ライフサイエンスコーパス: cerebral hemisphere

1 induced by controlled cortical impact on one cerebral hemisphere.

2 ctions of PV are with S2 and PV of the other cerebral hemisphere.

3 mm min(-1), respectively; n = 5) across the cerebral hemisphere.

4 f the laminar architecture of the developing cerebral hemisphere.

5 zed by epilepsy and degeneration of a single cerebral hemisphere.

6 at extend over nearly the full length of the cerebral hemisphere.

7 gion near the temporal pole of the mammalian cerebral hemisphere.

8 stinguish it from the medial boundary of the cerebral hemisphere.

9 activity of the right (language nondominant) cerebral hemisphere.

10 ning across the lateral surface of the right cerebral hemisphere.

11 zations can spread widely across the injured cerebral hemisphere.

12 y movable microelectrodes spanning an entire cerebral hemisphere.

13 died in a patient who was born with only one cerebral hemisphere.

14 r degeneration primarily affecting the right cerebral hemisphere.

15 r patients with lesions situated in the left cerebral hemisphere.

16 losum is the major commissure connecting the cerebral hemispheres.

17 ions between the ectoderm and the developing cerebral hemispheres.

18 in and incorporate into the neocortex of the cerebral hemispheres.

19 onal transfer of information between the two cerebral hemispheres.

20 nvolved receive their motor output from both cerebral hemispheres.

21 in, and biological features of, normal human cerebral hemispheres.

22 fiber tract that connects the left and right cerebral hemispheres.

23 and astrogliosis in dorsal striatum in both cerebral hemispheres.

24 predominantly in the posterior region of the cerebral hemispheres.

25 n the mammalian brain, linking the bilateral cerebral hemispheres.

26 ural and functional connectivity between the cerebral hemispheres.

27 rved postmortem chimpanzee (Pan troglodytes) cerebral hemispheres.

28 rized by overgrowth of either one of the two cerebral hemispheres.

29 of the leptomeninges over large areas of the cerebral hemispheres.

30 olves incomplete or failed separation of the cerebral hemispheres.

31 acterized by an incomplete separation of the cerebral hemispheres.

32 n of axonal projections that connect the two cerebral hemispheres.

33 cerebral arteries serving the left and right cerebral hemispheres.

34 non-motor cortical regions within and across cerebral hemispheres.

35 needed for the expansion and bifurcation of cerebral hemispheres.

36 hic affecting the spine, cranial nerves, and cerebral hemispheres.

37 ined as the incomplete separation of the two cerebral hemispheres.

38 e neuroendocrine system from any part of the cerebral hemispheres.

39 oss after seizures and (b) with a more focal cerebral hemisphere abnormality usually due to vascular

40 Does complete removal of a cerebral hemisphere affect either of these processes?

41 matter, in terms of tissue volume, from the cerebral hemispheres after traumatic brain injury.

42 trol was found in language areas of the left cerebral hemisphere along the Sylvian fissure.

43 most of the external morphology of the right cerebral hemisphere and a fragment of fossilized face th

44 bral nuclei form the ventral division of the cerebral hemisphere and are thought to play an important

45 Innervated regions in the cerebral hemisphere and brainstem fall into nine general

46 cessing was strongly lateralized to the left cerebral hemisphere and involved a network of regions in

47 ade to demonstrate the medial surface of the cerebral hemisphere and the medial wall of the lateral v

48 omotopic and other locations in the opposite cerebral hemisphere and to a surrounding array of eight

49 g on the neurons and neuroglial cells in the cerebral hemispheres and associated fiber tracts of the

50 imals exhibit a reduction in the size of the cerebral hemispheres and associated structures.

51 fferent and afferent connections between the cerebral hemispheres and between the cortex and thalamus

52 ificant age-related differences in volume of cerebral hemispheres and caudate nuclei (controls, but n

53 ray of cerebral cortical layering, fusion of cerebral hemispheres and cerebellar folia, and aberrant

54 sensory-motor functions, and suprasegmental cerebral hemispheres and cerebellum.

55 The corpus callosum connects cerebral hemispheres and is the largest axon tract in th

56 s; in mice lacking Foxg1, development of the cerebral hemispheres and olfactory epithelium (OE) is se

57 ereby limits neuronal trafficking across the cerebral hemispheres and reduces input to cortical inhib

58 is a reduction in white matter volume in the cerebral hemispheres and structural abnormalities in mye

59 rectomy (i.e. surgical removal of one entire cerebral hemisphere) and 10 age- and sex-matched control

60 l cells (sensory ganglia and outer aspect of cerebral hemispheres) and glial cells (radial glia, sate

61 izures, progressive degeneration of a single cerebral hemisphere, and autoimmunity directed against g

62 ch-motor regions of the non-dominant (right) cerebral hemisphere, and extend this theory to include t

63 t of marginal zone components, fusion of the cerebral hemispheres, and scalloping of the dentate gyru

64 fibre tract in the brain, connecting the two cerebral hemispheres, and thereby facilitating the integ

65 The cerebellum and cerebral hemispheres appear to have evolved reciprocally

66 s originating from the contralesional intact cerebral hemisphere are capable of sprouting into the de

67 The human left and right cerebral hemispheres are anatomically and functionally a

68 the rest of the brain (and, conversely, the cerebral hemispheres are smaller with respect to the cer

69 The two cerebral hemispheres are specialised for different cogni

70 Diffuse astrocytomas of the adult cerebral hemispheres are unique among tumours in human b

71 amining the connectional organization of the cerebral hemispheres as a whole (right and left cerebral

72 n the perisylvian area of the left and right cerebral hemispheres, as well as in the frontal and occi

73 developed marked infarcts in the ipsilateral cerebral hemisphere at 24 hr and showed significant loss

74 by sleeping with only one eye closed and one cerebral hemisphere at a time.

75 ight ratios of ipsilateral and contralateral cerebral hemispheres at 12 hrs, 24 hrs, or 2, 3, or 7 da

76 ight ratios of ipsilateral and contralateral cerebral hemispheres at 48 hrs postischemia.

77 re consistent with the known predominance of cerebral hemisphere axonal injury in cardiac arrest and

78 usion, fibrin accumulates in the ipsilateral cerebral hemisphere, based upon immunoblotting, and loca

79 hyperintensities in the white matter of the cerebral hemispheres, brainstem, cerebellum, and cervica

80 ntral nervous system (CNS) that were high in cerebral hemispheres but progressively decreased toward

81 ive of edema in the posterior regions of the cerebral hemispheres, but the changes often involved oth

82 These data suggest both cerebral hemispheres can benefit from supportive sentenc

83 sed by about 50% the weight loss of the left cerebral hemisphere caused by hypoxia-ischemia in neonat

84 Brain structures investigated included the cerebral hemispheres, cerebral cortex, diencephalon, cau

85 Maps in each cerebral hemisphere code information from the opposite s

86 Nearly every tissue section from bilateral cerebral hemispheres contained either macroscopic or mic

87 e stimulus and that may be controlled by the cerebral hemisphere contralateral to the limb.

88 Virtually all parts of the cerebral hemispheres contribute to a triple descending p

89 of 50 fetuses, and the medial surface of the cerebral hemisphere could be traced posteriorly around t

90 The surgical disconnection of the cerebral hemispheres creates an extraordinary opportunit

91 the corpus callosum, cortical axons from one cerebral hemisphere cross the midline to reach their tar

92 that resulted in holoprosencephaly (a single cerebral hemisphere), cyclopia (a single midline eye), a

93 In ECMO animals, cerebral blood flow (cerebral hemispheres) decreased from a baseline measurem

94 brain, or it can alternate over time between cerebral hemispheres, depending on the species.

95 Although the left and right human cerebral hemispheres differ both functionally and anatom

96 coarse coding hypothesis postulates that the cerebral hemispheres differ in their breadth of semantic

97 Schizophrenia may involve the two cerebral hemispheres differentially.

98 omatic mutations that affect each developing cerebral hemisphere differently with more neurons than e

99 onous activation of cortical loci in the two cerebral hemispheres during development leads to the sta

100 ient and symmetrically in the cortex of both cerebral hemispheres except for precentral gyri in the s

101 As the cerebral hemispheres expand, they extend caudally, passi

102 human forebrain, and in its severe form, the cerebral hemispheres fail to completely separate into tw

103 of the human forebrain and midface where the cerebral hemispheres fail to separate into distinct left

104 itudinal changes in network activity in each cerebral hemisphere, focusing specifically on the "presy

105 ls of N434A, but not H435A, decreased in the cerebral hemispheres following bilateral injection into

106 h with defects in neurulation, fusion of the cerebral hemispheres, formation of the great forebrain c

107 And yet, even though each cerebral hemisphere has its own set of capacities, with

108 A recent study of a child born with one cerebral hemisphere has revealed an extreme developmenta

109 Within the cerebral hemispheres, hsp110 is present in neurons in al

110 demonstrated along the medial surface of the cerebral hemisphere in 36 (72%) of 50 fetuses, and the m

111 processing in the left compared to the right cerebral hemisphere in nondeficit schizophrenia.

112 ning across the lateral surface of the right cerebral hemisphere in persons at high risk.

113 n arises from the dominant role of the right cerebral hemisphere in regulating attention.

114 Understanding the role of the unaffected cerebral hemisphere in the motor recovery process has be

115 Imaging of the surface of the cerebral hemispheres in both explant cultures and brains

116 ions ultimately disrupt the formation of the cerebral hemispheres in dorsal regions.

117 In addition, defects in development of the cerebral hemispheres in Foxg1(-/-) mice are not rescued

118 cle that discussed the separate roles of the cerebral hemispheres in humans.

119 us callosum (CC) connects the left and right cerebral hemispheres in mammals and its development requ

120 size and anatomical connectivity across the cerebral hemispheres in persons with Tourette's disorder

121 genetic determination of the left and right cerebral hemispheres in the nonright-handed twin pairs i

122 nferior frontal and temporal regions of both cerebral hemispheres in the titled and untitled conditio

123 Each cerebral hemisphere initially processes one half of the

124 d to provide a model for the organization of cerebral hemisphere inputs to this network.

125 Since the medial wall of the cerebral hemisphere is commonly spared following stroke,

126 The left cerebral hemisphere is dominant for language, and many a

127 For instance, in humans the left cerebral hemisphere is largely responsible for language

128 Because the medial wall of the cerebral hemisphere is often spared following brain inju

129 either the unmyelinated axon of the immature cerebral hemispheres is relatively resistant to traumati

130 ted with progressive destruction of a single cerebral hemisphere, is an autoimmune disease in which o

131 Cerebral hemisphere lambda1 was lower in cardiac arrest

132 Following intra-nasal delivery, low cerebral hemisphere levels of variants were obtained at

133 ends in part on multiple regions of the left cerebral hemisphere, located outside the classic languag

134 within the distributed motor system in both cerebral hemispheres, more so in patients with greater i

135 Tumor locations were diencephalon (n = 58), cerebral hemisphere (n = 3), and cerebellum (n = 17).

136 Understanding the principles of cerebral hemisphere neural network organization is essen

137 s, SD 14.7) with 156 paired watershed vessel/cerebral hemisphere observations.

138 re stereotactically implanted into the right cerebral hemisphere of Fischer rats.

139 r, were transplanted into the spinal cord or cerebral hemisphere of immunosuppressed normal and myeli

140 ulated in ischemic region rather than normal cerebral hemisphere of MCAO rats.

141 surface area and volume of V1 in one or both cerebral hemispheres of 15 neurologically normal human b

142 a pleiotropic role in the development of the cerebral hemispheres of the brain.

143 Cerebral hemispheres of the offspring were examined at t

144 metry of venous drainage in the pathological cerebral hemisphere on CT and MRI dynamic angiography.

145 te a differential role of the left and right cerebral hemispheres on immune functions in humans.

146 gliomas, we injected hMSCs directly into the cerebral hemisphere opposite an established human glioma

147 ted changes were greater in magnitude in the cerebral hemisphere opposite the more clinically affecte

148 iencephalon, but also in the olfactory bulbs/cerebral hemispheres, optic tectum/tegmentum, retina, an

149 Virtually all of the cerebral hemisphere projects on the upper brainstem beha

150 occipital-temporal scalp areas of the right cerebral hemisphere regardless of the visual field of st

151 rtals and Cro-Magnon 1, who have the largest cerebral hemispheres relative to cerebellum volume of an

152 e hypothesis that asymmetric routing between cerebral hemispheres represents an important mechanism f

153 VAF and caudal SRAF in the right cerebral hemisphere responded maximally to midline horiz

154 ephalon failed to bulge or separate into two cerebral hemispheres, resulting in holoprosencephaly.

155 typically bilaterally distributed across the cerebral hemispheres, show similarity to known white mat

156 ured cerebral volume on four contiguous 5 mm cerebral hemisphere slices at each time point, using an

157 o cortical sulci over the convexities of the cerebral hemispheres, sparing the brainstem, cerebellum

158 elencephalon, the embryonic precursor of the cerebral hemispheres, specialized cell types form a midl

159 tion, the development of the patient's right cerebral hemisphere terminated.

160 They also learn better with the left cerebral hemisphere than with the right hemisphere.

161 ducted a cytoarchitectonic analysis by using cerebral hemispheres that were cut at oblique angles and

162 The microprobes were inserted through the cerebral hemisphere, the superior colliculus and the mid

163 The larger units of analysis, including the cerebral hemispheres, the major grey and white matter st

164 aschitic hemisphere-that is, the ipsilateral cerebral hemisphere (THGr(Ce)) and the contralateral cer

165 notypic features such as failure of anterior cerebral hemisphere to divide, hydrocephalus and cleft p

166 ntly better for patients with cerebellar and cerebral hemisphere tumors (n = 75) than those with tumo

167 ction (GTR) was attempted for cerebellar and cerebral hemisphere tumors, with biopsy or less aggressi

168 rder characterized by an enlarged, malformed cerebral hemisphere, typically causing epilepsy that req

169 ose of this study was to examine how the two cerebral hemispheres use perceptual information about wo

170 n neurons (CPN), whose axons connect the two cerebral hemispheres via the corpus callosum (CC).

171 ns that connect homotopic regions of the two cerebral hemispheres via the corpus callosum and that ar

172 allosal projection neurons (CPN) connect the cerebral hemispheres via the corpus callosum, integratin

173 MRI measured affected and non-affected cerebral hemisphere volumes for HME and non-HME cases, i

174 eter measured with the medial surface of the cerebral hemisphere was 10.7 mm, compared with the true

175 male cats anaesthetized with chloralose, one cerebral hemisphere was exposed and the middle cerebral

176 rotid ligation, perfusion of the ipsilateral cerebral hemisphere was markedly diminished, suggesting

177 r each case, the entire hippocampus from one cerebral hemisphere was sliced into 5mm slabs (5-7 slabs

178 During mammalian evolution, expansion of the cerebral hemispheres was accompanied by expansion of the

179 metries of input from the two eyes into each cerebral hemisphere, we measured ocular dominance column

180 Both cerebral hemispheres were actively involved in speech pr

181 nes and early members of the genus Homo, the cerebral hemispheres were large in proportion to the cer

182 The cerebral hemispheres were segmented semi-automatically,

183 nce between blood flow in the right and left cerebral hemispheres when autoregulation was impaired in

184 f the BF-1 gene results in hypoplasia of the cerebral hemispheres, which is more severe in structures

185 wavefronts selectively over the ipsilateral cerebral hemispheres with a velocity of 3.8 +/- 0.70 mm

186 zation are present in the left vs. the right cerebral hemisphere, with the left hemisphere showing a

187 n brain is composed of two broadly symmetric cerebral hemispheres, with an abundance of reciprocal an

188 was hypothesized that disconnection between cerebral hemispheres would disrupt mental simulation of