ライフサイエンスコーパス: agonist-induced

1 Notably, agonist-induced 3-phosphorylated phosphoinositide produc

2 effect of these compounds on CB(1) receptor agonist-induced [(35)S]GTPgammaS binding, inhibition, an

3 These data showed that agonist-induced 5-HT(1A)R internalization does exist in

4 Thrombin, a G protein-coupled receptor agonist, induced a biphasic expression of cyclin D1 in p

5 Feeding or treatment with an FXR agonist induced Abcg5/8 and Scarb1 expression in WT, but

6 rolongs the AP by 25% and abolishes the GPCR agonist-induced acceleration of the AP repolarization.

7 d for re-priming, had only a minor effect on agonist-induced accumulation of nonphosphorylated protei

8 we show that cSrc inhibition also blocks the agonist-induced acrosome reaction and that this inhibiti

9 increasing K(+) concentrations inhibited the agonist-induced acrosome reaction as well as the increas

10 cyte-derived dendritic cells (MoDCs) and TLR agonist-induced activation assessed by cytokine producti

11 R4.60A resulted in a total ablation of agonist-induced activation in both the beta-arrestin tra

12 lpha(IIb)beta(3) or P-selectin exposure upon agonist-induced activation in platelet-rich plasma or wh

13 ed processes allowed greater growth and made agonist-induced activation more effective.

14 AZD8529 potentiated agonist-induced activation of mGluR2 in the membrane-bin

15 depletion from the PM was achieved either by agonist-induced activation of phospholipase C beta or wi

16 n vitro, M8-B blocked cold-induced and TRPM8-agonist-induced activation of rat, human, and murine TRP

17 Agonist-induced activation of Rho GTPase signaling leads

18 l assays, we identified residues involved in agonist-induced activation of TAS2R10, and investigated

19 effects of dopamine-2 receptor (D2R) and its agonist-induced activation on trafficking of Ca(V)2.2 is

20 ecent structures of the muOR in inactive and agonist-induced active states (Huang et al., ref.

21 These data point towards an agonist-induced adaptive response by KOR, the dynamics o

22 rthermia-susceptible muscle, we investigated agonist-induced adenosine formation in lymphocytes as an

23 tail of MOPr was identified as a mediator of agonist-induced affinity changes in MOPr.

24 PKC downstream of 12-LOX inhibition rescued agonist-induced aggregation and integrin activation.

25 nd dynamin dependent and could be modeled as agonist-induced aggregation of transiently expressed GFP

26 he association of a PEAR1 variant with multi-agonist-induced aggregation.

27 pathway for ASMCs with respect to sustaining agonist-induced airway contraction and the underlying Ca

28 ay that mediates both swelling-activated and agonist-induced amino acid release in brain glial cells.

29 These LXR agonists induced an increased matrix metalloproteinase-1

30 Our data identify an agonist-induced and Ca(2)(+)-dependent protein-protein i

31 reas protein kinase-C can also contribute to agonist-induced and heterologous phosphorylation.

32 Here we show that HKL blocks agonist-induced and pressure overload-mediated, cardiac

33 Moreover, KOR agonist-induced antinociceptive tolerance observed in vi

34 for 'self' are either eliminated through TCR-agonist-induced apoptosis (negative selection) or restra

35 ptor substates in favor of the active state, agonist-induced arrestin recruitment is accompanied by a

36 cells with ASM activated by IL-33 increased agonist-induced ASM contraction, and in vivo IL-33 induc

37 pathways mediating this Ca(2+) influx during agonist-induced ASMC contraction are not well defined.

38 hese studies show that photolysis but not by agonists induced astrocytic Ca(2+) signaling triggers gl

39 y IDO1 activity or treating mice with a GCN2 agonist induced autophagy and protected mice from nephri

40 ate that the mTOR pathway is involved in KOR agonist-induced aversion.

41 We show that BQCA potentiates agonist-induced beta-arrestin recruitment to M1 mAChRs.

42 th reduced beta-arrestin2 levels and delayed agonist-induced beta-arrestin2 recruitment to the membra

43 palmitoylation of Cys-265 is negligible, but agonist-induced beta2AR activation results in enhanced S

44 Other agonists induced borderline-normal aggregation.

45 Our findings reveal how PAF-R agonists induced by chemotherapy treatment can promote t

46 p38 Mapk activation but also plays a role in agonist-induced C-terminal and linker region phosphoryla

47 1 residues resulted in 58+/-3.8% decrease in agonist-induced C3aR phosphorylation there was no change

48 Here we investigated the involvement of agonist-induced Ca(2+) entry and STIM1 and Orai1 protein

49 The decline in extracellular K(+) evoked by agonist-induced Ca(2+) in Bergmann glia transiently incr

50 However, resting Ca(2+) levels, agonist-induced Ca(2+) increases, store-operated Ca(2+)

51 Agonist-induced Ca(2+) oscillations are accompanied by o

52 As a result, agonist-induced Ca(2+) oscillations are critically depen

53 Abstract Agonist-induced Ca(2+) oscillations in many cell types a

54 the roles of CB2R agonist, GW405833 (GW) in agonist-induced Ca(2+) oscillations in pancreatic acinar

55 through InsP3Rs and consequent reduction of agonist-induced Ca(2+) oscillations in SMCs.

56 Agonist-induced Ca(2+) oscillations underlie this contra

57 affect the ability of BH4-Bcl-2 to suppress agonist-induced Ca(2+) release in the cytosol or to prev

58 dimers were fully functional as indicated by agonist-induced Ca(2+) release.

59 s also impaired, as indicated by reduced RyR agonist-induced calcium release from the ER and RyR-medi

60 hereas p11 overexpression potentiates mGluR5 agonist-induced calcium responses, overexpression of mGl

61 ceptor, the concentration-response curve for agonist-induced cAMP accumulation was shifted to the lef

62 ive allosteric modulation of the orthosteric agonist-induced cAMP accumulation, [(35)S]GTPgammaS bind

63 static beta2AR redox states are vital toward agonist-induced cAMP formation and subsequent CREB and G

64 However, the molecular cascade coupling agonist-induced cannabinoid receptor activation to insul

65 The compounds modulated the hypertrophic agonist-induced cardiac gene expression.

66 ct; it increases agonist binding, yet blocks agonist-induced CB1 signaling.

67 vated ARC neurons was assessed by monitoring agonist-induced cellular activity via calcium imaging in

68 raft plasma membrane markers) to analyze the agonist-induced changes in compartmentalization of AT(1)

69 sensors serve the dual purpose of detecting agonist-induced changes in GPCR-G protein interactions,

70 ired-end tag sequencing of P300, we observed agonist-induced changes in long-range chromatin interact

71 that of the nAChR and GLIC, does not undergo agonist-induced channel gating, although it does not exh

72 ound alpha-Btx molecules required to prevent agonist-induced channel opening remains unknown.

73 nding indicates that BEL could suppress hPXR agonist-induced chemoresistance.

74 ls, SOCE mediated by ORAI1 was necessary for agonist-induced chloride secretion and activation of the

75 intra- and interdimer cross-links such that agonist-induced closure of the LBD "clamshells" is trans

76 ion function-2 (AF-2) helix 12 mechanism for agonist-induced coactivator interaction and NR transcrip

77 h lacks the last 101 residues, revealed that agonist-induced confinement was abolished and that the a

78 ubject to various interpretations, including agonist-induced conformational change versus selective s

79 t GalphaiAGS3 and GalphaiAGS4 directly sense agonist-induced conformational changes in the receptor,

80 rings from Iqgap1-/- mice generated greater agonist-induced contractile force, even after removal of

81 ase, Ca(2+) influx, PKC and ROCK in alpha(1)-agonist-induced contraction and phosphorylation of key p

82 individuals with asthma exhibited increased agonist-induced contraction.

83 SAR218645 potentiated mGluR2 agonist-induced contralateral turning.

84 Here, c-Abl silencing inhibited the agonist-induced cortactin phosphorylation and the associ

85 hetic TLR7 and TLR9 agonists, as well as TLR agonist-induced costimulatory molecule expression and TN

86 e (ACh): agonist sensitivity (EC50), maximal agonist-induced current (Imax), and time constant (tau)

87 TLR agonist-induced cytokine production was measured in huma

88 The ontogeny of TLR8 agonist-induced cytokine responses was defined in rhesus

89 n autologous plasma; levels of alum- and TLR agonist-induced cytokines and costimulatory molecules we

90 Imaging and preclinical studies have shown agonist-induced D2R internalization can be imaged with p

91 duced confinement was abolished and that the agonist-induced decrease in diffusivity was reduced subs

92 IGF-1R, but protecting the receptor against agonist-induced degradation.

93 l membrane compartmentalization in selective agonist-induced degradation.

94 G protein-coupled receptor kinases (GRKs) in agonist-induced desensitization of the mu-opioid recepto

95 s lack the phosphorylation sites involved in agonist-induced desensitization of the other two subtype

96 nthol followed by its washout did not affect agonist-induced desensitization, suggesting that menthol

97 expression, activation, and internalization/agonist-induced desensitization.

98 r disrupting endocytic trafficking prevented agonist-induced deubiquitination of the GCGR.

99 iated gene inactivation, exhibited defective agonist-induced down-regulation.

100 r of SL biosynthesis partially prevented CB2 agonist-induced effects on cell viability and motility.

101 es constitutive internalization, whereas the agonist-induced effects were imperceptible.

102 essed as an intrabody, it robustly inhibited agonist-induced endocytosis of a broad set of GPCRs with

103 alendronate treatment functionally reversed agonist-induced endogenous beta2AR loss as indicated by

104 f proteins represent a major pathway for the agonist-induced entry of calcium associated with the gen

105 x metalloprotease inhibitor, GM6001, blocked agonist induced Erk activation within seconds, strongly

106 Agonist-induced Erk phosphorylation was preceded by rapi

107 In contrast, it acts as an enhancer of agonist-induced ERK phosphorylation.

108 The agonist-induced exocytosis of WPB from BOECs and formati

109 of membrane fusion to control the extent of agonist-induced exocytosis.

110 panded Treg cells with rapamycin and an RARA agonist induced expression of alpha4beta7 and had suppre

111 t Galpha(13), but not Galpha(q/11), controls agonist-induced expression of hypertrophy-specific genes

112 Intracerebroventricular injection of GPR17 agonists induced food intake, whereas administration of

113 sociated MOR-1Bs has been demonstrated in mu agonist-induced G protein coupling, adenylyl cyclase act

114 agonist binding nonetheless antagonized the agonist-induced G-protein coupling to the CB1 receptor,

115 ks trafficking at early endosomes eliminated agonist-induced GCGR deubiquitination.

116 erapeutic concentration, can antagonize hPXR agonist-induced gene expression and chemoresistance.

117 The decrease in the rate of agonist-induced GIRK conductance was receptor selective

118 Agonist-induced GPCR shedding from the ciliary surface m

119 Other GPCRs showed agonist-induced GPCR/14-3-3 interaction signal increases

120 ction signal increases that occur later than agonist-induced GPCR/beta-arrestin interaction signals,

121 endent fashion with SNPs in Hap -6A favoring agonist-induced GR binding.

122 tor (alpha = 16.55) and potent antagonism of agonist-induced GTPgammaS binding.

123 or G-protein association, thereby preventing agonist-induced guanine nucleotide exchange.

124 plays biased antagonism whereby it inhibits: agonist-induced guanosine 5'-O-(3-[(35)S]thio)triphospha

125 eater chromatin-GR binding with increased GR agonist-induced hAGT expression in liver and renal tissu

126 5-HT(2A)R agonist-induced head-twitch behavior was also augmented

127 ngs may represent the first demonstration of agonist-induced heterodimerization of the H1R and H2R.

128 Depleting Intu blocked Smo agonist-induced Hh pathway activation, whereas the expre

129 10 (PtdIns 4,5-P2-binding peptide) inhibited agonist-induced HLHCGR and cAMP accumulation but not ARF

130 tion in mouse or human platelets resulted in agonist-induced hyperactivation and increased calcium en

131 Bile acids and a TGR5-selective agonist induced hyperexcitability of dorsal root ganglia

132 mice, as well as enhanced sensitivity to KOR agonist-induced hypolocomotion and analgesia-G protein s

133 rolactin response, but also blunted 5-HT(1A) agonist-induced hypothermia and increased 5-HT(2A) recep

134 from NT subjects led to a blunting of D(5) R agonist-induced increase in cAMP production and decrease

135 to internalize and bind GTP, blunting of the agonist-induced increase in cAMP production and decrease

136 m locus coeruleus neurons were made, and the agonist-induced increase in potassium conductance was me

137 e GIRK2 channel in Ts brain upon the GABAB R agonist-induced infantile spasms phenotype in the Ts mou

138 d GIRK2 channel is necessary for the GABAB R agonist-induced infantile spasms phenotype in the Ts mou

139 agonist tertiapin-Q also rescued the GABAB R agonist-induced infantile spasms phenotype in Ts mutants

140 esis that GIRK2 is necessary for the GABAB R agonist-induced infantile spasms phenotype in Ts.

141 mber of Kcnj6 in Ts mice rescued the GABAB R agonist-induced infantile spasms phenotype.

142 screen 39 potential A(3)R, antagonists using agonist-induced inhibition of cAMP.

143 elet adhesiveness is critically dependent on agonist-induced inside-out activation of heterodimeric i

144 so enhanced islet GLP1R expression and GLP1R agonist-induced insulin secretion and glucose tolerance.

145 Although agonist-induced integrin alphaIIbbeta3 affinity regulati

146 thermore, CB1R(DeltaH9) is more sensitive to agonist-induced internalisation and less efficient at do

147 DP1 receptor (DP1) to the cell surface after agonist-induced internalization and that L-PGDS overexpr

148 ected by the three-residue mutation, with no agonist-induced internalization observed even in the pre

149 Concomitantly, agonist-induced internalization of alpha2AAR is signific

150 The distribution and lack of agonist-induced internalization of D2 receptors on dopam

151 ells, we confirmed that AP-2 is required for agonist-induced internalization of endogenous PAR4.

152 face and facilitate resensitization, whereas agonist-induced internalization of PAR1 is critical for

153 In this study we found that agonist-induced internalization of the dopamine D2 recep

154 Agonist-induced internalization, intracellular trafficki

155 PAR1 displays both constitutive and agonist-induced internalization.

156 PAR1 displays constitutive and agonist-induced internalization.

157 4 cell FPR1 was atypical in that it resisted agonist-induced internalization.

158 nodine receptor (RyR), plays a major role in agonist-induced intracellular calcium ([Ca(2+)]cyt) dyna

159 Model results show that agonist-induced intracellular calcium dynamics can be mo

160 nel activation, while Ca2+ store content and agonist-induced IP3 production were unaltered.

161 eatment, GRKs, but not PKC, were involved in agonist-induced KOPR internalization.

162 Specifically, we demonstrate that the agonist-induced linker region phosphorylation of Smad2 a

163 (TG) hydrolysis, and its deficiency enhanced agonist-induced lipolysis in vivo CTRP2-deficient mice a

164 Cocaine-induced and quinpirole (D2 receptor agonist)-induced locomotion was enhanced in rats that co

165 LD not only failed to potentiate orthosteric agonist-induced LTD but also blocked M(1)-dependent LTD

166 estigated the role of cingulin in control of agonist-induced lung EC permeability via interaction wit

167 hat central administration of senktide (NK3R agonist) induced luteinizing hormone (LH) secretion in p

168 Agonist-induced lysosome secretion ex vivo was also impa

169 enetic ablation of CB2 had any effect on CB2 agonist-induced macrophage chemotaxis.

170 i/o-coupled GPCR must be responsible for CB2 agonist-induced macrophage migration.

171 Particulate beta-glucan (a DECTIN-1 agonist) induced mast cell degranulation in mesenteric w

172 D5 receptors reversed priming, whereas D1/D5 agonists induced mechanical hypersensitivity exclusively

173 duce mGluR1 association with lipid rafts and agonist-induced, mGluR1-dependent activation of extracel

174 We examined agonist-induced mGluR5 signaling in the postmortem dorso

175 Rap1b to vesicular membranes that mimic the agonist-induced microenvironment.

176 H4-Bcl-XL peptide via electroporation limits agonist-induced mitochondrial Ca(2+) uptake and protects

177 role for GRK2 (and potentially also GRK3) in agonist-induced MOPr desensitization in the LC, but leav

178 to study the involvement of GRK2/3 in acute agonist-induced MOPr desensitization.

179 a Galphaibetagamma heterotrimer-biased CXCR4 agonist, induced more robust phosphorylation of Ser-346/

180 in NOP-eGFP and NOP-eYFP mice, NOP receptor agonists induced multisite phosphorylation and internali

181 ysiological mechanism acting in concert with agonist-induced MYPT1 phosphorylation to inhibit MLCP ac

182 Furthermore, cues associated with a KOR agonist-induced negative affective state were assessed f

183 H23390 administration into the OFC plus GABA agonist-induced neural inactivation of the contralateral

184 sion of the M-current and prevents resultant agonist-induced neuronal hyperexcitability.

185 influx in skin and lung Arthus reactions and agonist-induced neutrophilia in the peritoneum, whereas

186 Importantly, agonist-induced NFAT activation is reduced in p65 null m

187 These mice exhibited lowered agonist-induced nitric oxide synthase (NOS) activity and

188 RXR agonists induced no beneficial effects in the E4FAD-HP i

189 ntibodies to the NOP receptor, we found that agonist-induced NOP receptor phosphorylation occurred pr

190 sidue is selective for only GPCR but not RTK agonist-induced nuclear export and proteolytic degradati

191 ylation and COX-2 expression, whereas an EP4 agonist induced only transient increases in CREB phospho

192 found GPCR/14-3-3 interaction signals can be agonist-induced or agonist-inhibited.

193 d symptom remission after 2-3 months of GnRH agonist-induced ovarian suppression (leuprolide) then re

194 he effects of gonadotropin-releasing hormone agonist-induced ovarian suppression on mood, sleep, sexu

195 0 muM; lungs, 20 muM; IC50, 29 nM) decreased agonist-induced oxidant generation.

196 Tymp deficiency also significantly decreased agonist-induced P-selectin expression.

197 ine the involvement of individual kinases in agonist-induced P-UAEC proliferation.

198 TLR2 or TLR4 agonist induced PAI-2 expression, which subsequently sta

199 lex-2 (AP-2), whereas AP-2 and epsin control agonist-induced PAR1 internalization.

200 sidues of the tyrosine-based motif disrupted agonist-induced PAR4 internalization.

201 ociated protein stathmin in the mediation of agonist-induced permeability in EC cultures and vascular

202 The role of TMEM16F in apoptosis- or agonist-induced phosphatidylserine (PS) exposure was stu

203 rmeability transition pore (mPTP) formation, agonist-induced phosphatidylserine exposure and alphaIIb

204 Increased PAR1 expression also enhanced agonist-induced phosphoinositide hydrolysis and endothel

205 o and in vivo studies also revealed a 5-HT1A agonist induced phosphorylation of FGFR1 and extracellul

206 hly selective CK2 inhibitor, greatly reduced agonist-induced phosphorylation of beta-cell M3Rs, indic

207 hat receptor internalization is required for agonist-induced phosphorylation of extracellular signal-

208 Agonist-induced phosphorylation of G protein-coupled rec

209 Agonist-induced phosphorylation of the parathyroid hormo

210 r kinases 2 and 3 (GRK2/3) cooperated during agonist-induced phosphorylation, which, in turn, facilit

211 oss of negative signals from PKCalpha due to agonist-induced PKCalpha down-regulation and (b) positiv

212 for Hsp70/Hsc70 and Hsp90 in the control of agonist-induced PKCalpha processing.

213 The present study examines the impact of agonist-induced PKCbetaII activation on contractile func

214 Exposure of macrophages to inflammasome agonists induced PKR autophosphorylation.

215 Chronic pain enhanced KOR agonist-induced place aversion in a sex-dependent manner

216 ction of CIB1, and its ability to facilitate agonist-induced plasma membrane localisation of sphingos

217 e rs11202221 and rs6566765 associations with agonist-induced platelet aggregation are novel.

218 In this first GWAS of agonist-induced platelet aggregation in African American

219 n of IL-6 to the thrombocytosis, exaggerated agonist-induced platelet aggregation, and enhanced extra

220 A+ interacts with platelet TLR4 and promotes agonist-induced platelet aggregation.

221 Agonist-induced platelet surface activated glycoprotein

222 Moreover, agonist-induced PM translocation of Epac1 leads to disso

223 tic potentiation induced by oxytocin, Avpr1b agonist-induced potentiation of CA2 synapses relies on N

224 se HPV is usually studied in the presence of agonist-induced preconstriction ('pretone').

225 Sustained agonist-induced production of the second messengers InsP

226 3 showed robust efficacy in antagonizing KOR agonist-induced prolactin secretion and in tail-flick an

227 osphorylated PKCalpha is a direct target for agonist-induced proteasomal degradation via an Hsp-regul

228 tation is recorded immediately downstream of agonist-induced receptor activation.

229 onformation at rest, and only GBR1 closes on agonist-induced receptor activation.

230 Agonist-induced receptor internalization followed a clat

231 r466 and Ser470 led to 40+/-1.3% decrease in agonist-induced receptor phosphorylation but this was as

232 ls stably expressing the M3-MR did not alter agonist-induced receptor phosphorylation or receptor int

233 work tested the hypothesis that lifetimes of agonist-induced receptor-arrestin clusters at the cell s

234 four residues to alanine partially decreased agonist-induced recruitment of arrestin3 without alterin

235 Basal and agonist-induced regulation of alpha2AAR-Galphai2YFP(C352

236 rthermore, overexpression of FBXO17 inhibits agonist-induced release of keratinocyte-derived cytokine

237 The Nfkb1(SSAA) mutation prevented the agonist-induced release of TPL-2 from its inhibitor p105

238 r acute activation of Kv3.1 using a specific agonist induced resilience to depression.

239 C-terminal residues had little impact on the agonist-induced response.

240 antagonist binding to the receptor, and the agonist-induced response.

241 Structural characterization of the PAF-R agonists induced revealed multiple oxidized glycerophosp

242 Parallel beta3 AR agonists-induced reversal of Na(+)-K(+) pump inhibition

243 has been implicated in the amplification of agonist-induced Rho signaling, leading to increased vasc

244 These novel M(1) allosteric agonists induced robust electrophysiological effects in

245 KOR agonist-induced ROS generation resulted from the early a

246 Agonist-induced rosette formation is blocked by pertussi

247 icient in syntaxin-11 had a robust defect in agonist-induced secretion although their morphology, act

248 We show that agonist-induced sensitisation is independent of the agon

249 Agonist-induced sensitisation may provide an explanation

250 binding but acted as an inhibitor of CB(1)R agonist induced signaling, including beta-arrestin2 tran

251 7 transmembrane biogenic amine receptors in agonist-induced signaling has not yet been clarified des

252 Therefore, agonist-induced signaling in this system involves two di

253 he impact of such preassociated complexes on agonist-induced signaling is poorly understood.

254 wn was performed, in human ASM cultures, and agonist-induced signaling was assessed.

255 romatic residue at position VI:09, unchanged agonist-induced signaling was observed upon Ala substitu

256 s are required for the full dynamic range of agonist-induced signaling, as 5-HT(7) receptors spontane

257 ors with G(s) heterotrimers is necessary for agonist-induced signaling.

258 ken the hydrophobic core, showed significant agonist-induced signaling.

259 stration of CL-316,243, a selective beta3-AR agonist, induced significant increases in non-rapid-eye

260 We found that selective Avpr1b agonists induced significant potentiation of excitatory

261 PAR4-agonist induced slower release of fewer molecules, where

262 e signal transduction process in response to agonist -induced smooth muscle contraction.

263 Finally, muscarinic agonist-induced smooth muscle contraction also exhibited

264 Our results demonstrate that agonist-induced SNO contributes to junctional membrane p

265 BEL attenuated the agonist-induced steroid receptor coactivator-1 interacti

266 that low [Na(+)] is required to allow large agonist-induced structural changes in A2AR, and that pat

267 Identifying agonist-induced structural changes underlying nAChR acti

268 We also show that BQCA potentiates agonist-induced subcellular trafficking.

269 Cold- and beta3-adrenoceptor agonist-induced sympathetic activation leads to angiogen

270 Gemcitabine in combination with a CD40 agonist induced T-cell-dependent regression of subcutane

271 TLR agonist-induced TAG storage is a multifaceted process th

272 In all cases, agonist-induced tagged 5-HT(1A)R endocytosis was prevent

273 ntrast, sustained exposure (for 24 h) to all agonists induced tagged-5-HT(1A)R endocytosis in raphe s

274 We found that isolated ZP or alpha7 agonists induced the AR in sperm from WT but not alpha7-

275 Intranasal exposure with receptor agonists induced the release of IL-33 and subsequent eos

276 SYK inhibition in vivo represses beta-agonist-induced thermogenesis and oxygen consumption.

277 ivator, is phosphorylated in response to the agonist-induced TLR signaling.

278 induced traces, as well as the modulation of agonist-induced traces by anesthetic, either coapplied o

279 well, including both anesthetic-induced and agonist-induced traces, as well as the modulation of ago

280 Our results provide the first data on the agonist-induced trafficking of native GPR17 in oligodend

281 tty acid in synaptic membranes, enhances the agonist-induced transition to the desensitized state in

282 signaling to protein synthesis, deficits in agonist-induced translational control, protein synthesis

283 The TPR domain of AGS3 was required for agonist-induced translocation of AGS3 from the cell cort

284 Agonist-induced translocation of AGS3 to the GA altered

285 The agonist-induced translocation of AGS3 was reversed by th

286 This phosphorylation event inhibits agonist-induced translocation of Epac1 to the plasma mem

287 Agonist-induced turnover of palmitate occurs predominant

288 antiviral responses and was critical for TLR agonist-induced, type 1 IFN-dependent suppression of inf

289 particle treatment prevented the cannabinoid agonist-induced up-regulation and enhanced 5-HT2A recept

290 identify the role of GRK5 in the cannabinoid agonist-induced up-regulation and enhanced activity of 5

291 Interestingly, we found that cannabinoid agonist-induced up-regulation of GRK5 involves CB2 recep

292 r ERK1/2 inhibitor prevented the cannabinoid agonist-induced up-regulation of GRK5.

293 lephrine (100 mumol/L), an alpha1 adrenergic agonist, induced upregulation of Nox4 (1.5-fold; P<0.05)

294 in B cells is correlated with impaired TLR7 agonist-induced upregulation of activation markers CD69

295 owed that adenosine or an ADORA2A or ADORA2B agonist induced V-ATPase translocation from vesicles to

296 ed the time-of-day variations in response to agonist-induced vasoconstriction, myosin phosphorylation

297 e to troglitazone, a high-affinity PPARgamma agonist-induced vasorelaxation in UtA preconstricted wit

298 Expression of T210A Plk1 inhibited the agonist-induced vimentin phosphorylation at Ser-56 and c

299 The agonist-induced VPAC2 shedding is selective, as shown by

300 Sisley et al. reveal that GLP-1R agonist-induced weight loss requires GLP-1Rs in the CNS,