ライフサイエンスコーパス: neuroanatomy

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

2 and cross-species differences in functional neuroanatomy.

3 as begun to rekindle interest in fundamental neuroanatomy.

4 anatomy may also be extremes of typical male neuroanatomy.

5 as the sole method of establishing cognitive neuroanatomy.

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

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

8 als of cognitive neuropsychology and applied neuroanatomy.

9 it parallel changes in their adult olfactory neuroanatomy.

10 social mammal with complex human-like brain neuroanatomy.

11 defined with reference to human behavior and neuroanatomy.

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

13 rences from macaques can be applied to human neuroanatomy.

14 orly understood due to exceptionally complex neuroanatomy.

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

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

17 estimated probabilistically on the basis of neuroanatomy alone.

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

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

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

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

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

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

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

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

26 WF correlations between neuroanatomy and general cognitive ability were essentia

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

28 The functional neuroanatomy and intracellular signaling mechanisms unde

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

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

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

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

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

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

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

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

37 pplication of relationships between cellular neuroanatomy and synaptic connectivity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 However, neuroanatomy-based cladistics suggesting close phylogene

55 Neuroanatomy benefits from quantification of neural stru

56 Differences in neuroanatomy between discordant monozygotic twins might

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

110 The functional neuroanatomy of aversive anticipation was probed through

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 The neuroanatomy of stick insects is compared to that studie

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

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

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

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

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

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

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

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

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

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

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

148 The neuroanatomy of the proposed circuit is discussed as wel

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

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

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

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

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

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

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

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

157 The neuroanatomy of these neurons has been mapped in conside

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

182 The precise functional neuroanatomy underlying generation and representation of

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

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

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

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

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

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

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

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

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

192 A comparison of the neuroanatomy with other orthopteroid insects highlights

193 By combining quantitative neuroanatomy with targeted genetic manipulation of synap

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