ライフサイエンスコーパス: ganglion cell axon

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

2 r, pathfinding and synaptogenesis of 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 astrocytes, some of which comes from retinal ganglion cell axons.

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

7 cylindrical structures oriented parallel to ganglion cell axons.

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

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

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

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

12 intermediate targets for pathfinding retinal ganglion cell axons.

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

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

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

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

17 etermined growth patterns of Xenopus retinal ganglion cell axons.

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

19 muli is being conveyed by myelinated 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 Strikingly, nonelectroporated retinal ganglion cell axons also mistarget in the tract region,

23 w that microglia regulate pruning of retinal ganglion cell axons and are important for proper behavio

24 Retinal ganglion cell axons and axonal electrical activity have

25 ted in the regeneration of zebrafish retinal ganglion cell axons and promoted regeneration and sprout

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

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

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

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

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

31 ese OPCs impaired precise control of retinal ganglion cell axon arbor size during formation and matur

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

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

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

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

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

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

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

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

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

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

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

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

44 and global distribution of OS and DS retinal ganglion cell axon boutons using in vivo two-photon calc

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

46 Our research demonstrates surviving retinal ganglion cell axons can re-establish terminal fields, ac

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

48 ons on one side of the animal and in retinal ganglion cell axons crossing to the tectum on the opposi

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

50 lusters were defined as locations from where ganglion cell axons enter the optic nerve head within a

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

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

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

54 through which vasculature enters the eye and ganglion cell axons exit.

55 rvating their central brain targets, retinal ganglion cell axons fasciculate in the optic tract and t

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

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

58 mammalian visual system, individual retinal ganglion cell axons form clustered terminal boutons cont

59 and EphB1 knockout mice, mistargeted retinal ganglion cell axons form dense islands of axon terminals

60 Retinal ganglion cell axons forming the optic nerve (ON) emerge

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

62 Retinal ganglion cell axons from double knockout mice were more

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

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

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

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

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

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

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

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

71 cerebellar parallel fiber growth and retinal ganglion cell axon guidance.

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

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

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

75 o automatically and accurately count retinal ganglion cell axons in optic nerve (ON) tissue images fr

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

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

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

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

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

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

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

83 Cue stimulation of growing Xenopus retinal ganglion cell axons induces rapid dissociation of riboso

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

102 Retinal ganglion cell axons project retinotopically to their pri

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

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

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

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

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

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

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

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

111 Retinal ganglion cell axons show intense L1 immunoreactivity as

112 We show that in the absence of Dcc, some ganglion cell axons stalled at the optic disc, whereas o

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

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

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

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

117 of metabolically labeled mRNAs from retinal ganglion cell axon terminals in mouse.

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

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

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

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

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

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

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

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

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

127 in the developing Xenopus brain, and retinal ganglion cell axons turned to follow this gradient.

128 Mitochondria within retinal ganglion cell axons underwent systematic ultrastructural

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

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

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

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

133 studies showing age-related loss of retinal ganglion cell axons, we showed a significant decline in

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

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

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

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