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1 rexia and body weight loss without affecting locomotor activity.
2 he Drosophila brain control daily rhythms in locomotor activity.
3  but emphasize their importance in promoting locomotor activity.
4 cts in the forced swim test without altering locomotor activity.
5 mbens triggered MAPK signaling and modulated locomotor activity.
6 A release in the dorsal striatum or baseline locomotor activity.
7 d adiposity without affecting food intake or locomotor activity.
8 play, but not social exploratory behavior or locomotor activity.
9 depression of spontaneous or cocaine-induced locomotor activity.
10  mice were normal in development and general locomotor activity.
11 of L2 flexor-related and L5 extensor-related locomotor activity.
12  spontaneous alternation, but did not affect locomotor activity.
13 O) mice display a longer circadian period of locomotor activity.
14 aytime versus nighttime feeding behavior, or locomotor activity.
15 s that are a major source of rhythmicity and locomotor activity.
16 s would be sufficient to produce coordinated locomotor activity.
17 ircadian rhythmicity of body temperature and locomotor activity.
18  that is sufficient to initiate and maintain locomotor activity.
19  the spinal networks to generate coordinated locomotor activity.
20 nse characterized by a transient increase in locomotor activity.
21 otype in new directions by examining in-cage locomotor activity.
22 omotor activity and inhibits novelty induced locomotor activity.
23 e same drug concentrations that gave maximal locomotor activity.
24 ure interacts with thermoregulation, but not locomotor activity.
25 t mice does not develop because of increased locomotor activity.
26 o nausea/malaise or prolonged suppression of locomotor activity.
27 ithout affecting normal pain sensitivity and locomotor activity.
28 the generation of ultradian rhythms (URs) of locomotor activity.
29 rics, including hearing, vision, weight, and locomotor activity.
30 gnificant attenuation in amphetamine-induced locomotor activity.
31 ed within clock neurons for normal circadian locomotor activity.
32 , like BTR, is controlled independently from locomotor activity.
33 al adaptations and decreases the baseline of locomotor activity.
34 ts on water maze escape, place preference or locomotor activity.
35 ut affecting nicotine self-administration or locomotor activity.
36 food intake, fat uptake or absorption, or in locomotor activity.
37 xhibited by SHRs, while having no effects on locomotor activity.
38 inemia, and hepatic steatosis and normalized locomotor activity.
39 tor outputs to modulate circadian control of locomotor activity.
40 uced only a partial reduction on spontaneous locomotor activity.
41 ithout affecting baseline visual function or locomotor activity.
42 d circadian behavioral rhythms and decreased locomotor activity.
43 ty, but did not affect plus maze behavior or locomotor activity.
44 spension test but spared anpirtoline-induced locomotor activity.
45 s food intake and body weight and normalizes locomotor activity.
46  reduces AMPH-stimulated dopamine efflux and locomotor activity.
47 lmitate, decreased food intake and increased locomotor activity.
48 or does it translate to a non-weight-bearing locomotor activity.
49  progressive ratio test but had no effect on locomotor activity.
50 chitecture that may account for the enhanced locomotor activity.
51  a high-fat diet, while not altering general locomotor activity.
52  in mice, decreasing methamphetamine-induced locomotor activity.
53 ected 0.2% saccharin self-administration nor locomotor activity.
54 ress-induced potentiation of cocaine-induced locomotor activity.
55 the overall effect to a 19.2% improvement of locomotor activity.
56 V1 interneurons are essential for high-speed locomotor activity.
57 erneurons is rhythmically modulated with the locomotor activity.
58 ervous system (SNS) and increase CR-specific locomotor activity.
59 argets of maternal rest that modulate larval locomotor activity.
60 c Drosophila increased survival and improved locomotor activity.
61  INs, each likely playing different roles in locomotor activities.
62 eeding, and drinking were validated, but not locomotor activities.
63 logical circadian rhythms and increase their locomotor activity 2-3h prior to the next scheduled feed
64 epressive-like behaviors and increased basal locomotor activity (41%).
65 icle improves significantly sensorimotor and locomotor activity 7 and 14 days after stroke, reduces i
66 microglia marker) positive cells and reduced locomotor activity 72 h after transient forebrain ischem
67 ing neuronal damage and behavioral deficits (locomotor activity, 8-arm radial maze task).
68 oned to regulate dopamine (DA) signaling and locomotor activity, a canonical measure of basal ganglia
69 as adjusted their energy expenditure, Tb and locomotor activity according to season and also time of
70 r show bursts of morning (M) and evening (E) locomotor activity and a "siesta" in the middle of the d
71 et restfulness were characterised by minimal locomotor activity and a low theta/delta ratio in the lo
72                                              Locomotor activity and anxiety-like behavior were increa
73 he treatment period, animals were tested for locomotor activity and anxiety-like behavior.
74 cy did not induce significant alterations of locomotor activity and anxiety-related indices in the no
75 months, and were distinct from reductions in locomotor activity and anxiety.
76 s of Cdk5 in dorsolateral striatum increased locomotor activity and attenuated motor learning.
77  wherein radiotelemetry determined home cage locomotor activity and body temperature at 23 degrees C
78 clozapine, and risperidone were assessed for locomotor activity and catalepsy.
79  necessary and sufficient for normal evening locomotor activity and daytime sleep profiles, respectiv
80 lphaB-expressing mice also exhibit decreased locomotor activity and decreased dopamine-regulated CREB
81 vo, suppression of TSC1 expression increased locomotor activity and decreased habituation in a hippoc
82 f qrfp or its receptors results in increased locomotor activity and decreased sleep during the day.
83 h behavioral state, increasing robustly with locomotor activity and decreasing with rest.
84 en known to be involved in the regulation of locomotor activity and development of psychosis.
85 g two distinct behavioral paradigms: general locomotor activity and directed, visually guided navigat
86 epileptogenesis were associated with altered locomotor activity and distorted circadian rhythm.
87  liver microsomes and compared to cocaine in locomotor activity and drug discrimination paradigms in
88 10-30 mg/kg i.p.) dose-dependently increased locomotor activity and electrical brain-stimulation rewa
89                                              Locomotor activity and elevated plus maze test/forced sw
90 in both HFD and/or OVX groups, and decreased locomotor activity and energy expenditure after OVX can
91 leads to increased food intake and decreased locomotor activity and energy expenditure, and ultimatel
92 rioration at >61 days and exhibited abnormal locomotor activity and enhanced tremor.
93  of LXRbeta function leads to abnormality in locomotor activity and exploratory behavior, signs of an
94 tat (5, 50, or 100 mg/kg) on novelty-induced locomotor activity and found that it blunted exploration
95                        Therefore, we assayed locomotor activity and immobility-defined sleep in a new
96 exposed to E. coli as neonates had increased locomotor activity and impaired motor coordination as ju
97 of neural circuitry is reflected in enhanced locomotor activity and in the inability of the larvae to
98 d CNO dose-dependently decreases spontaneous locomotor activity and inhibits novelty induced locomoto
99 uate the participation of D2R in spontaneous locomotor activity and motor learning.
100  of the dorsal mPFC enhanced cocaine-induced locomotor activity and occluded behavioral sensitization
101 rain regions associated with impulsivity and locomotor activity and of alpha7-nAChRs in hypothalamic
102   Viability and behavioral alteration in the locomotor activity and place preference, after IL treatm
103 yond the dopaminergic system may also affect locomotor activity and psychosis.
104 w that 5-HT and octopamine jointly influence locomotor activity and quiescence in feeding and fasting
105 T did not significantly reduce the increased locomotor activity and rearing behavior observed in the
106 w A53T mice develop age-dependent changes in locomotor activity and reduced anxiety-like behavior.
107 rosophila also resulted in severely impaired locomotor activity and reduced lifespan, mirroring patie
108 ncreased spontaneous and amphetamine-induced locomotor activity and reduced spontaneous alternation,
109                    We quantified spontaneous locomotor activity and responsiveness to sensory stimuli
110 the excitability of SCN neurons, we examined locomotor activity and SCN firing in mice lacking Kv1.4
111 resetting, these mice exhibited consolidated locomotor activity and skipped the timed rest period (si
112 cemaker neurons to brain areas that regulate locomotor activity and sleep.
113 nsequently, the mutant mice were impaired in locomotor activity and spatial memory and were resistant
114  supersensitive; adenylate cyclase activity, locomotor activity and stereotypy were exaggerated in DR
115 ly I:C and postnatal LPS produced changes in locomotor activity and temperature patterns, increases i
116  M peak is associated with courtship-related locomotor activity and the A peak is due to an artifact
117 without corresponding changes in spontaneous locomotor activity and was transient, which has only bee
118 ads to a lean phenotype, increased nocturnal locomotor activity, and activation of brown adipose tiss
119 record electroencephalogram, electromyogram, locomotor activity, and body temperature, and the effica
120       Assessments of in vivo neurochemistry, locomotor activity, and cardiovascular parameters were c
121 rgy expenditure, respiratory exchange ratio, locomotor activity, and food intake.
122 d lead to decreased glucose levels, enhanced locomotor activity, and improved cognition.
123 ing antinociception, hypothermia, catalepsy, locomotor activity, and in the drug discrimination parad
124 ed ventricles and impaired social behaviour, locomotor activity, and learning and memory.
125 7% decrease in lifespan, reduced spontaneous locomotor activity, and no lifespan increase when reared
126 test which provides a measure of anxiety and locomotor activity, and object placement, a measure of s
127 further differed in body weight, spontaneous locomotor activity, and prepulse inhibition of startle.
128 cortex, and a deficit in social interaction, locomotor activity, and prepulse inhibition.
129 cephalography (EEG), electromyography (EMG), locomotor activity, and subcutaneous temperature.
130 ctivity-promoting E cells paralleled evening locomotor activity, and the LUC profile from sleep-promo
131 ral health, olfactory abilities, exploratory locomotor activity, anxiety-like behaviors and pain resp
132 ct effects on thermoregulatory processes and locomotor activity are likely mediated by different mech
133               Pacemaker neurons critical for locomotor activity are not necessary for TPR; instead, t
134 in confer an approximately 24-hr rhythm onto locomotor activity are unclear, but involve the neuropep
135 xpenditure, such as feeding, metabolic rate, locomotor activity, arousal, growth and reproduction.
136 own morphants showed a significantly reduced locomotor activity as well as distorted muscle integrity
137   Rats treated with Tamoxifen recovered some locomotor activity at 21 and 28 DPI, which could be rela
138 TH-induced decreases in body temperature and locomotor activity at 23 degrees C were also attenuated
139  effectively suppresses phencyclidine-evoked locomotor activity at doses that do not impair neuromusc
140 and partial agonist RO5263397 on sleep/wake, locomotor activity, body temperature, and cataplexy were
141             L-Tsc1 KO mice displayed reduced locomotor activity, body temperature, and hepatic trigly
142 d that HCRT neuron-ablated larvae had normal locomotor activity, but demonstrated an increase in slee
143          Clozapine also dramatically reduced locomotor activity, but in the absence of catalepsy.
144 e did not affect general or morphine-induced locomotor activity, but markedly increased cocaine-induc
145 (GABA) neuronal activation similarly induced locomotor activity, but with striking differences in mod
146 s) altered clock gene expression and reduced locomotor activity by disrupting the central and periphe
147  The present results indicate that increased locomotor activity can be correlated to TH protein expre
148 ng or lengthening of the circadian period of locomotor activity can be obtained either by targeting d
149                                 In contrast, locomotor activities, central box duration and sucrose p
150  cocaine injections (20 mg/kg) paired with a locomotor activity chamber (Paired) or home cage (Unpair
151 (5, 8, 10, and 15 mg/kg) every 12 hours in a locomotor activity chamber and a challenge dose of 5 mg/
152 mor (tremulous jaw movements), and decreased locomotor activity compared with administration of TBZ a
153 ant-induced behaviors relevant to addiction: locomotor activity, conditioned place preference, anxiet
154 sion of either protein caused an increase in locomotor activities consistent with enhanced synaptic r
155 nd SCN input and, when activated, suppresses locomotor activity, consistent with the behavioral hyper
156                               The effects on locomotor activity could be reversed by direct delivery
157              EEG, EMG, body temperature, and locomotor activity data were collected continuously duri
158 der, older age (> 7 postnatal weeks), higher locomotor activity, daytime recordings, and recent blood
159 both larvae and adult fruit flies, including locomotor activity, degeneration of dopaminergic neurons
160 ind that the overexpression of QRFP inhibits locomotor activity during the day, whereas mutation of q
161 ns and spiking activity coordinated with the locomotor activity expressed by the lumbar cord.
162                  Despite a large decrease in locomotor activity, FL-PGC-1alpha(-/-) mice exhibited th
163         WT mice showed a marked reduction in locomotor activity following acute administration of hal
164 ar (dHb-IPN) pathway expedites the return of locomotor activity following an unexpected negative stim
165  null allele of Csnk1e showed an increase in locomotor activity following MA administration.
166 flick test for nociception, and a measure of locomotor activity for general arousal.
167 ly measures standing, feeding, drinking, and locomotor activities from 3D trajectories.
168 ional outcomes up to 3 weeks after stroke on locomotor activity, grip strength, sensory neglect, gait
169 inant human IGF1 (rhIGF1) improves lifespan, locomotor activity, heart rate, respiration patterns, an
170 aggressiveness (resident-intruder test), and locomotor activity (horizontal and vertical).
171 ic neurons of Drosophila and observe reduced locomotor activity, impaired survival and an age-depende
172 LG-IH also altered metabolic expenditure and locomotor activities in male offspring, and increased nu
173 We also demonstrate that clozapine decreases locomotor activity in a 5-HT(2A)-dependent manner, in th
174 DH44 PI-Hugin SEZ circuit controls circadian locomotor activity in a daily cycle but has minimal effe
175 cond test 7 dpf fish revealed an increase in locomotor activity in all MeHg exposures tested.
176 ndent behavioral flexibility, and heightened locomotor activity in an open field arena.
177           There were no group differences in locomotor activity in an open field on the copulation te
178                                              Locomotor activity in an open field was also elevated.
179 QTL) mapping of methamphetamine (MA)-induced locomotor activity in C57BL/6J (B6) x DBA/2J (D2)-F(2) m
180 tylcholine (ACh) activation markedly reduced locomotor activity in DD mice.
181 lized PER1 and PER2 expression and circadian locomotor activity in ENT1 KO mice.
182                        We examined circadian locomotor activity in ENT1 KO vs WT littermates and foun
183  that electromyograms (EMGs) obtained during locomotor activity in mice were effective for identifica
184 oventricular application of insulin promoted locomotor activity in MUFA-fed mice, whereas SFA-mice we
185 od pressure without affecting SCN-controlled locomotor activity in murine models.
186  in real-time place preference and increased locomotor activity in open-field testing.
187  timing of clock gene expression and reduced locomotor activity in parallel with increased lung infla
188 ally, Gal-1 deficiency did not change normal locomotor activity in post-natal animals.
189 ly decreased spontaneous and cocaine-induced locomotor activity in rats expressing KORD to midbrain (
190 (cAMP response element binding protein), and locomotor activity in rats raised in enriched (EC), impo
191 n of DeltaFosB-T149D in NAc leads to greater locomotor activity in response to an initial low dose of
192     Compound (-)-34 was also able to elevate locomotor activity in the above PD animal model signific
193                         Chronic E2 decreased locomotor activity in the open field and enhanced perfor
194 gy expenditure (EE) and a 3-fold decrease in locomotor activity in the unfed state.
195 lead to manganese dyshomeostasis and altered locomotor activity in zebrafish with CRISPR-induced slc3
196  place within the neural network controlling locomotor activity, including spinal interneurons.
197  energy expenditure as a result of increased locomotor activity, increased thermogenesis in brown adi
198 more severe impairments, including decreased locomotor activity, inferior cued water maze performance
199 admill, we show that vestibular influence on locomotor activity is modulated independently in each li
200  During walking, the vestibular influence on locomotor activity is phase-dependent and modulated in b
201 , we find that QRFP overexpression decreases locomotor activity largely in a light-specific manner.
202 nduced behaviour in C. elegans and increased locomotor activity levels when injected into the central
203 ptin and amino acid signaling, and increased locomotor activity, likely attributable to increased mel
204 regions of rat mPFC, in appetitive trace and locomotor activity (LMA) procedures.
205         EEG, EMG, body temperature (Tb), and locomotor activity (LMA) were recorded in Taar1 KO, OE,
206 es influence body weight and cocaine-induced locomotor activity (LMA).
207 I3 interneurons are not necessary for normal locomotor activity, locomotor circuits rhythmically inhi
208  (vSPZ) is critical for rhythms of sleep and locomotor activity (Lu et al. [] J Neurosci 21:4864-4874
209 ression of clock genes, circadian rhythms of locomotor activity, lung function, and inflammatory and
210 ensure that their sensory responsiveness and locomotor activity match environmental demands.
211      Rats exhibited increases in spontaneous locomotor activity, measured by implanted radiotelemetry
212 firing rate with bioluminescence imaging and locomotor activity monitoring.
213  were associated with the morning or evening locomotor activities occurred ~4 hours before their resp
214                                  Analysis of locomotor activity of diquat dibromide and the neurotoxi
215 as first-generation medications suppress the locomotor activity of Egr3(-/-) and WT mice to a similar
216                       The BP, heart rate and locomotor activity of rats was analyzed and urinary sodi
217 n be conveniently estimated by measuring the locomotor activity of the flies using techniques and ins
218       These changes correlate with increased locomotor activity of the Mecp2-deficient animals, sugge
219 (VS) are sufficient to synchronize the daily locomotor activity of wild-type Drosophila melanogaster.
220    Sound stimulus during the day reduced the locomotor activity of wild-type sibling larvae, while HC
221 Exposure to light during the night decreased locomotor activity of wild-type siblings, but induced an
222 g RNA knockdown, serum parameters, circadian locomotor activity, Oil Red O staining, transient transf
223               GluN3A KO mice showed impaired locomotor activity on a variety of motor function tests,
224                                              Locomotor activity or food reinforced operant responding
225 raperitoneally) had no significant effect on locomotor activity or intracranial self-stimulation.
226 e with CNO-mediated changes in ANS function, locomotor activity or motor coordination.
227  are observed at doses that do not influence locomotor activity or reinstatement responding following
228 reinstatement to cocaine, but did not affect locomotor activity or reinstatement to sucrose seeking.
229  seeking without affecting operant learning, locomotor activity, or reinstatement of natural reward s
230 penditure, with no change in caloric intake, locomotor activity, or thyroid hormone levels.
231 anges (PS bouts, SWS time, body temperature, locomotor activity) persisted after the CSDS regimen had
232 piny neurons (iMSNs) is sufficient to impair locomotor activity, phenocopying DA depletion models of
233                    Memory, behavioral tasks, locomotor activity, presence of human antibodies specifi
234  mir-124 mutants exhibit profoundly abnormal locomotor activity profiles, including loss of anticipat
235 e report the use of animal models, including locomotor activity, protection, and rescue experiments i
236 hythms of clock gene expression in the lung, locomotor activity, pulmonary function, inflammatory, pr
237 neurons had increased energy expenditure and locomotor activity; reduced body weight, fat mass, and f
238 re includes the de facto assumption that any locomotor activity reflects an absence of fear.
239 played enhanced spontaneous and drug-induced locomotor activity, relative to control transplanted Mit
240 tive sensory feedback to the coordination of locomotor activity remains less clear.
241 y disrupted or restored dopamine content and locomotor activity, respectively.
242 Kiss1r KO females displayed markedly reduced locomotor activity, respiratory rate, and energy expendi
243                   During ad libitum feeding, locomotor activity resumed its arrhythmic state, but per
244                                  Analysis of locomotor activity revealed no major differences in dail
245 ination (narrow bean traverse and gait), and locomotor activity revealed no significant differences b
246                           Light pulses delay locomotor activity rhythm during the early night and adv
247 est period induces phase delays of circadian locomotor activity rhythm.
248 eactivity and injections of SIFamide delayed locomotor activity rhythms circadian time-dependently, S
249 ct of translation control genes on circadian locomotor activity rhythms in flies.
250                      As in previous studies, locomotor activity rhythms in older mice required more d
251 tion of the Drosophila homolog HDAC4 impairs locomotor activity rhythms of flies and decreases period
252 in neuronal remodeling, which contributes to locomotor activity rhythms.
253 e start of foraging of 3.3 h, and whole-hive locomotor-activity rhythms were delayed by an average of
254 re sufficient to drive motivated feeding and locomotor activity similar to LHA (GABA) neurons, but wi
255 rmance, and between striatal 5-HT levels and locomotor activity strongly implicate regionally-specifi
256                                              Locomotor activity, Tb (measured in the rumen) and the l
257                                              Locomotor activity tests were performed once a week for
258 ng self-administration of 0.2% saccharin and locomotor activity tests.
259 ie prion inocula showed a faster decrease in locomotor activity than similar flies exposed to scrapie
260 its have markedly shorter (0.5 h) periods of locomotor activity than wild-type (WT) mice.
261                 Ultradian (~4 hr) rhythms in locomotor activity that do not depend on the master circ
262             Through non-linear conversion of locomotor activity to "Locomotor Inactivity During Sleep
263 rotonin in inhibiting endogenously generated locomotor activity to neurons located in the posterior m
264  locomotor output of animals from horizontal locomotor activity to vertical activity, further highlig
265      Comparative analysis of cocaine induced locomotor activity using PANs and thick acupuncture need
266                               LS3 suppresses locomotor activity via a BK channel-specific mechanism i
267                                              Locomotor activity was also affected in some cases.
268                                A decrease in locomotor activity was also observed in mice treated sys
269                               Interestingly, locomotor activity was decreased in the hybrid peptide g
270 ncillary effects on behavioral activation as locomotor activity was either unaffected, as in the case
271                        Significantly reduced locomotor activity was exhibited in B6.TH-tabw2 congenic
272 ousing conditions when the nicotine-mediated locomotor activity was expressed as a percent change fro
273 was increased to near that of wild type, and locomotor activity was improved.
274                               Interestingly, locomotor activity was increased in [dA(2)]GLP-1/GcG mic
275 aperitoneal) every other day for 14 days and locomotor activity was measured.
276 nificantly increased during daytime, overall locomotor activity was not significantly different.
277                                    Increased locomotor activity was observed after 4-MMC administrati
278 ved neurologic deficit score and spontaneous locomotor activity was observed, and the stroke infarct
279                                      Maximal locomotor activity was obtained after treatment with a h
280              Capsaicin's effect on S4-evoked locomotor activity was potent until the lumbar 5 (L5) se
281                                              Locomotor activity was unaltered by vector administratio
282                 In addition, cocaine-induced locomotor activity was used as a general 'read out' of m
283                              Phase shifts of locomotor activity were analyzed in grass rats transferr
284 microstructural analysis of food intake, and locomotor activity were assessed.
285 ained improvements in motor coordination and locomotor activity were observed, even after onset of ne
286                     No associated changes in locomotor activity were observed.
287  dystonic movements or postures or change in locomotor activity were observed.
288                        Several parameters of locomotor activity were shifted early in the disease tim
289 owever, mGluR5(KD-D1) animals showed reduced locomotor activity when placed in a novel environment, a
290 intoxication, low doses of ethanol stimulate locomotor activity whereas high doses induce sedation.
291 muscimol dose dependently reduced open-field locomotor activity, whereas 300 ng of picrotoxin caused
292 e also show that QRFP overexpression reduces locomotor activity, whereas animals that lack QRFP signa
293 : hypocretin and cgrp stimulated spontaneous locomotor activity, whereas galanin and nociceptin atten
294 hat Nematostella exhibits rhythmic circadian locomotor activity, which is persistent in constant dark
295 irect comparison of luciferase activity with locomotor activity, which was assayed in the same flies
296 This effect was not explained by a change in locomotor activity, which was unaffected by STN-HFS.
297 AP-DNSynCAM1 mice) exhibit disrupted diurnal locomotor activity with enhanced and more frequent episo
298 or behavior; while LHA (Gal) neurons induced locomotor activity without compulsivity.
299 tudies, GluN2B inhibitors reduce MA-mediated locomotor activity, without affecting basal activity.
300 ts of imidacloprid on queens (egg-laying and locomotor activity), worker bees (foraging and hygienic

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