ライフサイエンスコーパス: neuroanatomical

1 l injury, and are associated with widespread neuroanatomical abnormalities and adverse early neurodev

2 Neuroanatomical abnormalities in gray matter volume in t

3 itive impairments in sustained attention and neuroanatomical abnormalities in the right inferior fron

4 , we were able to determine that the primary neuroanatomical abnormalities that precede dyslexia are

5 Despite increasing evidence that neuroanatomical abnormalities underlie pathological anxi

6 altered vocalization, anxiety-like behavior, neuroanatomical abnormalities, and growth impairment.

7 f the affected cognitive domains, as well as neuroanatomical abnormalities, resemble symptoms and sig

8 delian genotype ratios, and exhibit no gross neuroanatomical abnormalities.

9 d the association between imaging markers of neuroanatomical abnormality and poor cognitive and motor

10 The findings extend a functional neuroanatomical account of disorders characterized by cl

11 However, the specific effect of neuroanatomical aging on the efficiency of economic deci

12 ely define a 4-dimensional categorization of neuroanatomical alterations in mild cognitive impairment

13 Moreover, it remains unclear whether neuroanatomical alterations linked to ADHD are also pres

14 oimaging studies indicate disease-associated neuroanatomical alterations, the behavioural correlates

15 Neuroanatomical analysis and two-photon calcium imaging

16 Neuroanatomical analysis revealed a reduced density of d

17 The results are discussed with reference to neuroanatomical and behavioral studies of various specie

18 The key neuroanatomical and behavioural links bridging vocal lea

19 However, the neuroanatomical and biochemical substrates through which

20 In this study, we tested for neuroanatomical and cognitive endophenotypes in a group

21 motional-affective/motivation) with specific neuroanatomical and cognitive substrates.

22 e context of other brain structures in which neuroanatomical and connectional modularity have functio

23 ent advances in mouse genetics combined with neuroanatomical and electrophysiological techniques have

24 entiviral re-expression, in combination with neuroanatomical and electrophysiological techniques, hav

25 isms that mediate these effects by employing neuroanatomical and electrophysiological techniques.

26 inherited transgenerationally at behavioral, neuroanatomical and epigenetic levels.

27 derstood why tauopathies vary greatly in the neuroanatomical and histopathological patterns of tau ag

28 In this study, we used neuroanatomical and imaging approaches to delineate the

29 Here, through neuroanatomical and immunohistochemical analysis, we ide

30 drawal symptom in abstinent smokers, yet the neuroanatomical and molecular bases underlying it are un

31 We report a profound disruption of cortical neuroanatomical and molecular features upon loss of Lhx2

32 These results provide a neuroanatomical and molecular substrate for relapse beha

33 Although neuroanatomical and neurofunctional networks involved in

34 an increasing literature aiming to establish neuroanatomical and neuropathological (e.g. amyloid and

35 Functional, neuroanatomical and transcriptional consequences of comp

36 llular analyses coupled to mouse behavioral, neuroanatomical, and molecular phenotyping, we provide m

37 roject (HCP) and an objective semi-automated neuroanatomical approach, we delineated 180 areas per he

38 Using neuroanatomical approaches with tract tracing and electr

39 autoantibodies related to narcolepsy using a neuroanatomical array: rat brain sections were processed

40 between orexin and depression, few specific neuroanatomical associations have been made.

41 In order to assess neuroanatomical associations of performance on auditory

42 Neuroanatomical associations were assessed using blinded

43 ere has been recent motivation to search for neuroanatomical asymmetries in nonhuman primates in orde

44 ic plasticity, it has remained unexplored if neuroanatomical asymmetries linked to human language dom

45 pirical existence of this scale, implicit in neuroanatomical atlases, combined with advances in compu

46 the findings suggest candidate cognitive and neuroanatomical bases for these salient but under-apprec

47 dependence in smokers, yet the mechanism and neuroanatomical bases for withdrawal symptoms are unclea

48 The neuroanatomical bases of autism spectrum disorder remain

49 hese results provide first glimpses into the neuroanatomical bases of early childhood stuttering, and

50 We studied the structural neuroanatomical basis for impaired self-awareness among

51 how humans infer hierarchical identity, the neuroanatomical basis for perceiving key social dimensio

52 What is the neuroanatomical basis for the decline in brain function

53 These findings provide the neuroanatomical basis for the interaction between distal

54 agnetic resonance imaging study assessed the neuroanatomical basis for these effects.

55 s of advanced Parkinson's disease, but their neuroanatomical basis is incompletely understood.

56 ly common disorder after stroke, its precise neuroanatomical basis is still unknown.

57 and contribute preliminary evidence for the neuroanatomical basis of individual differences in moral

58 ies addressed this question by examining the neuroanatomical, behavioral, and pharmacological mechani

59 y with predictive probabilities for the male neuroanatomical brain phenotype.

60 The pattern of neuroanatomical change observed in our alcohol-dependent

61 y has specifically investigated whether such neuroanatomical changes also occur at this level in huma

62 e brain and suggests caution in interpreting neuroanatomical changes as being related to a potentiall

63 ntal illness enables a clearer definition of neuroanatomical changes associated with subsets of human

64 These neuroanatomical changes help explain functional phenotyp

65 Here, we investigated the neuroanatomical changes in a transgenic rat model for a

66 We conclude that fairly small neuroanatomical changes in specific regions of the LFPN

67 We identified neuroanatomical changes in the brains of mice deficient

68 This conclusion is reinforced by evidence of neuroanatomical changes in the same set of patients with

69 These neuroanatomical changes may be critical for the generati

70 use model recapitulates most of the hallmark neuroanatomical changes observed in 22q11.2 deletion car

71 f this transition are unknown, including the neuroanatomical changes that made flight possible [1].

72 dy examined the neurochemical mechanisms and neuroanatomical changes underlying coexisting behavioral

73 However, the neuroanatomical changes were not associated with changes

74 r, offspring neuroendocrine, epigenetic, and neuroanatomical changes, in an attempt to determine the

75 Here, our goal is to provide the first neuroanatomical characterization of GFP expression in th

76 effects on energy intake, elucidating a key neuroanatomical circuit driving pathological anorexia an

77 neurons that project to the CeA, outlining a neuroanatomical circuit that is activated by cisplatin.

78 logy, induced by pharmacologic modulation of neuroanatomical circuits using designer receptors exclus

79 dividuals with classical Alzheimer's disease neuroanatomical, cognitive, cerebrospinal fluid biomarke

80 Passive frame theory begins to isolate the neuroanatomical, cognitive-mechanistic, and representati

81 The complex neuroanatomical connections of the inferior colliculus (

82 It also makes strong neuroanatomical connections with areas of the mesolimbic

83 region to region in the brain through direct neuroanatomical connections.

84 at examined white matter measures reflecting neuroanatomical connectivity (fractional anisotropy) in

85 sor imaging/diffusion spectrum imaging-based neuroanatomical connectivity into the brain model, the r

86 The afferent and efferent neuroanatomical connectivity of the subregions of the hi

87 not reducible to specific brain regions and neuroanatomical connectivity.

88 in network that is inherently present in the neuroanatomical connectivity.

89 The hypothesis is based on a fundamental neuroanatomical constraint: an axon must pass close to t

90 om within sub-cellular, cellular, tissue and neuroanatomical contexts.

91 Our results provide potential neuroanatomical correlates for impaired familiarity perc

92 The neuroanatomical correlates mediating vestibular sensatio

93 tricity can provide novel insights about the neuroanatomical correlates of a diverse set of traits, r

94 Neuroanatomical correlates of auditory spatial processin

95 Our findings extend previous studies of the neuroanatomical correlates of cognitive and affective em

96 In this study, we investigate the neuroanatomical correlates of dysglycemia in very young

97 Our study highlights key neuroanatomical correlates of schizophrenia genetic risk

98 Here, we explored the neuroanatomical correlates of sensation seeking and impu

99 common in children born prematurely, robust neuroanatomical correlates of these impairments remain t

100 We examined the neuroanatomical correlates of this specific error type i

101 her, these results provide insights into the neuroanatomical correlates supporting the development of

102 sible neurodevelopmental origins but unknown neuroanatomical correlates.

103 d Herculano-Houzel assign power functions to neuroanatomical data and present a model to account for

104 Building upon neuroanatomical data and studies investigating direct ne

105 lbs of the brain in vertebrates, but no such neuroanatomical data exists for vultures.

106 these considerable advances in connectomics, neuroanatomical data must be integrated with neurophysio

107 he scaling law obtained from the comparative neuroanatomical data, which strengthens the case for the

108 to high-throughput analysis of many forms of neuroanatomical data.

109 s indirect, there is close correspondence to neuroanatomical data.

110 riety of behavioral, neurophysiological, and neuroanatomical data.We argue that these models hold the

111 Neuroanatomical defects and abnormal neocortical RZRbeta

112 As a result, the severity of the neuroanatomical defects and learning and memory deficits

113 Overexpression of BBS7 rescues head size and neuroanatomical defects of kctd13 morphants, whereas sup

114 We first provide a neuroanatomical description of the motoneurons and muscl

115 rmore, disease stage significantly moderated neuroanatomical diagnosis as recurrently-ill patients ha

116 Neuroanatomical diagnosis was correct in 80% and 72% of

117 nd current IQ, but little is known about the neuroanatomical differences among these cognitive subgro

118 The challenge was based on supposed neuroanatomical differences between humans and other pri

119 including the psychological, behavioural and neuroanatomical differences between male and female case

120 ort (ADNI) to elucidate the heterogeneity of neuroanatomical differences between subjects with mild c

121 Yet, the neuroanatomical differences engendered by population his

122 The reported neuroanatomical differences in dyslexia may be causal to

123 (ODD) (comorbidity rates up to 60%) on these neuroanatomical differences is scarcely studied, while O

124 in type 1 diabetes (T1D) describe widespread neuroanatomical differences related to exposure to glyce

125 Despite these striking neuroanatomical disparities, we observed reliable space-

126 ional genetic techniques has facilitated the neuroanatomical dissection of the melanocortinergic netw

127 us-specific information, questioning assumed neuroanatomical distinctions between storage and control

128 The HF and LF male rats exhibited neuroanatomical distinctions that were not observed in H

129 use of the Mchr1-cre mouse for outlining the neuroanatomical distribution and neurochemical phenotype

130 Although the neuroanatomical distribution of catecholaminergic (CA) n

131 Furthermore, we provide the neuroanatomical distribution of JH receptors in both the

132 BM)-chimeric mice were used to determine the neuroanatomical distribution of peripheral myeloid cells

133 ociation tracts had an anterior and superior neuroanatomical distribution.

134 The genetic bases of neuroanatomical diversity appear to be relatively indepe

135 tect genetic variants with a large effect on neuroanatomical diversity, but those currently identifie

136 markers within the context of the wide human neuroanatomical diversity.

137 ches that are being creatively combined with neuroanatomical, electrophysiological and behavioral tec

138 Second, our study is the first to integrate neuroanatomical, electrophysiological, and behavioral ev

139 However, little neuroanatomical evidence consistent with this account ha

140 Electrophysiological and neuroanatomical evidence for reciprocal connections with

141 and nucleus accumbens (NAc); however, direct neuroanatomical evidence of OT regulation of DA neurons

142 This study provides strong neuroanatomical evidence that catecholamines are importa

143 ization and integration of results from many neuroanatomical experiments.

144 The neuroanatomical extent of the 1953 operation could not b

145 ronic pain is predetermined by corticolimbic neuroanatomical factors.

146 Recently, a uniquely human neuroanatomical feature has been demonstrated in the str

147 We describe an atypical neuroanatomical feature present in several primate speci

148 ar cortex is an example of a relatively rare neuroanatomical feature that has become more common in e

149 Neuroanatomical features derived from voxel-based morpho

150 To date, unequivocal neuroanatomical features have been demonstrated neither

151 We first introduce the neuroanatomical features of AIC and existing findings on

152 tion have been linked to divergence in gross neuroanatomical features of sensory pathways.

153 his neuroblast affects molecular properties, neuroanatomical features, and functional inputs of proge

154 om that of its primate relatives by specific neuroanatomical features, especially the strong linkage

155 hing statistics to be linked to larger scale neuroanatomical features.

156 provides a brief historical review of these neuroanatomical findings, which were relevant to the stu

157 To test the species generality and neuroanatomical foundations of this hypothesis, we asked

158 Adolescence is a time of extensive neuroanatomical, functional, and chemical reorganisation

159 Because the pulvinar's neuroanatomical geometry makes it unlikely to be a direc

160 ss phyla, mushroom body-like centers share a neuroanatomical ground pattern and proteins required for

161 resses the GLP-1R and represents a potential neuroanatomical hub connecting the nucleus tractus solit

162 The prefrontal cortex is a critical neuroanatomical hub for controlling motivated behaviours

163 strates that the habenula acts as a critical neuroanatomical hub that connects and regulates brain re

164 imensions of our conscious experience, their neuroanatomical implementations were clearly dissociable

165 We used neuroanatomical,in vitroandin vivoelectrophysiological,

166 Our findings suggest that neuroanatomical information may provide generalizable di

167 ology enables the synthesis of molecular and neuroanatomical information through the use of transgeni

168 gene expression data, connectivity data and neuroanatomical information with powerful search and vie

169 Preserved neuroanatomical integrity in these networks is associate

170 ences in neurocognitive function and altered neuroanatomical integrity.

171 des the first systematic immunohistochemical neuroanatomical investigation of the systems involved in

172 sis, this study integrates over 5 decades of neuroanatomical investigations into a multiscale, multil

173 prise depends on the integration of previous neuroanatomical knowledge, partly through the developmen

174 led out for special attention in the earlier neuroanatomical literature, we undertook to examine them

175 The neuroanatomical localization most likely relates to insu

176 Elucidating the neuroanatomical localization of LRRK2 will further defin

177 s fNIRS studies have suffered from imprecise neuroanatomical localization, we rely on the most rigoro

178 Mendelian disorders according to the primary neuroanatomical location affected: skeletal muscle, card

179 trodes, and it has been used to identify the neuroanatomical loci and to compute the distance to the

180 such, the mPOA is a logical candidate for a neuroanatomical locus modulating activity in the mesolim

181 These results provide a neuroanatomical map of NLGN and NRXN expression patterns

182 echanisms of mouse MCH neurons, we performed neuroanatomical mapping and characterization followed by

183 Functional neuroanatomical mapping revealed that vagal preganglioni

184 ng genetic neuronal targeting and functional neuroanatomical mapping we tested the hypothesis that pa

185 Advances in neuroanatomical mapping, genetically specific neuronal m

186 characterize neurobehavioural correlates of neuroanatomical measures implicated in the pathophysiolo

187 To elucidate the neuropharmacological and neuroanatomical mechanisms underlying this phenomenon, w

188 and instrumental settings involves distinct neuroanatomical mechanisms.

189 While neuroanatomical methods enable high-resolution mapping o

190 Modern neuroanatomical methods have allowed the identification

191 e used behavioral, electrophysiological, and neuroanatomical methods to demonstrate the feasibility o

192 nt study, physiological, pharmacological and neuroanatomical methods were used to explore the autonom

193 hnical difficulties with currently available neuroanatomical methods.

194 L-R reversals do not necessarily represent a neuroanatomical mirror image.

195 Neuroanatomical models hypothesize a role for the dorsal

196 oaches ranging from in vivo imaging to novel neuroanatomical, molecular, epigenomic, and computationa

197 Here, we used neuroanatomical, neuropharmacological, and chemogenetic

198 rous genomic loci that are associated with a neuroanatomical or neurobehavioral phenotype.

199 ed an experiment to inquire whether specific neuroanatomical or socioecological measures predict succ

200 nt from the motor system, although the exact neuroanatomical origin is unknown.

201 on, Rudebeck et al. provide insight into the neuroanatomical origins of a subset of these signals.

202 f 5HT neurons in the dorsal raphe, a defined neuroanatomical pathway, and a behavioral phenotype that

203 c information is plausibly relayed along the neuroanatomical pathways alluded to above.

204 The presence in primates of dedicated neuroanatomical pathways for specific sensorimotor integ

205 Furthermore, the neuroanatomical pathways that express NMUR2 and its ultr

206 etely understood but plausibly could include neuroanatomical pathways to and from central vestibular

207 Cre driver lines with expression in specific neuroanatomical pathways within the cerebral cortex and

208 This neuroanatomical pattern is consistent with an existing,

209 ted diversity in brain structure, as well as neuroanatomical patterns associated with low or high ASD

210 Together, our neuroanatomical, pharmacologic, and neuronal activity da

211 between KCTD13, a key driver of the mirrored neuroanatomical phenotypes of the 16p11.2 CNV, and cilio

212 using magnetic resonance imaging (MRI)-based neuroanatomical phenotyping.

213 an RCT in vivo evidence for the presence of neuroanatomical plasticity in humans.

214 In the present study, spontaneous neuroanatomical plasticity of severed bulbospinal system

215 lt humans provides an opportunity to examine neuroanatomical plasticity resulting from altered sensor

216 lassifier will enable substantially improved neuroanatomical precision for studies of the structural

217 es, rather than dyslexia per se, whereas the neuroanatomical precursors are predominantly in primary

218 ions in the brain, we have characterized its neuroanatomical profile from embryonic stages to adultho

219 atterns: (i) individuals with largely normal neuroanatomical profiles, who also turned out to have th

220 -imaging studies show a relationship between neuroanatomical properties and learning for adults expos

221 The neuroanatomical reality of the SNS-SS feedback loops sug

222 The lateral hypothalamus (LH) is a neuroanatomical region essential for appetitive and cons

223 ata highlight the cerebellum as an important neuroanatomical region in alcohol consumption phenotype

224 increased neuroinflammation in at least one neuroanatomical region in dementia patients, most usuall

225 t these call types are processed in distinct neuroanatomical regions and establish a functional link

226 localized, in the absence of Lewy bodies, to neuroanatomical regions mildly affected in Parkinson's d

227 ray matter into ventral, lateral, and dorsal neuroanatomical regions was observed.

228 acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.

229 tion in major depression due to an increased neuroanatomical schizophrenia likeness of these patients

230 brain maturation may strongly impact on the neuroanatomical separability of major depression and sch

231 Our results demonstrate that neuroanatomical shape can be significantly heritable, ab

232 Neuroanatomical shape descriptors, however, can represen

233 omprehensive analysis of the heritability of neuroanatomical shape measurements across an ensemble of

234 be made, are critical in view of their close neuroanatomical similarity to humans in brain regions im

235 It is encoded in specific neuroanatomical sites that activate a specific repertoir

236 To examine possible neuroanatomical sources of cognitive deficits, we used a

237 To test for neuroanatomical specificity, 16 specific tracts were add

238 patterns specific to developmental stage and neuroanatomical structure.

239 ovel technique to study shape asymmetries of neuroanatomical structures across subcortical and cortic

240 ative dose effect of sex chromosome genes on neuroanatomical structures and cognitive abilities.

241 ourse of Lithium therapy and have identified neuroanatomical structures influenced by norepinephrine.

242 , here we analyse 134 specimens from various neuroanatomical structures of whole autopsy brains from

243 our species coupled with a growing number of neuroanatomical studies across primates provide an unpre

244 Neuroanatomical studies and experimental diffusion-anato

245 Neuroanatomical studies are rarely frontline news, but t

246 whole-brain data sets has opened the door to neuroanatomical studies at an unprecedented scale.

247 Nonhuman primate neuroanatomical studies have identified a cortical pathw

248 Neuroanatomical studies have long indicated that cortico

249 ly related to functional questions raised by neuroanatomical studies of Ramon y Cajal over a century

250 PHC function in humans have been informed by neuroanatomical studies of these regions obtained in ani

251 he mammalian cerebral cortex in experimental neuroanatomical studies.

252 In sum, our neuroanatomical study demonstrates that a small group of

253 ells of the prefrontal cortex, providing the neuroanatomical substrate for a potential interaction.

254 Here we describe a neuroanatomical substrate for familiarity signaling, the

255 t the goldfish heart possesses the necessary neuroanatomical substrate for fine, region-by-region aut

256 portant for mood disorders and constitutes a neuroanatomical substrate for investigating the underlyi

257 amic area (LHA) was identified as a critical neuroanatomical substrate for motivated behavior.

258 The present study is aimed at providing a neuroanatomical substrate for the function of the lagena

259 Seeking to define a neuroanatomical substrate for these findings, we showed

260 lucinations in Parkinson's disease and whose neuroanatomical substrates may involve mesial temporal l

261 es and limited sample sizes, findings on the neuroanatomical substrates of ADHD have shown considerab

262 iousness achieves this function, and (c) the neuroanatomical substrates of conscious processes.

263 potentials and structural MRI to reveal the neuroanatomical substrates of early status recognition.

264 se three systems appear to map onto distinct neuroanatomical substrates, and depend on unique computa

265 d nouns and scrutinized their timecourse and neuroanatomical substrates.

266 rability causes developmental alterations in neuroanatomical systems and behaviors that are relevant

267 review summarizes both the efficacy and the neuroanatomical targets for DBS in four common neuropsyc

268 a combination of multichannel recording and neuroanatomical techniques to elucidate the laminar basi

269 Initial studies use neuroanatomical techniques to reveal that angiotensin ty

270 rain has been assessed previously by several neuroanatomical techniques.

271 The enormous potential of modern molecular neuroanatomical tools lies in their ability to determine

272 these projections, we used new computational neuroanatomical tools to identify 29 distinct functional

273 ues, we made small, single injections of the neuroanatomical tracer biotinylated dextran amine (BDA)

274 ng and electrophysiological mapping to guide neuroanatomical tracer injections into distal digit tip

275 We injected neuroanatomical tracers into the primary somatosensory a

276 Here we employed neuroanatomical tracers to map projections from the clau

277 trode recordings and injected with different neuroanatomical tracers to reveal patterns of thalamic p

278 Small amounts of neuroanatomical tracers were injected in these represent

279 comparing it against published results using neuroanatomical tracers.

280 Here we used a combination of neuroanatomical tracing and chemogenetic approaches to m

281 ddressed these issues using a combination of neuroanatomical tracing and chemogenetic approaches.

282 vivo and in vitro electrophysiological, and neuroanatomical tracing methods to define midbrain peria

283 ue cortical connectome derived from complete neuroanatomical tracing studies, a recent study in PLOS

284 ct (HC) and low-contact (LC) offspring using neuroanatomical tracing techniques.

285 this system in rats along with conventional neuroanatomical tracing with cholera toxin B to identify

286 Here, we used neuroanatomical tracing, immunofluorescence, and confoca

287 Here, neuroanatomical tracing, immunohistochemical, and behavi

288 ound that 139H is transported along the same neuroanatomical tracks as HY TME, adding to the growing

289 from the peripheral nervous system and along neuroanatomical tracts within the central nervous system

290 Findings indicate that neuroanatomical traits potentially impacted by bipolar d

291 tative MRI technique to better elucidate the neuroanatomical underpinnings of individual differences

292 and to identify the patterns of sex-related neuroanatomical variability associated with low or high

293 Moreover, the patterns of neuroanatomical variability carrying low or high ASD pro

294 n about how genetic variation contributes to neuroanatomical variability, and whether particular geno

295 sistent, stereotyped procedure may be due to neuroanatomical variation in the patients.

296 We found five independent patterns of neuroanatomical variation that related to clinical facto

297 ssed with the FreeSurfer software to compare neuroanatomical volumes and cerebral cortical thickness

298 and brain morphometry, including subcortical neuroanatomical volumes and regional cortical thickness.

299 In this cross-sectional study, neuroanatomical volumes associated with extinction in ma

300 widespread regions and significantly smaller neuroanatomical volumes, including total gray matter, ce