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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
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
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
74 cy did not induce significant alterations of locomotor activity and anxiety-related indices in the no
77 wherein radiotelemetry determined home cage locomotor activity and body temperature at 23 degrees C
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.
85 g two distinct behavioral paradigms: general locomotor activity and directed, visually guided navigat
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
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
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
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
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
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,
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
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
123 ing antinociception, hypothermia, catalepsy, locomotor activity, and in the drug discrimination parad
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.
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
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
142 d that HCRT neuron-ablated larvae had normal locomotor activity, but demonstrated an increase in slee
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
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
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
164 ar (dHb-IPN) pathway expedites the return of locomotor activity following an unexpected negative stim
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
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
179 QTL) mapping of methamphetamine (MA)-induced locomotor activity in C57BL/6J (B6) x DBA/2J (D2)-F(2) m
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
187 timing of clock gene expression and reduced locomotor activity in parallel with increased lung infla
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
195 lead to manganese dyshomeostasis and altered locomotor activity in zebrafish with CRISPR-induced slc3
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
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
211 Rats exhibited increases in spontaneous locomotor activity, measured by implanted radiotelemetry
213 were associated with the morning or evening locomotor activities occurred ~4 hours before their resp
215 as first-generation medications suppress the locomotor activity of Egr3(-/-) and WT mice to a similar
217 n be conveniently estimated by measuring the locomotor activity of the flies using techniques and ins
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
225 raperitoneally) had no significant effect on locomotor activity or intracranial self-stimulation.
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
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
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
239 played enhanced spontaneous and drug-induced locomotor activity, relative to control transplanted Mit
242 Kiss1r KO females displayed markedly reduced locomotor activity, respiratory rate, and energy expendi
245 ination (narrow bean traverse and gait), and locomotor activity revealed no significant differences b
248 eactivity and injections of SIFamide delayed locomotor activity rhythms circadian time-dependently, S
251 tion of the Drosophila homolog HDAC4 impairs locomotor activity rhythms of flies and decreases period
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
259 ie prion inocula showed a faster decrease in locomotor activity than similar flies exposed to scrapie
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
270 ncillary effects on behavioral activation as locomotor activity was either unaffected, as in the case
272 ousing conditions when the nicotine-mediated locomotor activity was expressed as a percent change fro
276 nificantly increased during daytime, overall locomotor activity was not significantly different.
278 ved neurologic deficit score and spontaneous locomotor activity was observed, and the stroke infarct
285 ained improvements in motor coordination and locomotor activity were observed, even after onset of ne
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
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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