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1 diate zone of the subcortical telencephalon (subpallium).
2 ry neurons originate from progenitors in the subpallium.
3  develop from the dorsal pallium and ventral subpallium.
4 before dorsal Wingless signals, and a larger subpallium.
5 ptal nuclei derive from both the pallium and subpallium.
6 ike, and septal-like subdivisions within the subpallium.
7 ons of) the dorsal as well as of the ventral subpallium.
8  primordium by tangential migration from the subpallium.
9 ir embryonic site of origin, the pallium and subpallium.
10 duced in number and grew no farther than the subpallium.
11  has two major subdivisions, the pallium and subpallium.
12 ain tegmentum and profuse innervation of the subpallium.
13 regionalization of the reptilian pallium and subpallium.
14  medial ganglionic eminence of the embryonic subpallium and express the transcription factor Nkx2-1.
15 e cortical interneurons are generated in the subpallium and migrate tangentially over a long distance
16 l cell types in the pallium and eight in the subpallium and nominated novel marker genes.
17 plementary expression of dlx2a, dlx5a in the subpallium and tbr1, neurod in the pallium.
18 linergic-positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleo
19 ) cells were observed in the olfactory bulb, subpallium, and preoptic area of the telencephalon.
20 tor expression patterns in porcine embryonic subpallium are similar to rodents, delineating a distinc
21 ly) into postmitotic zones of the peripheral subpallium (as does Dlx2a and Lhx6) as well as (tangenti
22  mutants, cortical pioneer axons entered the subpallium at the appropriate time, but most stopped gro
23 dentify the boundary between the pallium and subpallium based on the complementary expression of dlx2
24 ns (which do not express Gbx2) grew into the subpallium but did not enter the diencephalon.
25 lium and in a restricted zone of the ventral subpallium, comparable to the known restricted septal ex
26 nic cortex and were scattered throughout the subpallium, consistent with the cell polarity abnormalit
27 t Chrna2 is specifically expressed in medial subpallium-derived amygdalar nuclei from early developme
28 on of the postnatal SVZ and demonstrate that subpallium-derived Dlx2-expressing cells give rise to as
29 enriched for pathways including striatum and subpallium development, mechanosensory response, dopamin
30 itors, mimicking human forebrain pallium and subpallium development.
31 ct regions of the telencephalon (pallium and subpallium), diencephalon, mesencephalon, hindbrain, spi
32                           After reaching the subpallium, each projection may require a molecularly in
33  showed that only RG cells isolated from the subpallium (ganglionic eminence) generate CalR(+) or GAB
34 l telencephalon, neural progenitors from the subpallium generate the majority of inhibitory medium sp
35  and medial ganglionic eminence (MGE) in the subpallium has been well studied; however, so far the ro
36 In the larval zebrafish, subdivisions of the subpallium have been proposed using conserved developmen
37  all other dorsal thalamic nuclei are to the subpallium, however.
38     The conserved expression of CARTp in the subpallium, hypothalamus, and dorsal vagal complex of bi
39  of many CNS regions, including the pallium, subpallium, hypothalamus, diencephalon, optic tectum, mi
40 CART-immunoreactive fibers were found in the subpallium, hypothalamus, midbrain, and brainstem.
41 sent a new model for the subdivisions of the subpallium in teleost fish.
42  identify transcriptional changes within the subpallium in the absence of Arx.
43 ed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic
44  the olfactory bulb (OB), all regions of the subpallium (including the dorsal, ventral, central, and
45 comprehensive regional fate map of the mouse subpallium, including sources for specific subtypes of a
46 rneurons are both generated in the embryonic subpallium, including the medial ganglionic eminence (MG
47 , Dlx2a is generally expressed in all of the subpallium, including the ventricular zones of (all thre
48 n the dorsal subdivision (Sdd) of the dorsal subpallium, interpreted here as the homologue of the mam
49 bdivision (Sdv) of the precommissural dorsal subpallium, interpreted here as the homologue of the mam
50 ventricular zone (SVZ) that extends from the subpallium into the dorsal pallium.
51 diencephalic populations DC2 and DC4) to the subpallium is considered the zebrafish correlate of the
52  preoptic area of the telencephalon, and the subpallium is devoid of these cells.
53                                          The subpallium is well described and highly conserved.
54 ogenitor domains of the mouse basal ganglia (subpallium, MGE, and CGE).
55 e central vocal and auditory networks in the subpallium, preoptic area (POA), anterior hypothalamus,
56 velopment of the human forebrain pallium and subpallium, respectively.
57 d their inappropriate expression of normally subpallium-restricted developmental controls, conferring
58 ly lying posterior subdivision of the dorsal subpallium (Sdp; possible homologue of the subpallial am
59              Their close interactions in the subpallium suggest that they may use each other for guid
60 rthermore expressed in the zebrafish ventral subpallium (Sv, septum), and in the supra-/postcommissur
61  the dorsal (i.e. pallium) and ventral (i.e. subpallium) telencephalon.
62                            In the developing subpallium, the fate decision between neurons and glia i
63 y bulb (homologous to mammalian A16) and the subpallium, the hypothalamic groups (A12, A14), the pret
64  major source of excitatory neurons, and the subpallium, the major source of inhibitory neurons.
65 g- and Nkx2.1-positive domain in the lamprey subpallium was thought to be similar to mouse mutants in
66 resses dorsal molecular markers, whereas the subpallium, which primarily consists of the GABAergic ba