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1 activity contributes to withholding of self-movement.
2 the preoptic DA neurons in the initiation of movement.
3 conversion of chemical energy to mechanical movement.
4 earning without affecting reward learning or movement.
5 ogress made in China's nascent environmental movement.
6 iotemporal heterogeneity in transmission and movement.
7 was again greater after a twitch than a wake movement.
8 sms that take place during CLas cell-to-cell movement.
9 uromuscular networks controlling posture and movement.
10 e influence of reproductive state and age on movement.
11 l conditions, including darkness and passive movement.
12 ich suggests a link between capture and gene movement.
13 also had more beta desynchronization during movement.
14 heral, and have little influence over normal movement.
15 various processes might affect polarity site movement.
16 ay and the birth of the modern environmental movement.
17 not fully utilize the potential of the Maker Movement.
18 at these patterns are highly stable to fibre movement.
19 essary and sufficient for SRBP1 cell-to-cell movement.
20 direction of penile penetration and/or semen movement.
21 ent in processing verbs describing body part movements.
22 ng automated detection of slow waves and eye movements.
23 e brain keeps an internal record of physical movements.
24 tensioning of the body, such as subtle wrist movements.
25 ift covertly, decoupled from programming eye movements.
26 gns value to things, and how it controls our movements.
27 he hippocampus coordinates memory-guided eye movements.
28 ng to a tight coupling between head and wing movements.
29 ear movements, movement sequences and aiming movements.
30 ious phenomena observed during goal-directed movements.
31 their contributions to its diverse reaching movements.
32 eld (FEF) carries such a CD for saccadic eye movements.
33 hormone metabolism with early embryonic cell movements.
34 he possibility that durotaxis underlies cell movements.
35 n, execute, and consolidate skilled reaching movements.
36 tation of statewide restrictions on internal movement (0.1% per day; 95% CI -0.04% to 0.3%; P = 0.14)
38 es are regulated to coordinate multicellular movements, a conserved feature in twitching bacteria.
43 mitant changes of their values correspond to movement along the constant speed goal equivalent manifo
44 gger barrel activity; when we controlled for movement amplitude, barrel activity was again greater af
46 in feedback correction in the middle of the movement and a reduction in motor noise near the target.
49 e is critical for preventing their continued movement and introduction, but screening a sufficient fr
51 pendent switch in the response of V1 to head movements and identifies a circuit in which SOM cells ar
53 improved mechanistic understanding of animal movements and their roles in ecological processes and fo
56 lamus that differentiated tic from voluntary movement, and this physiological feature could potential
57 bio-logging has the potential to reveal how movements, and hence life-history trade-offs, vary over
58 , laminae II/III INs generate paw withdrawal movements, and laminae III/IV INs modulate dynamic corre
59 ochondrial dynamics, stimulate mitochondrial movements, and promote organelle accumulation at the cor
60 hIs are essential for the control of complex movements, and they suggest a therapeutic potential of s
64 NCE STATEMENT Motor coordination and skilled movements are driven by the permanent discharge of neuro
67 speed and direction, as well as pursuit eye movements, are significantly impaired at 0.015% BAC, sug
68 haracterization of spontaneous polarity site movement as a search process and use a mechanistic compu
73 moose, bear, and wolf habitat selection and movement behaviour in response to anthropogenic habitat
74 elopment is the origin of stochastic nuclear movement between apical and basal surfaces of neuroepith
75 onous, variable local control, together with movement between populations, elevates long-term regiona
76 and coding schemes supporting relations and movements between spatial locations in mammals are "recy
77 ntify plausible mechanisms of nomadic animal movement by comparing the performance of multiple moveme
79 quantum theory, we found that a synchronous movement can occur during CO-CO collisions, whereby a bu
81 ion occurs through coordinated vertical cell movement: cells towards the periphery of the placode mov
83 d disruptions to three critical circuits for movement control: the cerebral cortex, the cerebellum, a
89 f an effective stimulus to the start of head movement decreased with repeated stimuli and this effect
90 weak in BBS, as expected where year-to-year movement degrades the link between local population grow
91 y differentiated linguistic and transitional movements, demonstrating encoding of language-relevant a
92 der, hyposmia, constipation), characteristic movement difficulty (eg, tremor, stiffness, slowness), a
94 ese well-known aetiologies, a range of other movement disorder syndromes may also present with SIBs,
95 se of a progressive, pediatric-onset spastic movement disorder with variable clinical presentation.
97 e seizure types, severe developmental delay, movement disorders, and elevated risk of sudden unexpect
99 ntial comorbidity between the disorders, and movement disturbances are common in patients with SCZ be
100 ntribution of preparatory neural activity to movement duration (MD) variability is greater for smalle
101 s information sheds light on possible proton movements during heme-catalyzed oxygen activation, as we
106 om kinematic features, 70% accuracy from eye movement features and 78% accuracy from combined feature
109 ions with statewide restrictions on internal movement from the unique associations with the first soc
110 striatal subfields are involved in voluntary movement generation and cognitive and emotional tasks, b
116 Finally, the perceived directionality of the movement (i.e. towards or away from the observer) was fo
118 rain circuits implicated in the selection of movements, impaired operation of GABA signaling within t
120 Thus, SNr may regulate the active avoidance movement in downstream areas that mediate the behavior,
122 ings extend the recent work examining animal movement in response to changing phenology from migrator
123 We found higher beta power during rest and movement in the GPi, which also had more beta desynchron
126 cy are related to the preparation of adapted movements in human, and whether such effects generalise
129 n illusions, rather than the distribution of movements in the environment (the "slow world" prior) as
130 s been at the crossroads of human population movements in the Pacific for the past three millennia.
131 or integration during unconstrained reaching movements in the presence of variable environmental forc
138 al link between sensorimotor beta bursts and movement initiation and suggest that neurofeedback train
143 ntary suppression of beta bursts to speed up movement initiation.SIGNIFICANCE STATEMENT This double-b
144 measure of the neural interaction underlying movement-initiation and -cancellation, opening new avenu
145 ch space use has been studied restrict their movements into a constrained spatial area: their home ra
147 circuits, which are essential for voluntary movements, involves both guidance molecule- and activity
148 hus, the pattern generator for dexterous arm movement is distributed across multiple, strongly intera
150 duals tended to successfully imitate unusual movement kinematics while autistic individuals tended to
152 measurements, and it was possible to detect movements <1 nm of the domains with respect to each othe
153 ks permitted by our device, including linear movements, movement sequences and aiming movements.
154 Tac1 neurons obliterates both non-rapid eye movement (NREM) and rapid eye movement (REM) sleep, stro
156 EG source-localization, during non-rapid eye movement (NREM) sleep and rapid eye movement (REM) sleep
157 her learning is facilitated by non-rapid eye movement (NREM) sleep or by REM sleep, whether it result
159 els of the shared ligand CCL7 to control the movement of a key population of CCR1-expressing macropha
160 clear actin-myosin-based pathway driving the movement of activated genes to the nuclear periphery.
162 uctures and the structure of apo-hGGT reveal movement of amino acid residues within the active site a
163 This increased contractility also impaired movement of basal progenitors during hair placode morpho
166 nvolving the one-dimensional decoding of the movement of finger groups and in an offline two-dimensio
167 that management interventions to facilitate movement of gametes along short ecological gradients wou
168 on event involved a massive and asymmetrical movement of genes from a distantly related AFC lineage i
169 aging, we directly observe the intercellular movement of GFP and a subset of endogenous proteins thro
171 logical glass contains information about the movement of goods and ancient economies, yet our underst
173 with well-defined entry and exit routes, the movement of leukocytes in the peritoneal cavity is large
174 ed by circular membrane flow and anterograde movement of lipid vesicles, resulting in cell polarizati
175 droplet magnetofluidics (DM) to automate the movement of magnetic beads between small volumes of reag
177 powerful method to size dependently control movement of microparticles and cells in paper using surf
178 etions; 2) single/multigene deletion; and 3) movement of mobile genetic elements (including prophages
179 se fascinating molecules are responsible for movement of molecules, organelles, cells, and whole anim
180 Xenopus egg extracts and observed outward co-movement of MTs, endoplasmic reticulum (ER), mitochondri
181 edance spectroscopy (EIS) (which measure the movement of only the charged, i.e., dissociated, ions) w
183 The resulting electric forces cause the movement of pore water ions in opposite directions, lead
184 n-DNA product requires a global scissor-like movement of protein and DNA, delivering the scissile pho
187 lied across the globe, we find that downward movement of SOC along the soil profile reduces SOC loss
189 fastest diffusion has been attributed to the movement of the halides, largely neglecting the contribu
191 he ECD-TMD interface is characterized by the movement of the histidine 98 residue, which is, after ac
196 ng in siRNA production and the intercellular movement of these siRNAs to reinforce TE silencing in sp
197 r exposure may contribute to controlling the movement of toxic ions to leaves and, therefore, can be
198 protein-conducting channels that facilitate movement of transmembrane segments, cytosolic and lumina
199 and invasion, which in turn facilitates the movement of tumor epithelial cells toward nutrient-rich
201 passage, yet, given the abundance, diet, and movements of ducks in nature, our results have major imp
202 erized how walking Drosophila coordinate the movements of individual limbs (DeAngelis et al., 2019).
203 tance (NLC) represents voltage sensor charge movements of prestin (SLC26a5), the protein responsible
205 substrate translocation and release involve movements of the bulky transport domain through the lipi
206 e if microgravity can create deformations or movements of the eye or optic nerve, and if such changes
208 ing sleep, significantly improved fine motor movements of the limb corresponding to the sensorimotor
211 a decoy transmitter enabled us to track the movements of traffickers, and thus gain a better underst
212 rgets, sensory organs make small unexplained movements on top of the primary task-related motions.
213 ts indicate that TARK1 functions in stomatal movement only in response to biotic elicitors and suppor
215 els impact the onset or severity of abnormal movements or neuropathological features in DYT1 mouse mo
217 nferior quality accounting for overall price movements (other orchards growing same variety that year
221 ion, eroded the benefits of informed nomadic movements, particularly for movements based on resource
222 refers to the altered muscle activations and movement patterns in scapulae along with some abnormal a
223 heory predicts that animals evolve efficient movement patterns to enhance encounter rates with specif
225 n system complete with a mobile stage for XY movement, peristaltic pumps equipped with perfusion line
228 recorded over the motor cortex during a pre-movement preparatory phase were, on average, significant
229 tics and coordination between gross and fine movements progressively changed with repeated manipulati
230 n when Parkinson's patients perform stepping movements, raising the question whether the STN is invol
231 ecies-specific changes in terrestrial mammal movement rates in response to increasing temperature.
232 availability) might affect the abundance and movement rates of animals following each of these rules.
233 isruption of the corticostriatal transfer of movement-related cues and their striatal integration wit
234 summarize recent findings on the presence of movement-related signals in sensory areas and discuss ho
235 logy of each muscle is determined, such that movements relying upon contraction of many muscles are b
237 provided during training enhanced rapid eye movement (REM) sleep time, increased oscillatory activit
239 apid eye movement (NREM) sleep and rapid eye movement (REM) sleep, in six medication-refractory focal
240 non-rapid eye movement (NREM) and rapid eye movement (REM) sleep, strongly consolidating the waking
242 atal oscillatory activity is associated with movement, reward, and decision-making, and observed in s
244 ent by comparing the performance of multiple movement rules along a continuum from nomadism to reside
245 es in KB together with changes in polar bear movements, seasonal ranges, body condition, and reproduc
249 pping preceded by both imagined and executed movements showed a reduced response in the superficial l
250 ecome less synchronized during non-rapid eye movement sleep after sleep deprivation at the network an
251 ther highlight the prospect of non-rapid eye movement sleep as a therapeutic target for meaningfully
253 an include prodromal features (eg, rapid eye movement sleep behavior disorder, hyposmia, constipation
254 , but also a disinhibition of REM (rapid eye movement) sleep, demonstrated as a shortening of REM lat
256 establish the connections between herbivore movements, space-use, individual preference, and the spa
257 ce is to understand the relationship between movement speed and accuracy, known as the speed-accuracy
258 onal representations of spatial location and movement speed in the medial entorhinal cortex during th
261 sical activity as it relates to strength and movement strategy of the hip, knee and ankle, a model of
264 ctional connections among M1 units emerge at movement that are oriented along the same rostro-caudal
265 phant movements into two states: exploratory movements that are fast and directional, and encamped mo
267 lostella provides insights into transoceanic movements that have enabled it to become a worldwide pes
269 y in an NP size-dependent manner and that NP movement through alginate matrices is anisotropic and he
271 difference between the physical capacity for movement through the habitat and subsequent gene flow.
272 ANCE STATEMENT The cerebellum contributes to movements through signals generated by cerebellar output
274 y sample their environment with saccadic eye movements to bring relevant information into high-acuity
275 maller targets than larger targets, and that movements to smaller targets exhibit less variability in
277 monkeys conducted instructed walk-and-reach movements towards targets flexibly positioned in the cag
278 Our device can generate arbitrary virtual movement tracks, arbitrary time-varying forces or arbitr
280 s support the hypothesis that self-generated movements underlie adaptation to radical sensorimotor di
283 ences in behaviors, and metrics of nonlinear movement variability were used to quantify the complexit
285 multaneously encoded multiple actions (e.g., movement velocity, acceleration, distance to goal, and l
287 energy balance of all processes during fault movement, we present a framework that reconciles the dat
289 pen questions regarding the history of these movements, we generated genome-wide data for 11 ancient
290 ed hidden Markov models to test how wild dog movements were affected by the Human Footprint Index in
293 es have a strong influence over normal group movement, whereas subordinate males are passive, sociall
294 reveal a novel pathway for neural control of movement whereby the somatosensory cortex directly influ
296 r dynamics are also observed during grasping movements, which involve fundamentally different pattern
297 h residues of the B'-helix displayed outward movement with respect to the symmetry axis of the channe
299 sient head impacts, however, can elicit head movements with frequency content up to 300-400 Hz, raisi
301 um in the modulations given by different eye movements, with oculomotor transitions primarily acting