ライフサイエンスコーパス: ganglion cell axon

1 etermined growth patterns of Xenopus retinal ganglion cell axons.

2 astrocytes, some of which comes from retinal ganglion cell axons.

3 Neither protein is detected on ganglion cell axons.

4 d ovoid cells extended processes parallel to ganglion cell axons.

5 ease in optic nerve proteins associated with ganglion cell axons.

6 cylindrical structures oriented parallel to ganglion cell axons.

7 to the oriented cylindrical structure of the ganglion cell axons.

8 due to the oriented cylindrical structure of ganglion cell axons.

9 t that determines the pathway taken later by ganglion cell axons.

10 us NT-3 derives presynaptically from retinal ganglion cell axons.

11 intermediate targets for pathfinding retinal ganglion cell axons.

12 ted and myelinated zones of the same retinal ganglion cell axons.

13 tract, spinal motor, hippocampal and retinal ganglion cell axons.

14 expressed on both temporal and nasal retinal ganglion cell axons.

15 acts as a short range repellent for retinal ganglion cell axons.

16 e the pattern of central connections made by ganglion cell axons.

17 muli is being conveyed by myelinated retinal ganglion cell axons.

18 essential roles in the formation of retinal ganglion cell axons.

19 r, pathfinding and synaptogenesis of retinal ganglion cell axons.

20 We estimated cell production by counting ganglion cell axons after ganglion cell neurogenesis but

21 Antidromic activation of ganglion cell axons also increases the generation of Mul

22 Retinal ganglion cell axons and axonal electrical activity have

23 commissural trajectories, including retinal ganglion cell axons and spiral fiber axons, and that the

24 formed through interactions between retinal ganglion cell axons and target cells within the tectum h

25 al of sensory neurons and the maintenance of ganglion cell axons, and functions as a major determinan

26 otoreceptors, outer plexiform layer, retinal ganglion cell axons, and Muller cells.

27 ies of the crossing and non-crossing retinal ganglion cell axons approaching the disc.

28 ced the area and branchtip number of retinal ganglion cell axon arborizations within the optic tectum

29 In the adult mammal, retinal ganglion cell axon arbors are restricted to eye-specific

30 but less precise, while ipsilateral retinal ganglion cell axons are abnormally distributed in anteri

31 nization of the retinal neuroepithelium, and ganglion cell axons are found between pigmented and neur

32 In many species, retinal ganglion cell axons are myelinated in the optic nerve bu

33 The results demonstrated that intraretinal ganglion cell axons are predominantly varicose fibers in

34 When two spikes from a single ganglion-cell axon arrive within 30 milliseconds of each

35 Here we visualized individual retinal ganglion cell axons as they grew over the tectum in zebr

36 abnormal organization of the Pax2+ cells and ganglion cell axons at the nascent optic disc.

37 r vision relies on the divergence of retinal ganglion cell axons at the optic chiasm, with strictly c

38 tina, and abnormal axonal pathfinding of the ganglion cell axons at the optic chiasm.

39 , because it is sufficient to change retinal ganglion cell axon behavior from extension onto, to avoi

40 The gD accumulated in the proximal ganglion cell axon by 2 days and reached the most distal

41 erograde tracing techniques to label retinal ganglion cell axons combined with R-cadherin in situ hyb

42 ffusion, passive diffusion and activation of ganglion cells' axons en passant.

43 l coherence tomography (OCT) measures of the ganglion cell axons entering the optic nerve from corres

44 Retinal ganglion cell axons exit the eye, enter the optic stalk,

45 ng the developing optic disc, the site where ganglion cell axons exit the retina.

46 were present during the period when retinal ganglion cell axons first navigate through the optic tra

47 stem of the ferret, the terminals of retinal ganglion cell axons first segregate to form eye-specific

48 Retinal ganglion cell axons from 12/15-lipoxygenase-null mice we

49 Retinal ganglion cell axons from double knockout mice were more

50 At the optic chiasm, retinal ganglion cell axons from each eye converge and segregate

51 essential for the appropriate pathfinding of ganglion cell axons from the retina to the dorsal latera

52 g revealed a striking mistargeting of mutant ganglion cell axons from the ventral retina, which expre

53 ation probably lessens the risk of injury to ganglion cell axons from vascular compression.

54 ptic stalk and the initial misrouting of the ganglion cell axons give rise to retinal and optic disc

55 Retinal ganglion cell axons grew toward softer tissue, which was

56 l-dependent mechanism for stimulated retinal ganglion cell axon growth by epidermal growth factor rec

57 ed by AG1478 stimulated disinhibited retinal ganglion cell axon growth in central nervous system myel

58 data support a model in which dorsal retinal ganglion cell axons heading to the optic disc encounter

59 al branches were initially formed by retinal ganglion cell axons in both the superficial and internal

60 rograde degeneration of unmyelinated retinal ganglion cell axons in living rats for 4 weeks after int

61 y enhance regeneration of transected retinal ganglion cell axons in rats.

62 mission regulates the segregation of retinal ganglion cell axons in the lateral geniculate nucleus of

63 y (through synchronous activation of retinal ganglion cell axons in the optic nerve) substantially we

64 We found that the responses of retinal ganglion cell axons in the optic tract were never correl

65 atin regulated the normal pruning of retinal ganglion cell axons in their target field.

66 has been determined for mature mouse retinal ganglion cell axons in vivo.

67 gh both ligands may be able to guide retinal ganglion cells axons in vitro, they have different roles

68 llary acidic protein (GFAP) compartmentalize ganglion cell axons into bundles, forming "glial tubes,"

69 cell axon, these data suggest that damage to ganglion cell axons is not a sufficient condition to pro

70 amatic effects on the myelination of retinal ganglion cell axons, it has moderate effects on retinal

71 ss is completed before the reported onset of ganglion cell axon loss and retino-dLGN synapse eliminat

72 However, the majority of ganglion cell axons mapped to the appropriate rostrocaud

73 The early expression of PV and CB in ganglion cell axons might be related to optic nerve outg

74 Movement of viral DNA along ganglion cell axons occurs within capsid-like structures

75 of all species and in the ganglion cells and ganglion cell axons of all species except fish.

76 Intraretinal ganglion cell axons of seven human donors (1-85 years ol

77 lysis of ribosome-bound mRNAs in the retinal ganglion cell axons of the developing and adult retinote

78 ich is abnormally distributed in the retinal ganglion cell axons of transgenic mice expressing human

79 Here, we report that retinal ganglion cell axons of WT mice shed mitochondria at the

80 ent activities of slit-2 on cultured retinal ganglion cell axons, of semaphorin 3A on dorsal root gan

81 r, the projections of dorsal but not ventral ganglion cell axons onto the optic tectum showed profoun

82 Despite the nearly normal mapping of V ganglion cell axons onto the vibrissae follicles and bra

83 en Brn3b and Brn3c in regulating the retinal ganglion cell axon outgrowth.

84 Under these conditions, some temporal ganglion cell axons overshot their expected termination

85 serve as axon guidance molecules for retinal ganglion cell axon pathfinding toward the optic nerve he

86 Retinal ganglion cell axons project retinotopically to their pri

87 oduce the novel retinal projections, retinal ganglion cell axons projecting to the ventrobasal or med

88 orseradish peroxidase has shown that retinal ganglion-cell axons reach the optic nerve head in chrono

89 ereas reducing its function promoted retinal ganglion cell axon regeneration after optic nerve crush

90 t + short interfering CASP2-mediated retinal ganglion cell axon regeneration, Muller cell activation

91 in the retina and leads to enhanced retinal ganglion cell axon regeneration.

92 ic nerve lesion site promoting adult retinal ganglion cell axon regeneration.

93 re key mediators of ventral-temporal retinal ganglion cell axon retinocollicular mapping, by likely i

94 M) dataset and identified cohorts of retinal ganglion cell axons (RGCs) that innervated each of a div

95 Retinal ganglion cell axons show intense L1 immunoreactivity as

96 donors revealed that Xenopus laevis retinal ganglion cell axons stop growing in response to NO expos

97 hly concentrated in areas containing retinal ganglion cell axons, suggesting a role in regulating the

98 he developing chick retina and is present on ganglion cell axons suggests that it may be involved in

99 velopment and is required for normal ventral ganglion cell axon targeting to the optic nerve head.

100 Retinal ganglion cell axon terminals within the P and K layers w

101 erve extension, and branching of the retinal ganglion cell axon terminals, with the N-terminal region

102 e LGN during the final remodeling of retinal ganglion cell axon terminals.

103 ns have a major role in dorsoventral retinal ganglion cell axon termination along the mediolateral ax

104 detect immunoreactive profiles of trigeminal ganglion cell axons that contained many vesicular struct

105 e glaucomatous damage is known to affect the ganglion cell axon, these data suggest that damage to ga

106 e and probably contributes to the failure of ganglion cell axons to grow out of the eye.

107 Bst/+ mice is attributable to the failure of ganglion cell axons to reach the optic nerve head early

108 f Smad4 led to abnormal targeting of retinal ganglion cell axons to the optic nerve head, a phenotype

109 Mitochondria within retinal ganglion cell axons underwent systematic ultrastructural

110 It has previously been proposed that retinal ganglion cell axons use distinct guidance strategies in

111 hat both dorsal and ventral-temporal retinal ganglion cell axons utilize reverse signalling for topog

112 thetase/tyrosine hydroxylase expression) and ganglion cell axons via a TrkA receptor (TrkAR)-dependen

113 pe siblings, and the total number of retinal ganglion cell axons was increased to 226%.

114 However, after ganglion cell axons were crushed, synaptic receptors sho

115 Varicosities of the intraretinal ganglion cell axons were found throughout the retinas in

116 frequently accompanied by abnormal growth of ganglion cell axons, which failed to enter the optic ner

117 signaling was important for guiding retinal ganglion cell axons within the retina to the optic stalk