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1 the spinal cord dorsal horn by A delta and C primary afferent fibers.
2 nsory information arriving from Adelta and C primary afferent fibers.
3 mulation of capsaicin-sensitive, nociceptive primary afferent fibers.
4 t are sensed by vagal, spinal, and intrinsic primary afferent fibers.
5 rominently located near central terminals of primary afferent fibers.
6 GluR5/6/7-immunopositive terminals are from primary afferent fibers.
7 in behaviors, suggesting that ET-1 activates primary afferent fibers.
8 ciceptive)- and small (nociceptive)-diameter primary afferent fibers.
9 ls, small fusiform cells, granule cells, and primary afferent fibers.
10 y heterogeneous population of small diameter primary afferent fibers.
11 aicin-sensitive, substance P (SP)-containing primary afferent fibers.
12 rocessing in the terminals of small-diameter primary afferent fibers.
13 ) receptors associated with the membranes of primary afferent fibers.
14 s-like electrical stimulation of ipsilateral primary afferent fibers.
15 esence of mGlu1alpha receptors on peripheral primary afferent fibers and determine the behavioral eff
16 pal mediators of sensory information between primary afferent fibers and the spinal cord, activate Er
18 kly electric fish Eigenmannia, P- and T-type primary afferent fibers are specialized for encoding the
19 nd occasional terminals, presumed to be from primary afferent fibers, at the center of glomerular arr
20 tissue innervated by neuropeptide-containing primary afferent fibers chiefly from the trigeminal nerv
22 pil elements rather than in the terminals of primary afferent fibers, even though labeling overlapped
24 m-like brainstem structure that receives the primary afferent fibers from electroreceptors in the ski
25 hlear nuclei receive axosomatic endings from primary afferent fibers from the cochlea and have projec
26 ajor termination region for unmyelinated (C) primary afferent fibers; however, how the input it recei
28 a(2A)ARs are coexpressed on the terminals of primary afferent fibers in the spinal cord where they ma
29 ustained low-frequency stimulation (5 Hz) of primary afferent fibers in the tractus solitarius result
31 uropathic conditions, noxious stimulation of primary afferent fibers induces release of CatS from mic
32 t receive monosynaptic input from trigeminal primary afferent fibers innervating extracranial orofaci
33 ting of nerve growth factor (NGF)-responsive primary afferent fibers is thought to contribute to thei
34 ggest that receptor-Ca2+ channel coupling in primary afferent fibers may have little functional signi
35 PG), all induce long-lasting depression of A primary afferent fibers-mediated monosynaptic excitatory
36 esults imply that, in conjunction with local primary afferent fiber plasticity, injury-induced sprout
39 microscopy results, imply that unmyelinated primary afferent fibers terminating in the superficial d
40 ck is carried by action potentials of S-type primary afferent fibers that project to the inner cellul
41 IB4) is selectively taken up by unmyelinated primary afferent fibers that terminate in the outer part
42 er cell that relays sensory information from primary afferent fibers to higher order cells of ELLS.
43 ction patterns of peptidergic small-diameter primary afferent fibers to the cat sacrocaudal spinal co
44 n gene-related peptide (CGRP)-immunoreactive primary afferent fibers was selectively altered at speci
45 ated peptide (CGRP)-immunoreactive (CGRP-IR) primary afferent fibers were observed within the superfi