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1 ytes facilitate penetration through the glia limitans.
2 arance of the basement membrane and the glia limitans.
3 irect contacts with astrocytes near the glia limitans.
4 lial fibrillary acidic protein-positive glia limitans.
5 d with small blood vessels and with the glia limitans.
6 at terminate on blood vessels or on the glia limitans.
7 ial scar and the reconstitution of the glial limitans.
8 l disperse when located away from the sulcus limitans.
9 e lateral geniculate nucleus and the nucleus limitans.
10 h the ependyma, choroid plexus, and the glia limitans.
11 ells from localizing precisely at the sulcus limitans.
12 croglial reconstitution of the damaged glial limitans.
13 QP4, found in astrocyte foot processes, glia limitans and ependyma, facilitates water movement into a
14  removal of excess brain water through glial limitans and ependymal barriers.
15 n composed primarily of the superficial glia limitans and pial vessels, but trended toward a decrease
16 ecies (ROS) that ultimately breach the glial limitans and promote spread of the injury into the paren
17 d, from the ependymal layer to the pia-glial limitans, and from oligodendrocytes surrounding axons to
18 ; the dorsal, deep dorsal (DD), caudodorsal, limitans, and suprageniculate nuclei of MGd; and the MGm
19 in basement membrane and the underlying glia limitans are the key initial events of the cellular path
20 in basement membrane and the underlying glia limitans are the key initial events of the cellular path
21  Some cortical NeuN(+) neurons, GFAP(+) glia limitans astrocytes, Iba-1(+) microglia and S100beta(+)
22 arance of the basement membrane and the glia limitans at the cerebral cortical surface during develop
23 dherin localize preferentially to the sulcus limitans, but still disperse when located away from the
24  might serve to position cells at the sulcus limitans by counteracting their tendency to disperse dur
25 er (BBB) and then across the astrocytic glia limitans (GL).
26    Radial glial endfeet, which comprise glia limitans, grew out of the neural boundary.
27  that surround capillaries and form the glia limitans; however, the structural organization of AQP4 h
28 gues demonstrate that astrocytes of the glia limitans induce tight junction formation in response to
29 etween dorsal and ventral thalamus, the zona limitans interthalamica (ZLI).
30 egulating their penetration through the glia limitans into the parenchyma are less well studied, and
31 erior, nucleus of the optic tract, posterior limitans), into the superior colliculus, or into the vis
32 Sonic hedgehog (Shh) signaling from the zona limitans intrathalamica (ZLI) at the rostral border of t
33 ion the shh-positive signaling boundary zona limitans intrathalamica (ZLI) in the forebrain.
34                                     The zona limitans intrathalamica (ZLI) is located at the border b
35                     The position of the zona limitans intrathalamica (zli), a boundary-cell populatio
36                                     The zona limitans intrathalamica (ZLI), a narrow compartment in t
37  a set of brain enhancers active in the zona limitans intrathalamica (zli), a signaling center essent
38           The thalamic organizer is the zona limitans intrathalamica (ZLI), a transverse linear neuro
39 signaling centers, the cortical hem and zona limitans intrathalamica (ZLI), are merged, obliterating
40 rostral to caudal: the prethalamus, the zona limitans intrathalamica (ZLI), the thalamus and the pret
41 ntire thalamic ventricular zone and the zona limitans intrathalamica (ZLI).
42 nd an intervening boundary region - the zona limitans intrathalamica (ZLI).
43 h putative signalling properties -- the zona limitans intrathalamica (ZLI).
44 ling centres-the anterior neural ridge, zona limitans intrathalamica and isthmic organizer-are presen
45 n, PITX2 is expressed in neurons of the zona limitans intrathalamica and mammillary region and in gam
46 orebrain and have a caudal limit at the zona limitans intrathalamica, the boundary between dorsal and
47 o, including in a domain in or near the zona limitans intrathalamica.
48 cate that positioning of cells at the sulcus limitans is mediated in part by the differential express
49 iculate complex (MGC), suprageniculate (Sg), limitans (Lim), and medial pulvinar (PM) nuclei.
50 tures: posterior (Po), suprageniculate (Sg), limitans (Lim), and medial pulvinar (PM).
51  nuclei, including the suprageniculate (Sg), limitans (Lim), medial pulvinar (PM), and posterior nucl
52 a, margin of the lateral habenula, posterior limitans nucleus, superior colliculus, and periaqueducta
53 f the isthmic Muller cell I1 close to sulcus limitans of His.
54 osterior and medial pulvinar nuclei, nucleus limitans, pretectal area, nucleus of Darkschewitsch, mes
55  F-cadherin is first expressed at the sulcus limitans prior to the extensive cell movements that acco
56  in the arcuate nucleus/median eminence/glia limitans region.
57   The blood-brain barrier (BBB) and the glia limitans serve to prevent the migration of cells and oth
58 icate that the inducible barrier of the glia limitans should be further explored as a therapeutic tar
59 raoptic nucleus and associated ventral glial limitans (SON-VGL) under conditions that induce reversib
60 of PPC with features in common with the glia limitans that is formed by endfeet in other cortical are
61 ities in the pial surface basal lamina (glia limitans) that probably underlie the neuronal migration
62 stabilizes the basement membrane of the glia limitans, thereby supporting the cortical infrastructure
63 l changes in astrocytes of the ventral glial limitans (VGL) associated with a well-known model of cen
64 different regions, including one, the sulcus limitans, which partitions the caudal neural tube into a

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