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1 fibers) and vesicular monoamine transporter (sympathetic fibers).
2 ity in tyrosine hydroxylase-positive cardiac sympathetic fibers.
3 pinal nerve ligation, indicated sprouting of sympathetic fibers.
4 rowth factor (NGF) is trophic to sensory and sympathetic fibers.
5                               Postganglionic sympathetic fibers also showed abnormal recovery cycles
6  after tMCAO, tyrosine hydroxylase levels in sympathetic fibers and bone marrow noradrenaline levels
7 y of functional interaction between sprouted sympathetic fibers and sensory neurons, the present stud
8 rphology and structural relationship between sympathetic fibers and the DRG neurons by electron micro
9  and consists of the sprouting of peripheral sympathetic fibers, arising from the superior cervical g
10 s the temporal sequence in which sensory and sympathetic fibers arrived in the footpad was not affect
11                          Blockade of cardiac sympathetic fibers by thoracic epidural anesthesia may a
12 here, sporadically, patients with denervated sympathetic fibers develop chronic inflammation.
13 rocess which would transect the regenerating sympathetic fibers extending from the injury site -- did
14 generation is the sprouting of noradrenergic sympathetic fibers from the superior cervical ganglia in
15           The pharmacological suppression of sympathetic fiber function with systemic guanethidine si
16  expression resulted in an overproduction of sympathetic fibers in sympathetic target organs.
17     The confined location of early sprouting sympathetic fibers in the distal half of the L5 DRG conf
18 n) of neuropathic pain triggers sprouting of sympathetic fibers in the dorsal root ganglion (DRG).
19 ormal, suggesting that there is sprouting of sympathetic fibers in the DRG after peripheral nerve inj
20 udy examined the numbers and distribution of sympathetic fibers in the DRG and their sprouting routes
21         All these results indicate that many sympathetic fibers in the DRG are regenerating branches
22                     The numerical density of sympathetic fibers in the DRG of an injured segment was
23 ble interactions between sensory neurons and sympathetic fibers in the DRG of neuropathic rats.
24                                 Sprouting of sympathetic fibers in the DRG was extensive as early as
25               We conclude that the effect of sympathetic fibers in the L4/L5 gray rami in these model
26 injury site -- did not change the density of sympathetic fibers in the L5 DRG.
27 that transmitters released from the sprouted sympathetic fibers in the synovial membrane and upper de
28 eficits in the extension and arborization of sympathetic fibers in their final target fields, while n
29 ss but correlated with increased activity of sympathetic fibers innervating brown adipose tissue (BAT
30           Recently, a sprouting of autonomic sympathetic fibers into the upper dermis of the skin, an
31 rve fibers express p75 and trk A, and pulpal sympathetic fibers lack p75.
32 discharge characteristics, in the setting of sympathetic fiber loss associated with POTS, may contrib
33 e only 5-HT, whereas NE (perhaps secreted by sympathetic fibers) may be concentrated and repackaged f
34 ion along axons, particularly evident within sympathetic fibers of the vas deferens, reflecting a hig
35  neuronal reorganization in which peripheral sympathetic fibers, originating from the superior cervic
36                                        Those sympathetic fibers present in sweat glands expressed an
37                                     To label sympathetic fibers projecting to the gut muscle wall, de
38                     This tissue accommodates sympathetic fiber sprouting in the neonate but becomes i
39                                 Blocking the sympathetic fiber sprouting may provide a novel therapeu
40 sults show that in the absence of functional sympathetic fibers, the eye loses its ability to prevent
41 it acts as a guidance factor that encourages sympathetic fibers to follow blood vessels as they proje
42 e superior cervical ganglion, which supplies sympathetic fibers to the eye, and studied the immune re
43 a major component of the pathways that guide sympathetic fibers to their appropriate targets both in
44             In rats with intact innervation, sympathetic fibers travel to the orbit in association wi
45  instead a dense plexus of catecholaminergic sympathetic fibers was found commingled with sensory fib
46 all-diameter fibers, prior to dysfunction of sympathetic fibers, with depletion of skin NGF and the s
47 d that there is an increase in the number of sympathetic fibers within the dorsal root ganglion (DRG)