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1 l regions for action potential conduction in myelinated fibers.
2  morphometric changes in distal tibial nerve myelinated fibers.
3 y enters the brain and specifically binds to myelinated fibers.
4 fferent signal is carried by unmyelinated or myelinated fibers.
5 vantages for the high resolution staining of myelinated fibers.
6 f myelination and the domain organization of myelinated fibers.
7 s and maintained the axonal caliber of large myelinated fibers.
8 pport the earliest stages of regeneration of myelinated fibers.
9  receptor are juxtaposed along the course of myelinated fibers.
10 out affecting other structural properties of myelinated fibers.
11 esion leads to degeneration predominantly in myelinated fibers.
12 f the unmyelinated C-fibers and/or the small myelinated fibers.
13 hereas Cx32 staining was restricted to large myelinated fibers.
14 timeric complexes at juxtaparanodal zones in myelinated fibers.
15 ngs of unmyelinated fibers, and C2, of small myelinated fibers.
16 rves of transgenics showed a 60% increase in myelinated fibers.
17 ated axons relative to age-matched wild-type myelinated fibers, although connectivity and patterns of
18 aPOZ mice are impaired in the maintenance of myelinated fibers and are a promising model for studying
19              Electron microscopy showed well-myelinated fibers and axonal inclusions in the brain and
20 ly large myelinated fibers, bortezomib small myelinated fibers and cisplatin damaged all types of mye
21 copy to examine the number and morphology of myelinated fibers and size of myelinated CNS structures.
22 portance of sensory input in the building of myelinated fibers and suggest that this activity-depende
23 ion molecules between inflammatory cells and myelinated fibers and the apparent predominance of T hel
24 ls survived within the affected zone, as did myelinated fibers and the extrinsic calretinin- and tyro
25 Sensory modalities that involved large Abeta myelinated fibers and unmyelinated C fibers were most af
26 d itch matches the time for peak response in myelinated fibers, and (6) the time for peak itch sensat
27                To account for the beading of myelinated fibers, and axons of unmyelinated nerve fiber
28 rrant axonal regeneration, irregularly sized myelinated fibers, and fibrosis were frequently observed
29 e hypertrophy, onion bulb formation, loss of myelinated fibers, and occasional myelin thickening simi
30 sal roots, anti-GluR2/3 stains predominantly myelinated fibers; anti-GluR4 or anti-GluR2/4 stains pre
31 Striking color patterns unique to individual myelinated fibers are generated that facilitate their tr
32                                              Myelinated fibers are organized into distinct domains th
33 the sural nerve, where the large majority of myelinated fibers are sensory, approximately half of the
34                                     The mean myelinated fiber area in the regenerated cables of the d
35     Size-frequency histograms of regenerated myelinated fiber areas suggest a delay in the maturation
36 lements are the cell islands of layer II and myelinated fibers around the cell islands, the dispositi
37                             Visualization of myelinated fiber arrangements, cytoarchitecture, and pro
38 om examination of the axoplasm isolated from myelinated fibers as axoplasmic whole mounts and delipid
39 fibers at day 7, and the mean axonal area of myelinated fibers at 7, 14, and 21 days after injury, in
40  (NF186), a neuronal protein concentrated in myelinated fibers at nodes of Ranvier, and NF155, the ol
41 itaxel and vincristine affected mostly large myelinated fibers, bortezomib small myelinated fibers an
42                                              Myelinated fiber bundles of the spinal vestibular nucleu
43 des extensive Wallerian-like degeneration of myelinated fibers but relative sparing of unmyelinated f
44 ous and evoked neuronal hyperexcitability in myelinated fibers, coupled with development of neuropath
45 strated significantly decreased densities of myelinated fibers, decreased axonal areas, and increased
46 betic mice, resulted in significantly higher myelinated fiber densities and conduction velocities con
47              RESEARCH DESIGN AND Sural nerve myelinated fiber density (MFD), nerve conduction velocit
48 dex and reduced regeneration, as assessed by myelinated fiber density after acute crush of the sciati
49                                              Myelinated fiber density was normal.
50 motor and sensory conduction velocities; and myelinated fiber density.
51 city deficits, and reduction in tibial nerve myelinated fiber diameter, but not intraepidermal nerve
52  Ensheathed axons express low levels whereas myelinated fibers express high levels of NRG1 type III.
53                        In addition, 72.4% of myelinated fibers from the nerves that innervate the nas
54 , as well as microtubule disorganization, in myelinated fibers from vincristine-treated rats.
55 ld be determined along an extended length of myelinated fiber in the physiological condition.
56 osarcoma, and irregularity and disruption of myelinated fibers in areas infiltrated by oligodendrogli
57  were detected in the internodal axolemma of myelinated fibers in both control and MS brains.
58 neurons resulted in improved regeneration of myelinated fibers in both the dorsal root and the spinal
59 l lines of evidence for an important role of myelinated fibers in cowhage-induced itch: (1) a selecti
60 icroscopic comparison of the organization of myelinated fibers in lateral olfactory tract in the ante
61 of the paranodal junction of living or fixed myelinated fibers in mouse sciatic nerve.
62 bers and extensive ultrastructural damage of myelinated fibers in RTX-treated rats.
63 f IQCJ-SCHIP1 in vivo by studying peripheral myelinated fibers in Schip1 knock-out mutant mice.
64 ced by stimulation of unmyelinated and small myelinated fibers in the joint and surrounding tissue.
65 n neural processes that originate from three myelinated fibers in the underlying dermis.
66 urons that are not generally associated with myelinated fiber input from mechanical and proprioceptiv
67 tic neuropathies and axonal atrophy of large myelinated fibers, its role in small sensory nerve fiber
68 titative stereologic analysis showed reduced myelinated fiber length and density.
69  that the IC and MGC exhibit relatively high myelinated fiber length density (MFLD) values at birth a
70 ly aligned and right-sided obliquely aligned myelinated fibers, may represent a biologic mechanism fo
71 nt, number of oligodendrocytes, or number of myelinated fibers, nor was myelination delayed developme
72                                          The myelinated fibers of the auditory nerve can be divided i
73          Neuropathology showed loss of large myelinated fibers, onion bulb formations and focal foldi
74 ignificantly reduced the ratio of abnormally myelinated fibers (p = 0.00148) and secondary inflammati
75 y be selectively mediated by a low-threshold myelinated fiber pathway to the n. gracilis.
76 -established neuroprotective efficacy in the myelinated fiber population.
77                In addition, most of the fine myelinated fibers projecting from the corpus callosum in
78 , there was a 45% reduction in the number of myelinated fibers relative to controls, demonstrating a
79 on of the paranodal junctional region of CNS myelinated fibers shows that "transverse bands," a compo
80 ed itch: (1) a selective conduction block in myelinated fibers substantially reduces itch in a subgro
81  microscopy, each biopsy specimen had thinly myelinated fibers surrounded by minor onion bulbs.
82                The contribution of injury to myelinated fibers that was observed at P18 is probably a
83 ed fibers and cisplatin damaged all types of myelinated fibers to a similar degree.
84 in the axonal size-frequency distribution of myelinated fibers toward smaller axons in galactose-fed
85                 Fgfr2 is expressed by OLs in myelinated fiber tracks.
86 onal regeneration is normally limited within myelinated fiber tracts in the CNS of higher vertebrates
87 y (3) the proximity of damaged 5-HT axons to myelinated fiber tracts.
88  axons in the corpus callosum (percentage of myelinated fibers was 44.7% in cupr-water and 63% in cup
89 eous observation of neuronal cell bodies and myelinated fibers, we were able to correlate subnuclear
90 meter, myelin width, and the number of large myelinated fibers were decreased in the tibial nerves of
91                                     Varicose myelinated fibers were observed in the same regions as F
92 ot and TrV were composed primarily of larger myelinated fibers, whereas the periphery of the root and
93 t <or=60% of MT may be mediated via only the myelinated fibers, whereas vasodilation at >or=90% of MT
94         ST, however, was localized mainly in myelinated fiber (white matter) region of the cerebellum
95   The node of Ranvier is a tiny segment of a myelinated fiber with various types of specializations a
96 se novel connective tissues are comprised of myelinated fibers, with reduced myelin basic protein lev
97         We found evidence for two classes of myelinated fibers within the pinniped optic nerve, those
98 ect on neurite outgrowth and regeneration of myelinated fibers without affecting unmyelinated DRG neu
99 mount for action potential propagation along myelinated fibers, yet the mechanisms governing nodal de

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