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1 positive cell subpopulation derived from the lateral ganglionic eminence.
2 of newborn MSNs within their birthplace, the lateral ganglionic eminence.
3 ross the cortical-striatal boundary into the lateral ganglionic eminence.
4 rns of gene expression characteristic of the lateral ganglionic eminence.
5 bryonic neurons that populate the medial and lateral ganglionic eminences.
6 rkers characteristic of either the medial or lateral ganglionic eminences.
7 sed bromodeoxyuridine (BrdU) labeling in the lateral ganglionic eminence and frontal cortical neuroep
9 exhibit an increase in cell death within the lateral ganglionic eminence and rostral migratory stream
10 lial characteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumemb
11 rcine ventral mesencephalon or porcine fetal lateral ganglionic eminence cells were also performed.
13 is robustly expressed in the prethalamus and lateral ganglionic eminence-derived corridor and on cort
14 suggest that the ITCs arise from the dorsal lateral ganglionic eminence (dLGE) and migrate in the la
17 day 11 (E11, E0 = day of conception) when a lateral ganglionic eminence emerges surrounding the late
18 differentiation of neurons that populate the lateral ganglionic eminence express different combinatio
19 mbryonic forebrain progenitors of the dorsal lateral ganglionic eminence from Pax6 mutant Small Eye (
20 on corresponding to the mammalian medial and lateral ganglionic eminences generated medium spiny neur
21 the cytoarchitecture of the human SVZ at the lateral ganglionic eminence late in the second trimester
22 ment of the progenitor zones in the pallium, lateral ganglionic eminence (LGE) and medial ganglionic
23 on of Fgf3 in the subventricular zone of the lateral ganglionic eminence (LGE) at embryonic day 13.5
24 ferentiation phenotypes, particularly in the lateral ganglionic eminence (LGE) caudal ganglionic emin
26 nate reduction in the size of the Tlx mutant lateral ganglionic eminence (LGE) from embryonic day 14.
27 ors expressed in neuronal progenitors of the lateral ganglionic eminence (LGE) in the ventral telence
29 eas there is considerable agreement that the lateral ganglionic eminence (LGE) is the origin of stria
32 dial ganglionic eminence (MGE), but not from lateral ganglionic eminence (LGE) or neocortex, disperse
33 n of distinct neuronal subtypes derived from lateral ganglionic eminence (LGE) progenitors at specifi
34 ng the cell cycle of progenitor cells in the lateral ganglionic eminence (LGE), the neuroepithelial p
35 al GABAergic interneurons (GABA INs), or the lateral ganglionic eminence (LGE), which generate GABA I
36 specified such that they acquire a subset of lateral ganglionic eminence (LGE)-specific properties at
41 is expressed later in the forebrain itself (lateral ganglionic eminence; LGE) starting at E12.5, sug
42 s in the medial ganglionic eminences (MGEs), lateral ganglionic eminences (LGEs), and caudal ganglion
45 dult basal ganglia arise from the medial and lateral ganglionic eminences, morphologically distinct s
46 Cells of the corpus striatum arise from the lateral ganglionic eminence of the telencephalic neuroep
48 reted here as the homologue of the mammalian lateral ganglionic eminence (the adult caudatoputamen in
51 transcription factors normally found in the lateral ganglionic eminence, to prevent precocious diffe
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