ライフサイエンスコーパス: stereotypy

1 l across seasons, underlying changes in song stereotypy.

2 GABA interneurons and increasing behavioral stereotypy.

3 d behavior remarkable for its high degree of stereotypy.

4 s exhibited greater AMPH-induced rearing and stereotypy.

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

6 osomal activation is a general predictor for stereotypy.

7 ts may represent a neural correlate of motor stereotypy.

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

9 rone concentrations and with changes in song stereotypy.

10 avioral sensitization to amphetamine-induced stereotypy.

11 eased behavioral diversity characteristic of stereotypy.

12 attributed to a slower latency to enter into stereotypy.

13 nchronization became predictive of kinematic stereotypy.

14 assessment of inter- versus intra-individual stereotypy.

15 ayed autistic-like behaviours with a jumping stereotypy.

16 ts in ectopic branching and decreases branch stereotypy.

17 ing no effect on syllable or trill bandwidth stereotypy.

18 ference, behavioral sensitization, and motor stereotypy.

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

20 quent B cell receptor repertoire skewing and stereotypy.

21 stricted IGHV usage or B-cell receptor (BCR) stereotypy.

22 in the contralateral SC showed considerable stereotypy.

23 ous unilateral rotation, shuffling gait, and stereotypy.

24 et of methamphetamine-induced locomotion and stereotypy.

25 ppocampus-lesioned subjects began to exhibit stereotypies.

26 h, seizures, postnatal microcephaly and hand stereotypies.

27 fect, puerile behaviour and verbal and motor stereotypies.

28 erized by compulsive oral and forelimb motor stereotypies.

29 hypotonia, intellectual disability and motor stereotypies.

30 behaviors including social communication and stereotypies.

31 MeCP2 in SOM+ neurons exhibited seizures and stereotypies.

32 tor skills, intellectual impairment and hand stereotypies.

33 NMDAR antagonists on gamma oscillations and stereotypies.

34 Dystonia (34.2%), stereotypies (24.6%), and ataxia (16.2%) were the most p

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

36 ulse inhibition (PPI) and increased grooming stereotypies after a 30-min session of spatial confineme

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

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

39 ncentration-dependent THC-induced behavioral stereotypy akin to THC's effect in rats and the psychotr

40 5 mg/kg) rescued social behavior, normalized stereotypies and anxiety and blunted locomotor sensitiza

41 d spine density is associated with ASD -like stereotypies and cortico-striatal hyperconnectivity.

42 spoken language and hand use that, with hand stereotypies and impaired ambulation, constitute the fou

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

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

45 istration dose-dependently worsened grooming stereotypies and PPI deficits in partially CIN-depleted

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

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

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

49 The relationship between stereotypy and behavioural diversity was negative, but n

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

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

52 Decreased sequence stereotypy and combined syllables appeared within 1 week

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

54 llection, we analyzed neuronal morphological stereotypy and discovered that one set of mushroom body

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

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

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

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

59 o the actual frequency of BcR immunoglobulin stereotypy and major subsets, as well as the existence o

60 f connections between brains, revealed broad stereotypy and occasional variability in neuron count an

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

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

63 movements bilaterally, of nose movement, of stereotypy and variability in an active whisking to touc

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

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

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

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

68 ll as specific symptoms (verbal dysfunction, stereotypies, and hypersensoriality).

69 distinct ASD symptoms: language impairment, stereotypies, and hypersensoriality.

70 re language impairment, hypotonia, Rett-like stereotypies, and minor facial dysmorphisms (wide mouth,

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

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

73 ficiency to basal ganglia dysfunction, motor stereotypies, and social deficits.

74 ed a degradation of call acoustic structure, stereotypy, and individual uniqueness.

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

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

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

78 al development, sexual dimorphism, degree of stereotypy, and structural correlations to behavior or n

79 d novelty-induced hyperactivity, exaggerated stereotypy, and vertical exploration in both transgenic

80 haviours (social interaction and preference, stereotypies, anxiety, nociception) in Oprm1(+/+) and Op

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

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

83 Motor stereotypies are abnormally repetitive behaviors that ca

84 Orofacial stereotypies are critical to optimizing food rejection.

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

86 Primary motor stereotypies are relatively common in childhood and can

87 ere more likely to produce a cub, suggesting stereotypies are tied to behavioural but not physiologic

88 e gene deletion in the SST population caused stereotypies as well as learning and memory dysfunction.

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

90 tion had little effect on the development of stereotypies, as well as on body weight, glucocorticoid

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

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

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

94 morphological adaptations in mice displaying stereotypy behavior.

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

96 letion of D2R-SPNs in the NAc produced motor stereotypies but facilitated social behavior and impaire

97 ighly sexually motivated males were prone to stereotypy but also had high reproductive competence.

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

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

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

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

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

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

104 Motor stereotypies can occur in typical children and persist o

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

106 tactile sensitivity issues and sensorimotor stereotypies characteristic of RTT.

107 er, duplication carriers exhibited increased stereotypies compared to deletion carriers.

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

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

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

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

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

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

114 le variability, with sequential increases in stereotypy dependent upon neuromodulation.

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

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

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

118 The stereotypy emerges in the total response of the Kenyon c

119 Stereotypy encoding was observed in the core and was att

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

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

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

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

124 mice displayed social interaction deficits, stereotypies, hyperactivity, and occasionally spontaneou

125 ted toward a compromised welfare state (e.g. stereotypies, hypervigilance and aggressiveness) were al

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

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

128 o the brain, and lowered (+)-METH-associated stereotypies in a hyperlocomotion assay.

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

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

131 ent improved social preference but increased stereotypies in cocaine abstinent mice.

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

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

134 While the role of stereotypies in welfare assessment is well studied, few

135 gesting that the study of BcR immunoglobulin stereotypy in CLL has important implications for underst

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

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

138 cocaine-induced behavioral sensitization to stereotypy in mice.

139 ineffective against psychostimulant-induced stereotypy in naive animals.

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

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

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

143 d constraints with which convergence enables stereotypy in sensory responses despite random connectiv

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

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

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

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

148 , time-symmetric transitions, thus revealing stereotypy in the sequential patterns of state transitio

149 yon cells, mushroom body output neurons show stereotypy in their responses.

150 , improving success of reaching but limiting stereotypy in these animals.

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

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

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

154 Multivariate analysis showed that stereotypy increased with density of logs on the ground,

155 sychiatric manifestations including elevated stereotypy, increased anxiety-related traits, delayed ac

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

157 significantly reduced THC-induced behavioral stereotypy, indicating cannabinoid receptor 2 as a possi

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

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

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

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

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

163 We found that the stereotypy is enabled by the convergence of inputs from

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

165 This stereotypy is masked by the complex diversification proc

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

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

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

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

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

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

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

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

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

175 tion and synaptic structure related genes in stereotypy mice.

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

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

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

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

180 Motor stereotypies occurring in early-onset neuropsychiatric d

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

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

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

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

185 g with a quantification of the diversity and stereotypy of patterns at each level.

186 VC increased the pitch, amplitude, tempo and stereotypy of song, similar to the natural invigoration

187 The geometric complexity and stereotypy of spider webs have long generated interest i

188 Although the stereotypy of the behaviors and the complexity of the re

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

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

191 ity of red panda (n = 26), and the effect of stereotypy on their behavioural diversity in three India

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

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

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

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

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

197 to direct-pathway neuron disconnectivity in stereotypy remain poorly understood.

198 Stereotypies-repetitive, unvarying, functionless behavio

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

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

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

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

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

204 resulted in an enhanced amphetamine-induced stereotypy response.

205 e development and expression of the enhanced stereotypy response.

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

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

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

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

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

211 Oral stereotypies significantly increased in the rats infused

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

213 speed, personality change, disinhibition or stereotypy; six had pure memory impairment; and 12 had b

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

215 Movement disorders including stereotypies, spasticity and dystonia were also observed

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

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

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

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

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

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

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

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

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

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

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

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

228 o winter, and also with ambient temperature, stereotypy, tree density, and tree height used.

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

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

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

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

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

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

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

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

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

238 However, females that exhibited stereotypies were more likely to produce a cub, suggesti

239 Female stereotypies were negatively associated with all reprodu

240 Pronounced stereotypies were not observed in any of the experimenta

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

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

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

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

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

246 plasma ACTH and high rates of stress-induced stereotypies; whereas NSSI subjects with the s allele ex

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

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

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

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

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

252 The strong stereotypy within cohorts of brain regions allows genera