ライフサイエンスコーパス: pallium

1 (nest pallium), and the arcopallium (arched pallium).

2 ischemic penumbra regions (e.g. hippocampus, pallium).

3 hese abilities require dorsal telencephalon (pallium).

4 for CR cells on the edges of the developing pallium.

5 r include labeled cell bodies in the lateral pallium.

6 l) and medial (Dm) divisions of the goldfish pallium.

7 is restricted to regions close to the medial pallium.

8 ly dorsal thalamic nucleus projecting to the pallium.

9 ested to derive from ventral portions of the pallium.

10 entralmost pallial region, i.e., the ventral pallium.

11 re dispersed in the hypothalamus and ventral pallium.

12 traversing the basal ganglia, thalamus, and pallium.

13 orming a short recurrent pathway through the pallium.

14 into a smaller ventral pallium and a lateral pallium.

15 sal pallial part, not of the classic lateral pallium.

16 the macroarchitecture of the zebrafish adult pallium.

17 anding the organization and evolution of the pallium.

18 onsidered homologous to medial and/or dorsal pallium.

19 sition within the developing chicken lateral pallium.

20 general characteristic of the avian sensory pallium.

21 one of the main components of the sauropsid pallium.

22 ine a comprehensive regional fate map of the pallium.

23 ludes a medial, dorsal, lateral, and ventral pallium.

24 ingless, later foxg1 expression and a larger pallium.

25 5a in the subpallium and tbr1, neurod in the pallium.

26 input and output pathways of the gymnotiform pallium.

27 rto was considered to arise from the lateral pallium.

28 erstood, particularly as regards the roof or pallium.

29 not the case with RG cells isolated from the pallium.

30 rior neural plate that will give rise to the pallium.

31 lls with a rostral phenotype from the dorsal pallium.

32 extends from the subpallium into the dorsal pallium.

33 imary sensory input population (intercalated pallium); 2) a secondary intrapallial population (nidopa

34 1 and Neurog2 are coexpressed in the ventral pallium, a progenitor pool that first gives rise to Caja

35 over that distinct subdivisions in the avian pallium above and below the ventricle and the associated

36 rog2 have redundant functions in the ventral pallium, acting in two phases to first specify a CR cell

37 Watson/Puelles model into a smaller ventral pallium and a lateral pallium.

38 t, Tbr2 is expressed in all of the zebrafish pallium and in a restricted zone of the ventral subpalli

39 ventricular and subventricular zones of the pallium and migrate along radial glia fibers to reach th

40 We identify the boundary between the pallium and subpallium based on the complementary expres

41 hes, but cholinergic-positive neurons in the pallium and subpallium, and in the thalamus and cerebell

42 tures of their embryonic site of origin, the pallium and subpallium.

43 elencephalon has two major subdivisions, the pallium and subpallium.

44 ther, the septal nuclei derive from both the pallium and subpallium.

45 of these Emx1-lineage cells originate in the pallium and subsequently migrate to the developing stria

46 central (DC), and dorsal (DD) regions of the pallium and the intermediate region between DL and DC (D

47 bers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectu

48 ts adult derivatives develop from the dorsal pallium and ventral subpallium.

49 the striatum, the D1D and D3 throughout the pallium and within the mesopallium, respectively, and th

50 l boundary, which separates the dorsal (i.e. pallium) and ventral (i.e. subpallium) telencephalon.

51 lium (middle pallium), the nidopallium (nest pallium), and the arcopallium (arched pallium).

52 ated in the caudal pole of the telencephalic pallium, and a cell population that travels from the pre

53 c cells were observed in the olfactory bulb, pallium, and preoptic area of the telencephalon, and the

54 hy of secondary olfactory projections to the pallium are critical in evaluating these hypotheses, but

55 Nr4a2-labeled subplate cells in the lateral pallium at the site of the future insular cortex.

56 te that, upon mechanical injury to the adult pallium, axolotls can regenerate several of the populati

57 all along the urodele CNS (olfactory bulbs, pallium, basal ganglia, diencephalon, mesencephalic tegm

58 cal motor pathway and an anterior forebrain (pallium-basal ganglia-thalamo-pallial) loop.

59 we show that GINs migrate normally into the pallium, but fail to acquire proper layer position.

60 t of the claustrum primordium in the lateral pallium, but they migrate ventrally to reach the ventral

61 4-dimensional (3D + birthdating time) map of pallium construction in the adult teleost zebrafish.

62 This simple mode of pallium construction shares distinct traits with pallial

63 t from the basal ganglia, and input from the pallium (cortex in mammals) and torus semicircularis.

64 neurons receive direct projections from the pallium (cortex in mammals), which can increase the GPh

65 minantly in the dorsocentral division of the pallium (DC); the dorsolateral division of the pallium (

66 e connectivity of the subdivisions of dorsal pallium (DD) of an electric gymnotiform fish, Apteronotu

67 they migrate ventrally to reach the ventral pallium deep to the piriform cortex at E14.5 in the mous

68 nterior frontal cortex of mice with a dorsal pallium-derived, conditional knock-out (cKO) of Met.

69 llium (DC); the dorsolateral division of the pallium (DL) contained only weakly labeled neurons.

70 jor pathways are recursive: the dorsolateral pallium (DL) projects strongly to DDi, with lesser input

71 Apteronotus leptorhynchus, the dorsolateral pallium (DL) receives diencephalic inputs representing e

72 nections of DD are entirely intrinsic to the pallium: DL projects to DD (glutamatergic) and DD feeds

73 anscription factor largely restricted to the pallium during development.

74 Here, we show that the avian auditory pallium exhibits the same information-processing princip

75 The lizard medial pallium, expressing all genes, includes the medial and d

76 The ventral pallium, expressing Lhx9, but not Emx1, gives rise to th

77 Furthermore, like the mammalian pallium, expression in the ventral pallial subdivisions

78 , the hyperstriatum accessorium (HA) and the pallium externum (PE).

79 subdivisions in the dorsal and ventral avian pallium, forming mirror images to each other.

80 ound that Dbx1-positive cells of the ventral pallium generate the excitatory neurons of the basolater

81 now newly propose that the mammalian ventral pallium gives rise not only to all of the pallial amygda

82 nown connectivity, we propose that the avian pallium has four major cell populations similar to those

83 till uncertain for most of the telencephalic pallium in birds and thus the new pallial terminology is

84 had the tendency to descend into the ventral pallium in large aberrant fascicles.

85 s known about the development of the lateral pallium in mammals.

86 The region designated as the ventral pallium in the initial quadripartite model should theref

87 In addition, the avian auditory pallium is composed of adjacent information-processing r

88 In contrast, the teleost pallium is not well understood and its relation to that

89 igrating Nr4a2-negative cells in the ventral pallium; it is therefore developmentally distinct from t

90 ered a most ventrolateral part of the dorsal pallium (its ventrolateral subdivision).

91 tinct regions: (1) descending input from the pallium itself (dorsomedial and dorsocentral subdivision

92 connections between the accumbens and medial pallium just dorsal to it suggest a column-like organiza

93 brain areas including the dorsal and medial pallium, lateral and medial septum, bed nucleus of the s

94 e development of the progenitor zones in the pallium, lateral ganglionic eminence (LGE) and medial ga

95 ic ablation of MET signaling in mouse dorsal pallium leads to altered neuronal morphology indicative

96 Sensory-evoked potentials in this fish pallium may be more segregated than in elasmobranchs and

97 First, the avian medial pallium may correspond to part of the mammalian prefront

98 ed, with the highest densities in the medial pallium (mp; homolog of the mammalian hippocampus), accu

99 septum; amygdala; nucleus accumbens; ventral pallium; nucleus basalis Meynert; bed nucleus of the str

100 emonstration of steroid concentration in the pallium of a teleost forebrain.

101 The quadripartite model of the telencephalic pallium of amniotes offered by the Puelles school includ

102 gies between DL and DC and medial and dorsal pallium of tetrapods, respectively.

103 sic connections of the dorsal telencephalon (pallium) of gymnotiform fish.

104 In the dorsal telencephalon (pallium) of vertebrates, it remains unresolved which anc

105 al and organizational model of the zebrafish pallium-one which is the result of a complex outward-inw

106 addition there was almost no CARTp-ir in the pallium or the hippocampal formation, and little CARTp-i

107 and the VLS receives inputs from the lateral pallium-originated areas (e.g., the insula) [5, 6].

108 The VMS receives inputs from medial pallium-originated limbic structures (e.g., the medial p

109 e report that the germinal zone of the adult pallium originates from two distinct subtypes of embryon

110 the lateral septum, amygdala pars lateralis, pallium, preoptic area, hypothalamus, and dorsal mesence

111 medial amygdala, septal territories, medial pallium, preoptic area, lateral hypothalamus, thalamus,

112 erminate in all subpallial nuclei and in the pallium: sparsely in the medial pallial division (Dm); h

113 r of the olfactory bulbs, dorsal and lateral pallium, striatum, various subfields of the amygdala, be

114 x [5,6]; rather, they possess a neuron-dense pallium that is organized in clusters, in contrast to th

115 espectively) the hyperpallium (hypertrophied pallium), the mesopallium (middle pallium), the nidopall

116 ertrophied pallium), the mesopallium (middle pallium), the nidopallium (nest pallium), and the arcopa

117 progenitor domains in the telencephalon: the pallium, the major source of excitatory neurons, and the

118 ypothalamus, amygdala homologs of the dorsal pallium, the pineal organ, the inner ear, the pituitary,

119 communication information is conveyed to the pallium through complex indirect pathways that originate

120 an basal ganglia were renamed as part of the pallium, using prefixes that retain most established abb

121 at immediately flank the PSB are the ventral pallium (VP) and the dorsal lateral ganglionic eminence

122 ata indicate that progenitors in the ventral pallium (VP) contribute projection neurons to the LA and

123 Thus, the region of the lateral pallium was misidentified in the quadripartite model, as

124 earance of TH-ir cells in the telencephalon (pallium) was rather late (stage [S]31) with respect to t

125 cipient sensory neurons of the telencephalic pallium, whereas high egr1 upregulation occurred only in

126 atory neurons derive from progenitors in the pallium, whereas inhibitory neurons originate from proge

127 ain has a "limbic loop" involving the medial pallium, which also receives input from the avian equiva

128 a, and may belong to a distinct dorsolateral pallium, which extends from rostral to caudal levels.

129 The pallium, which primarily consists of glutamatergic corti

130 luence hypotheses on homologies of the avian pallium with other vertebrates.