ライフサイエンスコーパス: be inhibited by

1 The water permeability of SjAQP was inhibited by 1 mM HgCl2, 3 mM tetraethylammonium, 1

2 sible for co-metabolic transformation of PHE was inhibited by 1-octyne.

3 In primary hepatocytes, autophagy was inhibited by 3MA or autophagy-related protein 7 (Atg

4 by ATR signaling, involves Exo1 and BLM, and is inhibited by 53BP1/Rif1.

5 enzyme that mediates virus replication, can be inhibited by a panel of drugs that are commercially a

6 As are rapidly degraded when DNA replication is inhibited by a 3' to 5' pathway that requires extensi

7 Specific binding is inhibited by a L348R mutation in Munc18-1 and enhance

8 R transcription, but initiation at this site is inhibited by a negative regulatory sequence element,

9 x vivo treatment with URB597 and JZL184, and was inhibited by a CB1 antagonist.

10 lung CD4(+) T cells, and cytokine production was inhibited by a HLA-DR blocking Ab.

11 Moreover, the release of sVLDLR-N was inhibited by a metalloproteinase inhibitor, TAPI-1,

12 Cellular uptake was inhibited by a neutralizing antibody against alphav

13 terestingly, the PEX5(1-125)-DTM interaction was inhibited by a polypeptide comprising PEX5 residues

14 il adhesion to EC monolayers, an effect that was inhibited by a specific IKKbeta inhibitor.

15 tion of guinea pig and human vagus, and this was inhibited by a transient receptor potential ankyrin-

16 nses to evaporative cooling, and this effect was inhibited by a TRPM8 antagonist; behavioural respons

17 ction by T cells from peripheral lymph nodes was inhibited by A2aR activation (CGS-21680).

18 ltage-gated N-type calcium channels (Cav2.2) are inhibited by activation of G protein-coupled opioid

19 TGFBIp-induced lymphatic vessel sprouting was inhibited by addition of anti-integrin beta3 antibod

20 on type I signaling, and both mechanisms can be inhibited by administering specific molecules to prev

21 in mouse dorsal root ganglion (DRG) neurons is inhibited by agonists of the Gi-coupled micro opioid,

22 cycle arrest, and these anticancer functions are inhibited by AKT-induced phosphorylation and cytopla

23 Formation of NO and cGMP accumulation were inhibited by ALDH inhibitors chloral hydrate and da

24 Na(+) Curiously though, we found that SLO2.2 is inhibited by all divalent cations that activate SLO1,

25 f phenolics incorporation in melanoidins and are inhibited by amino groups through Maillard reaction.

26 trin, whereas both GABA-T and AGXT2 activity is inhibited by aminooxyacetic acid (AOA).

27 ding protein of the AAA+ ATPase superfamily, is inhibited by an unprecedented mechanism in which a li

28 ding of rhAPC to human neutrophils via VLA-3 was inhibited by an antagonistic peptide (LXY2).

29 V8-induced integrity damage was inhibited by an IL-1beta-mediated mechanism, indepen

30 However, C. bombi growth was inhibited by anabasine, eugenol, and thymol.

31 vation of lipoprotein lipase, an enzyme that is inhibited by angiopoietin-like 4 (ANGPTL4), has been

32 was mediated by CD1d, as maturation of moDCs was inhibited by anti-CD1d antibodies and Pru p 3-ligand

33 This ET-1 production was inhibited by anti-IFN-gamma and/or TNF-alpha antibod

34 itioned medium causing HSC chemotaxis, which was inhibited by anti-MIP1alpha.

35 ll-CM stimulated BMFs to produce IL-6, which was inhibited by anti-TGF-beta1 neutralizing antibody.

36 Immunosuppression by human Tregs can be inhibited by antibodies against GARP or against the i

37 Debris-stimulated tumors were inhibited by antiinflammatory and proresolving lipi

38 r and subsequent virulence factor expression is inhibited by apolipoprotein B, the structural protein

39 ron tolerance in OsPIP1;3 and OsPIP2;6 lines was inhibited by aquaporin inhibitors, silver nitrate an

40 s report, we expand the list of viruses that are inhibited by ARB and demonstrate that ARB suppresses

41 N-cadherin, and N-cadherin/LLGL1 interaction is inhibited by atypical protein kinase C-mediated phosp

42 tegrated in distinct functional circuits and were inhibited by aversive stimulation.

43 tion of fs120, but not fs188 cells, in vitro was inhibited by B20-4.1.1.

44 peptidoglycan when the native S. aureus PBPs are inhibited by beta-lactams.

45 more, expression of its close homolog Cyp1a1 was inhibited by beta-catenin.

46 tin cytoskeleton induced by Abeta42 in vitro was inhibited by bexarotene treatment.

47 The activity of this form of PP2A can be inhibited by binding of conserved Igo/ENSA proteins.

48 n of beta-catenin, and all of these pathways are inhibited by bis-indole-derived NR4A1 antagonists th

49 HIV fusion with the cell membrane can be inhibited by blocking coreceptor binding or by preven

50 ilize from cryptopatches, a process that can be inhibited by blocking GM-CSF, and mobilization preced

51 by the surface glycoprotein (GP), which can be inhibited by blocking TLR4 signaling.

52 c and degenerate phenotype in NP cells which is inhibited by blocking ASIC-3 activity, suggesting tha

53 We find that BMP production in enterocytes is inhibited by BMP signaling itself, and that BMP autoi

54 onal canonical WNT ligands, WISP2 expression was inhibited by BMP4 thereby allowing normal induction

55 This effect was inhibited by BoNT/A, supporting a role for Gbetagamm

56 activity of the Sst-GABA neurons in the DMV is inhibited by both melanocortin and mu-opioid agonists

57 in increased fatty acid (FA) oxidation that was inhibited by both chloroquine and 3-methyl adenine,

58 EPIC1 secretion was inhibited by brefeldin A (BFA), demonstrating that i

59 induced pro-inflammatory cytokine production was inhibited by buthionine sulfoximine, an inhibitor of

60 PycA is inhibited by c-di-AMP and these mutations prompted us

61 e first phosphorylation event on RSK1, which is inhibited by Ca(2+)-binding S100 proteins in malignan

62 gesting that binding of only one of the ABDs is inhibited by Ca(2+).

63 osphorylated CPK28 was Ca(2+)-responsive and was inhibited by Ca(2+)/CaM.

64 as higher after 420 nm and 540 nm, and could be inhibited by capsazepine and SKF96365, which also inh

65 is electrostatic, as its fungicidal activity is inhibited by cations.

66 ergic neurons in the nucleus accumbens (NAc) are inhibited by CB1 agonists and eCBs.

67 BCR-mediated signaling was inhibited by CC-115 and also in CLL samples obtained

68 Our previous studies have found WAVE1 to be inhibited by Cdk5-mediated phosphorylation in brain a

69 showed that proofreading DNA polymerases can be inhibited by certain primers.

70 the CPSF subunit Fip1, and this interaction is inhibited by CFIm68/59 hyper-phosphorylation.

71 This process is inhibited by chemokine receptor antagonists (CoRAs) t

72 n that an increase in plasma levels of FABP4 is inhibited by chloroquine treatment of mice.

73 drolyzed pro-EGF1020-1027, and this activity was inhibited by chymostatin and not GM6001.

74 This proteolysis was inhibited by chymostatin and not GM6001.

75 n was enhanced by extracellular proteins but was inhibited by cigarette smoke extract via oxidative d

76 Both folate and methotrexate transport were inhibited by classical antifolates but not by non-c

77 thermal quenching of Y2O3:Er(3+) microtubes is inhibited by co-doping with Tm(3+) or Ho(3+) ion, mor

78 enriched after Mrf4 RNAi and a MEF2 reporter is inhibited by co-transfected MRF4 and activated by Mrf

79 es in Tg(ERE:Gal4ff)(UAS:GFP) zebrafish that were inhibited by coexposure with ICI 182780, demonstrat

80 Alternative pathway activity is inhibited by complement factor H (FH).

81 as well as undecaprenyl diphosphate synthase were inhibited by compound 1.

82 OR transport is inhibited by conditional gene inactivation of the Hed

83 ependent apoptosis when NF-kappaB activation is inhibited by cycloheximide.

84 Pore opening can be inhibited by cyclosporin A mediated via cyclophilin D

85 Bone growth and remodeling is inhibited by denervation in adults and children, resu

86 omotetrameric model CaV channel CaVAb, which is inhibited by dihydropyridines and phenylalkylamines w

87 Transamidase activity is inhibited by direct inhibitor binding at the transami

88 This silencing was shown to be inhibited by DNA methylation in cancer cells.

89 Twinkle helicase is inhibited by DNA damage in a unique manner that is de

90 In type 1 dUTPases, Stl binding is inhibited by dUTP.

91 otein fibronectin and that this activity can be inhibited by E64c.

92 lation initiation intermediate complexes can be inhibited by eIF2B.

93 pinocytosis, and this increased fluid uptake was inhibited by EIPA and by soluble THY-1.

94 ich recent experiments have demonstrated can be inhibited by elevated membrane tension.

95 of dNTP synthesis, ribonucleotide reductase, is inhibited by endogenous levels of deoxyATP (dATP) pre

96 arteries, constriction to thrombin or A23187 was inhibited by endothelial-denudation, by ET-1 recepto

97 dosterone-mediated increase of TRPM7 current was inhibited by eplerenone, a mineralocorticoid recepto

98 This effect was inhibited by eritoran and by silencing CD14 or TLR4.

99 ies similar to the wild-type transporter and are inhibited by established GLUT5 inhibitors N-[4-(meth

100 flammatory cytokines IL-1beta and IL-18, can be inhibited by ethanol, and we sought to better underst

101 ivation, and secretion of phosphorylated ASC were inhibited by ethanol.

102 e discharges in the cortex and thalamus that were inhibited by ethosuximide.

103 in betaM3 and alpha4Met-269 in alphaM1 that was inhibited by etomidate but not by R-mTFD-MPAB establ

104 ecific to necroptosis as extrinsic apoptosis was inhibited by exposure to high levels of glucose.

105 tibacterial and antiviral functions of LL-37 were inhibited by exposure to, and interaction with, car

106 SOCE was inhibited by expression of sigma1R or an agonist of

107 For instance, TREK1 is inhibited by external acidification, whereas TREK2 is

108 The heteromer was inhibited by extracellular acidification and by spad

109 The binding could specifically be inhibited by Fab anti-C1q and C1q-derived peptides.

110 ticular is important for mood regulation and is inhibited by first-line drugs for treatment of depres

111 These effects are inhibited by forced elevation of NADH, reduced expre

112 ssociated DNA damage, and cell proliferation is inhibited by G1-S cell-cycle arrest.

113 MMP8 was inhibited by genetic and pharmacological approaches.

114 Conversely, MAPKs, which are inhibited by glucocorticoids, provide feedforward co

115 m attachment to and infection of HCT-8 cells were inhibited by glycosaminoglycans and were reduced af

116 ssed whether NOX activity in PCa cells could be inhibited by Graviola pulp extract (GPE) that contain

117 Transcription of MIR122 is inhibited by GRHL2, which is increased in livers of m

118 Dvl2 recruitment to the cell membrane was inhibited by Gsc in Xenopus animal cap assays and ke

119 However, in vivo tumor outgrowth was inhibited by >80% in a manner associated with reduce

120 Binding of Hic to hTSP-1 is inhibited by heparin and chondroitin sulfate A, indic

121 When VLDL particle assembly and secretion was inhibited by hepatic shRNA-induced apoB silencing or

122 Activity of the enzyme was inhibited by Hg(2+), Zn(2+) Co(2+) and Cu(2+), while

123 Moreover, alphaVbeta8 was inhibited by high concentrations of Mn(2+) and was s

124 uclear cells (PBMCs) and that activation can be inhibited by ibrutinib or idelalisib.IMPORTANCE EBV e

125 n and the Wnt/beta-catenin signaling pathway was inhibited by ICG-001, a beta-Catenin inhibitor, whic

126 A variety of viruses are inhibited by IFITMs at the virus entry step.

127 Notably, only NO production was inhibited by IFNalpha; production of other cytokines

128 GF-beta/Smad pathway of fibrosis and opacity was inhibited by IGF-1, and further with SAHA in particu

129 regulation requires STAT5 and its expression is inhibited by IL-4.

130 We show that FGFBP1 expression is inhibited by increased accumulation of the transformi

131 mately 2 mum), and yet only bacterial TrpRSs are inhibited by indolmycin.

132 ession of the tumor suppressor HNF4alpha may be inhibited by interactions of RBPs with the G4 motif i

133 Finally, BSIA in H69 cholangiocytes was inhibited by intracellular Ca(2+) chelation, aggrava

134 by Kv 1.5 stably expressed in HEK 293 cells were inhibited by intracellular dialysis of AMPK heterot

135 main (MTD), which, in unstressed conditions, is inhibited by intramolecular binding to the Vms1 leuci

136 Cross-linking was inhibited by itraconazole but not by ketoconazole, a

137 n this in vitro system, cross-linking of P-X was inhibited by itraconazole, but not by U18666A.

138 Ataxin-3's degradation is inhibited by its binding to the proteasome shuttle Ra

139 ted alphaB-crystallin, and its EMT induction was inhibited by knockdown of alphaB-crystallin.

140 d collagen 1-alpha expression in HSCs, which was inhibited by knockdown of ATG7, a critical autophagy

141 enously expressing TRPC4, channel activation was inhibited by knocking down PLCdelta1 levels and almo

142 thesize that the pUL89 endonuclease activity is inhibited by known RNase H inhibitors.

143 pore supported Ca(2+) and Na(+) uptake that was inhibited by known blockers of full-length channels.

144 sting that TP2 translocates as a monomer and is inhibited by lateral interactions in the membrane.

145 cules by BMP9/10 in the presence of TNFalpha was inhibited by LDN193189, which inhibits ALK2 but not

146 containing COPII vesicle budding from the ER was inhibited by LdSar1:T34N in an in vitro budding assa

147 d antigen presentation for T cell activation is inhibited by lipophilic pollutants through profound i

148 ontaining three copies of the alpha2 subunit are inhibited by low concentrations of physostigmine in

149 Proliferation was higher in BERKO NPCs and was inhibited by LY3201.

150 TCR signaling is inhibited by M. tuberculosis cell envelope lipoglycan

151 Finally, CXCL10-increased MMP-9 secretion was inhibited by methylprednisolone and also by compound

152 HPV could be inhibited by mitochondrial superoxide inhibitors prov

153 The influx was inhibited by MK-801, a specific pore blocker of N-Me

154 replication and that JCV DNA replication can be inhibited by MK2206, a compound that is specific for

155 The effect of LTE4 was inhibited by montelukast, a CysLT1 antagonist.

156 nes, Atg3, Atg5, and Atg7 were identified to be inhibited by MPA treatment.

157 ects of CCL2 and CCL21 on inflammatory cells were inhibited by MSC-Exo.

158 tored cap-dependent translation, which could be inhibited by mTOR inhibitors.

159 , but the activity of newly synthesized ULK1 is inhibited by mTOR.

160 bound signal with oxidation/reduction, which is inhibited by mutation of three tyrosine residues.

161 r-500 is found to require Ca(2+) and CaM and is inhibited by mutations that compromise binding of pho

162 ng for antibacterial therapy and reported to be inhibited by naphthoquinones.

163 ed CA-MRSA lyse by an unknown mechanism that is inhibited by necrostatin-1, an allosteric inhibitor o

164 bisphosphate carboxylase/oxygenase (rubisco) is inhibited by nonproductive binding of its substrate r

165 Indeed, we find that hEndoV cleavage is inhibited by normal intracellular ATP concentrations.

166 tudy, we revealed that Mo-DC differentiation was inhibited by NOX inhibitors and reactive oxygen spec

167 band of about 14.5 kDa and this recognition was inhibited by nPho d 2.

168 d down-regulation of antiapoptotic genes can be inhibited by overexpressing GLI1 in AA-sensitive cell

169 morphological signs of microglia activation are inhibited by P2X7R antagonists and (10)Panx1 and are

170 ith an increase in the protein amount, which was inhibited by p300 RNAi.

171 h through wingless production when apoptosis is inhibited by p35.

172 was significantly reduced, and this dilation was inhibited by paxilline but not by 4-aminopyridine, d

173 ced by uterotonics, and this reversal effect is inhibited by pertussis toxin and by genetic deletion

174 However, the increase was inhibited by pertussis toxin as well as by wortmanni

175 on, increase in the [Ca(2+)]c and cell death were inhibited by PF431396, a Ca(2+)-sensitive PYK2 inhi

176 (PFAAs) indicated that dechlorination could be inhibited by PFASs but that the inhibition depends on

177 enal transplantation, pulmonary tumor spread was inhibited by pharmacologic blockade of aldosterone e

178 Endoplasmic reticulum (ER) stress was inhibited by pharmacological (tauroursodeoxycholic a

179 We found that PgpB was inhibited by phosphatidylethanolamine (PE) in a comp

180 .1b, from the flowering plant Papaver rhoeas were inhibited by phosphorylation.

181 emonstrate that P. aeruginosa quorum sensing is inhibited by physiological levels of serum albumin, w

182 Both inward currents and 5-HT release were inhibited by Piezo2 small interfering RNA and antag

183 trus stage of the menstrual cycle of females was inhibited by pioglitazone, suggesting that an estrog

184 ion constituted a regulatable step and could be inhibited by Pirk, an endogenous feedback regulator o

185 2/Zn(2+) induced substantial cell death that was inhibited by PJ34 and DPQ, PARP inhibitors, 2-APB, a

186 olic Ca(2+) concentration ([Ca(2+)]c), which was inhibited by PJ34, a PARP inhibitor, and abolished b

187 Anaphylaxis was inhibited by platelet-activating factor receptor or

188 ranscription of four tRNA genes was shown to be inhibited by ppGpp.

189 Classical complement activation was inhibited by pretreatment of complement with an anti

190 Finally, E-2 effects were inhibited by pretreatment with the ASIC3 blocker AP

191 versely, hydrotropism, but not gravitropism, is inhibited by preventing differential cell-length incr

192 Ovulation was inhibited by preventing the periovulatory rise in th

193 l at the BBB level and these processes could be inhibited by probucol and L-thyroxine.

194 itionally, HCV infection and cell attachment were inhibited by PS but not by phosphatidylcholine (PC)

195 N cells), whose activity generates movement, are inhibited by Purkinje cells and excited by mossy fib

196 but not proinflammatory cytokine secretion, was inhibited by rapamycin in mDCs.

197 ell wall precursor, UDP-MurNAc-pentapeptide, is inhibited by region 3.2 of sigma subunit, possibly pr

198 Proximal cartilage formation was inhibited by removal of periosteum and could be reca

199 ATPase and ATP-dependent helicase activities are inhibited by Rev in a dose-dependent manner, althoug

200 ion 2 domain-containing phosphatase-1, which is inhibited by ROS.

201 Aa-induced IL-6 and IL-8 production was inhibited by rosuvastatin, particularly at higher do

202 xogenous interferon (IFN) administration can be inhibited by rotaviral replication both in vitro and

203 d by channels with characteristics of TRPA1, being inhibited by ruthenium red, isopentenyl pyrophosph

204 o-expression of the propeptide in trans SBT3 was inhibited by SBT3PP with a Kd of 74 nm for the enzym

205 hat both formate oxidation and CO2 reduction are inhibited by selective inhibitor binding to the Mo(V

206 ptake carriers of metformin and oxaliplatin, were inhibited by several clinically used TKIs.

207 3-ASC-caspase-1 inflammasome-induced pathway was inhibited by short hairpin RNA (shRNA), HBoV1-induce

208 FI6 When the expression of BIRC5 and/or IFI6 was inhibited by shRNA, the infected cells underwent apo

209 proteins in Nox4-deficient lung fibroblasts is inhibited by silencing of nuclear factor erythroid-de

210 Unwanted greening can be inhibited by simply changing the liquid sweetener.

211 sglutaminase activity in a manner that could be inhibited by small molecules targeting TG2 or TRX.

212 ein to non-physiological low pH in vitro and is inhibited by small molecule compounds, such as the dr

213 ves interaction between Smc ATPase heads and is inhibited by Smc3 acetylation.

214 nd to be partially dependent on IRE1b and to be inhibited by sodium 4-phenylbutyrate, suggesting that

215 nal proximal tubular epithelial cells, which was inhibited by sodium hydrosulfide (NaHS), a source of

216 nse to microenvironmental stiffening and can be inhibited by softening.

217 replication of EV-D68 in diverse cell types was inhibited by soluble ICAM-5 fragments.

218 Salt appetite was inhibited by spironolactone.

219 is a heat-stable ribonuclease whose activity was inhibited by Ssl2245 at optimal temperatures but not

220 ilution assays, subcutaneous tumor formation was inhibited by ST6Gal-I knockdown, whereas in a chemic

221 tion depended on cholesterol and podocin and was inhibited by stabilization of the actin cytoskeleton

222 ween MYC and mevalonate signaling, which can be inhibited by statin or 6-fluoromevalonate treatment.

223 store-operated PKC phosphorylation of TRPC1 was inhibited by STIM1 shRNA.

224 en TRPC1, STIM1, Galphaq and PLCbeta1, which were inhibited by STIM1 knockdown.

225 erated TRPC1 channel and PLCbeta1 activities were inhibited by STIM1 short hairpin RNA (shRNA) and ab

226 rmation in NSCLC cells, and these activities were inhibited by SU11274.

227 AGE-mediated autophagy is inhibited by suppression of PI3K and potentiated by t

228 d by overexpression of alphaB-crystallin but was inhibited by suppression of alphaB-crystallin.

229 ivity that desialylated PC12 cells and could be inhibited by Tamiflu, a neuraminidase (sialidase) inh

230 cancer cells promotes metastasis, which can be inhibited by targeting HIF-1alpha with RNA interferen

231 Early studies concentrated on molecules and were inhibited by template size complexity.

232 Ps have limited access to cleavage sites and are inhibited by tension on the fibril.

233 rin but that virion dissemination via plasma is inhibited by tetherin and is required for full MoMLV

234 by Ag stimulation, but Egr2 and 3 expression was inhibited by Th1-inducing cytokines.

235 Na(+) binding to the glutamate-bound state, are inhibited by the A334E substitution.

236 gma that all class I-III Fic domain proteins are inhibited by the inhibitory alpha-helix.

237 cate dose-dependent cytotoxic effects, which are inhibited by the nitric oxide synthase (NOS) inhibit

238 bserved to induce Ca(2+) influx, which could be inhibited by the addition of a naturally occurring ch

239 to-allergic volunteers and the binding could be inhibited by the addition of natural mosquito extract

240 lcium was higher after blue/green, and could be inhibited by the ion channel blocker, capsazepine.

241 th an oxidative phenotype are most likely to be inhibited by the mandelalides.

242 This translocation can be inhibited by the NTS-derived peptide (EPE) that block

243 Cell death could be inhibited by the singlet oxygen scavenger histidine i

244 This activity can be inhibited by the viral NS1 protein.

245 AM2 is inhibited by the amantadine class of antiviral drugs,

246 ssion in the anterior central brain of males is inhibited by the B isoform of Fru, whose DNA binding

247 y environmentally relevant Mn(III/IV) oxides is inhibited by the buildup of solid-phase Mn(II/III), s

248 egulators of NETs and show that the response is inhibited by the cell-cycle inhibitor p21(Cip).

249 e secondary immune response happens next and is inhibited by the CTLA4 pathway.

250 that in activated T cells, Ca(2+) clearance is inhibited by the endoplasmic reticulum Ca(2+) sensor

251 Hypoxic root bending is inhibited by the group VII ethylene response factor (

252 MITF transcriptional activity is inhibited by the histidine triad nucleotide-binding p

253 NKG2D expression in NK cells is inhibited by the histone deacetylase (HDAC) inhibitor

254 in a HIF1alpha methylation-dependent manner is inhibited by the LSD1/NuRD complex.

255 APC/C is inhibited by the Mitotic Checkpoint Complex (MCC), wh

256 he primary immune response appears first and is inhibited by the PD1-PDL1 axis, whereas the secondary

257 10) in late prophase I, the repair of which is inhibited by the presence of HORMAD1/2 on unsynapsed

258 ne to thiocholine where the activity of AChE is inhibited by the presence of organophosphate pesticid

259 The APC/C is inhibited by the spindle checkpoint in the presence o

260 in the presence of its complementary strand is inhibited by the stability of the template duplex.

261 sion also increases during filamentation and is inhibited by the transcription factors Sut1 and Sut2.

262 tions, the pacemaking activity in DA neurons is inhibited by the TRPC1-STIM1 complex.

263 In unstimulated cells, pathway activity is inhibited by the tumor suppressor membrane protein, P

264 inhibitors okadaic acid and microcystin, but is inhibited by the tyrosine phosphatase inhibitor ortho

265 Protein translation is inhibited by the unfolded protein response (UPR)-indu

266 mice, and its replication in cultured cells is inhibited by the zinc finger antiviral protein (ZAP),

267 sufficient to induce lysis, and ApoL1 lysis was inhibited by the antioxidant DPPD.

268 S. aureus occurred via an active process and was inhibited by the beta-lactam antibiotic oxacillin, w

269 Pressure-induced secretion was inhibited by the mechanosensitive ion channel antago

270 Activation of enteric neurons was inhibited by the nicotinic receptor antagonists hexa

271 Cell death was inhibited by the RIPK3 inhibitor, GSK872, and infect

272 Cell death by acute water stress was inhibited by the singlet oxygen scavenger histidine

273 ranscription factors Bcl6, E2A and TCF-1 but was inhibited by the transcriptional regulators Blimp1,

274 amycin-enhanced migration of TSC2-null cells was inhibited by the uPA inhibitor UK122, dexamethasone,

275 Here, we found that AKAV and SBV infections were inhibited by the addition of heparin or enzymatic r

276 These effects of CXCL12 on HMVP2 cells were inhibited by the CXCR4 antagonist AMD3100 as well a

277 itic extensions in 2D and 3D matrix cultures were inhibited by the GPR Q34A peptide compared with a w

278 ation of wild type gastric tissues and these were inhibited by the nitric oxide synthase inhibitor L-

279 Swelling-evoked [Formula: see text] signals were inhibited by the TRPV4 antagonist HC067047 (IC50 ap

280 of Cryptochrome (Cry) and Period (Per) genes is inhibited by their protein products.

281 InsR function was inhibited by three different mechanisms: InsR short

282 plasmacytoma variant translocation 1 (PVT1) was inhibited by transfection of primary ASMCs with smal

283 This effect was inhibited by transfection with siRNA anti-STAT3, sug

284 This redistribution was inhibited by treatment with nocodazole, colcemid, or

285 Falpha- or LPS-induced activation of WT PAEC was inhibited by treatment with rabbit anti-HMGB1 antibo

286 by protein ligation assays; this interaction is inhibited by trifluoperazine, a drug known to hamper

287 Store-operated TRPC1 channel activity was inhibited by TRPC1 and STIM1 antibodies and STIM1 sh

288 y increased in cells in which TRPM2 function was inhibited by TRPM2-S, and pretreatment of these cell

289 iring of Adelta-fibers (not C-fibers), which was inhibited by TRPV4 and P2X3 receptor antagonists.

290 t TBK1, a core kinase of antiviral pathways, is inhibited by tyrosine phosphorylation.

291 from the cell membrane to the cytosol, which were inhibited by U73122.

292 dicating that this decomposition pathway can be inhibited by use of substrates in which the olefin be

293 Activation of WNT signaling can be inhibited by various agents.

294 Myocyte KV currents are inhibited by vasoconstrictors, including angiotensin

295 The reaction catalysed by GABA-T is inhibited by vigabatrin, whereas both GABA-T and AGXT

296 of latent HIV-1 infection in CD4(+) T could be inhibited by viral-specific CD8(+) T cells, a result

297 onse to TNFalpha stimuli was detected, which was inhibited by vitamin D.

298 The cross-linked complex is inhibited by WASP's CA region, even though CA potentl

299 al neurons and of zebrafish single cell RGCs were inhibited by zebrafish M1-4, rat M1-4, and Nogo-A d

300 tivity of BbHtrA revealed that this protease is inhibited by Zn(2+) > Cu(2+) > Mn(2+).