ライフサイエンスコーパス: unmyelinated fiber

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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 ch matches the time for the peak response in unmyelinated fibers.

7 se to cowhage is different in myelinated and unmyelinated fibers, (5) the time of peak itch sensation

8 tion of the sciatic nerve revealed a loss of unmyelinated fibers and extensive ultrastructural damage

9 which is devoid of synapses and composed of unmyelinated fibers and glial cells.

10 ites that serve local high-energy demands of unmyelinated fibers and signal transmission.

11 ning for tyrosine hydroxylase (TH), were all unmyelinated fibers and some of them ended as growth con

12 rficial laminae: C1, likely to be endings of unmyelinated fibers, and C2, of small myelinated fibers.

13 ted to small-diameter myelinated axons, thin unmyelinated fibers, and small terminals that contained

14 It is argued that unmyelinated fibers are not blocked by the neurotoxins b

15 ated axons in the dorsal roots, although the unmyelinated fibers are preserved.

16 ements of conduction velocity indicated that unmyelinated fibers are responsible for glutamatergic si

17 resent on axons and Schwann cells of sensory unmyelinated fibers, but only on Schwann cells of sympat

18 ngs in hypertonic P18 kits decreased only in unmyelinated fibers, despite a loss in both myelinated a

19 es revealed early preferential loss of small unmyelinated fibers followed by prominent demyelination

20 ined the effects of C-peptide replacement on unmyelinated fiber function in the hind paw, sural nerve

21 old reduction in the density of regenerating unmyelinated fibers in LAR-/- nerves distal to the crush

22 l sprouting occurs, producing an increase in unmyelinated fibers in the corpus callosum.

23 1.2 channels were predominately localized in unmyelinated fibers in the cortex, hippocampus, spinal c

24 vier along adult CNS and PNS axons and along unmyelinated fibers in the PNS.

25 ever, although 65% of the AEN is composed of unmyelinated fibers, it has not been determined whether

26 There was no evidence of unmyelinated fiber loss or a decrease in the number of m

27 III, and IV are now known and there is clear unmyelinated fiber loss.

28 otion that altered potassium homeostasis and unmyelinated fibers may represent a potential vehicle fo

29 d restored the diabetes-induced reduction of unmyelinated fiber number (P < 0.01) and mean axonal siz

30 Myelinated and unmyelinated fibers of the lingual nerve were increased

31 the function of the adhesion molecule L1 in unmyelinated fibers of the peripheral nervous system (PN

32 eripherin (a marker of thinly myelinated and unmyelinated fibers) or calcitonin gene-related peptide

33 n of the labeling patterns suggests that AEN unmyelinated fibers project primarily to the ventral tip

34 c locations known to be innervated by small, unmyelinated fibers, suggesting that NGF modulated senso

35 he role of degeneration of myelinated versus unmyelinated fibers, we investigated the effects of an L

36 amatic proliferation in the Schwann cells of unmyelinated fibers, which resulted in the segregation o

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