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1 the control of interlimb coordination during locomotion.
2 ce backward locomotion compared with forward locomotion.
3 ce in tasks that reflect muscle strength and locomotion.
4 h were certainly well-adapted to terrestrial locomotion.
5 vivo measures of muscle oscillations during locomotion.
6 redictability of head movements (HMP) during locomotion.
7 to reconstruct the evolution of terrestrial locomotion.
8 speed, was invariant in rTg4510 mice during locomotion.
9 ard prediction error but also motivation and locomotion.
10 lance control is dynamically weighted during locomotion.
11 processes descending drive into coordinated locomotion.
12 Correspondingly, HMP increased with faster locomotion.
13 olytic phenotype, with no change in baseline locomotion.
14 rse modes of light-driven robotic underwater locomotion.
15 d and actual visual flow inputs generated by locomotion.
16 ers, and/or recruited the 'sensory' legs for locomotion.
17 VR upon manipulations of optic flow against locomotion.
18 imb during feeding and right hindlimb during locomotion.
19 aterials, making them less cumbersome during locomotion.
20 trength and rhythmicity of behaviors such as locomotion.
21 has important implications for their aquatic locomotion.
22 anical control mechanisms to maintain stable locomotion.
23 d on the injured side, resulting in impaired locomotion.
24 hat were similar during forward and backward locomotion.
25 rtex to reflect ongoing self-movement during locomotion.
26 n in Xenopus) disrupts contact inhibition of locomotion.
27 light energy into mechanical deformation and locomotion.
28 g to walking and further dropped with faster locomotion.
29 t DA in the medOB could modulate odor-evoked locomotion.
30 tic transitions accompanied with macroscopic locomotion.
31 o study locomotive transition and programmed locomotion.
32 rmal sarcomere organization and whole-animal locomotion.
33 romote shape reconfiguration, actuation, and locomotion.
34 of behaviors, most prominently goal directed locomotion.
35 e peripheral nerves, and reduction in larval locomotion.
36 vesicles, resulting in cell polarization and locomotion.
37 s entirely account for the change in a fly's locomotion.
38 al modularity via genome engineering affects locomotion.
39 outons in mouse primary visual cortex during locomotion.
40 tely contributes to slowing down spontaneous locomotion.
41 ctively drive slow-explorative or fast-speed locomotion.
42 ormed in vivo calcium imaging in mice during locomotion.
43 2a neuron-specific blockage of Mc4r promotes locomotion.
44 OE inhibits octavolateral hair cells during locomotion.
45 g that Somatostatin 1.1 inhibits spontaneous locomotion.
46 ral phenomena from polymer dynamics to snake locomotion.
47 recognize vibration events induced by human locomotion.
48 ntegration promotes cerebellar output during locomotion.
49 of biohybrid machines capable of untethered locomotion.
50 bular sense to the maturation of coordinated locomotion.
51 G), coordinate rhythmic movements underlying locomotion.
52 tabolism, growth, cytoskeletal structure and locomotion.
53 dent signaling and decreased cocaine-induced locomotion.
54 as spinal glial cell activation and reduced locomotion.
55 ft in the mode of cortical processing during locomotion.
56 eurons over other neuron populations rescues locomotion.
57 one of the primary considerations in animal locomotion.
58 understanding the adaptive origin of bipedal locomotion.
59 e unlikely to cause the observed decrease in locomotion.
60 ncreased walking speed, and improved skilled locomotion.
61 Size is a key to locomotion.
62 for applications in sensing, actuation, and locomotion.
63 n of fluke-powered, but forelimb-controlled, locomotion.
64 al skeleton has not been reported for lizard locomotion.
65 ting that this was their predominant mode of locomotion.
66 thout being inherently rewarding or altering locomotion.
67 in turn, provide facile pathways for proton locomotion.
68 se pumps to predict consequent head and body locomotion.
69 dditional excitability compared with forward locomotion.
70 dulation of electrosensory processing during locomotion.
71 utput necessary for limb coordination during locomotion.
72 pendent (or any other) principal features of locomotion.
73 adaptation of pterosaurs to a new method of locomotion.
74 botic feet and the study of foot function in locomotion.
75 tain their habitual motion path (HMP) during locomotion.
76 ing for synaptic transmission, survival, and locomotion.
77 thereby causing two effects that rate-limit locomotion: (1) impaired cell edge coordination during p
78 ms clear that transitioning between forms of locomotion(2,3)-from terrestrial to volant-challenged ea
80 in Drosophila including feeding initiation, locomotion, aggression, and courtship, among many others
83 spinal CPG transforms descending drive into locomotion and align its speed with the initial intentio
86 ve uncovered a neural mechanism for stopping locomotion and bring new insights into the function of t
90 iting VTA(Vgat) terminals in the LH elevated locomotion and decreased immobility time during the tail
91 rticles', which are incapable of independent locomotion and do not possess individual identity or add
98 RIM1 KO mice show heightened novelty-induced locomotion and impaired motor learning on the accelerati
99 ad minor but significant effects of reducing locomotion and intake of non-alcoholic palatable solutio
103 an essential player in the coupling of cell locomotion and phagocytosis in hemocytes, the Drosophila
104 deamination activity is necessary for normal locomotion and prevents age-dependent neurodegeneration.
105 the exploitation state, the animal inhibits locomotion and promotes hunting, generating small, local
106 ing swimming stress in both sexes, increased locomotion and reduced social interaction in male progen
107 ter in the Drosophila brain protects against locomotion and short-term memory function deficits in mu
108 ar in intact and spinal cats during backward locomotion and strategies were similar to forward locomo
109 ruitment of interneuronal populations during locomotion and suggest that the locomotor CPG is not a s
110 n the exploration state, the animal promotes locomotion and suppresses hunting, generating long-rangi
112 x2(+) interneurons are active during fictive locomotion and that their chemogenetic inhibition reduce
113 hat spinal networks controlling standing and locomotion and their interactions with sensory feedback
114 animals meet the metabolic O(2) demands for locomotion and thermogenesis in O(2)-thin air, but the d
115 ion from the environment required increasing locomotion and time investment, participants relied more
116 resentations to both local (current plane of locomotion) and global (gravity) cues across several exp
120 THC effects on behavioral assays of anxiety, locomotion, and place conditioning, as well as c-Fos exp
121 the visual thalamus and cortex, arousal and locomotion are associated with changes in the magnitude
122 muscle synergies during forward and backward locomotion are consistent with a shared spinal locomotor
123 These multifaceted roles of serotonin in locomotion are differentially mediated by a family of se
127 raphy (EMG) data during forward and backward locomotion at different treadmill speeds before and afte
128 roved thermotolerance and slightly increased locomotion at midlife, however, only soma-specific knock
129 g the spatial representation into equivalent locomotion-based ensemble versus optic-flow-based ensemb
130 s greater experimentation with wing-assisted locomotion before theropod flight evolved than previousl
132 lex superposition of signals that arise from locomotion, body orientation, swallowing, respiration, c
133 ngitudinal effects of alpha-syn pathology on locomotion, brain microstructure, and functional brain a
134 on that is congruent with self-motion during locomotion but are suppressed by other directions and co
136 inal sensorimotor circuits generate backward locomotion but require additional excitability compared
137 mp7 also regulates phagocytic processing and locomotion but uses pathways distinct from those of Trpm
138 ntegration critical for postural control and locomotion, but the nature and developmental organizatio
139 lates signal transduction important for cell locomotion, but the role of macrophage-specific FLNA dur
140 visceral activities, arousal, attention, and locomotion, but the specific roles of different ZI subdo
141 nergic neurons play a key role in modulating locomotion by releasing dopamine in the basal ganglia, s
142 In the absence of ORN activation, the fly's locomotion can be described by a random walk model where
144 due to the foot contacting the ground during locomotion, can be considered input signals to the body
147 he tail regresses during metamorphosis, when locomotion changes from an axial-driven mode in larvae t
162 The acquisition of terrestrial, limb-based locomotion during tetrapod evolution has remained a subj
163 rneurons, which are known to promote forward locomotion during wakefulness, act as major activators o
164 nct stimuli that were equivalent in terms of locomotion (e.g., freezing induced by looming and sound)
165 ve been selectively bred (b) for exploratory locomotion (EL), a behavioral phenotype correlated with
166 ion, a series of kinetic, kinematic, skilled locomotion, electrophysiologic, and immunohistochemical
172 environment and the presence of a partner on locomotion, grooming, singing, and other behaviors that
173 ore mechanistic understanding of terrestrial locomotion has been on how to generate and stabilize aro
174 neural pathways responsible for odor-evoked locomotion have been characterized in the sea lamprey (P
175 dopamine levels in the striatum and promote locomotion; however, their effects on striatal pathway f
176 essing neurons such as decreased spontaneous locomotion, impaired social interaction, and decreased m
178 ction of chemical cues is important to guide locomotion in association with feeding and sexual behavi
182 ovements and limb kinetics during overground locomotion in female adult rats showed that locally rewi
184 gur identified the neural circuits restoring locomotion in mice following spinal cord neurostimulatio
185 nation, spatial and contextual memories, and locomotion in mouse models for cerebellar ataxia, Alzhei
187 equires energy, yet animals need to increase locomotion in order to find and consume food in energy-d
190 Recapitulation of such multimodal aquatic locomotion in small-scale soft robots is challenging, du
193 dicating that arrestin recruitment can drive locomotion in the absence of D2R-mediated G protein sign
195 so shows that the spinal network controlling locomotion in the forward direction also controls locomo
196 analysis of multiple frequencies of fictive locomotion in the same spinal cord indicates that few ne
197 the vertebrae and ribs during slow treadmill locomotion in three savannah monitor lizards (Varanus ex
198 e Cambrian and Ordovician reveals amphibious locomotion in tidal environments and fills a gap between
202 e the transition from semiaquatic to aquatic locomotion, including development of a fusiform body and
204 ing in vivo two-photon imaging, we show that locomotion-induced Ca(2+) elevations in mouse astroglia
205 utside of lethargus, altered activity of the locomotion interneurons during lethargus favors strong R
207 ies have shown that behavioral state such as locomotion is an essential component of vision and can s
209 ting a new hypothesis that rib motion during locomotion may have been an exaptation for the evolution
210 rization, and severing is important for cell locomotion, membrane trafficking, and many other cellula
212 ing reconfigurable magnetic soft robots with locomotion modes of peristalsis, crawling, and rolling.
215 de range of cells, from bacteria to mammals, locomotion movements are a crucial systemic behavior for
218 levels of brain arousal and motor activity: locomotion, nonlocomotor movement, quiet wakefulness, an
220 study reveals how memory effects stymied the locomotion of a diversity of snakes in our previous stud
223 ging technological approaches to enhance the locomotion of micro/nanorobots in complex environments.
227 RM) in peripheral tissues, CD49a facilitates locomotion of virus-specific CD8 T cells, both in vitro
231 this phenomenon in light of the ambiguity of locomotion on energy balance and the different living co
232 ariance in rate of energy expenditure during locomotion, once speed and body size are accounted for.
233 any of these pathways on reward sensitivity, locomotion, or anxiety-like behavior, but inhibiting DRN
234 ng swimming, treadmill stepping, exploratory locomotion, or walking on an uncoated, slick surface.
235 y use optimal routes with respect to mode of locomotion, orientation and migration strategy, influenc
236 ted and carefully analyzed the kinematics of locomotion over a hundred of thousand bouts from hundred
237 ich are active during and can induce reverse locomotion-play a complex role and can act as inhibitors
238 etailed behavioral statistics describing the locomotion, pose, biting, and feeding dynamics of Aedes
240 ally active at the same frequency as fictive locomotion recorded from the ventral roots of the isolat
241 ases with increased prey activity, and rapid locomotion reduces attack rates and increases chances of
242 correlated with locomotion, the relevance of locomotion-related VIP neuron activity to visual coding
243 premise is that sensory cues consistent with locomotion reorganize spinal sensorimotor circuits.
245 the direction.SIGNIFICANCE STATEMENT Animal locomotion requires changing direction, including forwar
251 ode transition between circular and toroidal locomotion results from the onset of spiral tip meanderi
252 mble, in RSC, optic flow appears to override locomotion signals coherently in the population, when th
253 ation (OA) affect key ecological behaviours (locomotion speed and foraging success) and metabolic rat
255 MG, AVB and SIA control different aspects of locomotion speed as the animal navigates its environment
259 t the transition between forward and reverse locomotion states, perhaps when both forward (PVC) and r
262 of complex magnetically driven navigational locomotion such as passing through narrow channels and p
263 ensing, actuation, circuitry, and soft robot locomotion suggest the potential for versatile, tissue-l
264 lls are ENs whose activity is modulated with locomotion, suiting them to participate in sensorimotor
265 e reminiscent of human pathology and include locomotion, synapse morphology, and short-term memory de
266 uantified 26 phenotypes spanning morphology, locomotion, tactile sensitivity, and habituation learnin
267 cium imaging in a virtual reality (VR)-based locomotion task, we investigate how the integration of v
271 ay be linked to minimizing energetic cost of locomotion, the origin of the human-like pattern of pelv
272 rtex (V1) of mouse is highly correlated with locomotion, the relevance of locomotion-related VIP neur
273 estigated the role of somatostatin in innate locomotion through a genetic approach by knocking out so
276 aversive event can be conditioned to elicit locomotion to a safe location before the aversive outcom
278 is marked by a transition in hand use, from locomotion towards increasingly dexterous manipulation,
279 ased fear, impaired social interactions, and locomotion traits we associate with DA dysfunction and t
283 the cortex of awake, head-fixed mice during locomotion using polarography, spectroscopy, and two-pho
284 y harnessing this mode transition of the gel locomotion via coded illumination, we design programmabl
285 the impact of the sensory neuroprosthesis on locomotion, we created a novel ambulatory searching task
287 ous feeding and the impaired hindlimb during locomotion were both significantly greater in the treatm
288 the brain ventricles but to inhibit fictive locomotion when bath-applied in the spinal cord in vitro
289 tostatin has been previously shown to induce locomotion when injected in the brain ventricles but to
290 ransection, five/six cats performed backward locomotion, which required tonic somatosensory input in
291 d reward, but not to other movements such as locomotion, which were not linked to an explicit behavio
292 erformed forward locomotion but not backward locomotion while two others stepped backward but not for
293 timulation of this pathway enhances speed of locomotion, while inhibition decreases locomotor speed a
294 y of the system introduces a second circular locomotion with a small diameter caused by tip meanderin
297 otion and strategies were similar to forward locomotion, with shorter cycle and stance durations and
298 This paper shows that the center controlling locomotion within the spinal cord can produce a backward
299 ncy downregulated genes related to migration/locomotion without changes in genes associated with supp