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 receptor tyrosine kinases and the shared p75 neurotrophin receptor.

5 similar gamma-secretase cleavage is the 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 Schwann cell death via engagement of the p75 neurotrophin receptor.

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

13 tracellular neurotrophin binding site of 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 The p75 neurotrophin receptor, a member of the tumor necrosis fa

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

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

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

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

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

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

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

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

28 The expression of neurotrophin receptors and ligands by hematopoietic and

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

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

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

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

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

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

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

36 Neurotrophin receptors are emerging targets in oncology,

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

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

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

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

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

42 The TrkC neurotrophin receptor belongs to the functional dependen

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

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

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

46 Germline deletion of the p75 neurotrophin receptor causes dramatic axon guidance and

47 The neurotrophin receptor (CD271/NGFR/p75NTR) is a key regul

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

49 Neurotrophin receptors corresponding to vertebrate Trk,

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

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

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

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

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

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

56 Neurotrophin receptor expression was confirmed in a pane

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

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

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

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

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

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

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

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

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

66 5 kDa neurotrophin receptor (p75NTR) and two neurotrophin receptor homologs (NRH1, NRH2) constitute a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 NRAGE (neurotrophin receptor-interacting melanoma antigen) inte

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

86 p75 neurotrophin receptor is highly expressed during early n

87 The p75 neurotrophin receptor is important in multiple physiolog

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

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

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

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

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

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

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

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

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

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

98 Pathway analyses implicated p75 neurotrophin receptor/nerve growth factor signaling and

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

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

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

102 nt on the proper subcellular localization of neurotrophin receptor (NTR) to plasmalemmal signaling mi

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

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

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

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

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

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

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

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

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

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

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

114 The neurotrophin receptor p75 can induce apoptosis both in v

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

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

117 The neurotrophin receptor p75 is induced by various injuries

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

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

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

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

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

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

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

125 The neurotrophin receptor p75(NTR) negatively regulates spin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

148 The p75 neurotrophin receptor (p75(NTR)) has been proposed to me

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

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

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

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

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

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

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

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

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

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

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

160 During development, the p75 neurotrophin receptor (p75(NTR)) is widely expressed in

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

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

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

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

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

166 ular signaling networks regulated by the p75 neurotrophin receptor (p75(NTR)) substantially overlap w

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

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

169 Strikingly, mutant male mice lacking the p75 neurotrophin receptor (p75(NTR)) were resistant to the d

170 tingly, mutant male mice that lacked the p75 neurotrophin receptor (p75(NTR)) were seen to be resista

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

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

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

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

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

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

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

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

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

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

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

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

183 osin-related kinase receptors (Trks) and p75 neurotrophin receptors (p75) compete to regulate surviva

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 We discovered that the expression of the neurotrophin receptor p75NTR in PV cells inhibits the ma

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 The p75 neurotrophin receptor (p75NTR) is highly expressed in th

207 The p75 neurotrophin receptor (p75NTR) regulates numerous cellul

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

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

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

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

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

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

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

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

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

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

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

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

220 re, we demonstrate that mice lacking the p75 neurotrophin receptor, p75NTR, decrease their feeding an

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

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

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

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

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

226 p75 neurotrophin receptor plays an important role in the ner

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

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

229 The p75 neurotrophin receptor regulates neuronal survival, promo

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

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

232 chrome (DrBphP-PCM) to the kinase domains of neurotrophin receptors resulted in opto-RTKs controlled

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

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

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

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

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

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

239 unbalancing neurotrophin homeostasis via p75 neurotrophin receptor signaling.

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

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

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

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

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

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

246 Neurotrophin receptors (the receptor tyrosine kinases, T

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

262 Interestingly, APPL1-endosomes transport the neurotrophin receptor TrkB and mediate retrograde axonal

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

264 roitinase and fluoxetine are mediated by the neurotrophin receptor TRKB in parvalbumin-containing (PV

265 PNN removal requires intact signaling by the neurotrophin receptor TRKB in PV(+) neurons.

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

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

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

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

270 The neurotrophin receptor TrkB regulates dendritic structure

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

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

273 sion of extracellularly tagged transmembrane neurotrophin receptors TrkB and p75 on transfected neuro

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

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

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

277 The neurotrophin receptor, TrkB receptor tyrosine kinase, is

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

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

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

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

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

283 diameter myelinated neurons that express the neurotrophin receptor TrkC.

284 sfunction resulting from deficiencies in the neurotrophin receptor trkC.

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

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

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

288 The neurotrophin receptor tropomyosin-related kinase B (TrkB

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

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

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

292 The neurotrophin receptor tyrosine kinase TrkB is critical t

293 Trk neurotrophin receptor ubiquitination in response to liga

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

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

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

297 Here we show that the p75 neurotrophin receptor, which is abundantly expressed in

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