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 Although the neuroanatomical abnormalities have been identified in pa

3 ical disease course and different underlying neuroanatomical abnormalities than patients with the mor

4 riguingly, both visible gait alterations and neuroanatomical abnormalities throughout the brain diffe

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

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

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

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

9 We show that UPS induces several neuroanatomical alterations that were seen in both sexes

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

11 Neuroanatomical analysis and two-photon calcium imaging

12 Neuroanatomical analysis revealed a reduced density of d

13 Neuroanatomical analysis suggested greater lateral ventr

14 with extracellular stimulation and post hoc neuroanatomical analysis to investigate intrinsic and af

15 iple simultaneous patch-clamp recordings and neuroanatomical analysis.

16 This neuroanatomical and behavioral characterization of Y1R-e

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

18 However, the neuroanatomical and biochemical substrates through which

19 Lack of precision in both neuroanatomical and clinical boundaries have likely cont

20 nges in type 1 diabetes (T1D) and both their neuroanatomical and clinical features are less well char

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 This review provides a neuroanatomical and functional perspective of selected r

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

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

26 Here, through neuroanatomical and immunohistochemical analysis, we ide

27 We employed neuroanatomical and in vivo electrophysiological techniq

28 ent clinical and preclinical findings on the neuroanatomical and neurochemical adaptations triggered

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

30 of opioids, including sex differences in the neuroanatomical and neurophysiological characteristics o

31 ic startle response, consistent with altered neuroanatomical and physiological properties.

32 ulthood were able to correct electrographic, neuroanatomical and synaptic alterations of Ophn1 defici

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

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

35 ohistochemical approaches to investigate the neuroanatomical associations between tanycytes and neura

36 Neuroanatomical associations were assessed using blinded

37 her crustaceans, and with Hexapoda, specific neuroanatomical attributes of the protocerebrum, the mos

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

39 The neuroanatomical bases of autism spectrum disorder remain

40 The neuroanatomical basis behind acupuncture practice is sti

41 However, it is unknown whether a neuroanatomical basis exists for this variability.

42 we seek in the present work to decipher the neuroanatomical basis for an interplay between stress an

43 onological and lexical-semantic reading, the neuroanatomical basis for effects of lexicality (word vs

44 Altogether, our results lay the neuroanatomical basis for tanycyte/neural cell interacti

45 ivity in the nucleus accumbens represent the neuroanatomical basis for the impairment in aversive lim

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

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

48 ed the underlying experiential, genetic, and neuroanatomical basis of mutual eye gaze variation in ad

49 We review the central tenets and neuroanatomical basis of the global neuronal workspace (

50 foundation for a better understanding of the neuroanatomical basis of the stress-related feeding beha

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

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

53 cerebral cortical connections, together with neuroanatomical, brain imaging, and clinical observation

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

55 sence of fossil brain tissue, the underlying neuroanatomical changes as well as their genetic bases r

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

57 These neuroanatomical changes help explain functional phenotyp

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

59 We identified neuroanatomical changes in the brains of mice deficient

60 ous system (CNS) FAO did not result in gross neuroanatomical changes or systemic differences in metab

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

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

63 Group-level functional neuroanatomical changes were assessed using statistical

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

65 zygous mouse model (Kdm4b(+/-)), focusing on neuroanatomical changes.

66 Brain centers possessing a suite of neuroanatomical characters that define mushroom bodies o

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

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

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

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

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

72 ng approach to characterize the clinical and neuroanatomical complexity of CT in a larger, transdiagn

73 The complex neuroanatomical connections of the inferior colliculus (

74 associated with energy balance would possess neuroanatomical connections to permit coordination of mu

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

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

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

78 not reducible to specific brain regions and neuroanatomical connectivity.

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

80 Our results provide potential neuroanatomical correlates for impaired familiarity perc

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

82 -based morphometry was performed to identify neuroanatomical correlates of abnormal pain perception.

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

84 dult chimpanzees, and is the first to report neuroanatomical correlates of mutual eye gaze variation

85 Our study highlights key neuroanatomical correlates of schizophrenia genetic risk

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

87 Finally, we identify neuroanatomical correlates of SES that exist above and b

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

89 om a dimensional perspective and to identify neuroanatomical correlates of traits and behaviors that

90 tanding of their pathophysiologic causes and neuroanatomical correlates remains limited.

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

92 sible neurodevelopmental origins but unknown neuroanatomical correlates.

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

94 Building upon neuroanatomical data and studies investigating direct ne

95 Thus, it is not surprising that neuroanatomical data are available for only one genus wi

96 profound diversity among ctenophores, basal neuroanatomical data are limited to representatives of t

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

98 We analyzed behavioral and neuroanatomical data from 402 humans (212 males; 190 fem

99 Large-scale behavioral and neuroanatomical data from neurologic patients with focal

100 Neuroanatomical data indicate PPARgamma localization in

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

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

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

104 eletion of murine Trim9 or Trim67 results in neuroanatomical defects and striking behavioral deficits

105 e excitatory neurons of the forebrain caused neuroanatomical defects, fine motor deficits, increased

106 ciated with GDD/ intellectual disability and neuroanatomical defects.

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

108 transgenic shh-GFP line revealing increased neuroanatomical detail due to the progressed differentia

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

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

111 tlases provide a useful tool for identifying neuroanatomical differences and similarities between hum

112 Both neuroanatomical differences and the functional nausea-br

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

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

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

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

117 IFICANCE STATEMENT Whereas fMRI evidence for neuroanatomical dissociations between phonological and l

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

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

120 Morphological diversity and neuroanatomical distribution of pTDP-43 accumulations al

121 s older subjects), and relatively restricted neuroanatomical distribution of TDP-43 proteinopathy.

122 reveal that NCoR1 and SMRT share an overall neuroanatomical distribution, and are detected in both e

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

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

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

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

127 However, little neuroanatomical evidence consistent with this account ha

128 These findings provide novel neuroanatomical evidence for incorporating FPl in models

129 tion of 5-HT nuclei in teleosts and provides neuroanatomical evidence for serotonin as a modulator of

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

131 This work provides converging behavioral and neuroanatomical evidence that working memory is a key me

132 ization and integration of results from many neuroanatomical experiments.

133 this study, we evaluated the behavioural and neuroanatomical factors associated with better speech fl

134 ronic pain is predetermined by corticolimbic neuroanatomical factors.

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

136 To date, unequivocal neuroanatomical features have been demonstrated neither

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

138 Neuroanatomical features related to the enhanced sensory

139 nitrergic system of Neoceratodus shares many neuroanatomical features with tetrapods and particularly

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

141 t samples was based on plausible and similar neuroanatomical features.

142 The underlying neuroanatomical findings have not been described.

143 , or cognitive factors, each with a distinct neuroanatomical foundation.

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

145 ss clear, therefore we aimed to identify the neuroanatomical, functional, and behavioral features of

146 We describe the neuroanatomical-functional paradox in the context of tra

147 This neuroanatomical-functional paradox is likely to contribu

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

149 step towards parsing factors that influence neuroanatomical heterogeneity in ASD and is a potential

150 We report neuroanatomical heterogeneity in populations of the sero

151 (LDTg) expresses GLP-1Rs and functions as a neuroanatomical hub connecting the nucleus tractus solit

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

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

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

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

156 We used neuroanatomical,in vitroandin vivoelectrophysiological,

157 Our findings suggest that neuroanatomical information may provide generalizable di

158 Preserved neuroanatomical integrity in these networks is associate

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

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

161 is atlas can serve as a reference for future neuroanatomical investigations of subterranean mammals.

162 fine raphe subgroups based on both stringent neuroanatomical landmarks as well as quantitative cell m

163 at integrate the vast majority of Drosophila neuroanatomical light microscopy and electron microscopy

164 al pathway-tracing evidence was found in the neuroanatomical literature for the presence or absence o

165 The dataset was curated expertly from the neuroanatomical literature using experimental axonal pat

166 The neuroanatomical localization of g/Gwm provided the stron

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

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

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

170 molecular map that can be superimposed on a neuroanatomical map to permit molecular and genetic inte

171 Viral tracers are important tools for neuroanatomical mapping and genetic payload delivery.

172 In marked contrast to Fos immunoreactivity, neuroanatomical mapping of Neurobiotin-filled cells from

173 Functional neuroanatomical mapping revealed that vagal preganglioni

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

175 Advances in neuroanatomical mapping, genetically specific neuronal m

176 characterize neurobehavioural correlates of neuroanatomical measures implicated in the pathophysiolo

177 processes, our findings elucidate potential neuroanatomical mediators of the association between SES

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

179 een established many years ago using classic neuroanatomical methods, such as immunocytochemistry and

180 44 rats and will thus provide an appropriate neuroanatomical model for researchers working with this

181 and out-of-sample predictive accuracy of the neuroanatomical model, and its regional contributors.

182 Current neuroanatomical models of speech processing in adults pr

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

184 have coalesced around the view that distinct neuroanatomical networks subserve semantic and phonologi

185 nd sex-dependent patterns of CT, distributed neuroanatomical networks, and clinical profiles.

186 Here, we used neuroanatomical, neuropharmacological, and chemogenetic

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

188 s functional hierarchy is often reflected in neuroanatomical organization.

189 However, the neuroanatomical origins of interindividual variability i

190 Here we analyze 118 neuroanatomical parameters in 1,566 mutant mouse lines a

191 scriptionally-distinct clusters that exhibit neuroanatomical parcellation within MB subdivisions and

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

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

194 This neuroanatomical pattern is consistent with an existing,

195 onset neurodegeneration with a stereotypical neuroanatomical pattern of progression and an associated

196 male decrepit mice, we found a stereotypical neuroanatomical pattern of progression of the lesion alo

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

198 protein (eGFP) reporter mouse, combined with neuroanatomical, pharmacological, and behavioral approac

199 d identify 198 genes whose disruptions yield NeuroAnatomical Phenotypes (NAPs), mostly affecting stru

200 bust associations have been observed between neuroanatomical phenotypes and known genetic risk factor

201 to a causative understanding of the role of neuroanatomical plasticity for functional recovery is fu

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

203 Our work provides a complete neuroanatomical platform for future studies of the adult

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

205 atter Function will enable improved clinical-neuroanatomical predictions for brain lesion studies and

206 The present study investigates neuroanatomical predictors for trajectories of future al

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

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

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

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

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

212 ibuted to differences in the location of the neuroanatomical regions being stimulated.

213 We then analyzed 147 neuroanatomical regions for labeled boutons in every bra

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

215 ical and atypical APD administration induced neuroanatomical remodeling of regions rich in D3 recepto

216 tern similarity scores (a brain-MRI measured neuroanatomical risk for Alzheimer's disease), developed

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

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

219 Neuroanatomical shape descriptors, however, can represen

220 Neuroanatomical shape differences of the subcortex and f

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

222 These results highlight the neuroanatomical signature of interindividual variability

223 The present study exploratorily investigates neuroanatomical signatures for developmental trajectorie

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

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

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

227 ncogenic processes show striking age-related neuroanatomical specificity (highlighting their close in

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

229 A recent neuroanatomical staging scheme of amyotrophic lateral sc

230 n, magnetic resonance imaging, and classical neuroanatomical staining to provide a broad overview of

231 Employing a range of neuroanatomical stains, we detail the organization of th

232 Here, we describe the neuroanatomical structure of this center, called the ren

233 tion of homologies at multiple levels beyond neuroanatomical structure.

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

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

236 Neuroanatomical studies are rarely frontline news, but t

237 Nonhuman primate neuroanatomical studies have identified a cortical pathw

238 ears has allowed a resurgence of comparative neuroanatomical studies in humans and other primate spec

239 Neuroimaging-based neuroanatomical studies of ASD have often reported incon

240 Using male Agtr1a-Cre mice, neuroanatomical studies reveal that AT1aR neurons in the

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

242 or linking neuroimaging findings to a common neuroanatomical substrate and localizing therapeutic tar

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

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

245 rodent socioemotional behaviors and may be a neuroanatomical substrate for integration of emotion wit

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

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

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

249 These results lend insight into the causal neuroanatomical substrate of cervical dystonia, demonstr

250 ry modality, lending insight into the causal neuroanatomical substrate of hallucinations.

251 tiple different brain locations, leaving the neuroanatomical substrate unclear.

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

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

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

255 ol mental information, and that the critical neuroanatomical substrates of g and working memory inclu

256 Here, we investigate neuroanatomical substrates of melatonin-dependent vocal-

257 sion/anorexia nervosa) = 76) to identify the neuroanatomical substrates of optimal clinical response.

258 elf-administration procedures to investigate neuroanatomical substrates that mediate the effects of P

259 ed cognitions may be underpinned by distinct neuroanatomical substrates.

260 s along with elucidation of their respective neuroanatomical substrates.

261 We investigated neuroanatomical subtypes in a multi-institutional multi-

262 e used to identify distinct and reproducible neuroanatomical subtypes of schizophrenia.

263 Two distinct neuroanatomical subtypes were found.

264 covered two distinct and highly reproducible neuroanatomical subtypes.

265 Initial studies use neuroanatomical techniques to reveal that angiotensin ty

266 Advances in molecular neuroanatomical tools have expanded the ability to map i

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

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

269 We injected neuroanatomical tracers into specified locations in each

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

271 Small amounts of neuroanatomical tracers were injected in these represent

272 agC allowed the correlative visualization of neuroanatomical tracers within their ultrastructural vol

273 comparing it against published results using neuroanatomical tracers.

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

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

276 Anterograde and retrograde neuroanatomical tracing confirmed the connectivity of th

277 Neuroanatomical tracing identified a multiorder connecti

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

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

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

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

282 xes in male and female rats using a range of neuroanatomical tracing, reflex physiology, and chemogen

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

284 sing a combination of morphometric analysis, neuroanatomical tract-tracing, and intracellular neurona

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

286 Findings indicate that neuroanatomical traits potentially impacted by bipolar d

287 Previous neuroimaging studies examining the neuroanatomical underpinnings of 22q11.2DS show alterati

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

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

290 There is both clinical and neuroanatomical variability at the single-subject level

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

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

293 Neuroanatomical variation is not simply driven by brain

294 Neuroanatomical variation is plainly visible across bree

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

296 Four novel patterns of neuroanatomical variation that related to phenotypic var

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