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1 Wernicke-like brain region (the caudomedial nidopallium).
2 ateral magnocellular nucleus of the anterior nidopallium).
3 ar ridge and appears comparable to the avian nidopallium.
4 rsally into the intermediate and caudomedial nidopallium.
5 rom the lateral magnocellular nucleus of the nidopallium.
6 l mesopallium, nidopallium, and intercalated nidopallium.
7 ations in a specific part of the caudomedial nidopallium.
8 erior nidopallium, nor in other parts of the nidopallium.
9 ateral magnocellular nucleus of the anterior nidopallium.
10 and a minor projection from the caudomedial nidopallium.
11 e LMAN (lateral magnocellular nucleus of the nidopallium), a forebrain nucleus involved in learning b
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.
23 djacent nidopallial lamina, the intermediate nidopallium; and a contiguous portion of the ventral mes
24 per name) and the interfacial nucleus of the nidopallium, both show auditory gating, and they receive
29 urons in an endbrain association area termed nidopallium caudolaterale (NCL) from crows that assessed
30 neuronal activity in the telencephalic area nidopallium caudolaterale (NCL) while two crows (Corvus
31 corded the activity of single neurons in the nidopallium caudolaterale (NCL), a pallial association a
35 ateral magnocellular nucleus of the anterior nidopallium--DLM to LMAN) within the anterior forebrain
36 ve input from SHELL: the dorsal caudolateral nidopallium (dNCLSHELL ) and a region within the ventral
37 (AI), PoA, lateral, caudolateral and central nidopallium, dorsal and ventral mesopallium, and medial
38 ateral magnocellular nucleus of the anterior nidopallium) during juvenile vocal learning, and decreas
39 N (lateral magnocellular nucleus of anterior nidopallium), HVC, RA (robust nucleus of arcopallium), a
40 um); 2) a secondary intrapallial population (nidopallium/hyperpallium); 3) a tertiary intrapallial po
41 re generally not observed in the rest of the nidopallium, implying that steroids only act on the attr
42 N (lateral magnocellular nucleus of anterior nidopallium) is necessary for feedback-dependent song de
43 t LMAN (lateral magnocellular nucleus of the nidopallium) is required specifically for the generation
44 ateral magnocellular nucleus of the anterior nidopallium (LMAN) both project to the robust nucleus of
45 ateral magnocellular nucleus of the anterior nidopallium (LMAN) mediates song plasticity based on aud
46 ateral magnocellular nucleus of the anterior nidopallium (LMAN), but little is known concerning neura
47 ateral magnocellular nucleus of the anterior nidopallium (LMAN), HVC (proper name), and robust nucleu
48 ateral magnocellular nucleus of the anterior nidopallium (LMAN)] neurons of a songbird cortico-basal
49 ateral magnocellular nucleus of the anterior nidopallium (lMAN)] suggests a role in auditory learning
51 nd tectofugal pathway that terminates in the nidopallium medial to and separate from the entopallium.
53 Medial Magnocellular nucleus of the Anterior Nidopallium, MMAN; Nucleus Interface, NIf; nucleus Avala
55 xpressed with parvalbumin in the caudomedial nidopallium (NCM) and HVC shelf (proper name) but not in
57 rogens fluctuate in the auditory caudomedial nidopallium (NCM) during social interactions and in resp
58 dly induced within zebra finch caudal medial nidopallium (NCM) following novel song exposure, a respo
59 stimulation with birdsong in the caudomedial nidopallium (NCM) of the zebra finch (Taeniopygia guttat
60 s per unit length of dendrite in caudomedial nidopallium (NCM), a brain area activated by song percep
61 neous neuronal activation in the caudomedial nidopallium (NCM), a secondary auditory brain region tha
62 dorsal nidopallial shelf and the caudomedial nidopallium (NCM), the core or shell regions of dorsal t
63 brain, more specifically in the caudomedial nidopallium (NCM), the songbird analog of the mammalian
65 large bilateral lesions in the caudal medial nidopallium (NCM, a high auditory area) impaired recover
66 lium), the mesopallium (middle pallium), the nidopallium (nest pallium), and the arcopallium (arched
67 sually responsive region of the intermediate nidopallium (NI) lying between the nucleus interface med
68 inactivating the interfacial nucleus of the nidopallium (NIf) could eliminate all auditory-evoked su
69 ns in HVC and the interfacial nucleus of the nidopallium (NIf), suggesting that there is complex feed
71 d higher levels of 5-HIAA in the caudomedial nidopallium of the auditory forebrain than birds not exp
72 um, and lateral magnocellular nucleus of the nidopallium) of male zebra finches (Taeniopygia guttata)
73 ateral magnocellular nucleus of the anterior nidopallium) provides the output of a basal ganglia path
74 h inputs from sensory regions in surrounding nidopallium, suggesting that they function to integrate
75 es to each other, distinct from those of the nidopallium, the arcopallium, and the more distant divis
76 hus, left-sided dominance in the caudomedial nidopallium was specific for the song-learning phase and
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