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1 rves of transgenics showed a 60% increase in myelinated fibers.
2 the human brain require optimally sized and myelinated fibers.
3 that mediate domain-specific interactions of myelinated fibers.
4 red to vehicle, suggesting more functionally myelinated fibers.
5 morphometric changes in distal tibial nerve myelinated fibers.
6 y enters the brain and specifically binds to myelinated fibers.
7 l regions for action potential conduction in myelinated fibers.
8 fferent signal is carried by unmyelinated or myelinated fibers.
9 vantages for the high resolution staining of myelinated fibers.
10 f myelination and the domain organization of myelinated fibers.
11 s and maintained the axonal caliber of large myelinated fibers.
12 pport the earliest stages of regeneration of myelinated fibers.
13 receptor are juxtaposed along the course of myelinated fibers.
14 esion leads to degeneration predominantly in myelinated fibers.
15 f the unmyelinated C-fibers and/or the small myelinated fibers.
16 hereas Cx32 staining was restricted to large myelinated fibers.
17 timeric complexes at juxtaparanodal zones in myelinated fibers.
18 ngs of unmyelinated fibers, and C2, of small myelinated fibers.
19 out affecting other structural properties of myelinated fibers.
20 ated axons relative to age-matched wild-type myelinated fibers, although connectivity and patterns of
21 aPOZ mice are impaired in the maintenance of myelinated fibers and are a promising model for studying
23 ly large myelinated fibers, bortezomib small myelinated fibers and cisplatin damaged all types of mye
25 copy to examine the number and morphology of myelinated fibers and size of myelinated CNS structures.
26 portance of sensory input in the building of myelinated fibers and suggest that this activity-depende
27 ion molecules between inflammatory cells and myelinated fibers and the apparent predominance of T hel
28 ls survived within the affected zone, as did myelinated fibers and the extrinsic calretinin- and tyro
29 Sensory modalities that involved large Abeta myelinated fibers and unmyelinated C fibers were most af
30 d itch matches the time for peak response in myelinated fibers, and (6) the time for peak itch sensat
32 rrant axonal regeneration, irregularly sized myelinated fibers, and fibrosis were frequently observed
33 e hypertrophy, onion bulb formation, loss of myelinated fibers, and occasional myelin thickening simi
34 sal roots, anti-GluR2/3 stains predominantly myelinated fibers; anti-GluR4 or anti-GluR2/4 stains pre
35 Striking color patterns unique to individual myelinated fibers are generated that facilitate their tr
37 the sural nerve, where the large majority of myelinated fibers are sensory, approximately half of the
39 Size-frequency histograms of regenerated myelinated fiber areas suggest a delay in the maturation
40 lements are the cell islands of layer II and myelinated fibers around the cell islands, the dispositi
42 om examination of the axoplasm isolated from myelinated fibers as axoplasmic whole mounts and delipid
44 fibers at day 7, and the mean axonal area of myelinated fibers at 7, 14, and 21 days after injury, in
45 (NF186), a neuronal protein concentrated in myelinated fibers at nodes of Ranvier, and NF155, the ol
46 itaxel and vincristine affected mostly large myelinated fibers, bortezomib small myelinated fibers an
49 des extensive Wallerian-like degeneration of myelinated fibers but relative sparing of unmyelinated f
50 ous and evoked neuronal hyperexcitability in myelinated fibers, coupled with development of neuropath
51 strated significantly decreased densities of myelinated fibers, decreased axonal areas, and increased
52 betic mice, resulted in significantly higher myelinated fiber densities and conduction velocities con
54 dex and reduced regeneration, as assessed by myelinated fiber density after acute crush of the sciati
58 city deficits, and reduction in tibial nerve myelinated fiber diameter, but not intraepidermal nerve
60 Ensheathed axons express low levels whereas myelinated fibers express high levels of NRG1 type III.
64 to perceive innocuous pressures is lost when myelinated fiber function is experimentally blocked in h
66 osarcoma, and irregularity and disruption of myelinated fibers in areas infiltrated by oligodendrogli
68 neurons resulted in improved regeneration of myelinated fibers in both the dorsal root and the spinal
69 MPC onto injured axonal swellings and intact myelinated fibers in cases from individuals with confirm
70 l lines of evidence for an important role of myelinated fibers in cowhage-induced itch: (1) a selecti
71 is able to strongly and selectively bind to myelinated fibers in fixed mouse brain slices, and that
72 icroscopic comparison of the organization of myelinated fibers in lateral olfactory tract in the ante
77 ced by stimulation of unmyelinated and small myelinated fibers in the joint and surrounding tissue.
80 urons that are not generally associated with myelinated fiber input from mechanical and proprioceptiv
81 tic neuropathies and axonal atrophy of large myelinated fibers, its role in small sensory nerve fiber
83 that the IC and MGC exhibit relatively high myelinated fiber length density (MFLD) values at birth a
84 ly aligned and right-sided obliquely aligned myelinated fibers, may represent a biologic mechanism fo
85 nt, number of oligodendrocytes, or number of myelinated fibers, nor was myelination delayed developme
88 ignificantly reduced the ratio of abnormally myelinated fibers (p = 0.00148) and secondary inflammati
92 , there was a 45% reduction in the number of myelinated fibers relative to controls, demonstrating a
93 r hippocampus (serum 4%, CSF 6%); 3) against myelinated fibers (serum 2%, CSF 2%); 4) against cerebel
95 on of the paranodal junctional region of CNS myelinated fibers shows that "transverse bands," a compo
96 ed itch: (1) a selective conduction block in myelinated fibers substantially reduces itch in a subgro
100 in the axonal size-frequency distribution of myelinated fibers toward smaller axons in galactose-fed
102 and neurons in vivo and in vitro, as well as myelinated fiber tracts and a small number of macrophage
103 onal regeneration is normally limited within myelinated fiber tracts in the CNS of higher vertebrates
105 axons in the corpus callosum (percentage of myelinated fibers was 44.7% in cupr-water and 63% in cup
107 eous observation of neuronal cell bodies and myelinated fibers, we were able to correlate subnuclear
108 meter, myelin width, and the number of large myelinated fibers were decreased in the tibial nerves of
110 ot and TrV were composed primarily of larger myelinated fibers, whereas the periphery of the root and
111 t <or=60% of MT may be mediated via only the myelinated fibers, whereas vasodilation at >or=90% of MT
113 The node of Ranvier is a tiny segment of a myelinated fiber with various types of specializations a
114 se novel connective tissues are comprised of myelinated fibers, with reduced myelin basic protein lev
116 ect on neurite outgrowth and regeneration of myelinated fibers without affecting unmyelinated DRG neu
117 mount for action potential propagation along myelinated fibers, yet the mechanisms governing nodal de