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1 tem cells within the ventricular zone of the medial ganglionic eminence.
2 on and several transcriptomic changes in the medial ganglionic eminence.
3 suppression of Nkx2-1 leads to a loss of the medial ganglionic eminence.
4 tory interneurons derived from the embryonic medial ganglionic eminence.
5 e telencephalic ventricular zone and not the medial ganglionic eminence.
6 e cortical interneurons that derive from the medial ganglionic eminence.
7 n (1) prenatal interneurons derived from the medial ganglionic eminence, (2) in postnatal PV cells, a
9 pped to LHX6+/DLX+ lineages derived from the medial ganglionic eminence, a progenitor domain in the v
10 of-function analysis, Gsh2 expression in the medial ganglionic eminence after E10.5 may negatively re
11 -specific impairment in proliferation in the medial ganglionic eminence and caudal ganglionic eminenc
12 would reduce interneuron neurogenesis in the medial ganglionic eminence and diminish the population o
13 interneurons, are generated from the ventral medial ganglionic eminence and dorsal preoptic area base
14 arkers for inhibitory cells derived from the medial ganglionic eminence and few expressed VGAT, found
15 g neurogenesis, single-cell transcriptome of medial ganglionic eminence and neurobehavioural function
16 ed radial glial progenitors in the embryonic medial ganglionic eminence and preoptic area preferentia
17 me group, develops domains equivalent to the medial ganglionic eminence and rhombic lip, resembling t
18 upregulation of Dlx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the
19 tical interneurons that are derived from the medial ganglionic eminence, as most studies have examine
20 .1+ interneuron progenitors in the embryonic medial ganglionic eminence at E14 that was associated wi
22 an prefrontal cortex: glutamatergic neurons, medial ganglionic eminence-derived GABAergic neurons, an
24 hese data suggest that Satb1 is required for medial ganglionic eminence-derived interneuron different
25 s regulates the differentiation of two major medial ganglionic eminence-derived interneuron populatio
26 ous system neuroblastoma, FOXR2-activated to medial ganglionic eminence-derived interneurons, which c
27 essing 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking
31 x, future hippocampus as well as lateral and medial ganglionic eminences exhibited a 20-30% reduction
32 odevelopmental literature on embryonic mouse medial ganglionic eminence exists (with some additional
33 as predominantly localised in the developing medial ganglionic eminences, flanking a Fgf8-positive mi
35 ings, single-cell transcriptomic analyses of medial ganglionic eminence identified a distinct subpopu
37 of wild-type embryonic interneurons from the medial ganglionic eminence into the prefrontal cortex of
39 s and fates of cells born in the lateral and medial ganglionic eminences (LGE and MGE) in 13.5-day-ol
41 E STATEMENT Here we demonstrate that porcine medial ganglionic eminence, like rodents, exhibit a dist
42 c mice, that the first OLPs originate in the medial ganglionic eminence (MGE) and anterior entopedunc
43 Other precursors--including those from the medial ganglionic eminence (MGE) and OB--fail to generat
46 rth disrupts interneuron neurogenesis in the medial ganglionic eminence (MGE) and, more importantly,
47 Furthermore, Nkx2.1(+) progenitors in the medial ganglionic eminence (MGE) are misspecified such t
48 rgic interneuron precursors derived from the medial ganglionic eminence (MGE) can induce a second per
49 nsplanted GABAergic precursor cells from the medial ganglionic eminence (MGE) can migrate and differe
50 GABAergic progenitor cells derived from the medial ganglionic eminence (MGE) can reverse mechanical
52 have been described, a system modeling human medial ganglionic eminence (MGE) development, a critical
53 al interneurons originating in the embryonic medial ganglionic eminence (MGE) diverge into a range of
54 t inhibitory interneuron precursors from the medial ganglionic eminence (MGE) enhances GABAergic sign
57 d to GABAergic interneurons derived from the medial ganglionic eminence (MGE) impacts their synaptic
58 llium, lateral ganglionic eminence (LGE) and medial ganglionic eminence (MGE) in the subpallium has b
59 nic precursors of GABAergic neurons from the medial ganglionic eminence (MGE) into adult mouse spinal
60 tation of precursor cells from the embryonic medial ganglionic eminence (MGE) into early postnatal ne
61 ber of embryonic inhibitory neurons from the medial ganglionic eminence (MGE) into postnatal visual c
62 phalic GABAergic interneurons from the mouse medial ganglionic eminence (MGE) into the adult mouse sp
66 er, we report that mosaic elimination in the medial ganglionic eminence (MGE) of Smo, a key effector
67 ron subgroups originate primarily within the medial ganglionic eminence (MGE) of the subcortical tele
68 interneurons targeting cells by lineage from medial ganglionic eminence (MGE) or caudal ganglionic em
69 l interneurons tangentially migrate from the medial ganglionic eminence (MGE) or the adjacent preopti
70 e and comprises cryopreserved, post-mitotic, medial ganglionic eminence (MGE) pallial-type GABAergic
73 ere, we show that Prdm16 expression in mouse medial ganglionic eminence (MGE) progenitors is required
75 nNOS(+) IvCs and NGCs are both derived from medial ganglionic eminence (MGE) progenitors under contr
78 contrary, it resulted in a partial rescue of medial ganglionic eminence (MGE) properties, including i
79 atin (SST(+)) interneuron (IN) production in medial ganglionic eminence (MGE) secondary progenitors i
80 ice lacking ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE) showed marked deficits
81 nd Cdc42 in the ventricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice ca
82 ins inhibitory interneurons derived from the medial ganglionic eminence (MGE), a germinal zone in the
83 opment, several cIN subtypes derive from the medial ganglionic eminence (MGE), a transient ventral te
84 gration is regulated by blood vessels of the medial ganglionic eminence (MGE), an interneuron progeni
85 a transient embryonic structure known as the medial ganglionic eminence (MGE), but how the remarkable
86 nsplanted neuronal precursors from embryonic medial ganglionic eminence (MGE), but not from lateral g
87 l GABAergic interneuron progenitors from the medial ganglionic eminence (MGE), can overcome the mecha
88 tyric acid (GABA) interneurons, derived from medial ganglionic eminence (MGE), is implicated in disor
89 ing interneurons, which are derived from the medial ganglionic eminence (MGE), plays a role in the em
90 e-cell RNA sequencing on the mouse embryonic medial ganglionic eminence (MGE), the major birthplace f
91 Cell cycle regulation was examined in the medial ganglionic eminence (MGE), the major source of PV
92 n of GABAergic precursors from the embryonic medial ganglionic eminence (MGE), the source of neocorti
93 ebral cortical interneurons originate in the medial ganglionic eminence (MGE), where the signaling mo
94 ergic neurons, but not by progenitors in the medial ganglionic eminence (MGE), which generate cortica
95 GABA on apoptosis is mediated by inputs from medial ganglionic eminence (MGE)-derived but not caudal
96 /Ai14 embryos harboring tdTomato-fluorescent medial ganglionic eminence (MGE)-derived cortical GABAer
99 uired for the differentiation of a subset of medial ganglionic eminence (MGE)-derived neurons, but ar
101 during development represents an ancestral, medial ganglionic eminence (MGE)-derived striatal popula
102 SCs into telencephalic excitatory neurons or medial ganglionic eminence (MGE)-like inhibitory neurons
104 t the directed differentiation of hPSCs into medial ganglionic eminence (MGE)-like progenitors and th
111 we compared interneuronal progenitors in the medial ganglionic eminences (MGEs), lateral ganglionic e
112 rgic progenitors, derived from the embryonic medial ganglionic eminence, migrate long distances follo
113 mber of Nkx2.1+ and Dlx2+ progenitors in the medial ganglionic eminence of both humans and rabbits by
115 ing a role in oligodendrogenesis, within the medial ganglionic eminence of Nkx2.1 mutants, the early
117 0 d, and then patterned to NKX2.1-expressing medial ganglionic eminence progenitors by simple treatme
118 lanted embryonic inhibitory neurons from the medial ganglionic eminence reinstate ocular dominance pl
119 Inhibitory interneurons derived from the medial ganglionic eminence represent the largest cohort
120 reted here as the homologue of the mammalian medial ganglionic eminence (the adult pallidum in mammal
121 transplantation of cells from the embryonic medial ganglionic eminence (the major origin of cerebral
122 ion of ventral neurons characteristic of the medial ganglionic eminence, the embryonic structure whic
124 other hand, disrupting specification of the medial ganglionic eminence through loss of Nkx2.1 homeob
125 e embryonic basal telencephalon (lateral and medial ganglionic eminences) through loss of Dlx1/2 home
126 c interneurons, from their generation in the medial ganglionic eminence up to their settlement in the
128 mice severely impaired proliferation in the medial ganglionic eminence without grossly altering diff