ライフサイエンスコーパス: be antagonized by

1 ethanol and 1-butanol on cell-cell adhesion were antagonized by 1-pentanol (IC(50) = 715 microM) and

2 The serotonin effects were antagonized by 5 microM methysergide or 1-5 microM

3 tubule polymerization, and that these forces are antagonized by a C-terminal kinesin, Ncd, which gene

4 n fetal liver cells and this induction could be antagonized by a cyclooxygenase-2 inhibitor.

5 lating hormone (alphaMSH), MC1R function can be antagonized by a secreted factor, agouti signal prote

6 SS, the negative regulatory activity of ExsD is antagonized by a direct binding interaction with ExsC

7 During most of the cell cycle, Tem1 function is antagonized by a GTPase-activating protein complex, B

8 Furthermore, allosteric potentiation is antagonized by a neutral ligand at the MPEP site and

9 of bone morphogenetic protein (BMP) ligands is antagonized by a number of extracellular proteins, in

10 The activity of the pheromone is antagonized by a plasmid-encoded inhibitor peptide th

11 in bacteria outside the gamma-proteobacteria is antagonized by a protein called FliW.

12 rm, including bone morphogenic proteins, and is antagonized by a second secreted signal, Wnt proteins

13 TraR activity is antagonized by a second tumor-inducing plasmid-encode

14 q protein and adenylate cyclase activity and was antagonized by a cAMP-dependent protein kinase A and

15 transient outward, A-type K(+) current that was antagonized by a high concentration of 4-aminopyridi

16 ated interleukin-6 production, each of which was antagonized by a specific A2bR antagonist (PSB-603).

17 These effects of 8-bromo-cAMP were antagonized by a specific protein kinase A (PKA) in

18 rized by overexpression of Bcl-xL, which can be antagonized by ABT-737 leading to apoptosis.

19 exokinases from mitochondria, an effect that was antagonized by activated Akt.

20 ts, such as prostaglandin E(2) (PGE(2)), can be antagonized by activators of the ATP-sensitive potass

21 by endothelial cell adenosine A2B receptors is antagonized by adenosine reuptake into proximal tubul

22 This effect is antagonized by administration of protein synthesis in

23 Members of these melanocortin receptors are antagonized by agouti (ASP) and agouti-related prote

24 , a key component in the Sarm1-MAPK pathway, is antagonized by AKT signaling, which modulates the deg

25 he K(act) for wild-type PII, and this effect was antagonized by alpha-ketoglutarate.

26 OPN inhibited DUN-induced cell death, which was antagonized by alphavbeta3 monoclonal antibody.

27 T cell responses were antagonized by altered peptide ligands containing s

28 the immune response promoted by chemotherapy is antagonized by an immune-suppressive milieu, and the

29 The activity of the E3 ligase, SMURF2, is antagonized by an intramolecular, autoinhibitory inte

30 ulated bcl-x gene expression and this effect was antagonized by an inhibitor of NF-kappaB activity.

31 baseline [Ca(2+)](i) by 5.9 +/- 0.7-fold and were antagonized by an inhibitory cocktail containing 2-

32 Activating transient dimerization is antagonized by anions binding to a discrete site.

33 ebrain gene expression, an effect that could be antagonized by anterior mesendoderm, and promoted exp

34 tidomain' members Bax or Bak--a process that is antagonized by anti-apoptotic members of the Bcl-2 fa

35 ompared with fibroblasts and this inhibition was antagonized by antibodies against TNF alpha-related

36 dent on a twofold CXCR4 down-regulation that was antagonized by antigen-induced BCR signaling.

37 riatum, rich in dopamine D2 receptors, which are antagonized by antipsychotic medications, plays a ke

38 ke wild-type receptors, this channel opening was antagonized by application of either volatile anesth

39 The effects of NO donor exposure were antagonized by application of NO scavenger compound

40 Viagra effects were antagonized by application of NO scavengers, consis

41 The intrinsic pathway is antagonized by ARC-Bax binding, involving ARC's CARD

42 of non-NMDA receptor-mediated mEPSCs, which was antagonized by atropine but not mecamylamine.

43 t manner, Astrin, SKAP, and LC8 localization is antagonized by Aurora B such that they target exclusi

44 he MAKR2 inhibitory effect on TMK1 signaling is antagonized by auxin itself, which triggers rapid MAK

45 a bidirectional positive feedback loop that is antagonized by Bcl-2.

46 egulating mRNA translation and stability and are antagonized by binding to small noncoding RNAs.

47 Antibiotic efficacy can be antagonized by bioactive metabolites and other drugs

48 PDBu was antagonized by bisindolylmaleimide, a PKC inhibitor,

49 Conversely, when neuralin and BAMBI were antagonized by BMP4, astrocytic differentiation was

50 rate that human PAQRs from all three classes are antagonized by both 1(S),2(R)-d-erythro-2-(N-myristo

51 activation of c-Jun-N-terminal kinase, which was antagonized by both catecholamines and glucocorticoi

52 erestingly RIF1 accumulation at damage sites is antagonized by BRCA1 in S and G2 phases.

53 k DSB resection to promote NHEJ in G1, which is antagonized by BRCA1 in S phase to ensure a switch of

54 iate accumulation of RIF1 at DSBs in S phase is antagonized by BRCA1, and deletion of Rif1 suppresses

55 Induction of the CTGF promoter is antagonized by c-Jun or by MEKK1, suggesting that a p

56 We show that this activity is antagonized by C-rich motifs and correlated with prot

57 on between the N terminus of AC8 and PP2A(C) was antagonized by Ca(2+)/calmodulin.

58 A(1) adenosine receptors (A(1)Rs) are antagonized by caffeine and are most highly enriched

59 denosine in many physiological processes and is antagonized by caffeine.

60 phosphate (GTP) and does so in a manner that is antagonized by calcium.

61 -catenin destruction complex, whose activity is antagonized by canonical Wnt signaling.

62 nabled (Ena) via a conserved LPPPP motif and is antagonized by Capping Protein (CP).

63 dent model of acute inflammatory pain, which was antagonized by CB1 and CB2 receptor antagonists/inve

64 r high glucose, and the effects of all three were antagonized by CB1R blockade or siRNA-mediated knoc

65 soids required intrinsic S1P1 expression and was antagonized by CCR7.

66 autoinhibitory and that this negative effect is antagonized by Cdc42 to promote Ste20 kinase activity

67 teractions with the APC/C indicates how they are antagonized by Cdh1 phosphorylation.

68 a cell invasion mediated by this pathway can be antagonized by Cdk2/Cdc2 inhibitors in vitro and in v

69 cTNT and IR alternative exons, both of which are antagonized by CELF proteins.

70 loproteinase 2 (MMP2) and MMP9 activity that is antagonized by Chrdl1.

71 but not ATP-insensitive poisons was shown to be antagonized by ciprofloxacin.

72 h, synaptosomes and slices, the effect of KA was antagonized by CNQX, and persisted after pretreatmen

73 p193-induced apoptosis was antagonized by co-expression of Bcl-X(L).

74 , and inducible NO synthase, and this effect is antagonized by coinjection of the anti-inflammatory d

75 Vessel wall remodeling can be antagonized by common cardiovascular drugs that act i

76 ed IRF5 nuclear accumulation, and this could be antagonized by concomitant TLR2 signaling.

77 This activity is antagonized by Cortactin, a filament branch stabilize

78 mouse oligodendrocytes, an effect that could be antagonized by cotreatment with muscarine.

79 promote ciliogenesis and that this function is antagonized by CP110.

80 These effects were antagonized by CPT or adenosine deaminase (0.8 IU/m

81 ateral excitation, and that excitatory input is antagonized by crossed inhibition during contraversiv

82 lterations, referred to as neutrophil aging, were antagonized by CXCR4 (C-X-C chemokine receptor type

83 effect of PSD-95 is activity-independent and is antagonized by cypin, a nonsynaptic protein that regu

84 but not by gibberellin or abscisic acid, and is antagonized by cytokinin.

85 proliferation in early passage primary MEFs is antagonized by DNA damage checkpoint activation, cons

86 However, the actions of MAST3 are antagonized by dopamine and cAMP-regulated signaling

87 ine, but not epinephrine and norepinephrine, are antagonized by dopamine D4 antagonists.

88 by disruption of the actin cytoskeleton and is antagonized by dynamin.

89 The effects of shh ectopic expression could be antagonized by ectopic expression of chordin, an inhi

90 However, this mechanism can be antagonized by ectopically expressing a competitive i

91 racting partner of K17, and this interaction is antagonized by EGFR activation.

92 This activity of Gro is antagonized by EGFR signaling, which inhibits Gro-dep

93 This inhibition was antagonized by either L- or D-alanine.

94 stimulate follicle-stimulating hormone, and is antagonized by endocrine acting, gonadally derived in

95 Wnt activity is antagonized by endogenous proteins including dickkopf

96 etect both viral and bacterial pathogens but was antagonized by enteroviruses, such as rhinovirus and

97 This inhibitory activity of RVB2 is antagonized by Env through competitive interaction wi

98 The inhibition of RhoA activity by cadherins was antagonized by expression of a dominant negative p19

99 vity that is induced transiently by adhesion was antagonized by expression of dominant negative p190R

100 ts MST1/2, LATS1 and YAP, an effect that can be antagonized by ezrin.

101 This action of ethanol is antagonized by femtomolar concentrations of the neuro

102 receptor signaling to mediate cell repulsion is antagonized by fibroblast growth factor receptor (FGF

103 hol effects on both behavior and CNS neurons were antagonized by flumazenil (10 mg/kg in vivo; 10 muM

104 GDF11 is antagonized by follistatin (FST), which is also produ

105 d to endogenous activin A, and this response was antagonized by follistatin, as evidenced by changes

106 The process is antagonized by fragile X mental retardation protein (

107 tects myocytes from death, and this activity is antagonized by Fstl3.

108 , the activity of TnrA at the gltAB promoter was antagonized by glutamine synthetase under certain gr

109 in response to Aspergillus fumigatus conidia is antagonized by granulocyte-macrophage colony-stimulat

110 d downstream process of cell differentiation was antagonized by GW0742 in HL-60 cells that were pretr

111 We tested whether silencing establishment was antagonized by H3 K79 methylation or by the Dot1 pro

112 HIV-1 replication, and that this restriction is antagonized by HIV-1 Vpr.

113 These effects are antagonized by Hp, which binds free Hb and facilitat

114 The binding of hnRNP G to the exon is antagonized by hTra2beta.

115 factor, promyelocytic leukemia protein, and are antagonized by ICP0.

116 Induction of Th17 cells can be antagonized by IL-4 or IFN-gamma, but mechanisms thro

117 -gamma stimulation alone, and this induction was antagonized by IL-4 and granulocyte/macrophage colon

118 res a functional CsrS sensor protein and can be antagonized by increased extracellular Mg(2+), the ot

119 s under normoxia in LKB1-deficient cells and is antagonized by inhibition of mTOR complex I signaling

120 nse is triggered by cytoplasmic L1 cDNA, and is antagonized by inhibitors of the L1 reverse transcrip

121 This effect was antagonized by injection of osteoprotegerin fusion p

122 The action of TGF-beta on naive T cells is antagonized by interferon-gamma and IL-4, thus provid

123 0 involving interleukin-4, or interleukin-13 was antagonized by interferon-gamma.

124 Inactivation induced by Kvbeta1.3 was antagonized by intracellular PIP(2).

125 lity and cell-to-cell spread of bacteria but are antagonized by IpaH9.8, a bacterial ubiquitin ligase

126 In addition, IQGAP2 is antagonized by IQGAP1 to modulate the mechanoresponsi

127 As maximal expression of miR-216b is antagonized by Ire1, miR-216b accumulation reflects t

128 port Abeta at the BBB, in a process that can be antagonized by its putative natural ligand, desmoster

129 sized that the antioxidant function of Bcl-2 is antagonized by its interaction with the BH3 domains o

130 These actions are antagonized by JunB, which upregulates tumor suppres

131 es KaiC phosphorylation and this enhancement is antagonized by KaiB.

132 rces depend on Kid (kinesin-10) activity and are antagonized by Kif4A (kinesin-4), which functions to

133 adrenergic stimulation of the Ca(2+) current was antagonized by lavendustin A.

134 ced by ligation plus P. gingivalis infection was antagonized by local anti-RANKL antibody administrat

135 FadR DNA binding is antagonized by long chain acyl-CoAs, and thus FadR ac

136 d transduces Wnt-canonical signals which can be antagonized by LRP5 ligand, Dickkopf 1 (Dkk1).

137 These LT-IIb-B(5) activities were antagonized by LT-IIb; however, inhibitors of adeny

138 ibit endopolyploidization, but this function is antagonized by MAD1.

139 e receptors (RLR) is a crucial response that is antagonized by many viruses.

140 BMP-4 is essential for angiogenesis and is antagonized by matrix Gla protein (MGP) and crossvein

141 phosphorylation and transcriptional activity was antagonized by mitogen-activated protein kinase kina

142 to targeting c-Fos protein degradation that is antagonized by mitogenic stimulations.

143 Physical interactions between these proteins were antagonized by MMAC/PTEN consistent with their pote

144 As in MII, this phosphorylation is antagonized by Mos-mediated recruitment of PP2A to Em

145 o shown to depend on MEC1, but not TEL1, and were antagonized by MRE11.

146 ng compartment is independent of ephrins but is antagonized by MSP signaling.

147 mmatory program in PALF non-survivors (which is antagonized by NAC), while driving an anti-inflammato

148 ice after subcutaneous administration, which was antagonized by naloxone methiodide demonstrating act

149 The binding of CA200645 to tauD3 was antagonized by nanomolar concentrations of the A3 an

150 ssed SERINC5 restricts HIV-1 infectivity and is antagonized by Nef and analyzed both virions and prod

151 and p53 proteins; however, the p53 activity is antagonized by NF-kappaB signaling.

152 gers including death receptor ligand binding is antagonized by NFkappaB activation and potentiated by

153 This effect was antagonized by nifedipine but not omega-conotoxin GV

154 behavioral effects of nitrous oxide (N(2)O) were antagonized by non-specific inhibitors of nitric ox

155 The effects of RSV infection are antagonized by Nutlin-3, a specific chemical inhibit

156 moters are repressed by CepR2 and that CepR2 is antagonized by OHL.

157 progression and proper R8 specification, and are antagonized by other subfunctions of Broad-complex.

158 and flow cytometry reveal that SSA78 binding is antagonized by ouabain, supporting the interaction of

159 Such TLX-mediated suppression can be antagonized by overexpressing wild-type Sox2 but not

160 on component that is resistant to alphaCTxGI was antagonized by pancuronium (3-10 microM) and by a 4-

161 We predict that APOL genes are antagonized by pathogens by at least two distinct me

162 ta promoted the expression in a process that was antagonized by pharmacological and genetic interfere

163 d-1 receptor in AIY and RIF interneurons and is antagonized by pigment-dispersing factor (PDF).

164 els in the presence of PknA, and this effect was antagonized by PknA-K42N, a kinase-dead variant.

165 acts by promoting LIN-17 phosphorylation and is antagonized by planar cell polarity signaling compone

166 h a posttranslational modification of FoxM1b was antagonized by PLK1-mediated phosphorylation.

167 orks independently of their breakage, and to be antagonized by poly (ADP-ribose) polymerase/RECQ1-reg

168 ciated CDK1, and indirectly by Aurora B, and is antagonized by PP1-mediated dephosphorylation.

169 Cdc2-mediated phosphorylation of Emi2 was antagonized by PP2A, which could bind to Emi2 and pr

170 laxation which was insensitive to l-NAME but was antagonized by pretreatment with a VIP antagonist.

171 effect of quinpirole was dose dependent and was antagonized by pretreatment with domperidone (5 mg/k

172 This uncovering of the OXT response was antagonized by pretreatment with protein kinase A or

173 chondrial XIAP entry requires Bax or Bak and is antagonized by pro-survival Bcl-2 proteins.

174 enhanced degradation of MAP1B-LC, which can be antagonized by proteasome inhibitors.

175 er, ubiquitination of the 26S proteasome can be antagonized by proteasome-residing deubiquitinating e

176 a2-beta1 promotes inclusion of this exon and is antagonized by protein phosphatase (PP) 1.

177 demonstrate that Chk1 phosphorylation by ATR is antagonized by protein phosphatase 2A (PP2A).

178 mitotic kinase other than cdc2-cyclin B and is antagonized by protein phosphatase 2A.

179 and casein kinase 1epsilon (CK1epsilon) and was antagonized by protein phosphatase 1.

180 ion of a PI 3-kinase/Akt/mTOR pathway, which is antagonized by PTEN.

181 GS 21680 modulation was observed when D(2)Rs were antagonized by raclopride, suggesting that an acute

182 E2F transactivation is antagonized by retinoblastoma protein (pRb), which re

183 pf1 recruitment and subsequent RNA decay can be antagonized by retroviral RNA elements that promote t

184 inhibitor of mTOR, whose inhibitory activity is antagonized by Rheb in response to growth factor stim

185 The inhibitory action of FKBP38 is antagonized by Rheb, an oncogenic small GTPase, which

186 etween low-complexity domains of TDP-43 that are antagonized by RNA binding.

187 , inducing an adaptive defense response that is antagonized by RNA interference targeted against Nrf2

188 by RU486 and, second, repression of COX/PGES is antagonized by RU486.

189 Both enhancers are antagonized by RUNX/CBFbeta complexes, and SATB1 fur

190 This is antagonized by S1PR4 signaling, thus decreasing TLR-i

191 l-acyl carrier protein (ACP) or acyl-CoA and was antagonized by saturated acyl-ACP or acyl-CoA.

192 ult rats, SKF 38393-mediated phosphorylation was antagonized by SCH 23390, a D1-like receptor antagon

193 Wnt-Frizzled interactions can be antagonized by secreted Frizzled-related proteins (SF

194 een bromodomains and acetylated histones can be antagonized by selective small molecules that bind at

195 This pathway is antagonized by SH2-containing inositol 5'-phosphatase

196 toxicity in Mer(high) ALL cell lines, which was antagonized by short hairpin RNA-mediated knockdown

197 Hh signalling is antagonized by signals from the dorsal neural tube an

198 effect of pressure on the proliferation can be antagonized by silencing p27Kip1.

199 During apoptosis, XIAP is antagonized by SMAC, which is released from the mitoc

200 Bone morphogenetic proteins are antagonized by soluble binding proteins such as nogg

201 diated inhibition of endothelial cell growth is antagonized by soluble CD148 ectodomain as well as by

202 egative feedback loop of TLX expression that is antagonized by Sox2 in adult NSCs.

203 o keep the receptor silent, a state that can be antagonized by Sp1, SREBP, and inhibitors of histone

204 e in which pro-proliferative FGFR1 signaling is antagonized by SPRY1 to maintain satellite cell quies

205 CsrA activity is antagonized by sRNA(s) containing multiple CsrA bindi

206 This repression would normally be antagonized by Sry protein in XY embryos.

207 ed neurones, taurine induced a current which was antagonized by strychnine and by picrotoxin, but not

208 osphate (10 pmol) evoked a bradycardia which was antagonized by suramin (100 pmol).

209 Moreover, FOXP3 association with HDAC9 is antagonized by T cell stimulation and can be restored

210 ith their diminished expression of SOCS3 and is antagonized by T(reg)-specific induction of this regu

211 Furthermore, we show that NmFic activation is antagonized by tetramerization.

212 The expression and function of PEAR proteins are antagonized by the HD-ZIP III proteins, well-known p

213 These actions of ezrin are antagonized by the neurofibromatosis type 2 tumor-su

214 orm nuclear bodies and silence transcription are antagonized by the oncogenic antiphosphatase Sbf1 th

215 the activation of tyrosine kinases (TKs) can be antagonized by the action of protein-tyrosine phospha

216 B in infected cells and that this effect can be antagonized by the antiviral drug maribavir.

217 actions on the anti-HIV miRNAs and HIV could be antagonized by the opioid receptor antagonists (naltr

218 istal promoter site, but this activation can be antagonized by the regulator CysB.

219 at K68 and K71, which is a process that can be antagonized by the SIRT3 deacetylase.

220 H69 cleavage is antagonized by the 3 major host defense pathways defi

221 dent activation, a cooperative function that is antagonized by the activation of the conventional PKC

222 phosphatidyl inositol 3'-kinase/Akt pathway, is antagonized by the adenosine monophosphate (AMP)-acti

223 administered intraperitoneally at time zero is antagonized by the administration of astressin(2)-B b

224 We establish that downregulation of Cic is antagonized by the anterior patterning morphogen Bico

225 he metabolic switch induced by DC activation is antagonized by the antiinflammatory cytokine interleu

226 present in alpha4/6beta3delta receptors that is antagonized by the behavioral alcohol antagonist Ro15

227 This activity is antagonized by the chromosome passenger complex (CPC)

228 However, this signaling is antagonized by the chymase, mouse mast cell protease

229 We found that Huwe1 activity on TBP is antagonized by the deubiquitinase USP10, which protec

230 This activity is antagonized by the deubiquitinase Usp28, which is hig

231 ox containing complex) (Slimb), whose action is antagonized by the deubiquitinating enzyme fat facets

232 matic activity, DNA-binding activity of NrtR is antagonized by the effector ADP-ribose.

233 inoid CB(1) and CB(2) receptors; this target is antagonized by the endogenous compound N-arachidonoyl

234 We also demonstrate that PpsR is antagonized by the flavin-containing antirepressor, A

235 PKR and eIF2alpha Ser-51-dependent autophagy is antagonized by the herpes simplex virus neurovirulenc

236 es, and other enveloped virus particles, and is antagonized by the HIV-1 accessory protein, Vpu.

237 ces an autophagy response, but this response is antagonized by the HSV-1 neurovirulence gene product,

238 The neuroprotective effect of leptin is antagonized by the JAK2-STAT3 inhibitor AG-490, STAT3

239 methylation to promote its activation, which is antagonized by the Jumonji-family demethylase KDM4B.

240 s but, after the reproductive transition, it is antagonized by the MADS box transcription factor SQUA

241 tes in Escherichia coli, and phosphorylation is antagonized by the phosphatase activity.

242 Transcription by RNA polymerase II is antagonized by the presence of a nearby tRNA gene in

243 ect association of PABPC with importin alpha is antagonized by the presence of poly(A) RNA, supportin

244 dendritic cells and monocyte/macrophages but is antagonized by the primate lentiviral protein Vpx, wh

245 pression requires the activation of PI3K but is antagonized by the Ras-ERK pathway.

246 PAR-1 directly phosphorylates MEX-5 and is antagonized by the spatially uniform phosphatase PP2A

247 lex, and the SUMO E3 ligases PIAS1/PIAS4 and is antagonized by the SUMO protease SENP6.

248 CsrA activity is antagonized by the untranslated RNA CsrB, to which it

249 atidylethanolamine levels by the MSF1 domain is antagonized by the Ups2p LEA-like domain.

250 st probably mediated by protein kinase A and is antagonized by the ventralizing morphogen Sonic hedge

251 ty to fuse with target cells, an effect that is antagonized by the viral Nef protein.

252 or 5 (SERINC5) impairs HIV-1 infectivity but is antagonized by the viral Nef protein.

253 t chromosome interactions, but this activity is antagonized by the ZMM pathway to enable the formatio

254 d [3H]cAMP production (pEC50=8.57), and this was antagonized by the A3-selective antagonist MRS1220 (

255 sion with coinjection of 10 ng of Hsp70 cRNA was antagonized by the additional coinjection of Hsc70 c

256 The effect of Bay K 8644 was antagonized by the adenylyl cyclase inhibitor MDL 12

257 e hamster ovary cells, and the MCL-1S action was antagonized by the antiapoptotic MCL-1L.

258 DABK-induced leukocyte trafficking was antagonized by the B(1) receptor antagonist des-arg(

259 ltured Spodoptera Sf-9 cells, and this death was antagonized by the caspase inhibitors p35 or DIAP1.

260 te tactile and thermal hypersensitivity that was antagonized by the CCK2 receptor antagonist L365,260

261 The EET depletion by FABP was antagonized by the co-addition of arachidonic acid,

262 TFH cell programming by activin A was antagonized by the cytokine IL-2.

263 In addition, secretion of 5-HT was antagonized by the expression of a minigene encoding

264 diated by the glucocorticoid receptor, as it was antagonized by the glucocorticoid receptor antagonis

265 erentiation to the myofibroblastic phenotype was antagonized by the inhibition of hyaluronan synthesi

266 vate NF-kappaB and induce TNF-alpha and IL-8 was antagonized by the LT-IIb holotoxin.

267 uced by vagal stimulation, and the reduction was antagonized by the nitric oxide synthase inhibitor N

268 mate-stimulated cobalt uptake in taste cells was antagonized by the non-NMDA receptor antagonist CNQX

269 BMP7-induced protection was antagonized by the p42,44 MAPK kinase inhibitors PD9

270 (III) concentration in the testing media and was antagonized by the presence of the competing parent

271 ) response in a dose-dependent manner, which was antagonized by the selective 5-HT(2C) receptor antag

272 er diazoxide induced an outward current that was antagonized by the sulfonylurea receptor 1 (SUR1) ch

273 Allopregnanolone-induced proliferation was antagonized by the voltage-gated L-type calcium chan

274 nt inhibiting myosin light chain phosphatase were antagonized by the addition of recombinant S13D tel

275 of systemic A-134974 (10 micromol/kg, i.p.) were antagonized by the non-selective ADO receptor antag

276 ulation were absent in Ca2+ -free saline and were antagonized by the nonselective TRP channel antagon

277 ked in Muller cells by hypotonic stimulation were antagonized by the selective TRPV4 antagonist HC-06

278 permeability and cytoskeletal reorganization were antagonized by the selective TRPV4 blocker HC 06704

279 These effects were antagonized by the thioredoxin/thioredoxin reductas

280 he absence of AHLs; moreover, these proteins are antagonized by their cognate AHLs.

281 duction of phospho-ERK and growth inhibition were antagonized by thiol-containing anti-oxidants, but

282 These inhibitory actions of Tup11/12 are antagonized by three different types of transcriptio

283 tal effect of miR-146a deficiency in T cells was antagonized by TNF blockade, whereas phytochemical i

284 s stimulate lysine acetylation of APE1 which is antagonized by transcriptional upregulation of SIRT1.

285 that for the majority of these, PSF's effect is antagonized by TRAP150.

286 These effects were antagonized by treatment with rapamycin, indicating

287 own that the activity of the TWIST1 oncogene is antagonized by TRIM29 and now show that TRIM29 is nec

288 ion of nuclear factor-kappaB by TNF and this is antagonized by TRIP.

289 e global regulatory RNA binding protein CsrA is antagonized by two non-coding sRNAs, CsrB and CsrC, w

290 (iii) PGE(1)-induced increase of cAMP (which is antagonized by U46619 in an ADP-dependent manner) was

291 nd Fbw7-dependent HIF-1alpha degradation can be antagonized by ubiquitin-specific protease 28 (USP28)

292 bitor of 60S ribosomal subunit ribophagy and is antagonized by Ubp3.

293 gene, which, along with the daf-3 Smad gene, is antagonized by upstream receptors and receptor-regula

294 a predicted uricase, and DNA-binding by HucR is antagonized by uric acid, the substrate of uricase.

295 nated in vivo at multiple lysines, which can be antagonized by various deubiquitinases (DUBs) includi

296 The action of these floral repressors is antagonized by vernalization and the activity of a se

297 This infectivity block is antagonized by Vpu via PSGL-1 degradation.

298 Association between the portal and U(L)26.5 was antagonized by WAY-150138, a small-molecule inhibito

299 ail-nuclear Cat L-CUX1 drives EMT, which can be antagonized by Z-FY-CHO.

300 is model FtsA self-interaction at the Z ring is antagonized by ZipA, allowing unpolymerized FtsA to r