ライフサイエンスコーパス: high-affinity receptor

1 ositive feedback loop involving IL-2 and its high affinity receptor.

2 expressing a neurotrophin and its associated high-affinity receptor.

3 response requires the binding of IgE to its high-affinity receptor.

4 anisms of interaction between GM-CSF and its high-affinity receptor.

5 actions of neurotensin are mediated via its high-affinity receptor.

6 t complexes with the alpha subunit to form a high-affinity receptor.

7 ic mucosa against CWR-induced injury via its high-affinity receptor.

8 and in the presentation of growth factors to high affinity receptors.

9 of its mitogenic activity and its binding to high affinity receptors.

10 levels correlated with a larger fraction of high-affinity receptors.

11 st explained by a local spillover activating high-affinity receptors.

12 d selective clonal expansion of B cells with high-affinity receptors.

13 ents of these two neurotrophins and/or their high-affinity receptors along the tonotopic map, and the

14 bond abrogated cooperativity, resulting in a high affinity receptor and increased sensitivity of down

15 ods to understand why it is hard to design a high-affinity receptor and to explore the limits of affi

16 bFGF interacts with high-affinity receptors and heparan sulfate proteoglycan

17 This increased KAR function was mediated by high-affinity receptors and required activation of NMDA

18 otoxin involves extracellular binding to its high affinity receptors as a first step.

19 via interactions between substance P and its high affinity receptor, as evidenced by the absence of a

20 han a single Neu5Ac, appears to serve as the high-affinity receptor, as typhoid toxin possesses five

21 presence of CP105696, an antagonist for LTB4 high-affinity receptor, ATP was not able to reduce paras

22 play a role in arrestin transition into its high affinity receptor binding state.

23 were revealed as essential residues for the high affinity receptor binding.

24 _79, demonstrating selective blocking of the high affinity receptor binding.

25 terminal knob region that is responsible for high-affinity receptor binding and Ad tropism.

26 These include the restoration of high-affinity receptor binding by antiulcerogenic growth

27 lix of G(alpha), the extension of which is a high-affinity receptor binding element.

28 We suggest that heparin restores high-affinity receptor binding of basic fibroblast growt

29 Fiber is the high-affinity receptor binding protein that serves to me

30 ce is investigated using as a model an ultra-high-affinity receptor binding variant of human growth h

31 five YSA residues appear to be critical for high-affinity receptor binding.

32 0, and 180), which comprise a portion of the high-affinity receptor-binding epitope.

33 for leukotriene B4 have been identified: the high-affinity receptor BLT1 and the low-affinity recepto

34 Recently, leukotriene B4 and its high affinity receptor, BLT1, have been shown to mediate

35 (GABAA-Rs), or via continuous activation of high-affinity receptors by low concentrations of ambient

36 s with viruses that infect through different high-affinity receptors (CAR, CD46, and desmoglein-2), a

37 emoattractant protein (MCP)-1 (CCL2) and its high-affinity receptor, chemokine (C-C motif) receptor 2

38 Addition of a high-affinity receptor chimera, IL-1 trap, to cardiomyoc

39 he fraction of receptors associated with the high-affinity receptor class.

40 389 displayed an accumulation of the agonist high affinity receptor complex (RH = 26%).

41 12 is mediated through specific binding to a high affinity receptor complex composed of at least two

42 L-4 receptor alpha (IL-4Ralpha), a signaling high affinity receptor complex for IL-13 is generated.

43 T cells, IL-2 signals through a quaternary 'high affinity' receptor complex consisting of IL-2, IL-2

44 Its activities are mediated through a high-affinity receptor composed of two subunits, designa

45 is surface does not participate in essential high affinity receptor contacts, a finding inconsistent

46 We show that both high-affinity receptors (containing the beta2-subunit, b

47 ukocyte chemotaxis through activation of its high affinity receptor, CX(3)CR1.

48 This effect on the fraction of high-affinity receptors depended on the relative express

49 re to 10(-7) M fMLP, which saturates the PMN high-affinity receptor, did not elicit bactericidal rele

50 Further, the increase in the fraction of high-affinity receptors due to the presence of ErbB2 occ

51 ytes, and the vessel wall and interacts with high affinity receptors expressed in several tissues inc

52 affinity receptor families (GluK1-GluK3) and high-affinity receptor families (GluK4-GluK5) based on t

53 Fc epsilon 3-4) to a soluble fragment of the high-affinity receptor Fc epsilon RI alpha-chain (sFc ep

54 ytokine-primed monocytes, aggregation of the high-affinity receptor Fc gamma RI resulted in the activ

55 binding to and subsequent aggregation of the high-affinity receptor (Fc epsilon RI) by allergen plays

56 The regulation of the mast cell high affinity receptor, Fc epsilonRI, is poorly understo

57 are promoted by monomeric IgE binding to its high-affinity receptor, Fc epsilon RI.

58 requires the binding of IgE antibody to its high-affinity receptor, Fc epsilonRI.

59 impact on our view of the IgE binding to its high-affinity receptors, Fc epsilonRI.

60 Unique to the high-affinity receptor-Fc complex, however, is the confo

61 IgE binding to its high affinity receptor FcepsilonRI on mast cells and bas

62 teraction between IgE-Fc (Fcepsilon) and its high affinity receptor FcepsilonRI on the surface of mas

63 Binding of allergen-specific IgE to its high-affinity receptor FcepsilonRI on basophils and mast

64 emarkably stable interaction of IgE with its high-affinity receptor FcepsilonRI on basophils and mast

65 Monomeric IgE binding to its high affinity receptor (FcepsilonRI) results in a number

66 ergen-specific IgE antibodies bound to their high-affinity receptors (FcepsilonRI).

67 Fc structures and to the IgE-Fc bound to its high-affinity receptor, FcepsilonRI.

68 estores the ability of IgE-Fc to bind to its high affinity receptor, FcepsilonRIalpha.

69 cal blockade of ligand signaling through the high affinity receptor for activin, type II activin rece

70 esults demonstrate that beta2-chimaerin is a high affinity receptor for DAG through binding to its C1

71 Antigen-mediated cross-linking of the high affinity receptor for IgE (Fc epsilon RI), in the p

72 ation of the immunoglobulin E (IgE)-occupied high affinity receptor for IgE (Fc epsilon RI).

73 Polymorphisms in the beta chain of the high affinity receptor for IgE (Fc epsilon RI-beta, MS4A

74 This study demonstrates that the high affinity receptor for IgE (Fc epsilonRI) on rat bas

75 he cell surface-expressed gamma chain of the high affinity receptor for IgE (FcepsilonRI) can be phos

76 Aggregation of the high affinity receptor for IgE (FcepsilonRI) induces act

77 The human high affinity receptor for IgE (FcepsilonRI) is a cell s

78 When the high affinity receptor for IgE (FcepsilonRI) is extensiv

79 early event that follows aggregation of the high affinity receptor for IgE (FcepsilonRI) is the phos

80 Engagement of the high affinity receptor for IgE (FcepsilonRI) on mast cel

81 fibroblasts previously transfected with the high affinity receptor for IgE (FcepsilonRI) were furthe

82 receptor that responds to aggregation is the high affinity receptor for IgE (FcepsilonRI), which is r

83 Ca(2+) response to the cross-linking of the high affinity receptor for IgE (FcepsilonRI).

84 elta with Lyn required the activation of the high affinity receptor for IgE (FcsigmaRI) while the int

85 When the high affinity receptor for IgE and related receptors bec

86 s-linking of IgE bound to mast cells via the high affinity receptor for IgE triggers a signaling casc

87 The high affinity receptor for IgE, Fc epsilon receptor I (F

88 inhibit binding of IgE to both CD23 and the high affinity receptor for IgE, Fc epsilonRI, providing

89 structural role in signal initiation by the high affinity receptor for IgE.

90 The high affinity receptor for IgG (Fc gamma RI, CD64) is ex

91 Among them, FcgammaRI is the only high affinity receptor for IgG and thus is a potential t

92 previously determined that CRP binds to the high affinity receptor for IgG, FcgammaRI (CD64).

93 ngle nucleotide polymorphisms (SNPs) for the high affinity receptor for IgG, FcgammaRI.

94 We have recently described an additional high affinity receptor for IL-13, IL-13Ralpha2, whose fu

95 High affinity receptor for IL-5 (IL-5R), a predominant e

96 reflecting a low level of expression of the high affinity receptor for IL-7 (CD127) relative to conv

97 WIP in signaling pathways downstream of the high affinity receptor for immunoglobulin (Ig)E (Fcepsil

98 The high affinity receptor for immunoglobulin E (designated

99 Upon cross-linking by antigen, the high affinity receptor for immunoglobulin E (IgE), Fceps

100 We propose that NEMO functions as a high affinity receptor for linear ubiquitin chains and a

101 TrkA, the high affinity receptor for nerve growth factor (NGF), is

102 We conclude that RasGRP is a high affinity receptor for phorbol esters and diacylglyc

103 The only known high affinity receptor for RBP4, Stra6, is not expressed

104 ne-spanning tyrosine kinase that serves as a high affinity receptor for several members of the fibrob

105 and its closely related homologue GPR4 is a high affinity receptor for SPC with low affinity for lys

106 -coupled receptor 1 (OGR1) as a specific and high affinity receptor for SPC, and G2A as a receptor wi

107 cer G protein-coupled receptor 1 (OGR1) is a high affinity receptor for SPC, and its closely related

108 we have identified GPR4 as not only another high affinity receptor for SPC, but also a receptor for

109 ceptor from vascular endothelial cells, is a high affinity receptor for sphingosine 1-phosphate (SPP)

110 These results indicate that EDG-6 is a high affinity receptor for SPP, which couples to a G(i/o

111 us, 12-HETER represents the first identified high affinity receptor for the 12-(S)-HETE hydroxyl fatt

112 The TrkB receptor tyrosine kinase (RTK) is a high affinity receptor for the neurotrophins brain deriv

113 ting the presence of an alternative or novel high affinity receptor for these ligands.

114 mbrane of airway epithelia contains abundant high affinity receptors for AAV5.

115 ; in contrast, BCMA and BR3, the other known high affinity receptors for APRIL and BAFF, respectively

116 parations show that B104 cells expressed the high affinity receptors for bFGF, PDGF-AA and PDGF-BB.

117 In prior studies aggregation of the high affinity receptors for IgE, Fc epsilon RI, on a rat

118 have recently demonstrated the expression of high affinity receptors for SP (Neurokinin-1 (NK-1) rece

119 The plexins are high affinity receptors for the semaphorins and are resp

120 ed directed evolution to generate a panel of high affinity receptors for TSST-1.

121 ptor-1 (VEGFR-1) and VEGFR-2 are known to be high affinity receptors for VEGF, it is not clear which

122 A high-affinity receptor for 24p3 (24p3R) that is involved

123 splayed altered utilization of CEACAM1a, the high-affinity receptor for A59.

124 the discovery of cellular prion protein as a high-affinity receptor for Abeta oligomers, and the down

125 adenovirus receptor (CAR) is identified as a high-affinity receptor for adenovirus type 5.

126 and adenovirus receptor (CAR) is not only a high-affinity receptor for adenovirus, but also a tumor

127 It is also a high-affinity receptor for antiproliferative factor (APF

128 level of expression of full-length TrkB, the high-affinity receptor for BDNF, despite the fact that t

129 n demonstrate that the presence of TrkB, the high-affinity receptor for BDNF, in hippocampal neural p

130 ific ablation of TrkB, the gene encoding the high-affinity receptor for BDNF, is sufficient to elicit

131 we identified Plexin A4 (PLXNA4) as a novel, high-affinity receptor for CLU in the adult brain.

132 While CRF(1) is a high-affinity receptor for CRF, urocortin III binds with

133 triene B(4) receptor, was also shown to be a high-affinity receptor for cyclooxygenase-1 derived 12(S

134 ntegrated variant, confirming that YehU is a high-affinity receptor for extracellular pyruvate.

135 orphan member of the GFR-alpha family, is a high-affinity receptor for GDF15.

136 , and (iii) ErbB4 is a candidate for being a high-affinity receptor for HB-EGF on the surface of impl

137 c-Met, a high-affinity receptor for hepatocyte growth factor (HGF

138 The high-affinity receptor for human interleukin-5 (hIL-5) i

139 circulating IgE, increased expression of the high-affinity receptor for IgE (Fc epsilonRI), and great

140 s (MC) and basophils share expression of the high-affinity receptor for IgE (FcepsilonRI) but can be

141 Aggregation of the high-affinity receptor for IgE (FcepsilonRI) in mast cel

142 Cross-linking of the high-affinity receptor for IgE (FcepsilonRI) in RBL-2H3

143 Cross-linking of the high-affinity receptor for IgE (FcepsilonRI) leads to de

144 Activation of the high-affinity receptor for IgE (FcepsilonRI) on allergic

145 idermal Langerhans cells (LC) expressing the high-affinity receptor for IgE (FcepsilonRI) play a key

146 and T cells and for Fc receptors such as the high-affinity receptor for IgE (FcepsilonRI), a Src fami

147 Mast cells express a high-affinity receptor for IgE (FcepsilonRI).

148 re activated through receptors including the high-affinity receptor for IgE and KIT, specific tyrosin

149 mmation by virtue of their expression of the high-affinity receptor for IgE and release of potent pro

150 The high-affinity receptor for IgE expressed on the surface

151 High-affinity receptor for IgE stimulation of effector c

152 tients with atopic dermatitis (AD) carry the high-affinity receptor for IgE, FcepsilonRI, and are cru

153 to FcepsilonRIalpha, the alpha-chain of the high-affinity receptor for IgE, has been identified.

154 imulation of mast cells via FcepsilonRI, the high-affinity receptor for IgE, triggers a signaling cas

155 The high-affinity receptor for IgG (CD64 or FcgammaRI) is co

156 pregulation of interleukin (IL)-13Ralpha2, a high-affinity receptor for IL-13 that regulates tumor gr

157 risingly, we now find that expression of the high-affinity receptor for IL-15, IL-15R alpha, on T cel

158 e response initiated by cross-linking of the high-affinity receptor for immunoglobulin E (FcepsilonRI

159 Cross-linking of the high-affinity receptor for immunoglobulin E (FcepsilonRI

160 Like basophils, mast cells express the high-affinity receptor for immunoglobulin E (IgE) and ha

161 e stimulated following the activation of the high-affinity receptor for immunoglobulin E (IgE) in mas

162 We investigated how the high-affinity receptor for immunoglobulin E (IgE) modula

163 nd protein levels on stimulation through the high-affinity receptor for immunoglobulin E (IgE; Fcepsi

164 ctions are triggered via crosslinking of the high-affinity receptor for immunoglobulin E, F(c)epsilon

165 ated mast cell degranulation mediated by the high-affinity receptor for immunoglobulin E, FcepsilonRI

166 d-mediated cross-linking of FcepsilonRI, the high-affinity receptor for immunoglobulin E, on RBL-2H3

167 A high-affinity receptor for interleukin (IL)-13 (interleu

168 The 29-kDa nuclear protein is likely the high-affinity receptor for JH that mediates its genomic

169 The presence of soluble CD14, a high-affinity receptor for LPS and other bacterial ligan

170 mutant was related to expression of CD14, a high-affinity receptor for LPS and other microbial produ

171 myeloid leukocytes, which express BLT1, the high-affinity receptor for LTB4.

172 We recently identified GPR99 as a high-affinity receptor for LTE4 that mediates cutaneous

173 In the absence of the high-affinity receptor for MIP-2 (as in CXCR2-deficient

174 genetic ablation of Acvr2b, which encodes a high-affinity receptor for myostatin and activin A speci

175 he NTRK1 gene (also known as TRKA) encodes a high-affinity receptor for NGF, a neurotrophin involved

176 mplicated in nervous system plasticity, is a high-affinity receptor for Nogo, MAG, and OMgp.

177 Annexin II, recently described as a high-affinity receptor for PG, strongly co-localized wit

178 It functions as the high-affinity receptor for plasma retinol binding protei

179 sulin resistance, we studied the role of the high-affinity receptor for RBP4, STRA6 (stimulated by re

180 Here, we report that neuropilin (NRP)-2, the high-affinity receptor for SEMA3F and a coreceptor for c

181 Boc, a cell adhesion molecule that acts as a high-affinity receptor for Shh.

182 her Robo receptors, mammalian Robo3 is not a high-affinity receptor for Slits because of specific sub

183 erived G-protein-coupled receptor EDG-1 is a high-affinity receptor for the bioactive lipid mediator

184 Protease-activated receptor-1 (PAR-1) is the high-affinity receptor for the coagulation protease thro

185 The receptor tyrosine kinase c-MET is the high-affinity receptor for the hepatocyte growth factor

186 Protein kinase C (PKC) represents the major, high-affinity receptor for the phorbol esters as well as

187 We determined that sortilin is a high-affinity receptor for the proinflammatory cytokines

188 press protease-activated receptor (PAR)-1, a high-affinity receptor for thrombin, which is also activ

189 This renders SepL a high-affinity receptor for translocator/chaperone pairs,

190 VEGF receptor-1 (VEGFR-1 or Flt-1) is a high-affinity receptor for VEGF and is typically conside

191 of this type, which can rapidly evolve into high-affinity receptors for a broad range of structures,

192 rt" alphaIIbbeta3 integrins into "activated" high-affinity receptors for adhesive proteins.

193 High-affinity receptors for BN/GRP were found on tumors.

194 n of coagulation by (1) expressing specific, high-affinity receptors for coagulation proteases, zymog

195 ploit molecular diversity for PK-C and other high-affinity receptors for DAG and the phorbol esters.

196 Kremens are high-affinity receptors for Dickkopf 1 (Dkk1) and regula

197 nt microparticles that may express sustained high-affinity receptors for FVIII.

198 cell degranulation induced by aggregation of high-affinity receptors for IgE (FcepsilonRI) is negativ

199 C) activation via cross-linking of IgE-bound high-affinity receptors for IgE (FcepsilonRI) underlies

200 Activated SCF receptors and high-affinity receptors for IgE (FcvarepsilonRI) engage

201 y mast cells (MCs) on cross-linking of their high-affinity receptors for IgE by antigen that can ampl

202 Aggregation of high-affinity receptors for immunoglobulin E (Fc epsilon

203 al in the human host and therefore expresses high-affinity receptors for iron acquisition from host i

204 Trk receptors are high-affinity receptors for nerve-growth factor (trkA),

205 We showed previously that high-affinity receptors for pituitary adenylate cyclase-

206 Specific high-affinity receptors for SST were found on Dunning R-

207 CXCR1 is one of two high-affinity receptors for the CXC chemokine interleuki

208 demonstrated that resident CNS cells express high-affinity receptors for this neuropeptide (neurokini

209 c transformation of glial cells to produce a high affinity receptor form.

210 st glioblastoma cell transcripts, creating a high-affinity receptor form.

211 of Dns-C6-Cho, the apparent rates with which high-affinity receptors formed approximated those of ion

212 sed the Ki, suggesting that they disrupt the high affinity receptor-G protein interaction and stabili

213 onclude that recombinant hA(2A)AR can form a high-affinity receptor-G protein complex with alpha(s)be

214 bility but complexes with GMRalpha to form a high-affinity receptor (GMRalpha/beta).

215 ecting Dns-C6-Cho dissociation from low- and high-affinity receptors, had rates of 140 +/- 27 s-1 and

216 The disruption of the human immunolobulin E-high affinity receptor I (IgE-FcepsilonRI) protein-prote

217 s in layer V colabeled with their respective high-affinity receptors, i.e., trkA, trkB, and trkC, res

218 t IFN-gamma SC1 forms a 1:1 complex with its high-affinity receptor (IFN-gamma R alpha) with an affin

219 pendent on the interaction of IL-10 with its high-affinity receptor (IL-10R1).

220 of unbound IL-4 and IL-4 in complex with its high-affinity receptor (IL-4Ralpha).

221 d as a stable complex in the presence of its high affinity receptor, IL-15Ralpha.

222 Although IL-1beta binds to its high-affinity receptor, IL-1R, and upregulates proinflam

223 ontrols the expression and activation of its high affinity receptor in taste cells.

224 calize the diTC binding site and to design a high affinity receptor in the diTC-insensitive channel,

225 does not bind GM-CSF by itself, but forms a high-affinity receptor in association with GMRalpha.

226 rovides evidence for the role of NGF and its high-affinity receptor in the pathogenesis of psoriasis

227 nity receptors decreased while the number of high-affinity receptors increased in a Dns-C6-Cho concen

228 The latter is a very high affinity receptor (Kd = 50-100 pM) whose ligation t

229 s, alpha and beta, and ligand binding to the high-affinity receptor leads to signalling for the multi

230 for a detailed thermodynamic description of high-affinity receptor-ligand interactions involving poo

231 h their binding partners but together form a high affinity receptor.ligand complex.

232 and the group of alleles encoding A19), the high-affinity receptor/ligand pair KIR2DL2/HLA-C1, and t

233 armacophore features usually associated with high-affinity receptor ligands such as the heteroatom hy

234 In a search for high-affinity receptor ligands that might serve for deve

235 binding of soluble HLA-G to its alternative high-affinity receptor, LILRB1 (ILT2), appeared to be le

236 kotriene B(4) (LTB(4)), interacting with its high-affinity receptor, LTB(4) receptor 1 (BLT1), is kno

237 Specific growth factors acting through high-affinity receptors may be involved in maintaining t

238 on of the current showed two clear phases, a high-affinity receptor-mediated phase (IC50=14+/-2 nM) t

239 eurons (SGNs) in the inner ear; however, its high affinity receptor, neurokinin-1 (NK1), has not been

240 sion, secretion, or binding of Sema3A to its high-affinity receptor Neuropilin-1 (Npn-1).

241 ion and cell proliferation by binding of its high affinity receptor, neurotensin receptor-1 (NTR1).

242 function and also induce an elevation in the high affinity receptor, nicotinic therapy in autism may

243 l inflammation and healing by binding to its high-affinity receptor NTR1.

244 of the neuropeptide neurotensin (NT) and its high affinity receptor (NTR1) is increased during the co

245 led that VEGF induced a 2-3-fold increase in high affinity receptor number (5.0 x 10(4)/cell versus 2

246 irway infection, an effect that required the high-affinity receptor of IgE.

247 rotein (LIVBP or LivJ) serves as the primary high-affinity receptor of the Escherichia coli ABC-type

248 FVIII binds to specific, high affinity receptors on activated platelets (n = 484

249 gen-mediated aggregation of IgE bound to its high-affinity receptor on mast cells or basophils initia

250 The association of 125I-ABA to high-affinity receptors on Chinese hamster ovary (CHO)-h

251 We show that FGF-2 binds to low- and high-affinity receptors on LECs and is efficiently inter

252 ted that alpha-latrotoxin first binds to two high-affinity receptors on nerve terminals, neurexins an

253 mediates its biologic activities via binding high-affinity receptors on T and natural killer cells.

254 teracts with the blastocyst cell surface via high-affinity receptors other than ErbB1, (ii) the HB-EG

255 ochromocytoma clone (PC12) by activating the high affinity receptor, p140(trkA), linked to mitogen-ac

256 se-activating peptide (PACAP) and one of its high-affinity receptors (PAC1) are widely expressed in t

257 an neutrophils constitutively express Sema3E high-affinity receptor, PlexinD1.

258 CD14 is a high-affinity receptor protein for the complex of bacter

259 proteins have been described as the low- and high-affinity receptors, respectively, for the cytotoxic

260 s in collagen gel assays through a conserved high-affinity receptor, Ryk, which is expressed in CST a

261 ric acid secretion does not appear to be the high-affinity receptor since the neurotensin receptor an

262 of the pore, contribute to formation of the high-affinity receptor site for pore-blocking drugs, and

263 potentially cytolytic protein that is also a high-affinity receptor site specific antagonist for the

264 CCK-JMV, an agonist of the high affinity receptor state and antagonist of the low a

265 concentrations and may selectively label the high-affinity receptor state.

266 eceptor binding the agonist epibatidine (the high affinity receptor subtype, consisting primarily of

267 g Fibroblast Growth Factor-7 (FGF-7) and its high affinity receptor suggested that FGF-7 signaling ma

268 uggested that colicin N (ColN), which has no high-affinity receptor, targets highly abundant lipopoly

269 late the transcription of numerous genes via high affinity receptors that act in concert with chromat

270 More recently, human folate receptors (FRs), high affinity receptors that transport folate via endocy

271 of channel catfish to L-Arg are mediated by high-affinity receptors that are part of or closely coup

272 ock the binding of IL-2 to IL-2Ralpha of the high affinity receptor, the 7G7/B6 monoclonal antibody b

273 The targeted antibody functioned as a high affinity receptor to trap cell-permeable hapten-flu

274 plementation of H BiC (H-BiC) reveals that a high-affinity receptor-to-paramyxovirus H monomer stoich

275 ing of nerve growth factor (NGF) through its high-affinity receptor TrkA contributes to attention beh

276 shing a role for nerve growth factor and its high-affinity receptor TrkA in contextual memory consoli

277 position where nerve growth factor binds its high affinity receptor, TrkA, suggesting further paralle

278 ought to be the result of its binding to its high-affinity receptor, TrkA.

279 BDNF activates its high-affinity receptor TrkB and promotes neuronal surviv

280 be mediated through interactions with their high-affinity receptors TrkB (for BDNF and NT-4/5) and T

281 erived neurotrophic factor (BDNF) and of its high affinity receptor (trkB) mRNA was investigated in t

282 We examined the expression of BDNF and its high affinity receptor, trkB, in young and aged Sprague-

283 trophic factor (BDNF), and activation of its high affinity receptor, TrkB.

284 y interactions between secreted BDNF and its high-affinity receptor, TrkB.

285 Neurotrophin-3 (NT-3) and its high-affinity receptor TrkC play crucial trophic roles i

286 n-derived neurotrophic factor (BDNF) and its high-affinity receptor tropomyosin-related kinase B (trk

287 ous mutations of either human NGFbeta or its high-affinity receptor tropomyosin-related kinase recept

288 n-derived neurotrophic factor (BDNF) and its high affinity receptor, tropomyosin receptor kinase B (T

289 urotrophin family of growth factors, and its high-affinity receptor, tropomyosin receptor kinase B (T

290 d neurotrophin-3 (NT-3) and their respective high-affinity receptors, tropomyosin receptor kinase (tr

291 heir biological activities to activate their high affinity receptor tyrosine kinases.

292 rotrophins in vitro by transactivating their high-affinity receptor tyrosine kinases, the Trk recepto

293 n derived neurotrophic factor (BDNF) and its high affinity receptor, tyrosine kinase B (TrkB).

294 nase-type plasminogen activator (uPA) to its high-affinity receptor (uPAR) orchestrates uPAR interact

295 entified desmoglein-2 (DSG-2) as the primary high-affinity receptor used by adenoviruses Ad3, Ad7, Ad

296 lar endothelial growth factor (VEGF) and its high-affinity receptors VEGFR-1 and VEGFR-2 was investig

297 nding between bioactive rGIF derivatives and high-affinity receptors was 10-100 pM.

298 products for the full-length Trk A and Trk C high-affinity receptor were observed, as well as truncat

299 ses indicated two classes of high and medium-high affinity receptors with a kD of approximately 45 an

300 The high-affinity receptor with heparan sulfate modification