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1 y over 14 days), lower anxiety, and impaired sensorimotor gating.
2 limbic dopamine transmission, a modulator of sensorimotor gating.
3 flex, suggesting deficits in pre-attentional sensorimotor gating.
4 septum represent a key cell-type involved in sensorimotor gating.
5 DA receptors, specifically in the context of sensorimotor gating.
6 ibit clear apomorphine-induced reductions in sensorimotor gating.
7 ic basis for human population differences in sensorimotor gating.
8 ncluding cognitive inflexibility and reduced sensorimotor gating.
9 ncluding cognitive inflexibility and reduced sensorimotor gating.
10 rning and memory, anxiety-like behaviour and sensorimotor gating.
11      The LC hyperactivity is detrimental for sensorimotor gating.
12 n (PPI), a critical translational measure of sensorimotor gating.
13  behavioral responses, learning, memory, and sensorimotor gating.
14 alysis providing new molecular insights into sensorimotor gating.
15 and altered behaviors, including anxiety and sensorimotor gating.
16 ice exhibited abnormalities in cognition and sensorimotor gating.
17  inhibition (PPI), an operational measure of sensorimotor gating.
18 by subtle deficits in motor coordination and sensorimotor gating.
19 iated with exaggerated startle and deficient sensorimotor gating.
20 alities in prepulse inhibition, a measure of sensorimotor gating.
21 nstrating the importance of these neurons in sensorimotor gating.
22 ver, display changes in rearing behavior and sensorimotor gating.
23 ulatory mechanisms in startle plasticity and sensorimotor gating.
24  receptor in goldfish startle plasticity and sensorimotor gating.
25 nhibition (PPI) is an operational measure of sensorimotor gating.
26 ium channel activity in the mPFC to modulate sensorimotor gating.
27 rations in prepulse inhibition, a measure of sensorimotor gating.
28 ehavioral deficits in social interaction and sensorimotor gating.
29 central nervous system activity and impaired sensorimotor gating.
30 ragile X mental retardation protein regulate sensorimotor gating.
31  impaired cognitive processing, and impaired sensorimotor gating.
32  anxiety-related phenotype but no deficit in sensorimotor gating.
33 inhibition of acoustic startle, a measure of sensorimotor gating.
34 s mediating smooth pursuit eye movements and sensorimotor gating.
35 stimulus, provides an operational measure of sensorimotor gating (a process by which an organism filt
36                                              Sensorimotor gating abnormalities have been previously c
37 tive studies have led to the hypothesis that sensorimotor gating abnormalities may underlie thought d
38 f this portion of the DGCR is sufficient for sensorimotor gating abnormalities, but not sufficient to
39 s-dependent learning and memory and impaired sensorimotor gating, abnormalities observed in patients
40  and found that these mice have a deficit in sensorimotor gating accompanied by regional neurochemica
41 ramidal neurons, as well as abnormalities in sensorimotor gating, albeit without profound memory defi
42  stomatogastric nervous system, we show that sensorimotor gating also occurs at the level of the proj
43 ncreased compulsive-like behaviors, abnormal sensorimotor gating and altered responsiveness to stimul
44 septum represent a key cell type involved in sensorimotor gating and are relevant to pathologies asso
45 late several behavioral phenomena, including sensorimotor gating and aspects of motor activity.
46 fects on preconscious, automatic measures of sensorimotor gating and auditory sensory processing that
47 ockout (REGgamma-/-) mice exhibit late-onset sensorimotor gating and cognitive deficiencies including
48 macological inhibition of p110delta reversed sensorimotor gating and cognitive deficits.
49  to pathways controlling locomotor activity, sensorimotor gating and cognitive processes.
50 tor changes may be involved in disruption of sensorimotor gating and compulsive behavior relevant to
51 on in the hippocampus as well as deficits in sensorimotor gating and contextual memory, putative endo
52 rpose of this study was to examine automatic sensorimotor gating and controlled attentional modulatio
53 rther our understanding of the substrates of sensorimotor gating and could lead to better therapeutic
54   Prepulse inhibition (PPI) is an example of sensorimotor gating and deficits in PPI have been demons
55 n the treatment of subjects with compromised sensorimotor gating and enhanced motor responses to sens
56 ed amphetamine-driven changes in locomotion, sensorimotor gating and hallucination-like perception.
57 for p11 in modulating clozapine's effects on sensorimotor gating and hippocampal connectivity, offeri
58 nhibition (PPI) is an operational measure of sensorimotor gating and is deficient in several neuropsy
59 hat are deleted in patients have deficits in sensorimotor gating and learning and memory.
60 the prefrontal cortical circuitry regulating sensorimotor gating and locomotor behavior, both of whic
61 atal dopamine is implicated in regulation of sensorimotor gating and OCD pathophysiology.
62 ies, including hyperactivity, disturbance in sensorimotor gating and olfactory-associated behavior, a
63 zophrenia, as indexed by alterations both in sensorimotor gating and psychotomimetic-induced locomoto
64 e, LSD, and PCP on two behavioral parameters-sensorimotor gating and repetitive movements-were strong
65                                     Although sensorimotor gating and sensory gating are not identical
66 nents and in the neural circuits involved in sensorimotor gating and short-term memory.
67 culum, regions involved in the regulation of sensorimotor gating and short-term memory.
68                       To address this issue, sensorimotor gating and thought disturbance were measure
69 hizophrenic men were assessed on measures of sensorimotor gating and thought disturbance.
70  Locomotor activity, anxiety-like behaviors, sensorimotor gating, and aggressive behavior also were a
71 nto-striatal pathways resulting in defective sensorimotor gating, and consequently characteristic dif
72         These brain regions are important in sensorimotor gating, and impaired 'gating' may partly ex
73 y on stress sensitivity, cognitive function, sensorimotor gating, and prefrontal cortical transcripti
74  disturbances, such as hyperlocomotion, poor sensorimotor gating, and sensitivity to psychostimulants
75 ce, including cognitive impairment, abnormal sensorimotor gating, and sensitization to methamphetamin
76 al striatal dopamine dysfunction, cognitive, sensorimotor gating, and social behavioral deficits prec
77 e locomotor reactivity to novel environment, sensorimotor gating, anxiety, and cognition.
78  3 m of age, mutant mice displayed increased sensorimotor gating, anxiety, hypoactivity, and decrease
79 amatergic mGluR5 knockout mice are normal in sensorimotor gating, anxiety, motor balance/learning and
80 eactivity to a novel environment but not for sensorimotor gating, anxiety, motor coordination, severa
81  and simulations together indicate that this sensorimotor gating arises from the relative timing of t
82 isorders have been shown to have deficits in sensorimotor gating as assessed by prepulse inhibition o
83  that unmedicated OCD patients have impaired sensorimotor gating as measured by PPI.
84 baseline, DAT (-/-) mice exhibited deficient sensorimotor gating as measured by prepulse inhibition (
85 subjects have been shown to have deficits in sensorimotor gating as measured by prepulse inhibition,
86 ndividuals with fragile X also have impaired sensorimotor gating as measured using the prepulse inhib
87 otor activity, anxiety-related behavior, and sensorimotor gating, as well as handling-induced seizure
88 ormalities of information processing seen in sensorimotor gating associated with stress and stress-re
89 of ectopic dendrites in neurons and enhanced sensorimotor gating behavior in mice.
90 lterations in anxiety-like, stereotypic, and sensorimotor gating behaviors observed in adolescence no
91 These results also indicate that the site of sensorimotor gating can occur at the level of the projec
92 sts, and had similar olfactory, auditory and sensorimotor gating capabilities as wild-type mice.
93 t in prepulse inhibition (PPI), a measure of sensorimotor gating commonly deficient in individuals wi
94                                              Sensorimotor gating commonly occurs at sensory neuron sy
95 e first to demonstrate that BN have impaired sensorimotor gating compared with WKY, without impaired
96 udy was to examine the relationships between sensorimotor gating, compulsive behavior, and striatal d
97 ette syndrome (TS) is characterized by tics, sensorimotor gating deficiencies, and abnormalities of c
98 me degradation pathway may contribute to the sensorimotor gating deficiency and cognitive disorders i
99 ates prepulse inhibition (PPI), a measure of sensorimotor gating deficient in several illnesses inclu
100 ut not PND 35, suggesting the emergence of a sensorimotor gating deficit in early adulthood.
101          Finally, mice lacking IgSF21 show a sensorimotor gating deficit.
102                    SA-born WT mice exhibited sensorimotor gating deficits (males), increased reward p
103 anisms underlie abnormal social behavior and sensorimotor gating deficits and implicate Dvl1 in proce
104                                              Sensorimotor gating deficits and rearing are attenuated
105 phenotypic differences in an animal model of sensorimotor gating deficits in human neuropsychiatric d
106 o) proteins, alteration of which could cause sensorimotor gating deficits in schizophrenia.
107 eases tic-like responses and elicits TS-like sensorimotor gating deficits in the D1CT-7 mouse, one of
108                               The finding of sensorimotor gating deficits is particularly significant
109                                 In addition, sensorimotor gating deficits previously noted in Bdr mut
110 te maps associated anxiety-like, social, and sensorimotor gating deficits with volume of the dorsal a
111                                              Sensorimotor gating deficits, as measured by acoustic pr
112 s to have important roles in the reversal of sensorimotor gating deficits, as measured by prepulse in
113 itive effects on locomotor hyperactivity and sensorimotor gating deficits, but further produces syner
114  that the Pvalb/Gad1 Tg mice have pronounced sensorimotor gating deficits, increased novelty-seeking
115 .2(dp/+) mice did not exhibit the SZ-related sensorimotor gating deficits, psychostimulant-induced hy
116  a genetically transmitted susceptibility to sensorimotor gating deficits.
117 elevant to schizophrenia, including impaired sensorimotor gating, discrimination memory, and social b
118 ein levels; and a greater sensitivity to the sensorimotor gating-disruptive effect of amphetamine, co
119                These measures of sensory and sensorimotor gating have both been proposed as models fo
120 tle reflex amplitude, as well as significant sensorimotor gating impairments, as assessed by the prep
121                                  LSD altered sensorimotor gating in a human model of psychosis, suppo
122  failed to induce deficits in sociability or sensorimotor gating in adult KO mice.
123 sent results from a study examining abnormal sensorimotor gating in Fmr1KO mice.
124          Thus, we compared brain anatomy and sensorimotor gating in healthy people with Asperger's sy
125 , our results provide the first evidence for sensorimotor gating in larval zebrafish and report on th
126 amphetamine (AMPH)-induced sensitization and sensorimotor gating in rats, two preclinical procedures
127 the first data that demonstrate a deficit in sensorimotor gating in rodents caused by an inadequate a
128           We found a trend for disruption of sensorimotor gating in Sapap3-KOs using the translationa
129 ffer a useful animal model to study impaired sensorimotor gating in schizophrenia.
130 t studies carefully assessed drug effects on sensorimotor gating in SD versus W strains, across rat s
131 nstrated hypoactivity, anxiety, and impaired sensorimotor gating in the L825V/+ strain, particularly
132 ceptor antagonist can affect the deficits in sensorimotor gating in the NR1(neo/neo) mice.
133  has a significant, dose-dependent effect on sensorimotor gating in which lower doses (0.25-1.0 micro
134  transmitted deficit in prepulse inhibition (sensorimotor gating) in patients with schizophrenia spec
135  in Htr2B(-/-) mice, as shown by deficits in sensorimotor gating, in selective attention, in social i
136                                              Sensorimotor gating is a neural filtering process that a
137                                              Sensorimotor gating is often studied in humans and roden
138 titative and clinically important measure of sensorimotor gating is prepulse inhibition (PPI) of the
139  inhibition (PPI), an operational measure of sensorimotor gating, is deficient in schizophrenia patie
140 f the acoustic startle response-a measure of sensorimotor gating-is highly sensitive for manipulation
141  number of abnormal traits including reduced sensorimotor gating, lower density of dendritic spines i
142           These findings suggest that robust sensorimotor gating may represent a resiliency factor fo
143 his polymorphism is associated with impaired sensorimotor gating measured by prepulse inhibition--an
144  psychotic disorders (CPD) exhibit deficient sensorimotor gating (measured by prepulse inhibition (PP
145                                              Sensorimotor gating, measured by prepulse inhibition (PP
146 dorsal thalamus relay cells and (2) impaired sensorimotor gating, measured via paired-pulse inhibitio
147                    PPI reflects a nonlearned sensorimotor gating mechanism and also shows a robust ge
148 dence for within-gender differences in basic sensorimotor gating mechanisms and implicate the known n
149 eficit in social engagement, working memory, sensorimotor gating, native locomotor activity, and dopa
150 -like behaviors, motor function and balance, sensorimotor gating, novel object recognition, and spati
151         Prepulse inhibition (PPI), a form of sensorimotor gating, occurs when an auditory startle res
152 regions in their neurochemical modulation of sensorimotor gating of acoustic startle in the rat.
153 e has been used as an operational measure of sensorimotor gating or inhibition, and is reduced in sch
154        This study tested the hypothesis that sensorimotor gating performance is associated with risk/
155 ictive validity of animal PPI to model human sensorimotor gating phenomena but only limited studies h
156 ystems are involved in the modulation of the sensorimotor gating phenomenon known as prepulse inhibit
157 ry-adrenal axis stress response and impaired sensorimotor gating, phenotypic effects that were associ
158  exhibit deficits in automatic, preattentive sensorimotor gating (prepulse inhibition [PPI]) of the s
159 tal cortex 5-HT(2A)R expression and improved sensorimotor gating processes via 5-HT(2A)R.
160 frontal cortex dendritic spine structure and sensorimotor gating processes.
161 R) have been used as measures of sensory and sensorimotor gating, respectively.
162 ll as anxiety-related locomotor behavior and sensorimotor gating, revealing potential therapeutic app
163 s considerable interest in the regulation of sensorimotor gating, since deficits in this process coul
164 f picrotoxin caused locomotor hyperactivity; sensorimotor gating (startle prepulse inhibition) was un
165 ant to pathologies associated with disrupted sensorimotor gating such as schizophrenia.SIGNIFICANCE S
166 g that pathologies associated with disrupted sensorimotor gating, such as with schizophrenia, could b
167 ehavioral deficits in social interaction and sensorimotor gating tasks.
168 story of tics may have greater impairment in sensorimotor gating than the general OCD population.
169 on (PPI), which is an operational measure of sensorimotor gating that is deficient in schizophrenia p
170             Prepulse inhibition is a type of sensorimotor gating that is disrupted in some neuropsych
171  (PPI) of the startle reflex is a measure of sensorimotor gating that is reduced in humans with certa
172  of the startle response, a manifestation of sensorimotor gating that is reduced in humans with schiz
173 nhibition (PPI) is an operational measure of sensorimotor gating that is thought to probe preattentio
174 t brought the investigation of H1 effects on sensorimotor gating to human studies.
175 ed brain anatomy using quantitative MRI, and sensorimotor gating using prepulse inhibition of startle
176                                              Sensorimotor gating was abnormal, as measured by deficit
177                                              Sensorimotor gating was examined operationally via the u
178 creased, and acoustic, but not non-acoustic, sensorimotor gating was impaired in Tbx1 heterozygous mi
179                                              Sensorimotor gating was measured by prepulse inhibition
180                                    Moreover, sensorimotor gating was significantly impaired in Asperg
181 rs across working memory, fear processes and sensorimotor gating, we examined these functions between
182  impairments in social approach behavior and sensorimotor gating, whereas MIA offspring with a low in
183             PPI is an operational measure of sensorimotor gating which is strongly regulated by mesol
184 response (PPI) is a cross-species measure of sensorimotor gating, which is severely disrupted in pati
185 order (OCD) is associated with disruption of sensorimotor gating, which may contribute to difficultie
186 lse inhibition (PPI) is used as a measure of sensorimotor gating, with smaller PPI indicating less fi

 
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