ライフサイエンスコーパス: cortical field

1 ay a critical role in the differentiation of cortical fields (; ).

2 tational space across neurons in an auditory cortical field.

3 with each taste quality encoded by distinct cortical fields.

4 spine density in pyramidal neurons in these cortical fields.

5 ] and hippocampal [ventral subiculum (vSUB)] cortical fields.

6 ections with other architectonically defined cortical fields.

7 input to all neighboring frequency-organized cortical fields.

8 tional diversity between frequency-organized cortical fields.

9 om neuron to neuron and across five auditory cortical fields.

10 e about how normal aging affects these early cortical fields.

11 We found that V1 projects to 15 cortical fields.

12 ion with physiologically identified auditory cortical fields.

13 ouble-dissociation in map plasticity in both cortical fields.

14 ed in the tonotopic organization of auditory cortical fields.

15 al organization principle of primary sensory cortical fields.

16 fine-grained patterns of connectivity among cortical fields.

17 th similar patterns seen across all auditory cortical fields.

18 ct of locomotion is largely conserved across cortical fields.

19 ependent responses across different auditory cortical fields (ACFs).

20 raphy of connections of the primary auditory cortical field (AI) in the Mongolian gerbil with subcort

21 d a tonotopically organized primary auditory cortical field (AI) in the rat.

22 a specific pattern of connections with other cortical fields and brain structures, and together they

23 e-field calcium imaging to identify distinct cortical fields and cellular-resolution two-photon calci

24 d their termination patterns in the auditory cortical fields and layers.

25 eeded, these patterns of interconnections of cortical fields and thalamic nuclei suggest that the som

26 ce of connections between the other auditory cortical fields and the amygdala.

27 heir parents have differences in the size of cortical fields and the connections of somatosensory cor

28 ded under anesthesia in two primary auditory cortical fields and two tonotopically organized nonprima

29 l (MT) area, an early maturing dorsal stream cortical field, and which bypass the primary visual cort

30 und that S1 receives dense inputs from novel cortical fields, and that the density of existing cortic

31 ending series of ferret auditory and frontal cortical fields, and the dynamics of this representation

32 erior and mediolateral relationships between cortical fields appear to be invariant.

33 indicate that some aspects of development of cortical fields are not mediated by specific sensory inp

34 field correlated with the size of the other cortical fields as well as with the total size of the do

35 cal neuroepithelium to accommodate different cortical fields at early stages of development, although

36 use they interrupted connections of temporal cortical fields beyond the rhinal cortex that are also i

37 rtex with clear functional and architectonic cortical field boundaries, as well as discrete patterns

38 d labeled cells to histologically identified cortical field boundaries.

39 ation, such as the size and connections of a cortical field, can generate differences in behavior, wh

40 d that this response in a secondary auditory cortical field changes with experience to acquire a pitc

41 ity to sound timbre was reduced across three cortical fields compared with control animals, but maint

42 Further, we found that the size of each cortical field correlated with the size of the other cor

43 y of projections to areas 2 and 5 from other cortical fields could be determined.

44 childhood abuse and neuroplastic thinning of cortical fields, depending on the nature of the abusive

45 Theories of both cortical field development and cortical evolution propos

46 , to populations of neurons from 6 different cortical fields encompassing core and belt areas.

47 ame progressively more categorical in higher cortical fields, especially during task performance.

48 ls may supply the raw material necessary for cortical field evolution.

49 ivity to f(0) was found in all five auditory cortical fields examined, with most of those neurons exh

50 Each cortical field has a specific pattern of connections wit

51 nterhemispheric connections between auditory cortical fields have not been widely scrutinized.

52 or or non-selective responses in this second cortical field in naive animals.

53 ated dextran amine were performed in various cortical fields in cats (perirhinal, entorhinal, pre/inf

54 ish the location and organization of sensory cortical fields in macaque monkeys, a species with a rel

55 se loci have several features in common with cortical fields in monkey and human brains that contribu

56 populations of neurons in different auditory cortical fields in the macaque monkey carry sufficient i

57 The presence of multiple auditory cortical fields in the rat is consistent with auditory c

58 receiving pallidal input project to a motor cortical field, injections of the retrograde tracer Fluo

59 visual signals (gain fields) in two adjacent cortical fields, LIP and 7a, are referenced to the body

60 formed of multiple, functionally specialized cortical field maps (CFMs).

61 iled anatomic analyses to delineate its many cortical fields more clearly.

62 explain much of the phenotypic variation in cortical field number and organization in different mamm

63 tely yielded fewer neurons within developing cortical fields of Scz organoids.

64 between visual, somatosensory, and auditory cortical fields on the remaining cortical sheet.

65 The corticofugal projection from 12 auditory cortical fields onto the medial geniculate body was inve

66 l premotor cortex is a functionally distinct cortical field or group of fields in the primate frontal

67 e prelimbic and/or dorsal anterior cingulate cortical fields (PL and ACd, respectively).

68 in the spectral features of hippocampal and cortical field potential of Scn1a mice and of patients'

69 ress this, we examined electrocorticographic cortical field potential recordings from the human nonpr

70 oscillations apparent in posterior cingulate cortical field potentials are volume-conducted from the

71 Finally, we recorded cortical field potentials from three human subjects and

72 near methods could decode limb position from cortical field potentials in both monkeys.

73 mplitude of high broadband activity in human cortical field potentials indicates local processing and

74 We concurrently measured cortical field potentials via thinned-skull electroencep

75 potential amplitude, as reflected in global cortical field power.

76 ribe the number and internal organization of cortical fields present.

77 To gain insight into how cortical fields process somatic inputs and ultimately co

78 response, indicating that the birds' primary cortical field represents the segregated streams, but no

79 e quality is represented in its own separate cortical field, revealing the existence of a gustotopic

80 rate representation, we find that neurons in cortical fields rostral to AI predominantly use a monoto

81 he target of natural selection, variation in cortical field size across individuals may supply the ra

82 riation and examine the relationship between cortical field size and sensory processing abilities and

83 riability in body weight and primary sensory cortical field size, as defined by myeloarchitecture.

84 ze, cortical sheet size, and primary sensory cortical field sizes in the adult short-tailed opossum (

85 ize of the dorsolateral cortex or in primary cortical field sizes.

86 s suggest a functional dichotomy of auditory cortical fields: stimulus-determined mesial fields that

87 hese response types were observed across all cortical fields tested, but were largely absent from the

88 This is an avian cortical field that appears to contain a region comparab

89 d by progenitors specify an occipital visual cortical field that differentiates into V1 and V(HO); th

90 The neocortex of mammals is composed of cortical fields that have a unique organization associat

91 termine the degree of divergence from single cortical fields, the pattern of convergence from several

92 on in male mice might differ across auditory cortical fields, thereby contributing to the heterogenei

93 of single neurons in core and belt auditory cortical fields to both forward and reversed vocalizatio

94 acer (dextran biotin) injections in auditory cortical fields to describe the distribution of terminal

95 extends beyond reshaping of primary sensory cortical fields to respecification of the cortical origi

96 responses of individual neurons in different cortical fields to sounds that vary simultaneously acros

97 We found that individual neurons in each cortical field typically respond to just one sound categ

98 hitectonically defined nuclei to 14 auditory cortical fields was characterized qualitatively and quan

99 Functional boundaries of cortical fields were directly related to myeloarchitecto

100 pagates unconventional impulse excitation to cortical fields which have a critical role in providing

101 patches in layer IV within a poorly defined cortical field, which varies between hemispheres, rather

102 to determine the topographic organization of cortical fields with 55% concordance to electrophysiolog

103 species is the presence of multiple auditory cortical fields with topographically organized responses

104 d the results were used to localize auditory cortical fields within the STG.