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1  properties of the cerebellar granule cell's unmyelinated axon.
2 oform, Na(v)1.2, is found in the neighboring unmyelinated axon.
3 T-97, indicating that DOR-ir is localized to unmyelinated axons.
4 persistently expressed in gray matter and on unmyelinated axons.
5 rikarya and dendrites, and the remainder are unmyelinated axons.
6 aining the third FNIII domain was present in unmyelinated axons.
7 n of hippocampus, KT-LI was present in small unmyelinated axons.
8  higher percentage of smaller myelinated and unmyelinated axons.
9 lted in severe hypomyelination and increased unmyelinated axons.
10  yielded robust visualization myelinated and unmyelinated axons.
11 ibers, despite a loss in both myelinated and unmyelinated axons.
12 mitochondrial traffic in both myelinated and unmyelinated axons.
13 odium channel density and gating in proximal unmyelinated axons.
14 about 15% of PR-immunoreactive profiles were unmyelinated axons.
15 nd spines, with rare presynaptic labeling in unmyelinated axons.
16 ons, we investigated channel-noise limits in unmyelinated axons.
17 antly the presence of functional channels in unmyelinated axons.
18 nals forming symmetric synapses and in small unmyelinated axons.
19 f a few axon initial segments and many small unmyelinated axons.
20 es several new features of AP propagation in unmyelinated axons: (1) branches of a single axonal arbo
21  profiles, 87% were axon terminals and small unmyelinated axons, 12% were soma and dendrites, and 2%
22                    In dendrites, spines, and unmyelinated axons, a significantly larger proportion of
23       Digital segmentation of myelinated and unmyelinated axons allowed for determination of fiber si
24 y to TAI, the present study examines whether unmyelinated axons also respond differentially to FK506,
25 small- and medium-sized myelinated and small unmyelinated axons, although sensory nerve action potent
26 ad selective loss of small myelinated and/or unmyelinated axons and 2 had normal histology and fiber
27 ic level demonstrate that 32.4+/-2.9% of the unmyelinated axons and 21.6+/-4.7% of the myelinated axo
28 e hypothalamus only (13 of 13 cells) and had unmyelinated axons and a low discharge rate.
29          Alpha-2C-AR-IR was observed in some unmyelinated axons and astrocytic processes that were ap
30 e dendrites and the remainder were primarily unmyelinated axons and astrocytic processes.
31 icroscopy of this region revealed that small unmyelinated axons and axon terminals constituted 48% (9
32 xception of a small amount of GluD1-positive unmyelinated axons and axon terminals in the primate str
33 nfirmed the localization of endomorphin-2 to unmyelinated axons and axon terminals in the trigeminal
34 ely 50% of the ERalpha-labeled profiles were unmyelinated axons and axon terminals that contained num
35                                              Unmyelinated axons and axon terminals were also intensel
36 electron microscopy, KT-LI was restricted to unmyelinated axons and axon terminals, and was associate
37                VAChT immunoreactivity was in unmyelinated axons and axon terminals, and was most ofte
38 d to membranes of small synaptic vesicles in unmyelinated axons and axon terminals.
39 as most profiles with p75(NTR)-labeling were unmyelinated axons and axon terminals.
40 immunoreactive profiles were primarily small unmyelinated axons and axon terminals.
41 eurotrophins and tyrosine phosphorylation in unmyelinated axons and dendrites, where Na(V)1.2 channel
42 nistration of vincristine causes swelling of unmyelinated axons and disorientation of axonal microtub
43              Moreover, GPER1-IR was found in unmyelinated axons and glial profiles.
44 c profiles, but it was also present in small unmyelinated axons and in a few axon terminals and glia,
45 animals showed an increase in the density of unmyelinated axons and in myelin thickness in both nerve
46 chwann cell proliferation and death, loss of unmyelinated axons and marked heat and cold pain insensi
47 DAT and TH were localized primarily in small unmyelinated axons and morphologically heterogeneous axo
48 omy) of the rat is highly selective, sparing unmyelinated axons and myelinated sensory axons; Walleri
49 rbB-family receptors in interactions between unmyelinated axons and non-myelinating Schwann cells in
50    TH immunoreactivity was present mainly in unmyelinated axons and occasionally in myelinated axons.
51           alpha2A-AR-IR was also observed in unmyelinated axons and perikarya.
52 rm cortex layers, which are characterized by unmyelinated axons and perisynaptic astroglial envelopes
53  labeling in single coronal sections through unmyelinated axons and terminals.
54 athway, we increased the caliber of normally unmyelinated axons and the expression of numerous genes
55 dendrites, 46% were axon terminals and small unmyelinated axons, and 5% were glial processes.
56 tributed along the soma, proximal dendrites, unmyelinated axons, and axon terminals of stained neuron
57 N2D is predominantly expressed in dendrites, unmyelinated axons, and axon terminals within the STN.
58 also observed occasionally within dendrites, unmyelinated axons, and glial processes.
59 ositive C(1) neurons are barosensitive, have unmyelinated axons, and have a very low rate of discharg
60 abeling was seen in small axon terminals and unmyelinated axons, and the postsynaptic density (PSD) f
61 oss of unmyelinated axons, while sympathetic unmyelinated axons appeared normal.
62 siological evidence, however, indicates that unmyelinated axons are more vulnerable than myelinated a
63                                              Unmyelinated axons are not protected by glycogen and are
64 hough GLT1 is present on developing OLs when unmyelinated axons are prevalent in the developing rat c
65 all population of type II neurons with their unmyelinated axons are undetectable with most recording
66          The present study shows that 32% of unmyelinated axons at the dermal-epidermal junction are
67 rats, the present study demonstrates 1) that unmyelinated axons at the dermal-epidermal junction immu
68  labeling was also present in numerous small unmyelinated axons, axon terminals, and glial processes.
69      EM-1 immunoreactivity was identified in unmyelinated axons, axon terminals, and occasionally in
70                 We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed t
71 red for the detection of both myelinated and unmyelinated axons, but access to well-preserved human v
72 ium channels are uniformly distributed along unmyelinated axons, but are highly concentrated at nodes
73 oexpression, we studied large populations of unmyelinated axons by using quantitative single-label EM
74  function of slow-conducting, small-diameter unmyelinated axons (C fibers) during aglycemia.
75                   Gap junctions between fine unmyelinated axons can electrically couple groups of bra
76  that TRIF-dependent microglial clearance of unmyelinated axon debris facilitates axon outgrowth.
77 and rostrocaudal variation in myelinated and unmyelinated axon density was found.
78 conduction delays of action potentials in an unmyelinated axon depended on the history of activity an
79                                  Regenerated unmyelinated axons expressing calcitonin gene-related pe
80            Most craniosensory afferents have unmyelinated axons expressing TRP Vanilloid 1 (TRPV1) re
81  in this model may be the less myelinated or unmyelinated axons, extracellular matrix, or synaptic fi
82 noreactive (KOR-ir) neuronal structures were unmyelinated axons, followed by axon terminals, dendrite
83 ed a significantly higher density of labeled unmyelinated axons for both receptor subtypes.
84 ittle is known about repolarization in thin, unmyelinated axons forming en passant synapses, which re
85 an reversibly block action potentials in the unmyelinated axons from the marine mollusk Aplysia calif
86 gnificant decrease in microtubule density in unmyelinated axons from vincristine-treated rats.
87 (a) distinguished by frequent appositions of unmyelinated axons (from 15 to 35%) to the plasmalemmal
88 nderlying causes are unclear, but epidermal, unmyelinated axons have been shown to be the first to de
89 sults are specific to signal transmission in unmyelinated axons, I suggest that the conclusions are l
90 the passage of action potential spikes along unmyelinated axons in a simple nervous system.
91 utamate will activate a higher proportion of unmyelinated axons in glabrous skin than in hairy skin.
92 rastructural analysis of the cytoskeleton of unmyelinated axons in peripheral nerve during neuropathi
93 incristine-induced hyperalgesia, we analyzed unmyelinated axons in saphenous nerves of vincristine-tr
94 s further substantiate a distinctive role of unmyelinated axons in TAI, and suggest a highly efficaci
95 a significant 41 % decrease in the number of unmyelinated axons in the carotid sinus nerve, compared
96 ifferential susceptibility of myelinated and unmyelinated axons in the corpus callosum to Na(V)-depen
97 studies to assess large myelinated and small unmyelinated axons in the db/db type II diabetes mouse m
98 radish peroxidase, labeled as many as 52% of unmyelinated axons in the dorsal root.
99 (neurokinin INK1) receptor labels 32% of the unmyelinated axons in the glabrous skin of the rat hindp
100 rily on the plasma membrane of dendrites and unmyelinated axons in the hippocampus and cerebellum, wi
101 rade marker was found in both myelinated and unmyelinated axons in the NA-VL, as well as in nerve ter
102 ecently, vesicular release of glutamate from unmyelinated axons in the rat corpus callosum has been s
103 ral nervous system, Na(v)1.6 is localized in unmyelinated axons in the retina and cerebellum and is s
104 ction in glabrous skin and of myelinated and unmyelinated axons in the sural and medial plantar nerve
105                                          All unmyelinated axons in these images are individually anno
106  PRV infection induce electrical coupling in unmyelinated axons in vivo.
107 region that corresponded most closely to the unmyelinated axon initial segment, as defined by Golgi a
108 s, which resulted in the segregation of many unmyelinated axons into a 1:1 relationship with Schwann
109 FA)-induced inflammation, the proportions of unmyelinated axons labeled for NMDA, AMPA or KA receptor
110  an orientation consistent with granule cell unmyelinated axon labeling.
111 ing 12% were associated with glial and small unmyelinated axon-like structures.
112 ssociated with microstructural WM injury and unmyelinated axon loss at P1, diagnosed by diffusion ten
113 thin medium- to small-diameter dendrites and unmyelinated axons, most of the DAT gold particles are l
114   SP immunoreactivity was also identified in unmyelinated axons, myelinated axons, and nerve terminal
115  SP was readily identified in single-labeled unmyelinated axons, myelinated axons, and nerve terminal
116  generated by myelinated axons (N1 wave) and unmyelinated axons (N2 wave).
117             These myelin outfolds surrounded unmyelinated axons, neuronal cell bodies, and other myel
118         VIP immunoreactivity was confined to unmyelinated axons observed at several levels of the sen
119         The model replicates activity in the unmyelinated axon of the crustacean stomatogastric pylor
120  be explained in one of two ways: either the unmyelinated axon of the immature cerebral hemispheres i
121                                       In the unmyelinated axons of hippocampus, the conduction speed
122                                   The small, unmyelinated axons of olfactory sensory neurons project
123 ve fibre layer (RNFL) is composed largely of unmyelinated axons of retinal ganglion cells, and is acc
124        Expression also converts the normally unmyelinated axons of sympathetic neurons to myelination
125                    Here, we demonstrate that unmyelinated axons of the mouse central nervous system h
126 profound microtubule depolymerization in the unmyelinated axons of the peripheral nerve, we hypothesi
127 ontribution to the 440-nm reflectance of the unmyelinated axons of the toad RNFL and could make a sim
128 n whether adult-born OLs ensheath previously unmyelinated axons or remodel existing myelin.
129  were dendrites, and only 33 out of 215 were unmyelinated axons or terminals.
130 es of partially denervated Schwann cells and unmyelinated axons, or the byproducts of Wallerian degen
131  no systematic observations directed towards unmyelinated axon pathophysiology.
132                                              Unmyelinated axons persistently wrapped by oligodendrocy
133 odelling emphasises uncertainties about fine unmyelinated axon physiology but, when informed by biolo
134 ations in action potential propagation, with unmyelinated axons preferentially showing reduced action
135 age of their plasmalemmal surface apposed to unmyelinated axon profiles and an increased percentage o
136               In the sural nerve, 20% of the unmyelinated axon profiles immunostain for NMDAR1 and on
137  imaging techniques enables visualization of unmyelinated axons, regenerating axons, cytoskeleton ult
138 ition of the axonal cytoskeleton in shiverer unmyelinated axons relative to age-matched wild-type mye
139                                              Unmyelinated axons remained unchanged.
140 harmacological stimulation of myelinated and unmyelinated axons, respectively.
141 factory bulb-wide analysis of myelinated and unmyelinated axons revealed distinctive patterns of axon
142 daily to adult rats to examine its effect on unmyelinated axon-Schwann cell units in intact periphera
143 ce were smaller than wild-type mice, whereas unmyelinated axons showed no difference.
144 axonal excitability and synaptic function in unmyelinated axons.SIGNIFICANCE STATEMENT Voltage-gated
145              Examples include myelinated and unmyelinated axons, single strands of interconnected car
146 to the myelinated axons, the bundles contain unmyelinated axons, so that they also probably serve as
147 cant increase in the cross-sectional area of unmyelinated axons, suggesting swelling of axons.
148 and dendrites, but the proportion of labeled unmyelinated axons, terminals, and glia was higher than
149 nce of the large number of thin-diameter and unmyelinated axons that connect different cortical areas
150 e surprisingly incomplete and biased because unmyelinated axons, the most prevalent type of fibers in
151                                              Unmyelinated axons, the most prominent CST element durin
152 slow-conducting, and energetically expensive unmyelinated axons to large, fast-conducting, and energe
153 cross the CC, presumably in conjunction with unmyelinated axons, to colonize the contralateral hemisp
154                                        Thus, unmyelinated axon tracts are critical for patterning the
155 ial afferents is exclusively associated with unmyelinated axons, VR1 identifies C-fiber afferent path
156 s showed that regeneration of myelinated and unmyelinated axons was inhibited.
157 etwork of 30 multicompartmental neurons with unmyelinated axons was used to infer that: axon-axon gap
158 ure myelinating Schwann cells (SCs), whereas unmyelinated axons were aberrantly ensheathed in Remak b
159      Two phases of increase in the number of unmyelinated axons were observed at C7, while only one s
160 f other structures, including myelinated and unmyelinated, axons were also labeled.
161 oteinase 13 (MMP-13) induces degeneration of unmyelinated axons, whereas pharmacological inhibition o
162 ctive profiles were axon terminals and small unmyelinated axons, whereas the remainder were mainly de
163 he area occupied by glial cell processes and unmyelinated axons which significantly increased followi
164 ain conduction times are especially great in unmyelinated axons, which may transmit information via f
165 ice had reduced sensory function and loss of unmyelinated axons, while sympathetic unmyelinated axons
166       We find for example that for mammalian unmyelinated axons with 0.2 microm diameter (matching ce

 
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