ライフサイエンスコーパス: Broca's area

1 occurred in the left inferior frontal gyrus (Broca's area).

2 nsula and lateral premotor cortex and not of Broca's area.

3 subjects with PTSD showed decreased rCBF in Broca's area.

4 The pars triangular is a portion of Broca's area.

5 activation of the ventral temporal lobes and Broca's area.

6 o ventral premotor cortex, not the classical Broca's area.

7 racy in the left ventral premotor cortex and Broca's area.

8 correlation between left striate cortex and Broca's area.

9 dle temporal gyrus and the dorsal portion of Broca's area.

10 cortical networks, neither of which involves Broca's area.

11 lood oxygen level-dependent (BOLD) signal in Broca's area.

12 reas with premotor/motor areas, and not with Broca's area.

13 , in close topographical relationship to the Broca's area.

14 power in both Sylvian-parietal-temporal and Broca's areas.

15 logic cell counting in postmortem samples of Broca's area 44 in 9 schizophrenic patients and 14 norma

16 Broca's area, a cerebral cortical area located in the in

17 y identified by Broca and what is now called Broca's area, a finding with significant ramifications f

18 is discovery of language-specific regions in Broca's area advances our understanding of the cortical

19 ded during awake neurosurgical operations in Broca's area and in the dominant temporal lobe with the

20 tex in relation to bulbar disability, and in Broca's area and its homologue in relation to verbal flu

21 vation relative to the unaffected members in Broca's area and its right homolog, as well as in other

22 chronous delays led to increased activity in Broca's area and its right homologue, whereas disruptive

23 tion: storage for verbal materials activates Broca's area and left-hemisphere supplementary and premo

24 into alternating columns in the prospective Broca's area and orofacial motor cortex.

25 Heschl's gyrus, the parietal operculum, left Broca's area and the left arcuate fasciculus (similar to

26 s between FFG and phonology-related regions (Broca's area and the left inferior parietal lobule), and

27 The whole-brain MVPA revealed that Broca's area and the left pre-supplementary motor area e

28 ral prefrontal cortex (areas 45, 46 and 47), Broca's area and the right temporal (area 21) and right

29 ract that lies deep to posterior portions of Broca's area and the sensory-motor cortex, is a robust p

30 the input language resulted in activation of Broca's area and the supramarginal gyri, areas associate

31 nges were observed in the Brodmann areas 44 (Broca's area) and 45.

32 ing was restricted to left inferior frontal (Broca's area) and bilateral posterior perisylvian (Werni

33 ic activations in the left inferior frontal (Broca's area) and posterior superior temporal (Wernicke'

34 or prefrontal regions bilaterally (including Broca's area) and superior temporal regions bilaterally

35 rea, and the left inferior frontal gyrus, or Broca's area) and their homologous right-hemisphere area

36 mporoparietal components of Wernicke's area, Broca's area, and dorsal premotor cortex.

37 ask-relevant anatomic regions (sensorimotor, Broca's area, and superior temporal gyrus), these behavi

38 ft posterior middle temporal/fusiform gyrus, Broca's area, and/or Wernicke's area accounted for most

39 ions including frontopolar cortex (area 10), Broca's area (area 45), frontoinsular cortex (area FI),

40 inal patients and the increasing reliance on Broca's area as a major speech centre, we thought it imp

41 e, gets established rapidly, and consists of Broca's area as its hub.

42 assical theories of brain organization (e.g. Broca's area as speech output region) and provide a dist

43 imaging studies often rely on activation in Broca's area as verification that tasks have successfull

44 d by left-hemisphere speech areas, including Broca's area as well as the premotor and supplementary m

45 ur findings strongly indicate that a part of Broca's area (BA 44, pars opercularis) is critically imp

46 ive to the controls in a pre-motor region of Broca's area (BA 6/44).

47 BA 44 (part of Broca's area), BA 45 (part of Broca's area), BA 21 (inferior temporal cortex), BA 37 (

48 (including Wernicke's area), BA 44 (part of Broca's area), BA 45 (part of Broca's area), BA 21 (infe

49 Repetition of single words did not activate Broca's area but activity in three left-lateralised regi

50 word stimuli, neural activity is enhanced in Broca's area, but not in motor cortex.

51 rior temporal) as well as motor brain areas (Broca's area, cerebellum) in response to speech, and equ

52 Across species, Broca's area comprises Brodmann's areas 44 and 45.

53 reviously obtained cytoarchitectonic maps of Broca's area confirmed lack of homology between activati

54 ect fMRI, we find that both ideas are right: Broca's area contains two sets of subregions lying side

55 These unique data provide evidence that Broca's area coordinates the transformation of informati

56 In contrast, neural maturity in Broca's area correlated with children's verbal abilities

57 whether the electrophysiological activity of Broca's area correlates with the sound of the utterances

58 vity in the left ventral premotor cortex and Broca's area exhibited effective phoneme categorization

59 ith resting fMRI signals in the thalamus and Broca's area extending to Wernicke's area, supporting th

60 utational systems, and a common substrate in Broca's area for hierarchical processing has recently be

61 In this role, Broca's area formulates an appropriate articulatory code

62 We took the opportunity to study Broca's area homologue in a novel sample of 80 preserved

63 llustrate the interindividual variability of Broca's area homologue in the chimpanzee and support the

64 ly prior study documenting the morphology of Broca's area homologue in the chimpanzee, we report grea

65 t could be considered markers of the size of Broca's area homologue.

66 that the region of cortex commonly known as Broca's area (i.e., the posterior LIFG) serves to bias c

67 lumnar organization of cells in layer III of Broca's area in 11 human and 9 great ape specimens.

68 Contrary to classic notions of the role of Broca's area in speech, while motor cortex is activated

69 In humans, Broca's area in the frontal lobe and Wernicke's area in

70 ominant distribution of activation involving Broca's area in the generation tasks and a more bilatera

71 ions dorsal to the traditional boundaries of Broca's area in the inferior frontal sulcus and the post

72 Although it is widely accepted that Broca's area in the left inferior frontal gyrus plays an

73 issociation of language lateralization (e.g. Broca's area in the left, and Wernicke's area in the rig

74 r fMRI examinations showed activation of the Broca's area in the right hemisphere in 3/4 cases of low

75 gnificant cytoarchitectonic abnormalities in Broca's area in the same brains in which the dlPFC exhib

76 we have performed a morphometric analysis of Broca's area in the ventral frontal lobe.

77 ffective connectivity between Wernicke's and Broca's areas in the PPA patient group.

78 showed significantly increased activation in Broca's area, in addition to the well known visuospatial

79 No correlation was observed with Broca's area, insula, or sensorimotor cortex.

80 They demonstrate that cooling Broca's area interferes with speech timing but not speec

81 Anatomically, Broca's area is most often larger in the left hemisphere

82 cortex is activated during spoken responses, Broca's area is surprisingly silent.

83 The left inferior frontal gyrus (Broca's area) is generally believed to be critical for t

84 t ventrolateral prefrontal cortex (including Broca's area), left premotor cortex, and left and right

85 mal naming network and as such indicate that Broca's area may be a suitable candidate site for tDCS i

86 Broca's area mediates this cascade through reciprocal in

87 as the recurrence of the tumor near the left Broca's area might be the factors leading to reorganizat

88 e primary auditory cortex (p </= .001), left Broca's area (p </= .001), and cingulate gyrus (p </= .0

89 dings to reflect preferential recruitment of Broca's area, part of the neural substrate supporting si

90 independent datasets strongly indicate that Broca's area participates in categorical speech percepti

91 e whether the posterior, superior portion of Broca's area performs operations on phoneme segments spe

92 The posterior portion of Broca's area responded specifically to the sequence mani

93 Neighboring probes within Broca's area revealed distinct neuronal activity for lex

94 ize (RR, 2.0; 95% CI, 1.2-3.2) and injury to Broca's area (RR, 2.5; 95% CI, 1.3-5.0), internal capsul

95 the frontal-lobe language-sensitive regions (Broca's area), second languages acquired in adulthood ('

96 PF), left superior temporal region (ST), and Broca's area showed sustained activation during the memo

97 audate, as well as primary motor cortex, the Broca's area, superior temporal gyrus, insula, and claus

98 abolism, in the temporal and parietal lobes, Broca's area, thalamus, and hippocampus.

99 area; the inferior lateral premotor cortex (Broca's area); the anterior insula; and the cerebellum.

100 For Broca's area, the debate focuses on specialization for l

101 implicate anterior cortical regions such as Broca's area, the left anterior insula, and deep white m

102 d by left-hemisphere speech areas, including Broca's area, the premotor area, and the supplementary m

103 ntoparietal motor-related network (including Broca's area, the premotor region, the intraparietal sul

104 g the Sylvian fissure bilaterally including "Broca's area," the primary language area, by disrupting

105 uage network on epicentres in Wernicke's and Broca's areas; the explicit memory/emotion network on ep

106 patients are due entirely to dysfunction in Broca's area, thereby attributing all aspects of the dis

107 umptions, the range of locations ascribed to Broca's area varies broadly across studies.

108 lization index was calculated separately for Broca's area versus its right-hemisphere homolog and Wer

109 t the AF connects posterior brain areas with Broca's area via a relay station in the premotor/motor a

110 grade glioma (HGG) only the left hemisphere Broca's area was activated (LI=1).

111 Broca's area was also found when the same analysis was a

112 Broca's area was identified in the inferior frontal gyru

113 Broca's area was not robustly activated by any stimulus

114 In 4/5 of the cases activation in Broca's area was present- in 2 cases in the left hemisph

115 tems after the distraction, the DLPF, ST and Broca's area were also active.

116 Lesions in or near Broca's area were not associated with inter-hemispheric

117 ectly involved in language generation, or in Broca's area when the participants were executing a repe

118 iculus, a long associative bundle connecting Broca's area with Wernicke's area, and other language re

119 Brodmann's area 44 delineates part of Broca's area within the inferior frontal gyrus of the hu

120 Our data support the importance of Broca's area within the normal naming network and as suc