC) neur
97                              Four classes of efferent neurons were studied: descending corticofugal n
98 orphology and physiology of several types of efferent neurons with dendrites in the medial lobes.