ライフサイエンスコーパス: auditory area

1 areas, two visual areas, and a caudolateral auditory area.

2 vel of the SC or is relayed there from other auditory areas.

3 led a heterogeneity of function in secondary auditory areas.

4 icate that the temporal pattern is unique to auditory areas.

5 ch was source-localized to right-hemispheric auditory areas.

6 tlexical features distributed across various auditory areas.

7 ss-channel processing that exists in earlier auditory areas.

8 mplexity generated specific responses across auditory areas.

9 in the posterior-lateral part of high-level auditory areas.

10 erentially labeled hypothalamic and midbrain auditory areas.

11 ntaining frontal cortex, S1, V1, and primary auditory areas.

12 e impaired feedback connectivity to unimodal auditory areas.

13 ence of rapid synthesis of catecholamines in auditory areas.

14 ts, presumably defining two distinct primary auditory areas.

15 re found in both primary and secondary avian auditory areas.

16 een considered the domain of left-hemisphere auditory areas.

17 g the patterns of connections among the many auditory areas.

18 sponse than the tutor song or tone in higher auditory areas.

19 also had topographic connections with other auditory areas.

20 s were found between the orbital network and auditory areas.

21 ostaining were used to delimit the different auditory areas.

22 nd retrograde labeling in the aforementioned auditory areas.

23 s with superior temporal cortices, including auditory areas.

24 oral cortex contains multiple interconnected auditory areas.

25 own to entrain low-frequency oscillations in auditory areas [3, 4], and this entrainment increases wi

26 edicted a more normal histometric picture in auditory area 41.

27 elinated oval of cortex caudal to PV/S2, the auditory area (A), contained neurons that responded to c

28 core of primary areas, a surrounding belt of auditory areas, a lateral parabelt of two divisions, and

29 uring multielectrode penetrations of primary auditory area A1 in awake macaques revealed clear somato

30 ing (1.5 mm isotropic resolution) of primary auditory areas A1 and R in six human participants.

31 in the core are the human analogs of primate auditory areas A1 and R.

32 tory cortex (AC), which contains the primary auditory area (A1) and other auditory fields, encompasse

33 ase-encoded tonotopic methods to map primary auditory areas (A1 and R) within the "auditory core" of

34 or three subdivisions including the primary auditory area (AI), a surrounding belt of cortex with pe

35 in parallel to a core of three primary-like auditory areas, AI, R, and RT, constituting the first st

36 ross languages, beginning just outside early auditory areas and extending through temporal, parietal,

37 archical representations starting in primary auditory areas and moving laterally on the temporal lobe

38 rtical regions excluded several higher-order auditory areas and segregated maximally from the prefron

39 ies could be successfully decoded from early auditory areas and that learning-induced pattern changes

40 nly relatively light connections between the auditory areas and the medial network.

41 idalis (N.Ov), is situated between these two auditory areas, and its inactivation precludes the use o

42 ween cochleotopically organized thalamic and auditory areas, and suggest topographic relations betwee

43 nvolving SCm, Cg, secondary visual cortices, auditory areas, and the dysgranular retrospenial cortex

44 ponses, as indexed by the BOLD, to speech in auditory areas associated with phonological processing.

45 l breeder, (a) serotonergic fibers innervate auditory areas; (b) the density of those fibers is highe

46 ts slow speech-brain tracking bilaterally in auditory areas (below 2 Hz) and in turn increases left-l

47 Auditory areas can become recruited for visual and tacti

48 in the alternating condition in a secondary auditory area (caudomedial nidopallium, NCM) but not in

49 n, and accordingly organization, of cortical auditory areas caused by associative learning can be qui

50 The cytoarchitecture of the auditory area changes in a stepwise manner toward the ko

51 Additional injections into caudal lateral auditory area (CL) and Tpt showed similar connections wi

52 The caudal medial auditory area (CM) has anatomical and physiological feat

53 re" auditory cortex and a secondary "caudal" auditory area containing layer V pyramidal neurons that

54 ption, the electric cortical activity of the auditory areas correlates with the sound envelope of the

55 tal, occipital (visual areas), and temporal (auditory areas) cortical regions during rest (eyes/ears

56 ional specialization of somatomotor (and not auditory) areas determined lateralization in the dorsal

57 ve phase-locking to auditory speech signals, auditory areas do not show phase-locking to visual speec

58 of cross-modal plasticity in a higher-order auditory area does not reduce auditory responsiveness of

59 Other secondary auditory areas, dorsal and ventral to the core, do not d

60 In the primary forebrain auditory area field L (primary auditory cortex analog) o

61 ive fields (STRFs) of neurons in the primary auditory area field L of unanesthetized zebra finches.

62 ial nidopallium, NCM) but not in the primary auditory area (Field L2); in contrast, repetition suppre

63 e scale of several seconds-starting in early auditory areas, followed by language areas, the attentio

64 cally active region on the STG is a separate auditory area, functionally distinct from the HG auditor

65 re labeled; 5) the projections to nonprimary auditory areas had many laterally oriented axons; 6) the

66 ronounced caudally in the cortex assigned to auditory area I, only slightly reduced in the rostral ar

67 n the caudal medial nidopallium (NCM, a high auditory area) impaired recovery of the original pitch e

68 in the caudal mesopallium, a cortical-level auditory area implicated in discriminating and learning

69 caudal mesopallium (CM) is a cortical-level auditory area implicated in song discrimination.

70 re, the structural properties of a secondary auditory area in the left hemisphere, are capable to pre

71 s between the primary and secondary cortical auditory areas in brain slices from the mouse, and, in t

72 le sites in between the sites in the primary auditory areas in Heschl's gyrus and nonprimary auditory

73 We analyzed the MGB projections to 13 auditory areas in the cat using two retrograde tracers t

74 nsion of HVC that is closely associated with auditory areas in the caudomedial telencephalon.

75 Neuron B-LC3 linked the bilateral auditory areas in the protocerebrum.

76 itory areas in Heschl's gyrus and nonprimary auditory areas in the superior temporal gyrus.

77 onse to the playbacks showed, in addition to auditory areas, increased ZENK protein in several song c

78 imbic regions and between limbic and primary auditory areas, indicating the importance of auditory-li

79 ow that: 1) Local estradiol action within an auditory area is necessary for socially relevant sounds

80 been described in humans, and a second-level auditory area is shown to respond to somatosensory stimu

81 l multielectrode recordings from a forebrain auditory area known to selectively process species-speci

82 in cats and ferrets, although not all of the auditory areas known from these species could be identif

83 Third, modulatory properties of core auditory areas lack hemispheric lateralization.

84 nclear whether the cross-modally reorganized auditory areas lose auditory responsiveness.

85 e processing that could be realized in early auditory areas may shape speech understanding in noise.

86 re, callosal projections emanating from core auditory areas modulate A1 neuronal activity via excitat

87 We show that neurons in a forebrain auditory area of adult male zebra finches are selectivel

88 niculate (mMG) to determine if this critical auditory area of the HR conditioning circuitry receives

89 fMRI) to measure visually evoked activity in auditory areas of both early-deafened and hearing indivi

90 uts not only from somatosensory, visual, and auditory areas of cortex, but also from limbic regions,

91 Architecture of auditory areas of the superior temporal region (STR) in

92 id not observe changes in NF-M expression in auditory areas or in song control nuclei in the contexts

93 t be under the regulatory control of ZENK in auditory areas or in song control nuclei.

94 Several auditory areas overlapped with previously identified vis

95 Furthermore, disinhibition in auditory areas predicted abnormal auditory perception (a

96 Amygdala and auditory areas predominantly code emotion-related acoust

97 as highest in the anterior dorsal field, the auditory area previously shown to be innervated by a reg

98 roup suffered greater damage to two unimodal auditory areas: primary auditory cortex and the planum t

99 Midbrain auditory areas projected to both ipsilateral and contral

100 cingulate area (Cg), visual, oculomotor, and auditory areas provide strong input to the SCm, while pr

101 f Ta, containing two primary or primary-like auditory areas, received inputs from the ventral and mag

102 The organization of postthalamic auditory areas remains unclear in many respects.

103 But how posterior (and other) auditory areas represent acoustic space remains a matter

104 Neurons in secondary, but not primary, auditory areas respond preferentially to calls when they

105 In the younger monkey, different auditory areas show distinct patterns of onset and offse

106 The caudolateral auditory area shows the greatest age-related changes, su

107 ping alone can define areal borders, primary auditory areas such as A1 are best delineated by combini

108 lar, periventricular, and arcuate nuclei; in auditory areas, such as the ectorhinal and temporal cort

109 t projections ascending from lower to higher auditory areas; such a view, however, ignores the possib

110 ral cortex devoted to both somatosensory and auditory areas than the wild-caught Norway rat.

111 istinct cortical area, outside the classical auditory areas, that is specialized for the detection of

112 e zebra finches, neurons in a cortical-level auditory area, the caudal mesopallium (CM), can rapidly

113 atively inhibitory neurons of a higher-order auditory area, the caudomedial nidopallium (NCM).

114 dult primary auditory cortex and a secondary auditory area, the suprarhinal auditory field, was contr

115 Thus, the auditory areas themselves are the primary source of cort

116 th emerging results in both visual and other auditory areas, these findings suggest that neurons whos

117 resent study suggest that the right cortical auditory areas, thought to be specialized for spectral p

118 nd that this stream extends from the primary auditory area to the temporal pole.

119 st long-range parallel inputs from low-level auditory areas to apical areas in the frontal lobe of th

120 electively to the written version, and early auditory areas to the spoken version of the narrative.

121 cadic signals to yoke excitability states in auditory areas to those in visual areas, the brain can i

122 frequency within human primary and secondary auditory areas using fMRI.

123 Consequently, labeling in auditory areas was reduced by 36%.

124 Cerebral auditory areas were delineated in the awake, passively l

125 Interconnections within the medullary auditory areas were extensive.

126 s expected, connections with adjacent caudal auditory areas were stronger than connections with rostr

127 ustic signals lateralize to right-hemisphere auditory areas, whereas rapid temporal features (20-50 H

128 ustic information streams occurs in anterior auditory areas, whereas the segregation of sound objects

129 e to the talker's voice only appeared in the auditory areas with longer latencies, but attentional mo

130 The connections of RM favored rostral auditory areas, with no clear somatosensory inputs.

131 In contrast, the second auditory area within the circular sulcus has connections

132 Corticostriatal connections of auditory areas within the supratemporal plane and in ros