ライフサイエンスコーパス: nidopallium

1 Wernicke-like brain region (the caudomedial nidopallium).

2 ateral magnocellular nucleus of the anterior nidopallium).

3 rsally into the intermediate and caudomedial nidopallium.

4 ations in a specific part of the caudomedial nidopallium.

5 and a minor projection from the caudomedial nidopallium.

6 ar ridge and appears comparable to the avian nidopallium.

7 rom the lateral magnocellular nucleus of the nidopallium.

8 l mesopallium, nidopallium, and intercalated nidopallium.

9 erior nidopallium, nor in other parts of the nidopallium.

10 ateral magnocellular nucleus of the anterior nidopallium.

11 e LMAN (lateral magnocellular nucleus of the nidopallium), a forebrain nucleus involved in learning b

12 tralateral SHELL, dNCLSHELL , and regions of nidopallium adjacent to each.

13 s into the NIf (nucleus interfacialis of the nidopallium), an auditory forebrain area, blocks this st

14 ly, we found novel inputs to area X from the nidopallium and arcopallium, the mesencephalic central g

15 ed participation of the cortical caudomedial nidopallium and caudomedial mesopallium in the song-cont

16 h included two parts of the mesopallium, the nidopallium and hyperpallium, and the arcopallium and hi

17 sory (auditory/somatosensory) regions of the nidopallium and sensory regions of the intercollicular n

18 els of HSD17B4 mRNA in auditory (caudomedial nidopallium) and visual (hyperpallium apicale) regions t

19 s, the DVR is formed by an inner region, the nidopallium, and a more dorsal region, the mesopallium.

20 , formed by our revised ventral mesopallium, nidopallium, and intercalated nidopallium.

21 ateral magnocellular nucleus of the anterior nidopallium, and medial portion of the dorsolateral thal

22 s were LAMP-poor (e.g., field L, the lateral nidopallium, and somatic basal ganglia).

23 include the hippocampal complex, the medial nidopallium, and the ventromedial arcopallium.

24 djacent nidopallial lamina, the intermediate nidopallium; and a contiguous portion of the ventral mes

25 per name) and the interfacial nucleus of the nidopallium, both show auditory gating, and they receive

26 xpressed in the hippocampus and caudolateral nidopallium, but there were no sex differences.

27 We looked at two forebrain regions: the nidopallium caudale (NC), which plays a role in vocal co

28 lium) with their higher order telencephalon, nidopallium caudolateral (NCL) were simultaneously recor

29 gions - the hippocampus in reed warblers and nidopallium caudolateral in turtle doves.

30 y a role in navigation - the hippocampus and nidopallium caudolateral.

31 at for executive functioning in birds is the nidopallium caudolaterale (NCL) and the mammalian equiva

32 urons in an endbrain association area termed nidopallium caudolaterale (NCL) from crows that assessed

33 activity from the associative endbrain area nidopallium caudolaterale (NCL) of two male carrion crow

34 a key neural underpinning, the endbrain area nidopallium caudolaterale (NCL) represents sensory and m

35 ingle-cell recordings in the endbrain region nidopallium caudolaterale (NCL) showed a considerable pr

36 neuronal activity in the telencephalic area nidopallium caudolaterale (NCL) while two crows (Corvus

37 cording single-neuron activity in the crows' nidopallium caudolaterale (NCL), a brain structure criti

38 corded the activity of single neurons in the nidopallium caudolaterale (NCL), a pallial association a

39 Neurons in the avian nidopallium caudolaterale (NCL), an endbrain structure t

40 tion (hat1, hdac2, hdac4) in hippocampus and nidopallium caudolaterale brain regions.

41 es line lengths in individual neurons in the nidopallium caudolaterale, part of the telencephalon.

42 lular recordings of the prefrontal-like area nidopallium caudolaterale.

43 The nidopallium contains discrete areas that receive auditor

44 medial magnocellular nucleus of the anterior nidopallium), contributes to sequencing in adult male Be

45 We also suggest that the caudolateral nidopallium could be involved in weighing conflicting pi

46 ateral magnocellular nucleus of the anterior nidopallium--DLM to LMAN) within the anterior forebrain

47 ve input from SHELL: the dorsal caudolateral nidopallium (dNCLSHELL ) and a region within the ventral

48 (AI), PoA, lateral, caudolateral and central nidopallium, dorsal and ventral mesopallium, and medial

49 y located hyperpallium and ventrally located nidopallium during late development, suggesting that top

50 ateral magnocellular nucleus of the anterior nidopallium) during juvenile vocal learning, and decreas

51 re, we describe number neurons in the caudal nidopallium (functionally equivalent to the mammalian pr

52 at six time points across 24-h day in brain (nidopallium, hippocampus, and hypothalamus) and peripher

53 N (lateral magnocellular nucleus of anterior nidopallium), HVC, RA (robust nucleus of arcopallium), a

54 um); 2) a secondary intrapallial population (nidopallium/hyperpallium); 3) a tertiary intrapallial po

55 re generally not observed in the rest of the nidopallium, implying that steroids only act on the attr

56 ateral magnocellular nucleus of the anterior nidopallium), in shaping moment-by-moment output from a

57 er the upstream nucleus interfacialis of the nidopallium is lesioned and slows when HVC is cooled, de

58 N (lateral magnocellular nucleus of anterior nidopallium) is necessary for feedback-dependent song de

59 t LMAN (lateral magnocellular nucleus of the nidopallium) is required specifically for the generation

60 ateral magnocellular nucleus of the anterior nidopallium (LMAN) both project to the robust nucleus of

61 ateral magnocellular nucleus of the anterior nidopallium (LMAN) mediates song plasticity based on aud

62 ateral magnocellular nucleus of the anterior nidopallium (LMAN) specialized modules were less depende

63 ateral magnocellular nucleus of the anterior nidopallium (LMAN), but little is known concerning neura

64 ateral magnocellular nucleus of the anterior nidopallium (LMAN), HVC (proper name), and robust nucleu

65 ateral magnocellular nucleus of the anterior nidopallium (LMAN)] neurons of a songbird cortico-basal

66 ateral magnocellular nucleus of the anterior nidopallium (lMAN)] suggests a role in auditory learning

67 ateral magnocellular nucleus of the anterior nidopallium (LMAN)].

68 nd tectofugal pathway that terminates in the nidopallium medial to and separate from the entopallium.

69 stimuli, including the rostral hyperpallium, nidopallium, mesopallium, and lateral striatum.

70 Medial Magnocellular nucleus of the Anterior Nidopallium, MMAN; Nucleus Interface, NIf; nucleus Avala

71 lf (proper name) but not in the caudolateral nidopallium (NCL) or hippocampus.

72 The caudolateral nidopallium (NCL, the avian analogue of the mammalian pr

73 xpressed with parvalbumin in the caudomedial nidopallium (NCM) and HVC shelf (proper name) but not in

74 The caudal nidopallium (NCM) and subdivision L3 of field L were mor

75 Expression of ARC in caudomedial nidopallium (NCM) correlated with father-son song simila

76 rogens fluctuate in the auditory caudomedial nidopallium (NCM) during social interactions and in resp

77 dly induced within zebra finch caudal medial nidopallium (NCM) following novel song exposure, a respo

78 stimulation with birdsong in the caudomedial nidopallium (NCM) of the zebra finch (Taeniopygia guttat

79 s per unit length of dendrite in caudomedial nidopallium (NCM), a brain area activated by song percep

80 neous neuronal activation in the caudomedial nidopallium (NCM), a secondary auditory brain region tha

81 nd that the rostral region of the Cadomedial Nidopallium (NCM), a secondary auditory region of the av

82 ss this question in the songbird caudomedial nidopallium (NCM), an analogue of the mammalian secondar

83 a putative cortical locus is the caudomedial nidopallium (NCM), and one mechanism to facilitate audit

84 dorsal nidopallial shelf and the caudomedial nidopallium (NCM), the core or shell regions of dorsal t

85 brain, more specifically in the caudomedial nidopallium (NCM), the songbird analog of the mammalian

86 the L2 subfield of L (L2) and caudal medial nidopallium (NCM).

87 higher-order auditory area, the caudomedial nidopallium (NCM).

88 large bilateral lesions in the caudal medial nidopallium (NCM, a high auditory area) impaired recover

89 on in a secondary auditory area (caudomedial nidopallium, NCM) but not in the primary auditory area (

90 lium), the mesopallium (middle pallium), the nidopallium (nest pallium), and the arcopallium (arched

91 sually responsive region of the intermediate nidopallium (NI) lying between the nucleus interface med

92 aying nidopallial stripe called intermediate nidopallium (NI), and the dorsally adjacent mesopallium

93 inactivating the interfacial nucleus of the nidopallium (NIf) could eliminate all auditory-evoked su

94 ns in HVC and the interfacial nucleus of the nidopallium (NIf), suggesting that there is complex feed

95 ateral magnocellular nucleus of the anterior nidopallium, nor in other parts of the nidopallium.

96 to those in the prefrontal cortex and caudal nidopallium of adult animals.

97 d higher levels of 5-HIAA in the caudomedial nidopallium of the auditory forebrain than birds not exp

98 um, and lateral magnocellular nucleus of the nidopallium) of male zebra finches (Taeniopygia guttata)

99 ateral magnocellular nucleus of the anterior nidopallium) provides the output of a basal ganglia path

100 n LMAN (lateral magnocellular nucleus of the nidopallium) spontaneously exhibited synchronized bursts

101 h inputs from sensory regions in surrounding nidopallium, suggesting that they function to integrate

102 es to each other, distinct from those of the nidopallium, the arcopallium, and the more distant divis

103 hus, left-sided dominance in the caudomedial nidopallium was specific for the song-learning phase and

104 rder processing centers (the mesopallium and nidopallium), while highly proficient individuals increa

105 aligning putative cell types in avian caudal nidopallium with these molecular identities.