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1 netic and cellular basis of a model chordate central pattern generator.
2 t is thought to be controlled by a brainstem central pattern generator.
3 consistent with a postsynaptic effect on the central pattern generator.
4 and pattern-initiating neurons of the buccal central pattern generator.
5 ties of neuron B51, an element of the buccal central pattern generator.
6 in the Stomatogastric Ganglion, a well-known central pattern generator.
7 rhythmogenic core mechanism of the breathing central pattern generator.
8 n, a homologous key component of the singing central pattern generator.
9 t are sourced in a multifunctional brainstem central pattern generator.
10 y through integrated reflex pathways with no central pattern generator.
11 taneous swimming gait without the need for a central pattern generator.
12  and probe the organization of the mammalian central pattern generator.
13 inhibitory connectome within the respiratory central pattern generator.
14 ught to be produced by segmentally organized central pattern generators.
15 he interactions between functionally related central pattern generators.
16 rder control and indirect interactions among central pattern generators.
17 in sensory and neuromuscular circuits and in central pattern generators.
18 omous neural circuits known as pacemakers or central pattern generators.
19 ry bursts with properties similar to in vivo central pattern generators.
20 c and cholinergic components ensure that the central pattern generator activates motoneurones effecti
21                     When depolarized without central pattern generator activation, FTNs produced subt
22 tion of transplanted cells and maturation of central pattern generator activity synergistically.
23 splantation improved spinal conductivity and central pattern generator activity, and that treadmill t
24       These data suggest that independent of central pattern generator activity, intrapharyngeal nega
25 behavior that is thought to be governed by a central pattern generator and that is accompanied by hig
26 edback to the cervical enlargement of lumbar central pattern generator and/or hindlimb proprioceptive
27 roids on vocal patterning at two levels: (1) central pattern generators and (2) social behavior in na
28  blocks the depolarizing "ramp" input to the central pattern generator, and consequently the motor pr
29  with the lack of biophysical evidence for a central pattern generator, and recent experimental evide
30                            Sensory feedback, central pattern generators, and supraspinal structures c
31 e of the rhythmically active leech heartbeat central pattern generator are pairs of mutually inhibito
32 cending interneurons (dINs)] in the swimming central pattern generator are raised by depolarization d
33                  The study demonstrates that central pattern generators are capable of adapting oscil
34                                              Central pattern generators are neural circuits, which ge
35                                              Central pattern generators are neuronal circuits that wh
36                                              Central pattern generators are neuronal ensembles capabl
37                                              Central pattern generators are subject to extensive modu
38 A more modest focus of many neuroscientists, central pattern generators, are more tractable neuronal
39  Furthermore, the outputs of the respiratory central pattern generator as a whole are invariant to th
40 complex neural control system, the breathing central pattern generator (bCPG), that exhibits diverse
41 urately the dynamical response of biological central pattern generators (bCPGs).
42 not a necessary component of the respiratory central pattern generator but constitutes a defensive me
43 modulator myomodulin speeds up the heartbeat central pattern generator by reducing Na(+)/K(+) pump cu
44                       This suggests that the central pattern generator can maintain the locomotor per
45 propose that steroid-dependent modulation of central pattern generators can govern the overt expressi
46  rhythmic behavior one must characterize the central pattern generator circuit and quantify the popul
47 w that dopamine exerts potent effects on the central pattern generator circuit controlling locomotory
48 light activation of VALopA in neurons of the central pattern generator circuit for locomotion leads t
49 n handle this all by integrating a brainstem central pattern generator circuit in a larger network th
50 orsal swim interneurons of the Tritonia swim central pattern generator circuit.
51 or neurons of the reticular formation, where central pattern generator circuits controlling orofacial
52 he descending feedforward pathways and local central pattern generator circuits that control and gene
53  the presence of two distinct left and right central pattern generators, connected as coupled oscilla
54 f a pattern formation network of a two-level central pattern generator controlling locomotor activity
55 e stepping rhythm, it is difficult to reveal central pattern generator (CPG) adaptation.
56 ive components of the mouse spinal locomotor central pattern generator (CPG) and candidates for the r
57 ration of rhythmic behavior is operated by a central pattern generator (CPG) and does not require per
58 behavior is governed by a sexually dimorphic central pattern generator (CPG) and that fictive vocaliz
59  that early activity in the zebrafish spinal central pattern generator (CPG) and the earliest locomot
60 nx at the periphery, and the hindbrain vocal central pattern generator (CPG) centrally, that produce
61  between projection neurons and their target central pattern generator (CPG) circuit neurons.
62 the cervical and lumbar spinal enlargements, central pattern generator (CPG) circuitry produces the r
63 e inhibitory neurotransmitter for neurons in central pattern generator (CPG) circuits underlying swim
64                                          The central pattern generator (CPG) circuits underlying thes
65  dorsal swim interneurons (DSIs) of the swim central pattern generator (CPG) directly excite Pedal ne
66 ude that motoneurons provide feedback to the central pattern generator (CPG) during drug-induced loco
67   We explored the organization of the spinal central pattern generator (CPG) for locomotion by analys
68 amprey spinal cord/notochord can entrain the central pattern generator (CPG) for locomotion.
69 ed by a network of neurons termed the spinal central pattern generator (CPG) for locomotion.
70                                          The central pattern generator (CPG) for swallowing probably
71 s) are serotonergic neurons intrinsic to the central pattern generator (CPG) for swimming in the moll
72  In Melibe, it was previously shown that the central pattern generator (CPG) for swimming is composed
73  We found an example of such recovery in the central pattern generator (CPG) for the escape swim of t
74 ern, interneuron C2, a crucial member of the central pattern generator (CPG) for this rhythmic behavi
75 on of tongue control, the integration of the central pattern generator (CPG) for TP/R with other aero
76            We have previously identified the central pattern generator (CPG) for Xenopus tadpole swim
77        However, we could not find a definite central pattern generator (CPG) in the brain stem, which
78 eurons (DSIs) are members of the escape swim central pattern generator (CPG) in the mollusk Tritonia
79     We found no evidence that other swimming central pattern generator (CPG) interneurons are coupled
80 rization, the default state of the locomotor central pattern generator (CPG) is symmetrical, with ant
81 f neural characters comprising a vocal-sonic central pattern generator (CPG) morphotype is proposed f
82            Locomotor behavior is produced by central pattern generator (CPG) networks and modified by
83 ic contraction, are initiated by output from central pattern generator (CPG) networks in the CNS.
84                                              Central Pattern Generator (CPG) networks, which organize
85 riginate in the brain but are coordinated by Central Pattern Generator (CPG) neural networks in the s
86 hythm and, at these times, is a gastric mill central pattern generator (CPG) neuron.
87 rhythmic bursting in temperature-compromised central pattern generator (CPG) neurons by counteracting
88                       The characteristics of central pattern generator (CPG) outputs are subject to e
89 owever, it remains unclear how the locomotor central pattern generator (CPG) processes descending dri
90          The Aplysia multifunctional feeding central pattern generator (CPG) produces at least two ty
91 ntermediate reticular nucleus (IRt) form the central pattern generator (CPG) responsible for post-I a
92 e mammalian spinal cord contains a locomotor central pattern generator (CPG) that can produce alterna
93 he core interneuronal components of the limb central pattern generator (CPG) that coordinate flexor-e
94                             The multitasking central pattern generator (CPG) that drives consummatory
95  reticular nucleus (IRt) are components of a central pattern generator (CPG) that generates post-I ac
96 lled "whisking," are produced by a brainstem central pattern generator (CPG) that uses serotonin to i
97                                          The central pattern generator (CPG) underlying DV swimming h
98 mportant extrinsic modulatory actions on the central pattern generator (CPG) underlying rhythmic inge
99         If the input originates from a small central pattern generator (CPG) with dense divergent con
100 nal cord circuitry incorporating a two-level central pattern generator (CPG) with separate half-centr
101 icit distinct rhythmic motor patterns from a central pattern generator (CPG), but they can instead el
102 n the spinal cord, collectively known as the central pattern generator (CPG), coordinate rhythmic mov
103                       In the Aplysia feeding central pattern generator (CPG), identified interneuron
104 ere, we use the leech (Hirudo sp.) heartbeat central pattern generator (CPG), in which we can measure
105 gence relates to the formation of the spinal central pattern generator (CPG), the circuit that mediat
106                    Using the leech heartbeat central pattern generator (CPG), we selected three diffe
107 on depends on spinal interneurons termed the central pattern generator (CPG), which generates activit
108 imal locomotion is controlled, in part, by a central pattern generator (CPG), which is an intraspinal
109 ng function of B64 depend on the type of the central pattern generator (CPG)-elicited response rather
110 d in the spinal cord, known as the locomotor central pattern generator (CPG).
111 re controlled by a well characterized buccal central pattern generator (CPG).
112 uisqualic acid (l-QA), activated the pyloric central pattern generator (CPG).
113 ught to be regulated by an unknown brainstem central pattern generator (CPG).
114 have been assumed to reflect the output of a central pattern generator (CPG).
115 wer-level sensorimotor loops and a brainstem central pattern generator (CPG).
116 m neural circuits comprising the respiratory central pattern generator (CPG).
117 s colonic motor complexes, are controlled by central pattern generators (CPG) in the enteric nervous
118 ive collateral projections modulating lumbar central pattern generators (CPG).
119                                          The central pattern generators (CPGs) and motoneurons that c
120                                              Central pattern generators (CPGs) are circuits that gene
121 ebrates and invertebrates, chains of coupled central pattern generators (CPGs) are commonly evoked to
122       Modulatory interneurons that can drive central pattern generators (CPGs) are considered as good
123                                              Central pattern generators (CPGs) are lower in the funct
124 motor neuron activity.SIGNIFICANCE STATEMENT Central pattern generators (CPGs) are neural circuits th
125                                              Central pattern generators (CPGs) are neurons or neural
126 l pathways involved in retraining the spinal central pattern generators (CPGs) by afferent input in t
127                                     Although central pattern generators (CPGs) can produce rhythmic a
128                                              Central pattern generators (CPGs) control both swimming
129 e coordination between the spatially distant central pattern generators (CPGs) controlling forelimb a
130 otor behaviors requires modifications in the central pattern generators (CPGs) controlling muscle act
131 are commonly involved in the dynamics of the central pattern generators (CPGs) driving various rhythm
132 twork shares many functional properties with central pattern generators (CPGs) found in relatively si
133                       Neural networks called central pattern generators (CPGs) generate repetitive mo
134                                     The swim central pattern generators (CPGs) in both species are co
135 urons) is a potent activator of the hindlimb central pattern generators (CPGs) in rodent spinal cords
136 ent excitation and inhibition originating in central pattern generators (CPGs) may be used to control
137 ral mechanisms that underlie the function of central pattern generators (CPGs) presents a formidable
138                                              Central pattern generators (CPGs) produce neural-motor r
139               SIGNIFICANCE STATEMENT: Spinal central pattern generators (CPGs) produce the rhythmic o
140                                       Spinal central pattern generators (CPGs) produce the rhythmic o
141                                              Central pattern generators (CPGs) provide feedback to th
142  cord injury patients by reactivating spinal central pattern generators (CPGs) requires the elucidati
143 rder neurons provide commands to lower-level central pattern generators (CPGs) that autonomously prod
144 e control of spinal neural networks known as central pattern generators (CPGs) that comprise multiple
145 viously identified two anatomically distinct central pattern generators (CPGs) that drive the fast an
146  Locomotion relies on neural networks called central pattern generators (CPGs) that generate periodic
147                   During rhythmic movements, central pattern generators (CPGs) trigger bursts of moto
148                      Many well characterized central pattern generators (CPGs) underlie behaviors (e.
149     These networks, which are referred to as central pattern generators (CPGs), are ideal systems for
150 absence of sensory feedback, commonly called central pattern generators (CPGs), are involved in many
151      Oscillating neuronal circuits, known as central pattern generators (CPGs), are responsible for g
152                  Biological neural circuits, central pattern generators (CPGs), located at the spinal
153 ysfunction of synaptic neurotransmission and central pattern generators (CPGs), potentially a common
154                                              Central pattern generators (CPGs), specialized oscillato
155 In pacemaker-driven networks, including many central pattern generators (CPGs), this frequency range
156 perties with compact motor networks known as central pattern generators (CPGs).
157 derlying neural circuits and coordination of central pattern generators (CPGs).
158 s essential for the development of locomotor central pattern generators (CPGs).
159 action of rhythm generating networks, called central pattern generators (CPGs).
160 led to new insights about the functioning of central pattern generators (CPGs).
161                                              Central patterns generators (CPGs) are neural circuits t
162 ate spinal cord, a real understanding of how central pattern generators develop is hindered by our la
163 h bicuculline or by surgical ablation of the central pattern generator during early embryogenesis, we
164 iring in motoneurons and interneurons of the central pattern generator during swimming.
165  medulla, which contains key elements of the central pattern generator for breathing that are importa
166 omotor-related signal produced by the lumbar central pattern generator for locomotion selectively mod
167 g the frequency of interneuron firing in the central pattern generator for locomotion.
168 whisker premotor neurons, which might form a central pattern generator for rhythmic whisker protracti
169 tor cell (an interneuron that is part of the central pattern generator for swimming).
170  by different neural pathways, including the central pattern generator for walking, brainstem pathway
171 ent work that delineated the location of the central pattern generator for whisking has enabled pharm
172 uggests that insect thoracic ganglia contain central pattern generators for directed leg movements.
173 ing overground locomotion, suggesting normal central pattern generator function and supporting our hy
174           For example, neurons in crustacean central pattern generators generate similar firing patte
175 A computational model of the Aplysia feeding central pattern generator has, therefore, suggested that
176 ut the connections from cell Tr2 to the swim central pattern generator have not been identified.
177 xperimental preparations, sensory inputs and central pattern generators have now been shown to play d
178  The technology consists of silicon hardware central pattern generators (hCPGs) that may be trained t
179  interneurons are components of the hindlimb central pattern generator, helping to organize left-righ
180 xes (CMC) are considered to be controlled by central pattern generators housed in the myenteric plexu
181 y information from this stimulus to the swim central pattern generator, (ii) elicits the swim motor p
182 ne key identified interneuron of the singing central pattern generator in five cricket species.
183 iven by descending excitatory connections to central pattern generators in the spinal cord.
184 nal networks, such as those comprising motor central pattern generators; in turn, they receive feedba
185  stimulation (TANES), which can activate the central pattern generator, inducing active weight-suppor
186                 Stimulation of the ingestive central pattern generator input immediately triggers ing
187         Different stimuli activate different central pattern generator inputs.
188 and-like food-signaling cell type, a feeding central pattern generator interneuron, and a unique beha
189 tion of the electrically coupled neuron N3P (central pattern generator) interneurons does not affect
190 ext dependence by sequentially incorporating central pattern generators, intrinsic drives, and sensor
191 er movements and may be a key component in a central pattern generator involved in the generation of
192 e support for the concept that the locomotor central pattern generator is a modular network with spee
193 ample, although the regular oscillation of a central pattern generator is well characterized by its f
194 that the high reliability and flexibility of central pattern generators is determined by their redund
195 tive to sensory neurons, reflex circuits and central pattern generators is summarized.
196 llatory network can be traced to the role of central pattern generator located in the spinal cord.
197                     Spinal circuits known as central pattern generators maintain vertebrate locomotio
198 e inhibition of the contralateral scratching central pattern generator mediated by excitatory V0 neur
199  in activity in association with repetitive, central pattern generator mediated responses.
200 n systems such as the vertebrate respiratory central pattern generator, multiple pacemaker types inte
201              We experimentally demonstrate a central pattern generator network using capacitively cou
202 s can be regulated to make a self-assembling central pattern generator network; thus, network-level h
203 rates is based on a set of modules, like the central pattern generator networks (CPGs) in the spinal
204 ythmogenic neurons similar to those found in Central Pattern Generator networks of the central nervou
205                             We show that the central pattern generator neural network coordinately dr
206 ic excitation of the reciprocally inhibitory central pattern generator neurons LG (protraction) and I
207  of the macaque cerebral cortex and the swim central pattern generator of a mollusc) provides an inte
208                               In the feeding central pattern generator of Aplysia, the pattern-initia
209 may be attributed to damage inflicted on the central pattern generator of locomotion resulting in dys
210                                              Central pattern generators (one per limb) within the spi
211 ferently in determining different aspects of central pattern generator operation.
212 nderstand the cellular and synaptic bases of central pattern generator organization and reconfigurati
213                 To determine why elements of central pattern generators phase lock in a particular pa
214 s, apNPYergic reconfiguration of the feeding central pattern generator plays a role in the gradual tr
215                                              Central pattern generators produce many rhythms necessar
216  Neural networks in the spinal cord known as central pattern generators produce the sequential activa
217 jection network, neuromuscular junction, and central pattern generator, providing a platform for inve
218                                              Central pattern generators rather than afferent-evoked r
219 f the general role of serotonin in tonic and central pattern generator-related motor activity.
220  that this comodulation expands the range of central pattern generator's functional activity by navig
221            A local interneuron of a crayfish central pattern generator serves as a hub that integrate
222                                        Brain central pattern generators studies suggest that glia pla
223 hanges in some aspects of the circuitry of a central pattern generator, such as a several-fold increa
224 r a pattern formation network of a two-level central pattern generator that can be tested in neuromec
225 paration for copulation, is the product of a central pattern generator that consists of oscillators i
226                                          The central pattern generator that controls flying power in
227  LP neuron is part of the pyloric network, a central pattern generator that normally oscillates with
228  peripheral nerve activates an interneuronal central pattern generator that produces the long-lasting
229 s in particular are an integral component of central pattern generators that control respiration and
230  regulated by a spinal neuronal network, the central pattern generator, the activity of which is modu
231 haviors emerging from interactions between a central pattern generator, the body, and the physical en
232 ulation of an ingestive input to the feeding central pattern generator, the first few cycles of activ
233 We also show that the brainstem vocalization central pattern generator, the iRO, can create this brea
234 s modulatory premotor inputs to a vertebrate central pattern generator, the pacemaker nucleus in gymn
235                 In the mammalian respiratory central pattern generator, the preBotzinger complex (pre
236 neuron circuits collectively referred to as "central pattern generators." The contribution of proprio
237 in or detach the circuit from the locomotion central pattern generator to produce active and inactive
238 erent motor patterns generated by the buccal central pattern generator were induced by monotonic stim
239  these may be innate movements controlled by central pattern generators which become entrained by aud
240                  Networks in the ENS contain central pattern generators, which activate the 'hardwire
241                     It is often assumed that central pattern generators, which generate rhythmic patt
242  patterns are easily quantified and studied, central pattern generators will provide important testin

 
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