ライフサイエンスコーパス: unmyelinated axon

1 oform, Na(v)1.2, is found in the neighboring unmyelinated axon.

2 properties of the cerebellar granule cell's unmyelinated axon.

3 persistently expressed in gray matter and on unmyelinated axons.

4 rikarya and dendrites, and the remainder are unmyelinated axons.

5 aining the third FNIII domain was present in unmyelinated axons.

6 n of hippocampus, KT-LI was present in small unmyelinated axons.

7 higher percentage of smaller myelinated and unmyelinated axons.

8 ibers, despite a loss in both myelinated and unmyelinated axons.

9 mitochondrial traffic in both myelinated and unmyelinated axons.

10 odium channel density and gating in proximal unmyelinated axons.

11 about 15% of PR-immunoreactive profiles were unmyelinated axons.

12 nd spines, with rare presynaptic labeling in unmyelinated axons.

13 ons, we investigated channel-noise limits in unmyelinated axons.

14 antly the presence of functional channels in unmyelinated axons.

15 nals forming symmetric synapses and in small unmyelinated axons.

16 f a few axon initial segments and many small unmyelinated axons.

17 T-97, indicating that DOR-ir is localized to unmyelinated axons.

18 es several new features of AP propagation in unmyelinated axons: (1) branches of a single axonal arbo

19 profiles, 87% were axon terminals and small unmyelinated axons, 12% were soma and dendrites, and 2%

20 In dendrites, spines, and unmyelinated axons, a significantly larger proportion of

21 y to TAI, the present study examines whether unmyelinated axons also respond differentially to FK506,

22 small- and medium-sized myelinated and small unmyelinated axons, although sensory nerve action potent

23 ad selective loss of small myelinated and/or unmyelinated axons and 2 had normal histology and fiber

24 ic level demonstrate that 32.4+/-2.9% of the unmyelinated axons and 21.6+/-4.7% of the myelinated axo

25 e hypothalamus only (13 of 13 cells) and had unmyelinated axons and a low discharge rate.

26 Alpha-2C-AR-IR was observed in some unmyelinated axons and astrocytic processes that were ap

27 e dendrites and the remainder were primarily unmyelinated axons and astrocytic processes.

28 icroscopy of this region revealed that small unmyelinated axons and axon terminals constituted 48% (9

29 nfirmed the localization of endomorphin-2 to unmyelinated axons and axon terminals in the trigeminal

30 ely 50% of the ERalpha-labeled profiles were unmyelinated axons and axon terminals that contained num

31 Unmyelinated axons and axon terminals were also intensel

32 electron microscopy, KT-LI was restricted to unmyelinated axons and axon terminals, and was associate

33 VAChT immunoreactivity was in unmyelinated axons and axon terminals, and was most ofte

34 d to membranes of small synaptic vesicles in unmyelinated axons and axon terminals.

35 as most profiles with p75(NTR)-labeling were unmyelinated axons and axon terminals.

36 immunoreactive profiles were primarily small unmyelinated axons and axon terminals.

37 eurotrophins and tyrosine phosphorylation in unmyelinated axons and dendrites, where Na(V)1.2 channel

38 nistration of vincristine causes swelling of unmyelinated axons and disorientation of axonal microtub

39 Moreover, GPER1-IR was found in unmyelinated axons and glial profiles.

40 c profiles, but it was also present in small unmyelinated axons and in a few axon terminals and glia,

41 chwann cell proliferation and death, loss of unmyelinated axons and marked heat and cold pain insensi

42 DAT and TH were localized primarily in small unmyelinated axons and morphologically heterogeneous axo

43 omy) of the rat is highly selective, sparing unmyelinated axons and myelinated sensory axons; Walleri

44 rbB-family receptors in interactions between unmyelinated axons and non-myelinating Schwann cells in

45 TH immunoreactivity was present mainly in unmyelinated axons and occasionally in myelinated axons.

46 alpha2A-AR-IR was also observed in unmyelinated axons and perikarya.

47 rm cortex layers, which are characterized by unmyelinated axons and perisynaptic astroglial envelopes

48 labeling in single coronal sections through unmyelinated axons and terminals.

49 athway, we increased the caliber of normally unmyelinated axons and the expression of numerous genes

50 dendrites, 46% were axon terminals and small unmyelinated axons, and 5% were glial processes.

51 tributed along the soma, proximal dendrites, unmyelinated axons, and axon terminals of stained neuron

52 N2D is predominantly expressed in dendrites, unmyelinated axons, and axon terminals within the STN.

53 also observed occasionally within dendrites, unmyelinated axons, and glial processes.

54 ositive C(1) neurons are barosensitive, have unmyelinated axons, and have a very low rate of discharg

55 abeling was seen in small axon terminals and unmyelinated axons, and the postsynaptic density (PSD) f

56 oss of unmyelinated axons, while sympathetic unmyelinated axons appeared normal.

57 siological evidence, however, indicates that unmyelinated axons are more vulnerable than myelinated a

58 Unmyelinated axons are not protected by glycogen and are

59 hough GLT1 is present on developing OLs when unmyelinated axons are prevalent in the developing rat c

60 all population of type II neurons with their unmyelinated axons are undetectable with most recording

61 The present study shows that 32% of unmyelinated axons at the dermal-epidermal junction are

62 rats, the present study demonstrates 1) that unmyelinated axons at the dermal-epidermal junction immu

63 labeling was also present in numerous small unmyelinated axons, axon terminals, and glial processes.

64 EM-1 immunoreactivity was identified in unmyelinated axons, axon terminals, and occasionally in

65 We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed t

66 ium channels are uniformly distributed along unmyelinated axons, but are highly concentrated at nodes

67 oexpression, we studied large populations of unmyelinated axons by using quantitative single-label EM

68 function of slow-conducting, small-diameter unmyelinated axons (C fibers) during aglycemia.

69 Gap junctions between fine unmyelinated axons can electrically couple groups of bra

70 that TRIF-dependent microglial clearance of unmyelinated axon debris facilitates axon outgrowth.

71 and rostrocaudal variation in myelinated and unmyelinated axon density was found.

72 conduction delays of action potentials in an unmyelinated axon depended on the history of activity an

73 Regenerated unmyelinated axons expressing calcitonin gene-related pe

74 Most craniosensory afferents have unmyelinated axons expressing TRP Vanilloid 1 (TRPV1) re

75 in this model may be the less myelinated or unmyelinated axons, extracellular matrix, or synaptic fi

76 noreactive (KOR-ir) neuronal structures were unmyelinated axons, followed by axon terminals, dendrite

77 ed a significantly higher density of labeled unmyelinated axons for both receptor subtypes.

78 ittle is known about repolarization in thin, unmyelinated axons forming en passant synapses, which re

79 gnificant decrease in microtubule density in unmyelinated axons from vincristine-treated rats.

80 (a) distinguished by frequent appositions of unmyelinated axons (from 15 to 35%) to the plasmalemmal

81 sults are specific to signal transmission in unmyelinated axons, I suggest that the conclusions are l

82 the passage of action potential spikes along unmyelinated axons in a simple nervous system.

83 utamate will activate a higher proportion of unmyelinated axons in glabrous skin than in hairy skin.

84 rastructural analysis of the cytoskeleton of unmyelinated axons in peripheral nerve during neuropathi

85 incristine-induced hyperalgesia, we analyzed unmyelinated axons in saphenous nerves of vincristine-tr

86 s further substantiate a distinctive role of unmyelinated axons in TAI, and suggest a highly efficaci

87 a significant 41 % decrease in the number of unmyelinated axons in the carotid sinus nerve, compared

88 studies to assess large myelinated and small unmyelinated axons in the db/db type II diabetes mouse m

89 radish peroxidase, labeled as many as 52% of unmyelinated axons in the dorsal root.

90 (neurokinin INK1) receptor labels 32% of the unmyelinated axons in the glabrous skin of the rat hindp

91 rily on the plasma membrane of dendrites and unmyelinated axons in the hippocampus and cerebellum, wi

92 rade marker was found in both myelinated and unmyelinated axons in the NA-VL, as well as in nerve ter

93 ecently, vesicular release of glutamate from unmyelinated axons in the rat corpus callosum has been s

94 ral nervous system, Na(v)1.6 is localized in unmyelinated axons in the retina and cerebellum and is s

95 ction in glabrous skin and of myelinated and unmyelinated axons in the sural and medial plantar nerve

96 PRV infection induce electrical coupling in unmyelinated axons in vivo.

97 region that corresponded most closely to the unmyelinated axon initial segment, as defined by Golgi a

98 s, which resulted in the segregation of many unmyelinated axons into a 1:1 relationship with Schwann

99 FA)-induced inflammation, the proportions of unmyelinated axons labeled for NMDA, AMPA or KA receptor

100 an orientation consistent with granule cell unmyelinated axon labeling.

101 ing 12% were associated with glial and small unmyelinated axon-like structures.

102 ssociated with microstructural WM injury and unmyelinated axon loss at P1, diagnosed by diffusion ten

103 thin medium- to small-diameter dendrites and unmyelinated axons, most of the DAT gold particles are l

104 SP immunoreactivity was also identified in unmyelinated axons, myelinated axons, and nerve terminal

105 SP was readily identified in single-labeled unmyelinated axons, myelinated axons, and nerve terminal

106 generated by myelinated axons (N1 wave) and unmyelinated axons (N2 wave).

107 VIP immunoreactivity was confined to unmyelinated axons observed at several levels of the sen

108 The model replicates activity in the unmyelinated axon of the crustacean stomatogastric pylor

109 be explained in one of two ways: either the unmyelinated axon of the immature cerebral hemispheres i

110 In the unmyelinated axons of hippocampus, the conduction speed

111 The small, unmyelinated axons of olfactory sensory neurons project

112 ve fibre layer (RNFL) is composed largely of unmyelinated axons of retinal ganglion cells, and is acc

113 Expression also converts the normally unmyelinated axons of sympathetic neurons to myelination

114 profound microtubule depolymerization in the unmyelinated axons of the peripheral nerve, we hypothesi

115 ontribution to the 440-nm reflectance of the unmyelinated axons of the toad RNFL and could make a sim

116 n whether adult-born OLs ensheath previously unmyelinated axons or remodel existing myelin.

117 were dendrites, and only 33 out of 215 were unmyelinated axons or terminals.

118 es of partially denervated Schwann cells and unmyelinated axons, or the byproducts of Wallerian degen

119 no systematic observations directed towards unmyelinated axon pathophysiology.

120 Unmyelinated axons persistently wrapped by oligodendrocy

121 odelling emphasises uncertainties about fine unmyelinated axon physiology but, when informed by biolo

122 age of their plasmalemmal surface apposed to unmyelinated axon profiles and an increased percentage o

123 In the sural nerve, 20% of the unmyelinated axon profiles immunostain for NMDAR1 and on

124 ition of the axonal cytoskeleton in shiverer unmyelinated axons relative to age-matched wild-type mye

125 Unmyelinated axons remained unchanged.

126 harmacological stimulation of myelinated and unmyelinated axons, respectively.

127 daily to adult rats to examine its effect on unmyelinated axon-Schwann cell units in intact periphera

128 ce were smaller than wild-type mice, whereas unmyelinated axons showed no difference.

129 axonal excitability and synaptic function in unmyelinated axons.SIGNIFICANCE STATEMENT Voltage-gated

130 Examples include myelinated and unmyelinated axons, single strands of interconnected car

131 to the myelinated axons, the bundles contain unmyelinated axons, so that they also probably serve as

132 cant increase in the cross-sectional area of unmyelinated axons, suggesting swelling of axons.

133 and dendrites, but the proportion of labeled unmyelinated axons, terminals, and glia was higher than

134 nce of the large number of thin-diameter and unmyelinated axons that connect different cortical areas

135 Unmyelinated axons, the most prominent CST element durin

136 slow-conducting, and energetically expensive unmyelinated axons to large, fast-conducting, and energe

137 cross the CC, presumably in conjunction with unmyelinated axons, to colonize the contralateral hemisp

138 Thus, unmyelinated axon tracts are critical for patterning the

139 ial afferents is exclusively associated with unmyelinated axons, VR1 identifies C-fiber afferent path

140 s showed that regeneration of myelinated and unmyelinated axons was inhibited.

141 etwork of 30 multicompartmental neurons with unmyelinated axons was used to infer that: axon-axon gap

142 ure myelinating Schwann cells (SCs), whereas unmyelinated axons were aberrantly ensheathed in Remak b

143 Two phases of increase in the number of unmyelinated axons were observed at C7, while only one s

144 f other structures, including myelinated and unmyelinated, axons were also labeled.

145 ctive profiles were axon terminals and small unmyelinated axons, whereas the remainder were mainly de

146 he area occupied by glial cell processes and unmyelinated axons which significantly increased followi

147 ain conduction times are especially great in unmyelinated axons, which may transmit information via f

148 ice had reduced sensory function and loss of unmyelinated axons, while sympathetic unmyelinated axons

149 We find for example that for mammalian unmyelinated axons with 0.2 microm diameter (matching ce