ライフサイエンスコーパス: stereotypy

1 ing no effect on syllable or trill bandwidth stereotypy.

2 s exhibited greater AMPH-induced rearing and stereotypy.

3 r lab) had no effect on display structure or stereotypy.

4 osomal activation is a general predictor for stereotypy.

5 ts may represent a neural correlate of motor stereotypy.

6 and did not cause abnormal movement, such as stereotypy.

7 rone concentrations and with changes in song stereotypy.

8 avioral sensitization to amphetamine-induced stereotypy.

9 eased behavioral diversity characteristic of stereotypy.

10 attributed to a slower latency to enter into stereotypy.

11 ference, behavioral sensitization, and motor stereotypy.

12 res and frequencies of B-cell receptor (BcR) stereotypy.

13 quent B cell receptor repertoire skewing and stereotypy.

14 in the contralateral SC showed considerable stereotypy.

15 ous unilateral rotation, shuffling gait, and stereotypy.

16 et of methamphetamine-induced locomotion and stereotypy.

17 l across seasons, underlying changes in song stereotypy.

18 GABA interneurons and increasing behavioral stereotypy.

19 d behavior remarkable for its high degree of stereotypy.

20 h, seizures, postnatal microcephaly and hand stereotypies.

21 fect, puerile behaviour and verbal and motor stereotypies.

22 erized by compulsive oral and forelimb motor stereotypies.

23 MeCP2 in SOM+ neurons exhibited seizures and stereotypies.

24 tor skills, intellectual impairment and hand stereotypies.

25 NMDAR antagonists on gamma oscillations and stereotypies.

26 ppocampus-lesioned subjects began to exhibit stereotypies.

27 motivation to sing as well as song acoustic stereotypy, a measure of consistency over song rendition

28 oughly to the human putamen, led to tic-like stereotypies after either acute stress or d-amphetamine

29 sal ganglia) did not elicit sequential super-stereotypy after drug cessation.

30 nduce stereotypies, and more readily induced stereotypies and limbic seizure behaviors at high doses.

31 They exhibited limb and truncal stereotypies and orofacial dyskinesias upon weaning seda

32 is a function of newborns' spontaneous oral stereotypies and should be viewed within the context of

33 sioned subjects exhibited more self-directed stereotypies and the hippocampus-lesioned subjects displ

34 avioral response that included a decrease in stereotypy and a pronounced increase in locomotion.

35 , which are important to understand movement stereotypy and bilateral coordination in mice.

36 of a D1 receptor antagonist ameliorated the stereotypy and c-fos induction by C/L-DOPA.

37 Decreased sequence stereotypy and combined syllables appeared within 1 week

38 ties, including increased motor activity and stereotypy and deficits in social and sexual interaction

39 animal locomotion a tradeoff exists between stereotypy and flexibility: fast long-distance travellin

40 uding the criteria for identification of BCR stereotypy and its actual frequency as well as the ident

41 ems with the amount of MPD-induced behavior (stereotypy and locomotion) show that prenatal cocaine al

42 d to the shift in the relative expression of stereotypy and locomotion.

43 ntiated motor activity and elicited profound stereotypy and self-injurious behavior at 30 mg/kg.

44 agonist attenuated both the C/L-DOPA-induced stereotypy and the c-fos induction.

45 y have a larger impact on DA agonist-induced stereotypy (and possibly psychosis).

46 morine, attenuates behaviors (locomotion and stereotypies) and preprodynorphin (PPD) and substance P

47 ism, athetosis, dystonia, tremor, myoclonus, stereotypies, and akathisia.

48 ing while concomitantly increasing grooming, stereotypies, and ethological plus traditional measures

49 D1CT-7 mice at doses insufficient to induce stereotypies, and more readily induced stereotypies and

50 tion bearers showed a low incidence of motor stereotypies, and relatively high incidence of complex r

51 al activation included increased locomotion, stereotypy, and limbic seizures.

52 te the opposite view, in which discreteness, stereotypy, and long timescales emerge from the collecti

53 all animals were tested for their locomotor, stereotypy, and nucleus accumbens dopamine and DOPAC rel

54 nd social skills and the development of hand stereotypies, anxiety, tremor, ataxia, respiratory dysrh

55 mice, including those in locomotor activity, stereotypy, anxiety, and trace fear conditioning are als

56 Motor stereotypies are abnormally repetitive behaviors that ca

57 Orofacial stereotypies are critical to optimizing food rejection.

58 If correct, orofacial stereotypies are crucial to the maturation of aerodigest

59 Primary motor stereotypies are relatively common in childhood and can

60 quired to enhance the quality of song (i.e., stereotypy) as well as regulate context-specific vocaliz

61 er doses of methylphenidate produced intense stereotypy, as well as short- (5-day), but not long- (2-

62 oss of purposeful hand movements and speech, stereotypies, ataxia, seizures, mental retardation and a

63 lls and language, the onset of anxiety, hand stereotypies, autistic features, seizures and autonomic

64 ilar to RS, including hypoactivity, forelimb stereotypies, breathing irregularities, weight changes,

65 ystemic testosterone-induced changes in song stereotypy but not rate.

66 ontrast, amphetamine caused not only intense stereotypy, but also profound, long-lasting, dose-relate

67 These results suggest that song stereotypy, but not repertoire size, is a potential beha

68 s had no significant effect on locomotion or stereotypy, but they dramatically attenuated the locomot

69 The induction of high-intensity motor stereotypies by dopamine D1- and D2-class receptor agoni

70 Moreover, because stereotypies can compete with the salience of social sti

71 Motor stereotypies can occur in typical children and persist o

72 cy mediates socio-communicative deficits and stereotypies characteristic for autism.

73 tactile sensitivity issues and sensorimotor stereotypies characteristic of RTT.

74 were resistant to the expression of focused stereotypy compared to wild-type controls.

75 o not enhance acoustic features such as song stereotypy compared with birds receiving peripheral T th

76 or learning and biomechanics, proposing that stereotypies could provide a basis for both swallowing a

77 Consistent with these results, stereotypy could be induced in DD mice by a D1, but not

78 deficits, cognitive impairments and elevated stereotypy, decreased neurogenesis and synaptic plastici

79 ng) gene segment combinations, but that this stereotypy decreases dramatically as the zebrafish matur

80 ess, decreased concentration, hyperactivity, stereotypy, diarrhea, insomnia, and dry skin or pruritus

81 n several under-recognized conditions (motor stereotypy disorder, restless legs syndrome, and infanti

82 features, prevalence, and outcomes of motor stereotypy disorders in typically developing children.

83 Stereotypy encoding was observed in the core and was att

84 y integrating B-cell receptor immunoglobulin stereotypy (for subsets 1, 2, and 4) into the well estab

85 ssociative learning, this initial peripheral stereotypy gives way to functionally nonstereotyped circ

86 Studies on the mechanisms controlling motor stereotypies have focused on the role of dopamine in mod

87 g MeCP2-e1 deficient mice developed forelimb stereotypy, hindlimb clasping, excessive grooming and hy

88 , it remains unclear whether this anatomical stereotypy implies functional homogeneity, or whether in

89 emia based on B-cell receptor immunoglobulin stereotypy improves the Dohner hierarchical model and re

90 y role in reinforcement of post-feeding oral stereotypies in chickens subject to the same R treatment

91 Longitudinal data indicate that stereotypies in children with normal intelligence show a

92 n to the neurobiological basis of repetitive stereotypies in neurodevelopmental disorders, such as au

93 inhibition in P rats and increased locomotor stereotypies in NP rats.

94 compared to controls, whereas 5 mg/kg caused stereotypy in Dbh-/- mice, which is only observed in con

95 tal neurons is required for the induction of stereotypy in DD mice.

96 cocaine-induced behavioral sensitization to stereotypy in mice.

97 ineffective against psychostimulant-induced stereotypy in naive animals.

98 erns in CLL differ from those underlying BCR stereotypy in other B-cell malignancies.

99 ceptor agonist to induce different levels of stereotypy in rats.

100 Thus, whereas the expression of stereotypy in response to repeated METH treatment requir

101 monstrated substantial wiring and functional stereotypy in the fly olfactory system.

102 timulation causes a complex behavioral super-stereotypy in the form of excessive production and rigid

103 periments in Drosophila demonstrate striking stereotypy in the neural architecture of the olfactory s

104 Molecular genetics has revealed a precise stereotypy in the projection of primary olfactory sensor

105 Repeated METH-treatment elicits intense stereotypy in wild-type and D(3) mutants but not in D(2)

106 eptor agonist, with neither agonist inducing stereotypy in WT mice.

107 of behaviors (locomotion, rearing, grooming, stereotypies) including a microstructural analysis of in

108 ns (long days and elevated T), and that song stereotypy increases as nuclei within this circuitry gro

109 ortically in non-convulsant doses produced a stereotypy indistinguishable from that induced by amphet

110 ling, suggesting that the expression of oral stereotypies induced by amphetamine injections into the

111 assess striatal activity during the focused stereotypy induced by cocaine, both types of striatal un

112 and chronic COC rats, 18-MC potentiated the stereotypy induced by higher COC doses (20 and 40 mg/kg,

113 in the matrix predicted the degree of motor stereotypy induced by the drug treatments.

114 The issue of stereotypy is intertwined throughout and we also raise t

115 This stereotypy is masked by the complex diversification proc

116 These results imply that amphetamine-induced stereotypy is mediated in the cortex by the removal of t

117 Our earlier studies have shown that song stereotypy is persistently reduced in male zebra finches

118 ividual neurons neither glomerular order nor stereotypy is preserved in either region.

119 suggests that B-cell receptor immunoglobulin stereotypy is relevant from a clinical viewpoint, this a

120 tism's many sensorimotor features, including stereotypies, is unknown.

121 odes of repetitive motor activation (focused stereotypy) known to involve the mesostriatal dopamine s

122 Keven & Akins suggest that innate stereotypies like TP/R may participate in the acquisitio

123 effects of phencyclidine on working memory, stereotypy, locomotion, and cortical glutamate efflux.

124 how dopamine receptors facilitate particular stereotypies manifest in animal models of Tourette syndr

125 consider the possibility that early emerging stereotypies might help explain the foundations of the l

126 Motor impairments include stereotypies, motor delays, and deficits, such as dyspra

127 confirmed striatal deficits (hyperactivity, stereotypies, motor impairment in rotarod).

128 During amphetamine-induced focused stereotypy, motor-related neurons in the striatum respon

129 Here, we investigated the structural stereotypy of cortical barrel columns by measuring the 3

130 Our results show that, despite the stereotypy of Drosophila neuromuscular connections, dene

131 Sequential super-stereotypy of grooming chains may be particularly advant

132 The atlas quantifies the stereotypy of nuclear locations and provides other stati

133 two circuits reveal a high inter-individual stereotypy of the cell complement, neuronal projections,

134 The stereotypy of the innervation lies in the number of cont

135 at able to induce either striatal and limbic stereotypies or anxiolytic activity, thus outlining thei

136 significant decrease in the duration of the stereotypy phase as well as a profound increase and qual

137 f 2 mum on average, permitting assessment of stereotypy, potential connectivity and functional mappin

138 onse to the subsequent administration of non-stereotypy producing doses of amphetamine (0.5-1.5 mg/kg

139 knockout mice exhibited potentiated tic-like stereotypies, recapitulating core phenomenology of TS; t

140 toneuron dendrites, which contrasts with the stereotypy reported for presynaptic terminals of sensory

141 tal dopamine (DA) pathways in locomotion and stereotypy, respectively, we hypothesized that a persist

142 caine produced a progressive increase in the stereotypy response of rats to a challenge dose of cocai

143 ed animals showed an increased locomotor and stereotypy response to amphetamine after treatment with

144 st, apomorphine, would result in an enhanced stereotypy response to the subsequent administration of

145 resulted in an enhanced amphetamine-induced stereotypy response.

146 e development and expression of the enhanced stereotypy response.

147 s-induced increase in the locomotor, but not stereotypy, response to amphetamine.

148 evelopment and the expression of the altered stereotypy responsivity, though several dose- and time-r

149 tremors, dystonia, chorea, tics, myoclonus, stereotypies, restless legs syndrome, and various other

150 ich correlated with expression of behavioral stereotypy, resulted from an increased number of irregul

151 f a marked loss of the spectral and temporal stereotypy seen in crystallized song, including stutteri

152 Oral stereotypies significantly increased in the rats infused

153 of time spent engaged in continuous focused stereotypy simultaneous with a profound increase in ambu

154 luded a marked decrease in syllable sequence stereotypy, skewed syllable distribution within song bou

155 Secondary measures included the ABC stereotypy subscale, Repetitive Behavior Scale-Revised,

156 e spent engaged in typical cocaine-dependent stereotypies such as locomotion, sniffing, or gnawing, w

157 ate balance between individual variation and stereotypy, suggesting the existence of dedicated mechan

158 ype, both treatments elicit the same focused stereotypy (taffy pulling).

159 lesioned subjects consistently produced more stereotypies than the control subjects in a variety of c

160 h, social interactions, and repetitive motor stereotypies that are relevant to ASD.

161 d SCH23390 spent more time performing simple stereotypies that included intense scratching and biting

162 lly, early symptomatic mice showed increased stereotypies that were decreased by tetrabenazine treatm

163 songbirds exhibit a high degree of acoustic stereotypy that persists for days or months after the el

164 recedented BcR restriction (aptly coined as "stereotypy"), thus cementing the idea that antigenic ele

165 ehavioral response shifted away from focused stereotypy toward an increase in ambulation.

166 Like other orofacial stereotypies, TP/R emerges in the first phase and vanish

167 itions and dopamine-receptor-agonist induced stereotypies under normal conditions.

168 The emergence of stereotypies was examined in juvenile rhesus monkeys (Ma

169 key finding was that in the penumbra, spike stereotypy was maintained even during the seizure.

170 ion from hyperlocomotion to intense, focused stereotypy was observed that was correlated with an indu

171 g), rats were tested in photocell cages, and stereotypy was rated to determine preimmunization drug r

172 basolateral amygdalae and behavioral seizure stereotypy was simultaneously recorded digitally.

173 produce repetitive behaviors known as motor stereotypies, we applied psychomotor stimulants and a di

174 the mechanisms required for the induction of stereotypy, we examined the responses of dopamine-defici

175 tion failed to block the bicuculline-induced stereotypy; we conclude, therefore, that the stereotypic

176 Pronounced stereotypies were not observed in any of the experimenta

177 Rates of oral stereotypies were recorded by observers who were blind t

178 ate cyclase activity, locomotor activity and stereotypy were exaggerated in DRD mice in response to t

179 wever, amphetamine-stimulated locomotion and stereotypy were strongly enhanced, while amphetamine-sti

180 luding disinhibition, euphoria, or elaborate stereotypies, whereas dopamine deficiency can cause anxi

181 song maintenance, HVC promotes song syllable stereotypy, whereas LMAN promotes learning and acoustic

182 suppresses intake by inducing locomotion and stereotypy, which interfere with the appetitive phase of

183 with SKF38393 from inducing sequential super-stereotypy, which manifests as an exaggeration of the te

184 (RA), controls syllable and trill bandwidth stereotypy, while not significantly affecting higher ord

185 ot shell, attenuated methamphetamine-induced stereotypy, while treatment in either brain region had n

186 ations of CLL B-cell receptor immunoglobulin stereotypy, with a particular focus on 14 major stereoty