ライフサイエンスコーパス: subependymal

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 enged the initial report and postulated that subependymal GFAP(+) cells were the stem cells.

11 Aug 10, 2009, more than 35% of patients with subependymal giant cell astrocytoma (SEGA) associated wi

12 ed expression of these proteins in tuber and subependymal giant cell astrocytoma (SEGA) specimens in

13 xpression was assessed in tuber (n = 16) and subependymal giant cell astrocytoma (SEGA; n = 6) specim

14 the molecular and developmental basis of the subependymal giant cell astrocytoma in humans.

15 cm or greater, and either serial growth of a subependymal giant cell astrocytoma, a new lesion of 1 c

16 s (3q and 9p), one astrocytoma (6q), and two subependymal giant cell astrocytomas (16p and 21q).

17 ects with clinically definite TSC and either subependymal giant cell astrocytomas (n = 4) or a pilocy

18 Subependymal nodules (SENs) and subependymal giant cell astrocytomas (SEGAs) are common

19 rtical dysplasias, subependymal nodules, and subependymal giant cell astrocytomas (SEGAs).

20 s in TSC patients, renal angiomyolipomas and subependymal giant cell astrocytomas (SEGAs).

21 disease was more severe than TSC1, with more subependymal giant cell astrocytomas and angiomyolipomas

22 cy and safety of everolimus in patients with subependymal giant cell astrocytomas associated with tub

23 se results support the use of everolimus for subependymal giant cell astrocytomas associated with tub

24 se results support the use of everolimus for subependymal giant cell astrocytomas associated with tub

25 In the brain, growth of subependymal giant cell astrocytomas can cause life-thre

26 erruption of therapy resulted in regrowth of subependymal giant cell astrocytomas in one patient.

27 erved, which may be the murine equivalent of subependymal giant cell astrocytomas or tubers commonly

28 had at least 50% reduction in the volume of subependymal giant cell astrocytomas versus none in the

29 ent study, 25 TSC-related cortical tubers or subependymal giant cell astrocytomas, as well as tissue

30 findings are more likely to have concomitant subependymal giant cell astrocytomas, renal angiomyolipo

31 and CNS lesions include cortical tubers and subependymal giant cell astrocytomas, resulting in menta

32 Five to 15% of affected individuals display subependymal giant cell astrocytomas, which can lead to

33 me of 50% or greater relative to baseline in subependymal giant cell astrocytomas.

34 ally and significantly reduced the volume of subependymal giant cell astrocytomas.

35 arised tumours including angiomyolipomas and subependymal giant cell astrocytomas.

36 eaningful reduction in volume of the primary subependymal giant-cell astrocytoma, as assessed on inde

37 for surgical resection or other therapy for subependymal giant-cell astrocytoma.

38 iated with marked reduction in the volume of subependymal giant-cell astrocytomas and seizure frequen

39 ficacy end point was the change in volume of subependymal giant-cell astrocytomas between baseline an

40 ical resection is the standard treatment for subependymal giant-cell astrocytomas in patients with th

41 years of age or older with serial growth of subependymal giant-cell astrocytomas were eligible for t

42 Thus, concurrent suppression of subependymal glial differentiation and promotion of neur

43 Noggin, by suppressing subependymal gliogenesis and increasing progenitor avail

44 Subependymal GMH showed tendency to localize in the regi

45 Subependymal gray matter heterotopia was more common tha

46 g schizencephalic clefts, heterotopic bands, subependymal grey matter heterotopia, and the cortex ove

47 n manifestations such as cortical tubers and subependymal hamartoma/giant cell astrocytomas are major

48 at the predominant cellular phenotype of the subependymal hamartomas is astroglial and suggests that

49 terotopia, and the cortex overlying band and subependymal heterotopia.

50 most neurogenic zone of the adult brain, the subependymal layer (SEL) of the lateral ventricle.

51 ting, immature neurons in the olfactory bulb subependymal layer (SEL) undergo spontaneous and depolar

52 s in the adult brain occurs primarily in the subependymal layer (SEL), a zone where no particular org

53 ate that a regulatory region specific to the subependymal layer of the cerebral aqueduct and third ve

54 Midbrain tumors arose from the subependymal layer of the cerebral aqueduct.

55 The common finding of PNET arising from the subependymal layer of the diencephalon is unlikely to be

56 Intracranial tumors arising from the subependymal layer of the third ventricle also were obse

57 l retinal PNET and PNET originating from the subependymal layer of the third ventricle.

58 similarities between the Eker rat and human subependymal lesions.

59 lamina labyrinths or fractones derived from subependymal microglia.

60 Murine APC promotes subependymal neurogenesis in rodents in vivo after ische

61 t of the organism, therefore indicating that subependymal neurogenesis--as a system--is integrated in

62 ctural and functional characteristics of the subependymal neurogenic niche and to summarize the avail

63 In three of four patients with subependymal nodular heterotopia, nodules had lower [(11

64 Subependymal nodules (SENs) and subependymal giant cell

65 moderate-to-severe mental retardation, fewer subependymal nodules and cortical tubers, less-severe ki

66 Giant cells in tubers, SEGAs and subependymal nodules in the Eker rat model of TSC expres

67 s associated with focal cortical dysplasias, subependymal nodules, and subependymal giant cell astroc

68 elopmental brain lesions, such as tubers and subependymal nodules.

69 R5-RARE reporter transgene, defines neurons, subependymal, or ependymal cells in discrete locations t

70 regions, including the lamina terminalis and subependymal peri-third-ventricular region.

71 one of the median eminence, and formation of subependymal perivascular plexus.

72 data suggested some input of cells into the subependymal population during fractionated treatment, a

73 sternae of the GA in distal perisynaptic and subependymal processes, in perivascular foot plates of c

74 onal differentiation can mobilize endogenous subependymal progenitor cells to achieve substantial neu

75 BDNF and noggin proteins actively recruited subependymal progenitor cells to form new MSNs that matu

76 y acting to inhibit glial differentiation by subependymal progenitor cells, can potentiate adenoviral

77 euronal addition to the adult striatum, from subependymal progenitor cells.

78 In addition, subependymal, protuberant nests of cells, consisting pri

79 o-parietal areas of brain parenchyma, mostly subependymal region.

80 ially the leptomeningeal vessels, and in the subependymal regions of the ventricular system where the

81 labeling was prominent adjacent to CVOs, in subependymal regions, and in fiber tracts.

82 n-mammalian vertebrates, but only supra- and subependymal serotonergic plexuses are a commonly studie

83 t is possible that the radiation response of subependymal stem cells and not the apoptotic-sensitive

84 unoreactive puncta were located primarily in subependymal, subpial, and perivascular zones and were a

85 dult rodents, neural progenitor cells in the subependymal (SZ) zone of the lateral cerebral ventricle

86 ural precursor cells isolated from adult rat subependymal tissues.

87 in rapidly proliferating cells in the adult subependymal zone (SEZ) and early postnatal cerebellar e

88 of a neural stem cell niche in the postnatal subependymal zone (SEZ) and the rostral migratory stream

89 rogenitor cells (NPCs) residing in the adult subependymal zone (SEZ) are a potential source of expand

90 d ciliated ependymal (CE) cells, and special subependymal zone (SEZ) astrocytes as candidates for NSC

91 -aminobutyric A receptors (GABA(A)Rs) in the subependymal zone (SEZ) induces hyperpolarization and os

92 population of adult neural stem cells in the subependymal zone (SEZ) leads to persistently enhanced n

93 We examined the rostral subependymal zone (SEZ) of postnatal human brain for exp

94 The subependymal zone (SEZ) of the lateral ventricles is one

95 The subependymal zone (SEZ) of the lateral ventricles of the

96 d that a majority of NSCs in the young adult subependymal zone (SEZ) originated from these slowly div

97 The rodent subventricular/subependymal zone (SVZ/SEZ) houses neural stem cells (NS

98 rain harbors neuronal precursor cells in the subependymal zone (SZ).

99 at least 2 months after their genesis in the subependymal zone and are recruited primarily as GABAerg

100 n vivo fate mapping experiments in the adult subependymal zone and olfactory bulbs.

101 ate throughout the life of the animal in the subependymal zone and the subgranular zone of the dentat

102 ice in cortex, corpus callosum, hippocampus, subependymal zone area and thalamus.

103 Progenitors isolated from adult subependymal zone exhibit in vitro neurogenesis when sti

104 nce of neural stem cells (NSCs) in the brain subependymal zone of adult male and female mice.

105 mbryonic ventricular zone and persist in the subependymal zone of the adult brain.

106 neuroblasts migrate long distances from the subependymal zone of the lateral ventricles to the olfac

107 It is the subependymal zone of the lateral wall of the lateral ven

108 ted from neurospheres derived from postnatal subependymal zone or cerebellar cortex undergo a phenoty

109 rodent subventricular zone (SVZ; also called subependymal zone) generate doublecortin (Dcx)(+) neurob

110 n dopaminergic nerve terminals supplying the subependymal zone, acts as a niche component to sustain

111 Proliferative zones include the subependymal zone, from where progenitors migrate along

112 The subependymal zone--like a beating heart--continuously se

113 restricted to the lamina interna and lateral subependymal zone.

114 rentiated cortical neurons filling the adult subependymal zone; and that individuals with PH are at h