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1 in receptor terminals of both myelinated and unmyelinated fibers.
2 i-GluR4 or anti-GluR2/4 stains predominantly unmyelinated fibers.
3 rs, but only on Schwann cells of sympathetic unmyelinated fibers.
4 of myelinated fibers but relative sparing of unmyelinated fibers.
5 al role in the mediation of sensory input by unmyelinated fibers.
6 ssing pipeline for automated segmentation of unmyelinated fibers.
7 nd latency for myelinated fibers but not for unmyelinated fibers.
8 ch matches the time for the peak response in unmyelinated fibers.
9 se to cowhage is different in myelinated and unmyelinated fibers, (5) the time of peak itch sensation
10 hat the accumulation of D2 is predominant in unmyelinated fibers and a hallmark of bortezomib-induced
11 tion of the sciatic nerve revealed a loss of unmyelinated fibers and extensive ultrastructural damage
14 ning for tyrosine hydroxylase (TH), were all unmyelinated fibers and some of them ended as growth con
15 rficial laminae: C1, likely to be endings of unmyelinated fibers, and C2, of small myelinated fibers.
16 ted to small-diameter myelinated axons, thin unmyelinated fibers, and small terminals that contained
19 ements of conduction velocity indicated that unmyelinated fibers are responsible for glutamatergic si
20 nable quick and accurate characterization of unmyelinated fibers at scale and become instrumental in
21 resent on axons and Schwann cells of sensory unmyelinated fibers, but only on Schwann cells of sympat
22 -threshold mechanoreceptors in the skin with unmyelinated fibers called C tactile (CT) afferents.
23 ngs in hypertonic P18 kits decreased only in unmyelinated fibers, despite a loss in both myelinated a
24 es revealed early preferential loss of small unmyelinated fibers followed by prominent demyelination
25 ined the effects of C-peptide replacement on unmyelinated fiber function in the hind paw, sural nerve
26 old reduction in the density of regenerating unmyelinated fibers in LAR-/- nerves distal to the crush
27 al CNAP with all 1,759 myelinated and 13,283 unmyelinated fibers in NEURON required 286 and 15,860 CP
29 1.2 channels were predominately localized in unmyelinated fibers in the cortex, hippocampus, spinal c
31 ever, although 65% of the AEN is composed of unmyelinated fibers, it has not been determined whether
34 otion that altered potassium homeostasis and unmyelinated fibers may represent a potential vehicle fo
35 d restored the diabetes-induced reduction of unmyelinated fiber number (P < 0.01) and mean axonal siz
37 the function of the adhesion molecule L1 in unmyelinated fibers of the peripheral nervous system (PN
38 eripherin (a marker of thinly myelinated and unmyelinated fibers) or calcitonin gene-related peptide
39 n of the labeling patterns suggests that AEN unmyelinated fibers project primarily to the ventral tip
40 c locations known to be innervated by small, unmyelinated fibers, suggesting that NGF modulated senso
41 he role of degeneration of myelinated versus unmyelinated fibers, we investigated the effects of an L
43 pulation in minutes, including often omitted unmyelinated fibers which constitute 80% of the nerve.
44 amatic proliferation in the Schwann cells of unmyelinated fibers, which resulted in the segregation o