ライフサイエンスコーパス: intermediate zone

1 ice, showing migrating neurons halted in the intermediate zone.

2 olar to a bipolar neuronal morphology in the intermediate zone.

3 ecome multipolar and move nonradially in the intermediate zone.

4 r great distension mediolaterally across the intermediate zone.

5 mpaired orientation and migration across the intermediate zone.

6 the ventral horn and the lateral part of the intermediate zone.

7 migratory phase essential for entry into the intermediate zone.

8 , mainly where breakpoint criteria lacked an intermediate zone.

9 nd a second in a heterotopic position in the intermediate zone.

10 eral cortex and have sent out axons into the intermediate zone.

11 FOV), and a PAL-II with a relatively narrow intermediate zone (5.60 mm; 13 degrees H clear FOV).

12 H clear FOV), a PAL-I with a relatively wide intermediate zone (7.85 mm; 18 degrees H clear FOV), and

13 ks contains 4 layers: a ventricular zone, an intermediate zone, a homogeneous-appearing hippocampal p

14 Those few bipolar cells that reached the intermediate zone also exhibited a complete block in som

15 ns on cholinergic interneurons in the medial intermediate zone and C boutons on motoneurons.

16 n of Botch drives neural stem cells into the intermediate zone and cortical plate.

17 anal, as reported by others, but also in the intermediate zone and dorsal horn of the spinal gray mat

18 mice make ectopic projections rostral in the intermediate zone and frontal cortex.

19 l migration, resulting in increased cells in intermediate zone and less cells in CP, and decreases de

20 ess, multipolar to bipolar transition in the intermediate zone and locomotion in the cortical plate,

21 y (anti-adhesive, neurite repelling) and the intermediate zone and subplate (in which thalamic axons

22 ed a cell number reduction in upper laminae (intermediate zone and tectal plate), and at E9, they exh

23 In addition, cells in the intermediate zone and the cortical plate were also frequ

24 orm subcortical band heterotopias within the intermediate zone and then white matter.

25 At E17, axons course tangentially within the intermediate zone and turn or branch near the deepest la

26 synaptic activation of lamina VIII and other intermediate zone and ventral horn interneurones.

27 ns of the thoracic spinal cord (dorsal horn, intermediate zone and ventral horn).

28 ct cord evoked local field potentials in the intermediate zone and ventral horn, which is where T13 a

29 cular zone, the intervening white matter (or intermediate zone), and different sites of developing co

30 alyzed sections of cortex (ventricular zone, intermediate zone, and cortical plate [CP]) containing g

31 nerve regenerated into the ventral horn, the intermediate zone, and dorsal horn base, both in intact

32 HuD is expressed in migrating neurons of the intermediate zone, and mHuC is expressed in mature corti

33 ne expression between the ventricular zones, intermediate zone, and subplate, and distinct postnatal

34 he deep dorsal horn, the lateral part of the intermediate zone, and the dorsal two-thirds of the vent

35 plate of more dorsal cortex have entered the intermediate zone, and, by P5, they reach the primitive

36 migration increases with ascent through the intermediate zone (average 2-6.4 microns/hr) slowing onl

37 When they reached the ventral intermediate zone, axons slowed down, often coming to a

38 ewly born neurons at the subventricular zone/intermediate zone border.

39 uronal precursors at the subventricular zone/intermediate zone boundary at a transitional migratory p

40 entuates the known distinct character of the intermediate zone by showing for the first time that the

41 s were expressed by migrating neurons in the intermediate zone, characterized by a spindle-like shape

42 S/VZ) and the postproliferative compartment (intermediate zone/cortical plate/marginal zone) were exa

43 ent in many neurons in the ventricular zone, intermediate zone, developing cortical plate, and margin

44 In addition, most IE2(+) cells in the lower intermediate zone either showed multipolar morphology wi

45 us Reelin-expressing cells were found in the intermediate zone, except for regions containing somatic

46 However, scarce VGLUT2 terminals on intermediate zone excitatory premotor interneurons with

47 Addition of chNP to intermediate-zone explants did not enhance the Shh respo

48 Exposure of intermediate-zone explants to cGMP analogs enhanced thei

49 in a heterotopic position in the superficial intermediate zone, i.e., between the two cortical plates

50 r-related sites were sparsely connected with intermediate zone interneurons and tended to affect the

51 e neurons at 400 mum in the dorsal horn, 131 intermediate zone interneurons from approximately 800 mi

52 operties of excitatory and inhibitory spinal intermediate zone interneurons in pathways from group I

53 ow that individual excitatory and inhibitory intermediate zone interneurons may operate in a highly d

54 ongoing activities of T(10) dorsal horn and intermediate zone interneurons, and we determined the in

55 For 46 of the intermediate zone interneurons, we found significant pos

56 ression of FoxG1 during migration within the intermediate zone is essential for the proper assembly o

57 icular zone/subventricular zone (VZ/SVZ) and intermediate zone (IZ) of the dorsal telencephalon.

58 egion which included the lateral part of the intermediate zone (lateral to the large group I intermed

59 VIa during the following days; axons in the intermediate zone may give rise to radially directed bra

60 n measures showed that cutaneous neurons and intermediate zone neurons were related better to premoto

61 ween $50,000 to $100, 000/QALY or within the intermediate zone of acceptable cost-effectiveness ratio

62 ule and as two distinct fascicles within the intermediate zone of the cerebral cortex.

63 essed in extending neuronal processes in the intermediate zone of the developing cortex, a region tha

64 istance of 2 mm of choroidal melanoma in the intermediate zone of the fundus.

65 ral bed nucleus of the stria terminalis, and intermediate zone of the lateral septum, in which CRF1,

66 abeled neurons with much smaller soma in the intermediate zone of the medial RF, a few hundred microm

67 n differentiating neuronal precursors in the intermediate zone of the mouse and chick neural tube.

68 f GABA immunoreactive cells was found in the intermediate zone of the NST, medial to the solitary tra

69 All of the motor areas also terminate in the intermediate zone of the spinal cord (laminae V-VIII).

70 The intermediate zone of the spinal grey matter contains pre

71 om the cortex and thalamus first meet in the intermediate zone of the subcortical telencephalon (subp

72 ile smaller males and females co-occur in an intermediate zone of warmth.

73 c innervation in the marginal, subplate, and intermediate zones of the monkey occipital lobe as early

74 ecocious cells form tangential links between intermediate zones of the thalamus, ganglionic eminence,

75 e addition lens (PAL) with a relatively wide intermediate zone (PAL-I; 7.85 mm, 18 degrees H clear FO

76 ear FOV); and a PAL with a relatively narrow intermediate zone (PAL-II; 5.60 mm, 13 degrees H clear F

77 Generally, the intermediate zone possessed the lowest storage and loss

78 ) bands and fibrocartilaginous matrix in the intermediate zone, reminiscent of the native TMJ disc.

79 markably, development of the motor pool, not intermediate zone, RST projections paralleled RN motor m

80 In sections of day E14.5 mouse brain, the intermediate zone showed intensive staining for complex

81 icantly more collagen II and aggrecan in the intermediate zone than a low dose (50 mg microS/g of sca

82 In the intermediate zone, these migrating precursors move tange

83 in-expressing Cajal-Retzius cells and in the intermediate zone through which newly born cells migrate

84 the ventricular zone and migrate through the intermediate zone to enter into the cortical plate.

85 nes generate neurons that migrate across the intermediate zone to the overlying cortical plate, where

86 We hypothesized that the intermediate zone under mediolateral tension would exhib

87 observed across all species, such as a weak intermediate zone under mediolateral tension.

88 The area-of-focus intermediate zone was greater with the refractive than w

89 stricted projections, principally within the intermediate zone where they formed appositions with glu

90 ons far (>120 nm) from the interface and new intermediate zones where interfacial proximity renormali

91 an inflection point within a relatively flat intermediate zone, where factors causing overestimation

92 into the cerebral cortex, primarily via the intermediate zone, whereas cells from the LGE do not.

93 t densely in the dorsolateral portion of the intermediate zone, whereas those from the CMAv were conc

94 is also transiently present in fibers in the intermediate zone, which at this stage contains many tha

95 , yet is conspicuously less prominent in the intermediate zone, which contains migrating cortical neu

96 Cells in Qr and Qs migrate through the intermediate zone with no significant change in the inte

97 projections were present within the cervical intermediate zone, with a mature density of putative syn