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1 o effect on the density of the high-affinity NGF receptor.
2 ding is mediated by the p75 component of the NGF receptor.
3 te the expression of TrkA, the high-affinity NGF receptor.
4 in PC12nnr5 cells, which lack the p140(trk) NGF receptor.
5 n NGF actions were reflected at the level of NGF receptors.
6 ect cell expression of wild-type and mutated NGF receptors.
7 as a major mediator of signaling by FGF and NGF receptors.
8 al to SNT, the long-sought target of FGF and NGF receptors.
9 ffect of ethanol on the nerve growth factor (NGF) receptor.
15 rane region of the TrkA nerve growth factor (NGF) receptor and has been implicated in NGF signaling.
18 y NT-3 receptor, and trkA, the high-affinity NGF receptor, are both expressed from the early OLP thro
20 he MAP kinase cascade downstream of the TrkA NGF receptor but upstream or at the level of the B-Raf k
21 ED cells engineered to express the human p75 NGF receptor (D283p75) also did not undergo apoptosis.
22 sing both TrkC and TrkA/nerve growth factor (NGF) receptors, different morphological changes occur up
23 could suppress the increased, AF64A-induced NGF receptor expression in the medial septal nucleus.
25 this hypothesis, we measured NGF content and NGF receptor expression, p75(NTR) (low affinity neurotro
27 r necrosis factor (TNF)-nerve growth factor (NGF) receptor family have been shown to be important cos
30 oding the high-affinity nerve growth factor (NGF) receptor (GT1-trk) could also be persistently infec
31 tion of NGF and small molecule inhibitors of NGF receptors have been developed and tested in clinical
33 f RTA showed significantly more low affinity NGF receptor immunoreactive (p75NGFR-IR) neurons on the
34 a short-lasting hypertrophy of low affinity NGF receptor immunoreactive neurons within the nucleus b
35 Here we report that activation of the TrkA NGF receptor in oligodendrocytes negates cell death by t
38 al effects on both the low and high affinity NGF receptors in terms of cell body size and staining de
39 urotrophin receptor) and trkA (high affinity NGF receptor), in control and diabetic rat SMG, CG and s
40 embers Trk B and Trk C, and the low-affinity NGF receptor (INGFR) are all detected within both mature
42 sh the effect of C3 on the expression of the NGF receptor-IR elements, C3 was administered orally (25
43 evealed that AF64A induced the appearance of NGF-receptor-IR axonal varicosities in the rat medial se
47 a potential link to AD pathogenesis, TrkA, a NGF receptor, is expressed in cholinergic forebrain neur
48 lts reveal that IRAK is recruited to the p75-NGF receptor leading to formation of a complex between I
51 NGF in the keratinocytes and upregulation of NGF receptor (NGF-R) in the cutaneous nerves of psoriati
52 Mice carrying a mutation in the low-affinity NGF receptor (NGFR) gene possess deficits in sensory inn
54 educed the density of the low-affinity (p75) NGF receptor on PC12 cells, but had no effect on the den
55 o a complex with TrkA to dephosphorylate the NGF receptor on Ser/Thr residues and to potentiate its i
56 s of nerve growth factor (NGF) that bind the NGF receptor p140 TrkA was evaluated and compared with t
57 ly transfected with either the high affinity NGF receptor p140(trk) (3T3-Trk) or the low affinity NGF
59 on coexpression of the nerve growth factor (NGF) receptors p75(NTR) and TrkA, which bind NGF in cort
60 e the physiological role of the low affinity NGF receptor (p75) has not been clearly defined, this re
62 phic factor is a ligand for the low-affinity NGF receptor, p75, and for the high-affinity neurotrophi
64 have localized the binding sites of the two NGF receptors, p75 and TrkA, to other regions of the NGF
65 Immunotoxic lesions targeting low-affinity NGF receptor (p75NGF receptor)-bearing CBF neurons provi
66 osin receptor kinase A (TrkA) (high-affinity NGF receptor) pathway plays a role in the calcification
68 IgG-saporin, a specific immunotoxin for the NGF receptor-positive, cholinergic basal forebrain neuro
71 functions for the high affinity heteromeric NGF receptor site: (a) integration of both the MAPK and
72 d in aged animals, suggesting that decreased NGF receptor stimulation may be one factor contributing
74 nting the high-affinity nerve growth factor (NGF) receptor Trk A, its family members Trk B and Trk C,
75 on of the high-affinity nerve growth factor (NGF) receptor Trk occurs through multiple processes cons
76 NGF effect is mediated by the high affinity NGF receptor, Trk A and that neurotrophin binding to the
77 , and into PC12 variants expressing specific NGF receptor/Trk mutants, we show that transcriptional r
78 forms a novel multiprotein complex with the NGF receptor TrkA and the PI3K regulatory subunit p85, w
79 n of anti-NGF antibody, or inhibition of the NGF receptor trkA by k252a or antisense oligonucleotides
80 or the local activation of the high-affinity NGF receptor trkA was suggested by a strong inhibition o
82 differentiation and survival, associate with NGF receptor TrkA, and be tyrosyl-phosphorylated in resp
83 half of unmyelinated nociceptors express the NGF receptor TrkA, and half express the GDNF family liga
84 ssing neurons also express the high-affinity NGF receptor TrkA, and only a small proportion bind to I
85 PC12nnr5 cells, which lack the high affinity NGF receptor TrkA, ii) srcDN2 cells, which overexpress k
92 wn to bind to activated nerve growth factor (NGF) receptor TrkA and has been implicated in NGF-induce
96 Trypanosoma cruzi binds nerve growth factor (NGF) receptor TrkA, increasing receptor autophosphorylat
97 ript interacts with the nerve growth factor (NGF) receptor TrkA, regulating TrkA endocytosis and sign
100 most NB, while loss of nerve growth factor (NGF) receptor (trkA) gene expression correlates with an
101 ve shown that the activation kinetics of the NGF receptor, TrkA, and downstream protein kinases appea
102 al axons requires the kinase activity of the NGF receptor, TrkA, in both distal axons and cell bodies
104 ent on the levels of mRNA and protein of the NGF receptors, trkA and p75NTR, in normal and diabetic r
105 more, by expressing the nerve growth factor (NGF) receptor, TrkA, and the epidermal growth factor (EG
112 ably, we identified the nerve growth factor (NGF) receptor tyrosine kinase (NTRK1), a molecule not pr
113 ic antibodies to TRPV1; nerve growth factor (NGF) receptor tyrosine kinase A; glial cell line-derived
114 S12 associates with the nerve growth factor (NGF) receptor tyrosine kinase TrkA, activated H-Ras, B-R
117 f low and high affinity nerve growth factor (NGF) receptors was investigated in the basal forebrain d
119 cing the sensitisation of TRPV1 by TrkA, the NGF receptor, were characterised by observing the effect