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 erentially labeled hypothalamic and midbrain auditory areas.

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

4 e impaired feedback connectivity to unimodal auditory areas.

5 ence of rapid synthesis of catecholamines in auditory areas.

6 ts, presumably defining two distinct primary auditory areas.

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

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

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

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

11 also had topographic connections with other auditory areas.

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

13 ostaining were used to delimit the different auditory areas.

14 nd retrograde labeling in the aforementioned auditory areas.

15 s with superior temporal cortices, including auditory areas.

16 oral cortex contains multiple interconnected auditory areas.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 Auditory areas can become recruited for visual and tacti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 Several auditory areas overlapped with previously identified vis

74 Amygdala and auditory areas predominantly code emotion-related acoust

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

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

77 Midbrain auditory areas projected to both ipsilateral and contral

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 Interconnections within the medullary auditory areas were extensive.

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

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

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

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

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

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