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1 is in the adult brain via maintenance of the ependyma.
2 cilia of epithelial cells in the trachea and ependyma.
3 s expression on the luminal membranes of the ependyma.
4 vessels to terminate immediately beneath the ependyma.
5 es, and cellular necrosis was evident in the ependyma.
6 minating in bulbs immediately underneath the ependyma.
7 hannel Na(x) expressed by astrocytes and the ependyma.
8  induced signals were present in ventricular ependyma.
9  glia, especially astrocytes and ventricular ependyma.
10 ry epithelium, as well as choroid plexus and ependyma.
11  layer V and by glia in the white matter and ependyma.
12 rs reside underneath the lateral ventricular ependyma.
13 cin and probenecid increased accumulation in ependyma 4-5 times.
14 transduction of key brain tissues, including ependyma, after intracerebroventricular injection.
15 nin-1/CD133, is exclusively localized to the ependyma, although not all ependymal cells are CD133(+).
16 er of SVZ astrocytes interpolated within the ependyma and established contact with the ventricle.
17                     Among nonneuronal cells, ependyma and meninges lining the ventricular and subarac
18  -17, is expressed in adult rats and mice by ependyma and SVZ cells with long basal processes, and in
19 neumoniae can be detrimental to the ciliated ependyma and that antipneumolysin antibody may have a th
20 al nuclei within the hypothalamus and in the ependyma and the circumventricular organs that act as an
21 e, pia mater, and aspects of the ventricular ependyma and was relatively low within areas of white ma
22 dentified in radial glia, mature astrocytes, ependyma, and choroid plexus epithelium, but not in neur
23 lt CNS (retina, cerebellum, cerebral cortex, ependyma, and choroid) as well as the adult kidney epith
24 esent in epithelial cells of choroid plexus, ependyma, and meninges.
25 rked enhancement throughout her meninges and ependyma, and TTR amyloid deposition was confirmed by me
26 e show that astrocytes integrated within the ependyma are dividing, BrdU-labeled astrocytes that shar
27  on direct ependymal injury, indicating that ependyma are not a major source of endogenous neural ste
28 cerebral injection, subjacent to ventricular ependyma, as well as scattered in cerebral white and gra
29 bencephalon and spinal cord were seen in the ependyma, but many labeled cells were found in nonependy
30 al mitosis in the rhombencephalon was in the ependyma, but this finding was not true in the spinal co
31 ld-type pneumococci caused disruption to the ependyma, but this was not observed in rats infected wit
32 zone (SVZ) astrocytes are separated from the ependyma by the hypocellular gap.
33  We find here that connexin signaling in the ependyma changes after injury of the adult spinal cord,
34 noreaction product being associated with the ependyma, choroid plexus, and the glia limitans.
35                 This protein is expressed by ependyma, choroid plexus, astrocytes, and oligodendrocyt
36 l tissues including the nasal mucosa and the ependyma/choroid plexus in the brain.
37  in mouse brain in the meninges, ventricular ependyma, circumventricular organs, along the vasculatur
38 hat were near to but did not directly damage ependyma, contained no ependyma-derived cells.
39 as observed, greatest (38%) at 2 mm from the ependyma/CSF boundary and least at 10 mm (13%).
40 est (26%) in subventricular locations at the ependyma/CSF boundary and least with increasing distance
41 density increased by over 50% at 2 mm at the ependyma/CSF boundary and only by 15% at 10 mm and this
42                                        Thus, ependyma-derived CCN1 restricts NSC expansion in the adu
43 d not directly damage ependyma, contained no ependyma-derived cells.
44                           Here, we show that ependyma-derived matricellular protein CCN1 (cellular co
45 rush injuries across the entire spinal cord, ependyma-derived progeny remained local, did not migrate
46 ic epithelial cells of the mouse airways and ependyma destined to become MCCs.
47 lytic cycle genes within the brain stem, the ependyma (EP), containing the limbic and cortical areas,
48 antibodies, and never migrated away from the ependyma even at 5 weeks after BrdU injection.
49                                   Transduced ependyma expressed high levels of recombinant enzyme, wi
50  astrocyte foot processes, glia limitans and ependyma, facilitates water movement into and out of the
51 k connecting cilia, and ciliated ventricular ependyma fails to mature.
52 ty was detected in leukocytes traversing the ependyma from leptomeningeal infiltrates.
53                                              Ependyma have been proposed as adult neural stem cells t
54 wed by ventricular regions (caudate putamen, ependyma, hippocampus, 0.05-0.14 ml g(-1)).
55 an 86% decline in total NSCs/mm(2) of intact ependyma in 2-year old versus 3-month-old mice, with few
56 y was detected in the ciliated region of the ependyma in the central canal from early postnatal devel
57  foci of hyperintensity perpendicular to the ependyma, like a stack of coins.
58 ccessory hypothalamic neurosecretory nuclei, ependyma lining the ventricles and choroid plexus which
59                  Loss of p73 function in the ependyma may thus be one determining factor for chronic
60 and in the cerebral cortex, hippocampus, and ependyma of adult mouse brains.
61 t vimentin-immunopositive processes from the ependyma of the adjacent surface of the third ventricle.
62                                          The ependyma of the adult spinal cord is a latent stem cell
63 reactive cells were found exclusively in the ependyma of the basal region of the lateral ventricles (
64 r, a spike of mitotic activity occurs in the ependyma of the rhombencephalon and throughout the spina
65                                          CSF/ependyma-oriented gradient of reduction in NeuN(+) neuro
66 n the gene product after transduction of the ependyma, reduces Abeta plaque deposition, neurodegenera
67               A similar form of SVZ-mediated ependyma repair was also observed in young mice after mi
68 cible deletion of Foxj1-Ank3 from mature SVZ ependyma resulted in dramatic depletion of neurogenesis.
69                                        Adult ependyma-specific deletion of Ccn1 transiently enhanced
70 n of rAAV4betagal resulted again in striking ependyma-specific expression of transgene, with a notabl
71  epithelium of the choroid plexus and in the ependyma, such as asymmetrical cell shape and size, misp
72 h axons crossing ventral to a thick layer of ependyma surrounding the central canal.
73  undetectable in OX-42-positive cells in the ependyma, the external capsule, choroid plexus, and meni
74 served that, as they incorporated within the ependyma, they took on antigenic and morphologic charact
75 entricular zone by transducing the forebrain ependyma to constitutively express BDNF.
76 e in the early stages of the reaction of the ependyma to injury remain little understood.
77  neglected in the study of meningitis is the ependyma, which has been identified as a location of adu
78 particularly those of the choroid plexus and ependyma, which play critical roles in producing cerebro
79 r, baseline gliogenesis occurs mainly in the ependyma with substantial contribution by nonependymal a