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1  the cytoplasm of neuronal and non-neuronal (subependymal and choroid plexus epithelial) cell bodies
2 ntracranial lesions were found, of which the subependymal and subcortical hamartomas were most preval
3 ing GFAP-expressing cells in the adult mouse subependymal and subgranular zones stopped the generatio
4  progenitors were organized in niches in the subependymal area and a decline in their number was obse
5 severe hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.
6 s of the brain, in ventricular ependymal and subependymal cells and in peripheral tissues.
7    Optogenetic inhibition and stimulation of subependymal ChAT(+) neurons in vivo indicated that they
8  head circumference at birth and findings of subependymal cysts and lenticulostriate vasculopathy in
9 entriculomegaly, intraventricular adhesions, subependymal cysts, intracerebral calcifications, and mi
10                                              Subependymal demyelinated lesions with axonal loss and m
11 enged the initial report and postulated that subependymal GFAP(+) cells were the stem cells.
12 Aug 10, 2009, more than 35% of patients with subependymal giant cell astrocytoma (SEGA) associated wi
13 ed expression of these proteins in tuber and subependymal giant cell astrocytoma (SEGA) specimens in
14 xpression was assessed in tuber (n = 16) and subependymal giant cell astrocytoma (SEGA; n = 6) specim
15 the molecular and developmental basis of the subependymal giant cell astrocytoma in humans.
16 cm or greater, and either serial growth of a subependymal giant cell astrocytoma, a new lesion of 1 c
17 angiomyolipomas, dermatological findings and subependymal giant cell astrocytoma.
18 s (3q and 9p), one astrocytoma (6q), and two subependymal giant cell astrocytomas (16p and 21q).
19 ects with clinically definite TSC and either subependymal giant cell astrocytomas (n = 4) or a pilocy
20              Subependymal nodules (SENs) and subependymal giant cell astrocytomas (SEGAs) are common
21 s in TSC patients, renal angiomyolipomas and subependymal giant cell astrocytomas (SEGAs).
22 del characteristics of TSC hamartomas called subependymal giant cell astrocytomas (SEGAs).
23 rtical dysplasias, subependymal nodules, and subependymal giant cell astrocytomas (SEGAs).
24 disease was more severe than TSC1, with more subependymal giant cell astrocytomas and angiomyolipomas
25 cy and safety of everolimus in patients with subependymal giant cell astrocytomas associated with tub
26 se results support the use of everolimus for subependymal giant cell astrocytomas associated with tub
27 se results support the use of everolimus for subependymal giant cell astrocytomas associated with tub
28                      In the brain, growth of subependymal giant cell astrocytomas can cause life-thre
29 erruption of therapy resulted in regrowth of subependymal giant cell astrocytomas in one patient.
30 erved, which may be the murine equivalent of subependymal giant cell astrocytomas or tubers commonly
31  had at least 50% reduction in the volume of subependymal giant cell astrocytomas versus none in the
32 ent study, 25 TSC-related cortical tubers or subependymal giant cell astrocytomas, as well as tissue
33 findings are more likely to have concomitant subependymal giant cell astrocytomas, renal angiomyolipo
34  and CNS lesions include cortical tubers and subependymal giant cell astrocytomas, resulting in menta
35  Five to 15% of affected individuals display subependymal giant cell astrocytomas, which can lead to
36 me of 50% or greater relative to baseline in subependymal giant cell astrocytomas.
37 ally and significantly reduced the volume of subependymal giant cell astrocytomas.
38 arised tumours including angiomyolipomas and subependymal giant cell astrocytomas.
39 eaningful reduction in volume of the primary subependymal giant-cell astrocytoma, as assessed on inde
40  for surgical resection or other therapy for subependymal giant-cell astrocytoma.
41 iated with marked reduction in the volume of subependymal giant-cell astrocytomas and seizure frequen
42 ficacy end point was the change in volume of subependymal giant-cell astrocytomas between baseline an
43 ical resection is the standard treatment for subependymal giant-cell astrocytomas in patients with th
44  years of age or older with serial growth of subependymal giant-cell astrocytomas were eligible for t
45              Thus, concurrent suppression of subependymal glial differentiation and promotion of neur
46                       Noggin, by suppressing subependymal gliogenesis and increasing progenitor avail
47                                              Subependymal GMH showed tendency to localize in the regi
48                                              Subependymal gray matter heterotopia was more common tha
49 g schizencephalic clefts, heterotopic bands, subependymal grey matter heterotopia, and the cortex ove
50 n manifestations such as cortical tubers and subependymal hamartoma/giant cell astrocytomas are major
51 at the predominant cellular phenotype of the subependymal hamartomas is astroglial and suggests that
52 terotopia, and the cortex overlying band and subependymal heterotopia.
53                   We observed a substantial "subependymal-in" gradient of neuro-axonal loss and micro
54 ammatory degree either in large perivascular subependymal infiltrates, enriched in B cells, or within
55 eal tertiary lymphoid-like structures; large subependymal infiltrates, enriched in CD20(+) B cells an
56 most neurogenic zone of the adult brain, the subependymal layer (SEL) of the lateral ventricle.
57 ting, immature neurons in the olfactory bulb subependymal layer (SEL) undergo spontaneous and depolar
58 s in the adult brain occurs primarily in the subependymal layer (SEL), a zone where no particular org
59 ate that a regulatory region specific to the subependymal layer of the cerebral aqueduct and third ve
60               Midbrain tumors arose from the subependymal layer of the cerebral aqueduct.
61  The common finding of PNET arising from the subependymal layer of the diencephalon is unlikely to be
62         Intracranial tumors arising from the subependymal layer of the third ventricle also were obse
63 l retinal PNET and PNET originating from the subependymal layer of the third ventricle.
64  similarities between the Eker rat and human subependymal lesions.
65 al inflammation, compartmentalized either in subependymal lymphoid perivascular infiltrates or in CSF
66  lamina labyrinths or fractones derived from subependymal microglia.
67                          Murine APC promotes subependymal neurogenesis in rodents in vivo after ische
68 t of the organism, therefore indicating that subependymal neurogenesis--as a system--is integrated in
69 ctural and functional characteristics of the subependymal neurogenic niche and to summarize the avail
70               In three of four patients with subependymal nodular heterotopia, nodules had lower [(11
71                                              Subependymal nodules (SENs) and subependymal giant cell
72 moderate-to-severe mental retardation, fewer subependymal nodules and cortical tubers, less-severe ki
73             Giant cells in tubers, SEGAs and subependymal nodules in the Eker rat model of TSC expres
74 s associated with focal cortical dysplasias, subependymal nodules, and subependymal giant cell astroc
75 elopmental brain lesions, such as tubers and subependymal nodules.
76 R5-RARE reporter transgene, defines neurons, subependymal, or ependymal cells in discrete locations t
77 , the total (p = 0.20), ovoid (p = 0.31), or subependymal (p = 0.44) MRI thalamic lesion volumes corr
78 regions, including the lamina terminalis and subependymal peri-third-ventricular region.
79 one of the median eminence, and formation of subependymal perivascular plexus.
80  data suggested some input of cells into the subependymal population during fractionated treatment, a
81 sternae of the GA in distal perisynaptic and subependymal processes, in perivascular foot plates of c
82 onal differentiation can mobilize endogenous subependymal progenitor cells to achieve substantial neu
83  BDNF and noggin proteins actively recruited subependymal progenitor cells to form new MSNs that matu
84 y acting to inhibit glial differentiation by subependymal progenitor cells, can potentiate adenoviral
85 euronal addition to the adult striatum, from subependymal progenitor cells.
86                                 In addition, subependymal, protuberant nests of cells, consisting pri
87 o-parietal areas of brain parenchyma, mostly subependymal region.
88 ially the leptomeningeal vessels, and in the subependymal regions of the ventricular system where the
89  labeling was prominent adjacent to CVOs, in subependymal regions, and in fiber tracts.
90 n-mammalian vertebrates, but only supra- and subependymal serotonergic plexuses are a commonly studie
91 t is possible that the radiation response of subependymal stem cells and not the apoptotic-sensitive
92 ferase-positive (ChAT(+)) neurons within the subependymal (subep) region of the SVZ when these neuron
93 unoreactive puncta were located primarily in subependymal, subpial, and perivascular zones and were a
94 dult rodents, neural progenitor cells in the subependymal (SZ) zone of the lateral cerebral ventricle
95 ural precursor cells isolated from adult rat subependymal tissues.
96  in rapidly proliferating cells in the adult subependymal zone (SEZ) and early postnatal cerebellar e
97 of a neural stem cell niche in the postnatal subependymal zone (SEZ) and the rostral migratory stream
98 rogenitor cells (NPCs) residing in the adult subependymal zone (SEZ) are a potential source of expand
99 d ciliated ependymal (CE) cells, and special subependymal zone (SEZ) astrocytes as candidates for NSC
100  function reduced the number of qNSCs in the subependymal zone (SEZ) by inducing pre-mature activatio
101               Neural stem cells in the human subependymal zone (SEZ) generate neuronal progenitor cel
102 -aminobutyric A receptors (GABA(A)Rs) in the subependymal zone (SEZ) induces hyperpolarization and os
103 population of adult neural stem cells in the subependymal zone (SEZ) leads to persistently enhanced n
104 Z) of the hippocampal dentate gyrus, and the subependymal zone (SEZ) lining the lateral ventricles.
105                      We examined the rostral subependymal zone (SEZ) of postnatal human brain for exp
106                                          The subependymal zone (SEZ) of the lateral ventricles is one
107                                          The subependymal zone (SEZ) of the lateral ventricles of the
108 d that a majority of NSCs in the young adult subependymal zone (SEZ) originated from these slowly div
109                    The rodent subventricular/subependymal zone (SVZ/SEZ) houses neural stem cells (NS
110 rain harbors neuronal precursor cells in the subependymal zone (SZ).
111 at least 2 months after their genesis in the subependymal zone and are recruited primarily as GABAerg
112 n vivo fate mapping experiments in the adult subependymal zone and olfactory bulbs.
113 ate throughout the life of the animal in the subependymal zone and the subgranular zone of the dentat
114 ice in cortex, corpus callosum, hippocampus, subependymal zone area and thalamus.
115              Progenitors isolated from adult subependymal zone exhibit in vitro neurogenesis when sti
116 nce of neural stem cells (NSCs) in the brain subependymal zone of adult male and female mice.
117 mbryonic ventricular zone and persist in the subependymal zone of the adult brain.
118  neuroblasts migrate long distances from the subependymal zone of the lateral ventricles to the olfac
119                                    It is the subependymal zone of the lateral wall of the lateral ven
120 ted from neurospheres derived from postnatal subependymal zone or cerebellar cortex undergo a phenoty
121 f neuroblasts was significantly lower in the Subependymal Zone stem cell niche of lab mice when compa
122             Paradoxically, adult NSCs in the subependymal zone transcribe genes associated with both
123 rodent subventricular zone (SVZ; also called subependymal zone) generate doublecortin (Dcx)(+) neurob
124 n dopaminergic nerve terminals supplying the subependymal zone, acts as a niche component to sustain
125              Proliferative zones include the subependymal zone, from where progenitors migrate along
126                                          The subependymal zone--like a beating heart--continuously se
127 restricted to the lamina interna and lateral subependymal zone.
128 rentiated cortical neurons filling the adult subependymal zone; and that individuals with PH are at h

 
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