ライフサイエンスコーパス: neurotrophin receptor

1 the kinase-active Trk receptors and the p75 neurotrophin receptor.

2 ke receptor superfamilies, including the p75 neurotrophin receptor.

3 omponent of this receptor complex is the p75 neurotrophin receptor.

4 similar gamma-secretase cleavage is the p75 neurotrophin receptor.

5 receptor tyrosine kinases and the shared p75 neurotrophin receptor.

6 ate with the intracellular domain of the p75 neurotrophin receptor.

7 ota PKC.IRAK complex is recruited to the p75 neurotrophin receptor.

8 anism, supported by up-regulation of the p75 neurotrophin receptor.

9 actions of BDNF are mediated through the p75 neurotrophin receptor.

10 e induced by selective activation of the p75 neurotrophin receptor.

11 tracellular neurotrophin binding site of p75 neurotrophin receptor.

12 Schwann cell death via engagement of the p75 neurotrophin receptor.

13 or cell death decisions mediated by the p75 neurotrophin receptor.

14 f differentiation markers, and activation of neurotrophin receptors.

15 synthetic derivative LIGA20 activate various neurotrophin receptors.

16 small molecule agonists to transactivate Trk neurotrophin receptors.

17 S can physically associate with TrkA and p75 neurotrophin receptors.

18 least in part to differential trafficking of neurotrophin receptors.

19 of REM sleep by acting on one or more of the neurotrophin receptors.

20 The p75 neurotrophin receptor, a member of the tumor necrosis fa

21 The p75 neurotrophin receptor, a member of the tumor necrosis fa

22 Mechanistically, blockade of the p75 neurotrophin receptor abolished BDNF-induced postsynapti

23 udies provide a new reagent for altering p75 neurotrophin receptor actions after injury and suggest t

24 th factor (NGF) binding to both p75 and TrkA neurotrophin receptors activates the transcription facto

25 ta-catenin, Shh) and dermal papilla (p75 kDa neurotrophin receptor, alkaline phosphatase).

26 gulated intramembrane proteolysis of the p75 neurotrophin receptor (also known as p75 cleavage).

27 egulation of neurotrophins and their cognate neurotrophin receptors among other classes of transcript

28 ia the tyrosine receptor kinase B (TrkB)/p75 neurotrophin receptor and Fyn kinase in transfected cell

29 nteract through its TRAF domain with the p75 neurotrophin receptor and weakly with the lymphotoxin-be

30 Cav-1 concentrates glutamate and neurotrophin receptors and prosurvival kinases and regul

31 receptor expression, p75(NTR) (low affinity neurotrophin receptor) and trkA (high affinity NGF recep

32 the cell death mediator p75(NTR) (the common neurotrophin receptor), and its interaction with proapop

33 or induced apoptosis in cells expressing p75 neurotrophin receptor, and enhances neurite outgrowth in

34 d trkC-IgG) were used to block activation of neurotrophin receptors, and AADH-CNTF was used to antago

35 was blocked by exposure to the high-affinity neurotrophin receptor antagonist K252a, or an antagonist

36 Thus, both low- and high-affinity neurotrophin receptors are conspicuously present in neur

37 Our results indicate that Trk neurotrophin receptors are differentially regulated by u

38 lipid rafts, little is known about how these neurotrophin receptors are directed there or how localiz

39 Neurotrophin receptors are emerging targets in oncology,

40 We show that neurotrophin receptors are expressed early, being first

41 To determine which neurotrophins and neurotrophin receptors are expressed in taste buds, and

42 not fully understood how genes encoding Trk neurotrophin receptors are regulated.

43 However, the mechanisms by which neurotrophin receptors assemble such a sustained signali

44 eas they do not bind to the p75 low-affinity neurotrophin receptor at all.

45 In adulthood, p75 neurotrophin receptor becomes down-regulated and propofo

46 The TrkC neurotrophin receptor belongs to the functional dependen

47 es binding of pro-nerve growth factor to p75 neurotrophin receptor, blocks pro-nerve growth factor in

48 growth factor (NGF) in complex with the p75 neurotrophin receptor but is distinct from that of micro

49 osteoprotegerin, FOXC2 and FOXF2, BMP-2, p75 neurotrophin receptor, caspase-11, guanylate-binding pro

50 library for genes affecting the dynamics of neurotrophin receptor-containing endosomes in motor neur

51 Neurotrophin receptors corresponding to vertebrate Trk,

52 ssion of TrkC, a member of the Trk family of neurotrophin receptors, could drive tumorigenesis, invas

53 closely related to NRAGE, which mediates p75 neurotrophin receptor-dependent apoptosis, and necdin, w

54 of dynamin1 is a critical event coordinating neurotrophin receptor endocytosis and axonal growth.

55 kB (tropomyosin kinase receptor B), the main neurotrophin receptor expressed by neurons of the centra

56 lus propofol applications at the peak of p75 neurotrophin receptor expression after experimental trau

57 ricted to the developing nervous system when neurotrophin receptor expression peaks, indicate that BI

58 Neurotrophin receptor expression was confirmed in a pane

59 se is the lack of NO, which up-regulated p75 neurotrophin receptor expression, a receptor required fo

60 creased raft formation, neurotransmitter and neurotrophin receptor expression, NMDA- and BDNF-mediate

61 developmental-like programs and increase p75 neurotrophin receptor expression, probably to foster rep

62 the transcriptional machinery that specifies neurotrophin receptor expression.

63 tyrosine-related kinase B (TrkB) p75NTR (p75 neurotrophin receptor) facilitates stabilization of the

64 ceptor B (trkB) and a truncated form of this neurotrophin receptor, favoring the inactive form throug

65 hat Toll paralogs unrelated to the mammalian neurotrophin receptors function as neurotrophin receptor

66 S-HGGs, with recurrent fusions involving the neurotrophin receptor genes NTRK1, NTRK2 and NTRK3 in 40

67 The p75 neurotrophin receptor has been implicated in neurotrophi

68 Recent experiments suggest that Xenopus Neurotrophin Receptor Homolog 1 (NRH1) proteins act thro

69 tly, a closely related gene to p75NTR called neurotrophin receptor homolog-2 (NRH2) was identified; h

70 5 kDa neurotrophin receptor (p75NTR) and two neurotrophin receptor homologs (NRH1, NRH2) constitute a

71 rvival and are thought to lack high-affinity neurotrophin receptors (i.e., trks).

72 ntrast, optical density for low-affinity p75 neurotrophin receptor immunoreactivity in the VLDB did n

73 Neurons that were devoid of neurotrophin-receptor immunoreactivity were intermingled

74 myosin-related kinase B receptor (TrkB) is a neurotrophin receptor important for the synaptic plastic

75 eres with oligomerization of full-length p75 neurotrophin receptor in a dose-dependent manner.

76 lirin binds to and colocalizes with the TrkA neurotrophin receptor in neurons.

77 ceptor-associated kinase (IRAK) with the p75 neurotrophin receptor in PC12 cells.

78 Ubiquitination of the TrkA neurotrophin receptor in response to NGF is critical in

79 We found that TrkB is the most prominent neurotrophin receptor in the mouse SVZ, but only the tru

80 ence for either ChAT or the low-affinity p75 neurotrophin receptor in the nucleus basalis Meynert fai

81 mammalian neurotrophin receptors function as neurotrophin receptors in fruit flies.

82 tion with either fibroblast growth factor or neurotrophin receptors in neuronal development.

83 neurons that contain low- and high-affinity neurotrophin receptors in regions of the feline pons and

84 examined the expression of neurotrophins and neurotrophin receptors in the lesion/transplanted striat

85 -stimulating factor (M-CSF), the M-CSFR, and neurotrophin receptors in the NMDA-treated slices, as de

86 ic neurons but does modify the expression of neurotrophin receptors in these regions.

87 t-derived NGF promotes expression of the p75 neurotrophin receptor, in turn causing a reduction in th

88 Here we report that the neurotrophin receptor interacting factor (NRIF) is neces

89 functional interaction between TRAF6 and the neurotrophin receptor interacting factor (NRIF), two pro

90 In this study, we demonstrate that neurotrophin receptor-interacting factor (NRIF) mediates

91 NRAGE (neurotrophin receptor-interacting melanoma antigen) inte

92 Schwann cell factor 1 (SC1), a p75 neurotrophin receptor-interacting protein, is a member o

93 p75 neurotrophin receptor is highly expressed during early n

94 The p75 neurotrophin receptor is important in multiple physiolog

95 aline residue at position 264 in the rat p75 neurotrophin receptor is necessary for the ability of p7

96 Previously, we have shown that p75 neurotrophin receptor is required for glioma invasion an

97 Localization of Trk neurotrophin receptors is an important factor in directi

98 dings indicate that intracellular sorting of neurotrophin receptors is critical for postnatal neuroge

99 The expression of neurotrophins and neurotrophin receptors is essential for the proper estab

100 e tropomyosin-related kinase (Trk) family of neurotrophin receptors, is implicated in the growth and

101 Activation of the p75 neurotrophin receptor leads to a variety of effects with

102 neuronal cell death and abnormalities in Trk neurotrophin receptor levels.

103 y signals through the same Nogo receptor/p75 neurotrophin receptor/LINGO-1 (NgR1/p75/LINGO-1) complex

104 rotrophic factor ratio, which aggravates p75 neurotrophin receptor-mediated cell death.

105 BMP9 induced the p75 neurotrophin receptor (NGFR), a marker of BFCN, and Cntf

106 is and recent evidence suggests that the p75 neurotrophin receptor (NTR) contributes significantly to

107 We show that the p75 neurotrophin receptor (NTR) serves this role in retinal

108 while down-regulating the expression of p75 neurotrophin receptor (NTR), phospho-JNK, and Bcl-2-asso

109 rid library with the death domain of the p75 neurotrophin receptor (NTR), we identified the Sall2 tra

110 eurons mediated to a great extent by the p75 neurotrophin receptor (NTR).

111 gration and promotes myelination via the p75 neurotrophin receptor (NTR).

112 BDNF acts via TrkB and p75 neurotrophin receptors (NTR), and restoring its signalin

113 compound, EVT901, which interferes with p75 neurotrophin receptor oligomerization through direct int

114 unctionally blocking antibody toward the pan-neurotrophin receptor p75 (p75(NTR) ).

115 tivity for pro-nerve growth factor (proNGF), neurotrophin receptor p75 (p75(NTR)), and sortilin in th

116 hese effects are mediated by presynaptic pan-neurotrophin receptor p75 (p75(NTR)), the pro-BDNF recep

117 The neurotrophin receptor p75 (p75NTR) is a receptor of Abet

118 ceptors (tropomyosin-related kinase A [TrkA]/neurotrophin receptor p75 [p75(NTR)]).

119 The neurotrophin receptor p75 can induce apoptosis both in v

120 Activation of the neurotrophin receptor p75 has been shown to elicit oppos

121 Mice lacking the low-affinity neurotrophin receptor p75 have multiple peripheral neura

122 Efficient apical sorting of the neurotrophin receptor p75 is dependent on its O-glycosyl

123 The neurotrophin receptor p75 is induced by various injuries

124 lines of in vitro evidence suggest that the neurotrophin receptor p75 mediates or exacerbates Abeta-

125 Levels of the pan-neurotrophin receptor p75(NTR) and the BDNF receptor Trk

126 induce apoptosis in neuronal cells, via the neurotrophin receptor p75(NTR) and the sortilin receptor

127 The neurotrophin receptor p75(NTR) has been implicated in me

128 ed a marked upregulation of the proapoptotic neurotrophin receptor p75(NTR) in CA1, evident at 48 hr.

129 in PC-3 cells and siRNA directed against the neurotrophin receptor p75(NTR) in post-mitotic cultures

130 work has demonstrated an involvement of the neurotrophin receptor p75(NTR) in this process.

131 The neurotrophin receptor p75(NTR) negatively regulates spin

132 The pan-neurotrophin receptor p75(NTR) strongly inhibits activat

133 ases, may interact with the proapoptotic pan-neurotrophin receptor p75(NTR) to induce neuronal cytosk

134 kinase TrkA (also called NTRK1), the common neurotrophin receptor p75(NTR), and the proneurotrophin

135 how that the transmembrane domain of the pan-neurotrophin receptor p75(NTR), best known for regulatin

136 ability of SorCS2 to form complexes with the neurotrophin receptor p75(NTR), required for pro-brain-d

137 tion of saporin linked to an antibody to the neurotrophin receptor p75(NTR), which eliminates cells e

138 enomenon of pathological upregulation of pan-neurotrophin receptor p75(NTR).

139 ng with a signal-transducing coreceptor, the neurotrophin receptor p75(NTR).

140 NgR1) and a signal transducing subunit (the neurotrophin receptor p75).

141 rats also differ in their expression of the neurotrophin receptor p75.

142 gested to be a death-inducing ligand for the neurotrophin receptor p75.

143 pressed mRNA or protein for the low-affinity neurotrophin receptor p75.

144 n and induce their death via cleavage of the neurotrophin receptor p75.

145 ll number and the number of cells expressing neurotrophin receptors p75(NGFR) and trkA were assessed.

146 d immunoprecipitation with antibodies to the neurotrophin receptors p75, trkA, trkB, and trkC showed

147 for choline acetyltransferase (ChAT) or p75-neurotrophin receptor (p75(NTR) ).

148 ProNGF activates p75 neurotrophin receptor (p75(NTR)) and sortilin receptors

149 TAp73 is a transcriptional activator of p75 neurotrophin receptor (p75(NTR)) and that p75(NTR) mRNA

150 (BDNF) activate two distinct receptors: p75 neurotrophin receptor (p75(NTR)) and TrkB.

151 The p75 neurotrophin receptor (p75(NTR)) belongs to the tumor ne

152 trophic factor (BDNF)-activated TrkB and p75 neurotrophin receptor (p75(NTR)) by disrupting the endos

153 ole in Alzheimer's disease (AD), and the p75 neurotrophin receptor (p75(NTR)) has been implicated in

154 The role of the p75 neurotrophin receptor (p75(NTR)) in adult cholinergic ba

155 Expression of the p75 neurotrophin receptor (p75(NTR)) in primary melanomas is

156 Here we report that the p75 neurotrophin receptor (p75(NTR)) is a co-receptor of NgR

157 We show that cleaved p75 neurotrophin receptor (p75(NTR)) is a component of the n

158 The p75 neurotrophin receptor (p75(NTR)) is a member of the tumo

159 The p75 neurotrophin receptor (p75(NTR)) is a multifunctional re

160 Here we show that the p75 neurotrophin receptor (p75(NTR)) is a regulator of gluco

161 rve growth factor (NGF) signaling by the p75 neurotrophin receptor (p75(NTR)) is critical for neurona

162 distinct structural determinants in the p75 neurotrophin receptor (p75(NTR)) is crucial for the iden

163 The p75 neurotrophin receptor (p75(NTR)) is expressed on many ce

164 The p75 neurotrophin receptor (p75(NTR)) is highly expressed in

165 The p75 neurotrophin receptor (p75(NTR)) mediates neuronal death

166 The p75 neurotrophin receptor (p75(NTR)) mediates the death of s

167 be initiated by activation of either the p75 neurotrophin receptor (p75(NTR)) or the more selective t

168 xes with LINGO-1 and either the low-affinity neurotrophin receptor (p75(NTR)) or TROY to initiate gro

169 The p75 neurotrophin receptor (p75(NTR)) regulates a wide range

170 Here, we show that p75 neurotrophin receptor (p75(NTR)) undergoes hypoxia-induc

171 ron loss, distal axonal degeneration and p75 neurotrophin receptor (p75(NTR)) upregulation in the per

172 uctures of complexes formed by the DD of p75 neurotrophin receptor (p75(NTR)) with RhoGDI, for activa

173 e de novo expression of the low-affinity p75 neurotrophin receptor (p75(NTR)), a gene that plays crit

174 The p75 neurotrophin receptor (p75(NTR)), a member of the tumor

175 Here, we report that the p75 neurotrophin receptor (p75(NTR)), a TNF receptor superfa

176 mined the expression of the low affinity p75 neurotrophin receptor (p75(NTR)), an excellent marker of

177 This produced a substantial loss of both p75 neurotrophin receptor (p75(NTR))-positive and choline ac

178 GF, is a potent apoptotic ligand for the p75 neurotrophin receptor (p75(NTR))-sortilin complex.

179 aging in a complex with sortilin and the p75 neurotrophin receptor (p75(NTR)).

180 ed synapse elimination via activation of p75 neurotrophin receptor (p75(NTR)).

181 prevented by blocking antibodies against p75 neurotrophin receptor (p75(NTR)).

182 receptor tyrosine kinases (Trk) and the pan-neurotrophin receptor (p75) to regulate complex developm

183 g signals are generated by activation of p75 neurotrophin receptors (p75(NTR)).

184 cetyltransferase (ChAT) and the low-affinity neurotrophin receptor, p75(NTR) .

185 In recent studies, we have identified the neurotrophin receptor, p75(NTR), as a mediator of apopto

186 Here we demonstrate that a second neurotrophin receptor, p75(NTR), is expressed by establi

187 Expression of the neurotrophin receptor p75NTR is increased in the injured

188 We show that the neurotrophin receptor p75NTR, a tumor necrosis factor re

189 interplay with signaling promoted by the pan-neurotrophin receptor p75NTR.

190 s TrkA, TrkB and TrkC, as well as by the pan-neurotrophin receptor p75NTR.

191 ral cells via activation of the low affinity neurotrophin receptor p75NTR.

192 pheral nerves express elevated levels of the neurotrophin receptor p75NTR.

193 nase receptor TrkA, together with the common neurotrophin receptor p75NTR; both of which bind nerve g

194 neurotrophins bind with high affinity to p75 neurotrophin receptor (p75NTR) and lack the capacity to

195 s and mediates its effects by binding to p75 neurotrophin receptor (p75NTR) and sortilin.

196 binding to a receptor complex of the common neurotrophin receptor (p75NTR) and sortilin.

197 The 75 kDa neurotrophin receptor (p75NTR) and two neurotrophin rece

198 t with antisense oligonucleotides to the p75 neurotrophin receptor (p75ntr) decreased basal survival

199 t of the sympathetic nervous system, the p75 neurotrophin receptor (p75NTR) has a dual function: prom

200 Here, we investigate the involvement of p75 neurotrophin receptor (p75NTR) in Abeta-treated human ne

201 We investigated the role of the p75 neurotrophin receptor (p75NTR) in mediating neurotrophin

202 ur goal was to determine the role of the p75 neurotrophin receptor (p75NTR) in the loss of islet symp

203 myelin-associated glycoprotein recruited p75 neurotrophin receptor (p75NTR) into a complex with LRP1

204 Previously, we have shown that p75 neurotrophin receptor (p75NTR) is a novel mediator of in

205 The p75 neurotrophin receptor (p75NTR) is a proximate cell membr

206 Immunocytochemistry for the p75 low affinity neurotrophin receptor (p75NTR) or for calcitonin gene-re

207 Plasticity was rescued by inhibiting p75 neurotrophin receptor (p75NTR) signaling or its downstre

208 Here we show that the p75 neurotrophin receptor (p75NTR) undergoes presenilin-depe

209 They express the p75 neurotrophin receptor (p75NTR), which is known to signal

210 drinking produces a mobilization of DLS p75 neurotrophin receptor (p75NTR), whose activities oppose

211 he TrkA tyrosine kinase receptor and the p75 neurotrophin receptor (p75NTR).

212 t was triggered by overexpression of the p75 neurotrophin receptor (p75NTR).

213 (SCs) and an increased expression of the p75 neurotrophin receptor (p75NTR).

214 GF increased LDLR expression through the p75 neurotrophin receptor (p75NTR).

215 s in G1H mice that re-express the common p75 neurotrophin receptor (p75NTR).

216 e with and without the expression of the p75 neurotrophin receptor (p75NTR).

217 nchymal cells expressing both desmin and p75 neurotrophin receptor (p75NTR): HSCs in the liver parenc

218 ng cells (BTICs) and show that BTICs express neurotrophin receptors (p75NTR, TrkA, TrkB, and TrkC) an

219 rats by the recruitment of the low-affinity neurotrophin receptor, p75NTR, whose activities opposes

220 ed a mouse model with a mutation in the TrkA neurotrophin receptor (P782S) that results in reduced ub

221 he pro-brain-derived neurotrophic factor-p75 neurotrophin receptor pathway.

222 same set of transcription factors from a p75 neurotrophin receptor peptide (p75NTRp)-tagged adenoviru

223 indicate that the ubiquitination of the TrkA neurotrophin receptor plays a critical role in NGF-media

224 p75 neurotrophin receptor plays an important role in the ner

225 ppear to be mediated by the low-affinity p75 neurotrophin receptor, rather than a trk receptor.

226 fact that blockade of tyrosine kinase (Trk) neurotrophin receptors reduces basal GABRA4 promoter act

227 The p75 neurotrophin receptor regulates neuronal survival, promo

228 tyrosine receptor kinase A (TrkA) and TrkC, neurotrophin receptors required by DRG sensory neuron de

229 Furthermore, the p75 neurotrophin receptor restricts PSD formation, suggestin

230 d to nociceptors marked by expression of the neurotrophin receptor Ret.

231 ng trkA, trkB, and trkC, the identity of the neurotrophin receptor(s) undergoing phosphorylation was

232 t of NRAGE, a MAGE protein that mediates p75 neurotrophin receptor signaling and neuronal apoptosis.

233 Tat coactivator interactions interfere with neurotrophin receptor signaling in neuronal cells.

234 sults revealed new functions for proBDNF-p75 neurotrophin receptor signaling pathway in the control o

235 dopamine D1 receptors can be coupled to the neurotrophin receptor signaling to mediate the effects o

236 unbalancing neurotrophin homeostasis via p75 neurotrophin receptor signaling.

237 re, we demonstrate that EVT901 abrogates p75 neurotrophin receptor signalling by other ligands, such

238 a and other neurological disorders where p75 neurotrophin receptor signalling is affected.

239 Here, we identified the pro-neurotrophin receptor sortilin as major endocytic pathwa

240 cate that UCH-L1 is important for regulating neurotrophin receptor sorting to signaling endosomes and

241 gp120 were blocked by inhibitors of the p75 neurotrophin receptor, suggesting that proBDNF and gp120

242 hibition of the cell death domain of the p75 neurotrophin receptor (TAT-Pep5) and in mice lacking the

243 Neurotrophin receptors (the receptor tyrosine kinases, T

244 rocessing of synaptic vesicle components and neurotrophin receptors, the mechanism giving access to t

245 l and spatial protein expression patterns of neurotrophin receptors throughout the process of sensory

246 e, nicotinic acetylcholine receptor, and p75 neurotrophin receptor), thus demonstrating that pseudoty

247 dence for the CB1 receptor coupling the TrkB neurotrophin receptor to an axonal growth response in th

248 r-3 directly associates and recruits the p75 neurotrophin receptor to the axon-glial junction, formin

249 ility to redirect the apically localized P75 neurotrophin receptor to the basolateral membrane domain

250 nsduction pathways linking the activation of neurotrophin receptors to SG neuron nuclei.

251 hotyrosine immunoprecipitates identified the neurotrophin receptor TrkA (molecular weight approximate

252 Activation of the neurotrophin receptor TrkA by its ligand nerve growth fa

253 High expression of the neurotrophin receptor TrkA in neuroblastomas (NBs) is as

254 that LRP1 activation could phosphorylate the neurotrophin receptor TrkA in PC12 cells and increase ne

255 on axonal transport of mitochondria and the neurotrophin receptor TrkA, cargoes that are critical fo

256 ons that are marked by the expression of the neurotrophin receptor TrkA.

257 ss sensory neuron-associated markers such as neurotrophin receptors TrkA, TrkB, TrkC, and RET and the

258 rked changes in the expression levels of the neurotrophin receptors, TrkA and p75(NTR).

259 nsfected to overexpress one of the following neurotrophin receptors: TrkA, TrkC, and p75.

260 rs of the neural crest and expression of the neurotrophin receptor TrkB and its ligand, brain-derived

261 endritically localized mRNA encoding for the neurotrophin receptor TrkB has important ramifications f

262 -ERK-CREB-BDNF pathway as pre-treatment with neurotrophin receptor TrkB inhibitor ANA-12 and MEK inhi

263 isual cortical neurons in young rodents, the neurotrophin receptor TrkB is associated with PSD-95.

264 is study, we show that the expression of the neurotrophin receptor TrkB is induced on astrocytes in w

265 In mice in which the neurotrophin receptor trkB is knocked out selectively in

266 The neurotrophin receptor TrkB regulates dendritic structure

267 These data demonstrate that the neurotrophin receptor trkB undergoes phosphorylation in

268 ion resulting in a Y722C substitution in the neurotrophin receptor TrkB.

269 distribution of TRPC3 paralleled that of the neurotrophin receptor TrkB.

270 n and is mediated by the opposing actions of neurotrophin receptors TrkB and p75(NTR) .

271 om fresh human malignant gliomas express the neurotrophin receptors TrkB and TrkC, not TrkA, and they

272 Like ROS, the neurotrophin receptor, TrkB receptor tyrosine kinase, ha

273 The neurotrophin receptor, TrkB receptor tyrosine kinase, is

274 ell surface signaling receptors, such as the neurotrophin receptor, TrkB, have emerged as potential t

275 ncoded by Csf1, Nt3, and the tyrosine kinase neurotrophin receptor, TrkB.

276 ed inner ear sensory neurons fail to express neurotrophin receptors, TrkB and TrkC, suggesting that t

277 ach gene and with expression of the specific neurotrophin receptors, trkB and trkC.

278 on of gene expression, including that of the neurotrophin receptor TrkC, parvalbumin and Brn3b.

279 diameter myelinated neurons that express the neurotrophin receptor TrkC.

280 sfunction resulting from deficiencies in the neurotrophin receptor trkC.

281 outgrowth 4-fold and enhancing expression of neurotrophin receptors trkC and trkA.

282 During retrograde signaling, endocytosed neurotrophin receptors (Trks) activate the extracellular

283 broblast growth factor receptors (FGFRs) and neurotrophin receptors (TRKs) through their N-terminal p

284 broblast growth factor receptors (FGFRs) and neurotrophin receptors (TRKs) to common signaling target

285 with neurotrophins causes internalization of neurotrophin receptors (Trks).

286 The neurotrophin receptor tropomyosin-related kinase B (TrkB

287 We show that the neurotrophin receptor tropomyosin-related kinase C (TrkC

288 In this study, we report that two neurotrophin receptors (tropomyosin-related kinase TrkA

289 In cultured hippocampal neurons, neurotrophin receptor tyrosine kinase B (TrkB) signaling

290 The neurotrophin receptor tyrosine kinase TrkB is critical t

291 lesion formation, the neurotrophins and the neurotrophin receptor tyrosine kinases, trks B and C, ar

292 Trk neurotrophin receptor ubiquitination in response to liga

293 nity to test the hypothesis that trkB is the neurotrophin receptor undergoing phosphorylation.

294 of neurons expressing specific high affinity neurotrophin receptors was determined immunohistochemica

295 assays with cysteine-rich domains-fused p75 neurotrophin receptor, we confirmed that EVT901 interfer

296 Because this effect may be mediated by neurotrophin receptors, we sought to determine the distr

297 receptor agonist SKF38393, we found that Trk neurotrophin receptors were activated in embryonic day 1

298 involved in ectodomain shedding of p75NTR, a neurotrophin receptor with critical roles in neuronal di

299 and increasing the co-localisation of these neurotrophin receptors with retromer-associated sorting

300 -tagged raft-independent protein (the 75-kDa neurotrophin receptor; YFP-p75) was efficient even in th