ライフサイエンスコーパス: neuroanatomy

1 rences from macaques can be applied to human neuroanatomy.

2 orly understood due to exceptionally complex neuroanatomy.

3 tal nucleus" (RMTg) and report herein on its neuroanatomy.

4 and cross-species differences in functional neuroanatomy.

5 tical thickness, and, ultimately, functional neuroanatomy.

6 as begun to rekindle interest in fundamental neuroanatomy.

7 insights into normal and pathophysiological neuroanatomy.

8 anatomy may also be extremes of typical male neuroanatomy.

9 as the sole method of establishing cognitive neuroanatomy.

10 hat extent this heterogeneity is mirrored in neuroanatomy.

11 PS Powell was one of the founders of modern neuroanatomy.

12 sms to be isolated in terms of timing and/or neuroanatomy.

13 als of cognitive neuropsychology and applied neuroanatomy.

14 onmental contributions to SES differences in neuroanatomy.

15 ounting for each patient's unique functional neuroanatomy.

16 enues for an integrative approach to imaging neuroanatomy.

17 tructure and thus share a similar functional neuroanatomy.

18 n often be observed as changes in microscale neuroanatomy.

19 it parallel changes in their adult olfactory neuroanatomy.

20 social mammal with complex human-like brain neuroanatomy.

21 rities and differences in rodent and primate neuroanatomy.

22 defined with reference to human behavior and neuroanatomy.

23 PY-18, causes dramatic defects in C. elegans neuroanatomy.

24 been exploited in fields such as comparative neuroanatomy, abnormalities of the brain and mind, and e

25 on-human primates, suggesting differences in neuroanatomy across species.

26 estimated probabilistically on the basis of neuroanatomy alone.

27 ory signals generate evolutionary changes in neuroanatomy and behavior; however, few studies have inv

28 eal clade in which to study the evolution of neuroanatomy and behaviour.

29 atically reports of neural connectivity from neuroanatomy and brain imaging.

30 specific genetic factors can influence both neuroanatomy and cognitive capacity.

31 Nonhuman primate (NHP) neuroanatomy and cognitive complexity make NHPs ideal mo

32 structure (uncovered through advancements in neuroanatomy and connectomics) can impact on spatio-temp

33 to be an exceptional tool to study receptor neuroanatomy and correlate with NOP receptor function.

34 to be an exceptional tool to study receptor neuroanatomy and correlate with NOP receptor function.

35 a different purpose, they reveal details of neuroanatomy and cytoarchitecture.

36 transcriptomics in the context of advancing neuroanatomy and discuss how molecular neuroanatomy can

37 or improving our understanding of functional neuroanatomy and disruptions in psychiatric disorders.

38 atus of brain areas from the perspectives of neuroanatomy and electrophysiology.

39 equires a strong understanding of functional neuroanatomy and familiarity with the technical limitati

40 a nearly complete picture of the peripheral neuroanatomy and function of smell and taste in this ins

41 cies we now have a robust model of basic PVH neuroanatomy and function.

42 ven methods--commonplace in studies of human neuroanatomy and functional connectivity--provide a powe

43 WF correlations between neuroanatomy and general cognitive ability were essentia

44 ptor systems are situated within macro-scale neuroanatomy and how they shape emergent function remain

45 nt for autism found, clustering autism using neuroanatomy and identifying these strong connections ma

46 ging (MRI) provides useful information about neuroanatomy and improves detection of neuropathology.

47 use a simple model constrained by the known neuroanatomy and information processing properties of th

48 The functional neuroanatomy and intracellular signaling mechanisms unde

49 rovides important substrates for comparative neuroanatomy and molecular brain evolution studies.

50 fMRI and MEG, we characterize the functional neuroanatomy and neural dynamics of such scene-based obj

51 Thus, isolating the neuroanatomy and neurobiology of goal-directed action se

52 Our findings shed new light on the neuroanatomy and neurochemistry of ZI-located cells that

53 alysis assessed shared and disorder-specific neuroanatomy and neurofunction of inhibitory functions.

54 tative montages, which combined the cellular neuroanatomy and neurophysiology, suggested a circuit-le

55 to characterize different odorant receptors, neuroanatomy and odorant response properties of the earl

56 neering exploration of octopus arm molecular neuroanatomy and offering exciting new avenues in invert

57 Our results using combined neuroanatomy and optogenetic in vitro and in vivo show t

58 osaurus neglectus, in order to interpret the neuroanatomy and paleobiology of one of the last survivi

59 s proposed that is consistent with the known neuroanatomy and postulates differential projections of

60 The simple neuroanatomy and powerful genetic tools of C. elegans ha

61 able as they establish a causal link between neuroanatomy and resultant symptoms, lending insight int

62 TATEMENT Sex chromosome dosage (SCD) affects neuroanatomy and risk for psychopathology in humans.

63 promotes masculine sexual differentiation of neuroanatomy and sexual behavior in mammals.

64 Here, we investigated the links between neuroanatomy and sociality in free-ranging rhesus macaqu

65 generate a bilateral asymmetry in C. elegans neuroanatomy and suggest that left-right asymmetric epig

66 pplication of relationships between cellular neuroanatomy and synaptic connectivity.

67 Associations between neuroanatomy and task performance were assessed using ge

68 tems were considered based on their distinct neuroanatomy and their documented involvement in multipl

69 e then provided the first descriptions of DA neuroanatomy and tissue content in vole NAcc, and mating

70 uire high-resolution datasets to investigate neuroanatomy and validate the origins of image contrast

71 nclusion is consistent with nonhuman primate neuroanatomy and with existing face perception models.

72 being used to advance the field of molecular neuroanatomy, and also discusses emerging technologies t

73 ionships among X-chromosome gene expression, neuroanatomy, and cognitive-behavioral functions impaire

74 In Drosophila, the development, neuroanatomy, and function of intrinsic neurons of the M

75 osion of new information on the development, neuroanatomy, and possible functions of the mushroom bod

76 However, the mechanisms, underlying neuroanatomy, and specificity of this neuroanatomy are n

77 icroscopy are common techniques in arthropod neuroanatomy, and these methods often require time-consu

78 or the most part, the architecture, chemical neuroanatomy, and topological relationships of the compo

79 Digital Brain Zoo: datasets for comparative neuroanatomy; and Digital Pathologist: datasets for neur

80 in brain architecture using a computational neuroanatomy approach.

81 rlying neuroanatomy, and specificity of this neuroanatomy are not yet fully understood.

82 between organism and environment, not exotic neuroanatomy, are responsible for unique cognitive capac

83 that these lines will be valuable tools for neuroanatomy as well as for the elucidation of neuronal

84 at micro-CT is highly suitable for targeting neuroanatomy, as it reduces the risk of artifacts and is

85 This is because neonatal neuroanatomy, as opposed to genetic variation and sociod

86 al assumptions about sensorimotor functional neuroanatomy, as well as the role of alpha ERD as an ind

87 n particular, is there a distinct functional neuroanatomy associated with person knowledge?

88 into groups and measure the consistency with neuroanatomy at multiple levels.

89 However, neuroanatomy-based cladistics suggesting close phylogene

90 These indicate sex related sculpting of neuroanatomy begins early in development, before cortica

91 ongbirds using a comprehensive assessment of neuroanatomy, behavior, and neurophysiology.

92 Neuroanatomy benefits from quantification of neural stru

93 Differences in neuroanatomy between discordant monozygotic twins might

94 First, the authors compared neuroanatomy between outcome groups.

95 There are no differences in neuroanatomy between the three thoracic leg pairs, and t

96 , horse, and chimpanzee) widely differing in neuroanatomy, brain size, life span, and socioecology.

97 information will not only help inform feline neuroanatomy but also will serve as a reference standard

98 vestigated whether individual differences in neuroanatomy can also explain variation in moral judgmen

99 ncing neuroanatomy and discuss how molecular neuroanatomy can redefine mapping of the nervous system.

100 of the nervous system, such as behavior and neuroanatomy, can be utilized as a means to assess speci

101 ologists (n = 20) participating in the Emory NeuroAnatomy Carotid Training program underwent an instr

102 Early identification of such neuroanatomy changes can help to screen individuals acco

103 ociated with various phenotypic variables of neuroanatomy, cognition, lifestyle, sociodemographics, a

104 how differences in cognitive functioning and neuroanatomy compared with the general population.

105 dorsal raphe nucleus (DR) has a topographic neuroanatomy consistent with the idea that different par

106 recent anatomic studies of the periprostatic neuroanatomy continue to spur both advances and debate.

107 vely, maturational differences in functional neuroanatomy could exist despite similar performance.

108 tifying systematic individual differences in neuroanatomy could inform diagnosis and personalized int

109 lization hardware, software development, and neuroanatomy data enabled the translation of decades of

110 known about how they fit into the molecular neuroanatomy described above.

111 Together, these natural experiments in neuroanatomy, development, and genomics suggest that evo

112 ysis at the group level, when the underlying neuroanatomy does not represent the study population, gr

113 g the plasticity and diversity of functional neuroanatomy during development and suggest advances in

114 ns in branched mechanoreceptors, we combined neuroanatomy, electrophysiology and computation to analy

115 vention group and the control group in final neuroanatomy examination scores (mean [SD] score, 17.2 [

116 Left-right (L-R) asymmetries in neuroanatomy exist throughout the animal kingdom, with i

117 Through a combination of functional neuroanatomy, feeding, and electrophysiology studies in

118 In addition to defects in neuroanatomy, flies with reduced kismet expression show

119 olumetric postmortem investigations of human neuroanatomy for diagnostic, research, and educational p

120 Despite the importance of hemichordate neuroanatomy for testing hypotheses on deuterostome and

121 In this study, we characterized the neuroanatomy, frequency tuning, and neurophysiological r

122 ere traditionally attributed to differential neuroanatomy, functional differences might also arise fr

123 lex, exhibit left-right differences in their neuroanatomy, gene expression profiles and axonal projec

124 ith a better understanding of the functional neuroanatomy implicated in OCD, has resulted in improved

125 er, no past work has assessed whether infant neuroanatomy, important to stress regulation, moderates

126 eterogeneous neuroimaging findings to common neuroanatomy, improving localization of neuropsychiatric

127 GABA based on functional characteristics and neuroanatomy in a sample of 88 human participants (35 fe

128 ly informative in identifying the functional neuroanatomy in adolescents and young adults with BD (BD

129 ing and visualization of gene expression and neuroanatomy in an integrated manner.

130 Imaging revealed detailed neuroanatomy in brain, spinal cord, and DRG and was gene

131 d application of methods for high-throughput neuroanatomy in Drosophila using light microscopy.

132 nd pharmacological tools, as well as systems neuroanatomy in human fetuses and mouse models, to study

133 memory performance) would exhibit preserved neuroanatomy in key brain networks subserving memory.

134 in relation to what is known from classical neuroanatomy in laboratory animals.

135 of physical and mental health, cognition and neuroanatomy in male (n = 414) and female (n = 938) carr

136 ns the door to routine systematic studies of neuroanatomy in mouse models of human brain disorders.

137 he relationship between gene expressions and neuroanatomy in the developing mouse brain.

138 nsider the association between variations in neuroanatomy in velocardiofacial syndrome subjects and t

139 ed parallels with established mammalian HCRT neuroanatomy, including projections to the pineal gland,

140 te normal baseline synaptic transmission and neuroanatomy, indicating that ubiquitination may play a

141 a-IR may be utilized to study the functional neuroanatomy involved in the TNFalpha-mediated state-dep

142 Mapping neuroanatomy is a foundational goal towards understandin

143 However, it remains unclear if this neuroanatomy is causal, compensatory or otherwise correl

144 Information on chimpanzee neuroanatomy is essential for understanding the anatomic

145 Automated segmentation of CT neuroanatomy is feasible with a high degree of accuracy.

146 Although mature cerebellar neuroanatomy is well studied, understanding of its devel

147 ion with respect to connections and chemical neuroanatomy, it seemed of interest to determine whether

148 uia protensa, exhibiting the most compelling neuroanatomy known from the Cambrian.

149 urochemistry (dopamine, endogenous opioids), neuroanatomy (limbic system), and self-medication behavi

150 Our results merge insights from neuroanatomy, machine learning, and theoretical neurosci

151 we suggest that specific aspects of autistic neuroanatomy may also be extremes of typical male neuroa

152 indicating that, at least in some cases, the neuroanatomy may remain sufficiently intact so that corr

153 Evolutionary neuroanatomy must integrate two different sources of inf

154 evelopment may interact with rTMS, including neuroanatomy, neural circuit network topography, neuropl

155 cterized by subtle abnormalities of cortical neuroanatomy, neurochemistry and function.

156 f the traditional fields of neurophysiology, neuroanatomy, neurochemistry, and behavior, and we empha

157 cent studies addressing the neuropsychology, neuroanatomy, neurochemistry, and molecular biology of A

158 d, and contains reprints of contributions to neuroanatomy, neuropathology, and to disorders that affe

159 olution and the need to integrate studies of neuroanatomy, neurophysiology and behaviour.

160 rent state of understanding of human cardiac neuroanatomy, neurophysiology and pathophysiology in spe

161 n that incorporates integration of data from neuroanatomy, neurophysiology, and behavioral studies, u

162 rent state of understanding of human cardiac neuroanatomy, neurophysiology, pathophysiology in specif

163 We compared the neuroanatomy of 15 children (mean age:13+/-2) with WS an

164 Thus, we studied the neuroanatomy of 22qDS children using fully automated vox

165 e these questions by comparing the songs and neuroanatomy of 49 species from 17 families of songbirds

166 Here we investigate the developmental neuroanatomy of a putative basal arthropod, the pycnogon

167 ly little traditional work on the functional neuroanatomy of aggression.

168 el assay in mice for defining the functional neuroanatomy of appetitive conditioning and identify spe

169 In addition, we examined the neuroanatomy of ascending pathways from the antenna II a

170 However, it is unclear whether the neuroanatomy of ASD also shows a similar continuum in th

171 , the current study investigated the complex neuroanatomy of autism and linked between-group differen

172 We found that the neuroanatomy of autism differed between adult males and

173 al sex at the level of the brain: (i) is the neuroanatomy of autism different in males and females? a

174 rent in males and females? and (ii) does the neuroanatomy of autism fit predictions from the 'extreme

175 sign, and by spatial overlap analyses of the neuroanatomy of autism in males and females.

176 This makes the neuroanatomy of autism inherently difficult to describe.

177 Our results confirm the hypothesis that the neuroanatomy of autism is truly multidimensional, and af

178 e will be necessary for clarification of the neuroanatomy of autism.

179 The functional neuroanatomy of aversive anticipation was probed through

180 To translate our knowledge about neuroanatomy of bipolar disorder (BD) into a diagnostic

181 song learning during development affects the neuroanatomy of brain regions involved in song productio

182 development we re-examined the behaviour and neuroanatomy of Ccdc88a knockout pups.

183 d impressive developments in documenting the neuroanatomy of conditioned fear in animals.

184 In this study, we examined the neuroanatomy of dyslexic (14 males, four females) and co

185 cy associated with TS affects the functional neuroanatomy of early visual areas, and suggest that inv

186 parallelism observed in the adult olfactory neuroanatomy of ecological specialists extends more broa

187 Here we describe the external gross neuroanatomy of Einstein's entire cerebral cortex from 1

188 ly relevant research on the neurobiology and neuroanatomy of explore/exploit decision making, and dis

189 patients and 1256 controls), to unravel the neuroanatomy of FTD in schizophrenia and using virtual h

190 for persisting differences in the functional neuroanatomy of handwriting between right-handers and co

191 tching handedness, we studied the functional neuroanatomy of handwriting in 11 adult "converted" left

192 nner field strength, however, the functional neuroanatomy of hippocampal-dependent scene perception i

193 n of bodily arousal and suggest a functional neuroanatomy of how cognitive states are integrated with

194 This study investigated the functional neuroanatomy of inner speech and auditory verbal imagery

195 s of the heteromodal regions involved in the neuroanatomy of language.

196 pattern and timing by which the distinctive neuroanatomy of living birds was assembled.

197 al model was ultimately used to identify the neuroanatomy of long-term declarative memory (sometimes

198 ere we review this work with emphasis on the neuroanatomy of medial temporal lobe and diencephalic st

199 e of the nervous system based on the crossed neuroanatomy of motor and sensory systems.

200 ately converge into a unified picture of the neuroanatomy of musical expertise.

201 istent and controversies-free picture of the neuroanatomy of musical expertise.

202 sks and are surprising given the far simpler neuroanatomy of nautilus.

203 To review the neurophysiology and neuroanatomy of normal aging and the recent recommendati

204 ng learned about the neurophysiology and the neuroanatomy of normal aging.

205 maging was used to investigate the mediating neuroanatomy of obsessive-compulsive disorder symptoms.

206 Here, we exploit the unique functional neuroanatomy of olfaction with its ipsilateral stimulus

207 DPH diaphorase histochemistry to compare the neuroanatomy of precompetent (including specimens 6, 8,

208 ns during development alters the macroscopic neuroanatomy of primary or auditory association cortices

209 review the current literature evaluating the neuroanatomy of prostate and operative strategies for be

210 tures have been previously implicated in the neuroanatomy of schizophrenia.

211 different semantic features according to the neuroanatomy of sensory and motor systems.

212 , including the relative size and functional neuroanatomy of spinal projections.

213 The neuroanatomy of stick insects is compared to that studie

214 onance imaging to investigate the functional neuroanatomy of syntactic comprehension in 51 individual

215 for comparative study, we have described the neuroanatomy of the amphidial sensillae of P. trichosuri

216 shed animal model elucidating the functional neuroanatomy of the amygdala and hippocampus in emotiona

217 he authors sought to identify the functional neuroanatomy of the brain response to visual heroin-rela

218 of innate and learned guidance based on the neuroanatomy of the central complex (CX), adapted to con

219 , we undertook a detailed examination of the neuroanatomy of the chemosensory system of P. pacificus.

220 f OCD and offer additional insights into the neuroanatomy of the disorder that were not apparent from

221 ates, our templates better characterized the neuroanatomy of the EMA collision-sport athletes, reduce

222 ic maps and recent studies of the functional neuroanatomy of the FEF been determined.

223 ngs provide new insights into the functional neuroanatomy of the human amygdala and converge with con

224 mparative neuroimaging study of sex-specific neuroanatomy of the human and mouse brain.

225 The functional neuroanatomy of the human brain is known to vary between

226 re during development alters the macroscopic neuroanatomy of the human insula.

227 Here we characterize the neuroanatomy of the larval SEG in terms of tracts, commi

228 The functional neuroanatomy of the mammalian respiratory network is far

229 on the pre-Botzinger complex, the functional neuroanatomy of the neural circuits that generate expira

230 n leaving the deutocerebrum, we examined the neuroanatomy of the projection neuron pathways of three

231 The neuroanatomy of the proposed circuit is discussed as wel

232 a reliable tool for assessing the functional neuroanatomy of the respiratory network in health and di

233 (r) LFPs could be used to map the functional neuroanatomy of the respiratory network.

234 Neuroanatomy of the retina reflects adaptation and accli

235 es of the hemispheres, and another shows the neuroanatomy of the right (exposed) insula.

236 draw on recent discoveries in the functional neuroanatomy of the serotonergic dorsal raphe nucleus (D

237 hese studies examined the neurochemistry and neuroanatomy of the serotonin (5-HT) system innervating

238 been reported for this species, the relevant neuroanatomy of the serotonin system within mouse hypoth

239 ventral components, mirroring the functional neuroanatomy of the spinal cord and likely reflecting se

240 opamine agonism, and changes in the chemical neuroanatomy of the striatum that are consistent with al

241 In this study the neuroanatomy of the subgenual organ complex of stick ins

242 with Turner syndrome affects the functional neuroanatomy of the visual cortex.

243 and relates to individual differences in the neuroanatomy of these areas.

244 The neuroanatomy of these neurons has been mapped in conside

245 The shared functional neuroanatomy of these processes has been demonstrated in

246 The neurophysiology and neuroanatomy of these reflex pathways are well understoo

247 continued exploration of the transcriptional neuroanatomy of these unique neurons will be vital for p

248 er the previous knowledge on the microscopic neuroanatomy of this crucial reference species.

249 autonomic control of cardiac output, but the neuroanatomy of this system is not well understood.

250 ral information for analyzing the functional neuroanatomy of visual attention.

251 ) and atypical (clozapine (CLZ)) APDs on the neuroanatomy of wild-type (WT) and dopamine D3-knockout

252 d not cause gross alterations in hippocampal neuroanatomy or basal synaptic transmission.

253 awareness could not be explained by retinal neuroanatomy or previous studies of peripheral visual pr

254 el based on primate large-scale white matter neuroanatomy, our computational and mathematical results

255 Tac mice, in addition to displaying aberrant neuroanatomy, perform poorly on many behavioral tasks, r

256 Data from neurophysiology, neuroimaging, and neuroanatomy point to a division of labor within the med

257 Recent findings in neuroanatomy provide a basis for new approaches of cellu

258 group euarthropods, with gene expression and neuroanatomy providing strong evidence that the paired,

259 The way in which normal variations in human neuroanatomy relate to brain function remains largely un

260 How differences in neuroanatomy relate to the similarities in cognition bet

261 RI scans with the details of human brainstem neuroanatomy represented in atlases, which are mostly ba

262 However, the cerebral functional neuroanatomy representing and mediating peripheral auton

263 orphological evaluation of Bbs1 mutant brain neuroanatomy revealed ventriculomegaly of the lateral an

264 s that understanding the neurophysiology and neuroanatomy should be part of the standard working know

265 eings in physiology, cognitive capabilities, neuroanatomy, social complexity, reproduction, and devel

266 protein in the regulation of brain size and neuroanatomy, specifically in male mice.

267 iological recordings, and ex vivo functional neuroanatomy studies were performed.

268 rch into the brain led him to discoveries in neuroanatomy (such as those of the frontal sinus and men

269 The role of anxiety in Alzheimer's disease neuroanatomy, symptomology, and progression is used as a

270 l GMV ROIs were estimated with computational neuroanatomy techniques applied to high resolution, T1-w

271 f interest were estimated with computational neuroanatomy techniques applied to high-resolution, T1-w

272 w-dimensional space are more consistent with neuroanatomy than those in the original space.

273 ut do not affect sensory modalities or brain neuroanatomy that are requisite for conditioning.

274 r, we recently demonstrated using functional neuroanatomy that only a few limbic structures including

275 support behavior must respect the underlying neuroanatomy that shapes the functional properties of se

276 In addition, we observed changes in neuroanatomy that were caused by these 15 mutations, ind

277 From neuroanatomy, the topology of the mammalian brain can be

278 al recordings in brain slices with molecular neuroanatomy to identify distinct ion channel targets fo

279 distribution of these proteins as a tool in neuroanatomy to interpret developmental aspects of many

280 neurobiology, ranging from detailed in vivo neuroanatomy to the measurement of specific molecular ta

281 The precise functional neuroanatomy underlying generation and representation of

282 ttle, however, is known about the functional neuroanatomy underlying interoception in children.

283 Previously , we measured the cellular neuroanatomy underlying synaptic connectivity in Drosoph

284 cience is the extent to which the functional neuroanatomy underlying task performance differs in adul

285 The study of neuroanatomy using imaging enables key insights into how

286 n diffusion tensor imaging and computational neuroanatomy was developed to efficiently and quantitati

287 Inspired by classical neuroanatomy, we classified inhibitory neurons based on

288 Although Snx27(+/-) mice have grossly normal neuroanatomy, we found defects in synaptic function, lea

289 By neuroanatomy, we identified three major subtypes of DR n

290 nitive psychology, systems neuroscience, and neuroanatomy, we propose two accounts of how dimensional

291 ysis, and parallel perturbations to cortical neuroanatomy were identified via imaging.

292 By recasting neuroanatomy, which is traditionally viewed as a problem

293 cs, as well as developmental and comparative neuroanatomy, which together suggest that despite many e

294 HD, but also to researchers of computational neuroanatomy who may not have access to such large datas

295 Combining in vivo electrophysiology and neuroanatomy with behavioral testing, we show that G(PFC

296 ion-based maps were compared with underlying neuroanatomy with cytochrome oxidase staining.

297 A comparison of the neuroanatomy with other orthopteroid insects highlights

298 By combining quantitative neuroanatomy with targeted genetic manipulation of synap

299 mple principle to connect a concrete fact of neuroanatomy with the abstract concept of information: e

300 CT can provide additional insight into gross neuroanatomy without damaging rare and precious specimen