ライフサイエンスコーパス: be inhibited by

1 The vasodilatation was inhibited by 1 mum tetrodotoxin and 5 mum guanethidi

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

3 nt was smaller than open-channel current and was inhibited by 10 muM Zn(2+) Extreme hyperpolarization

4 The oxidation of fish oil was inhibited by 2-3 fold, compared to its unencapsulate

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

6 Wild type C. thermocellum is inhibited by 5 g/L n-butanol.

7 aneously implanted into immunodeficient mice was inhibited by 5-fluorouracil.

8 aneously implanted into immunodeficient mice was inhibited by 5-FU.

9 on of (67)Cu-CuSarTATE (5 MBq), tumor growth was inhibited by 75% compared with vehicle control.

10 Both transporters are inhibited by a common competitive mechanism with pot

11 SREBPs are inhibited by a complex composed of INSIG proteins, S

12 reveals the mechanism by which SidE ligases are inhibited by a SidJ-calmodulin glutamylase, and open

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

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

15 Ferroportin is inhibited by a peptide hormone, hepcidin.

16 access to the cluster and show that Mtb-DHAD is inhibited by a recently discovered herbicide, aspterr

17 S1P activation of nodose C-fibres is inhibited by a S1PR3 antagonist.

18 by a shift to pH 8 upon light adaptation and is inhibited by a shift to pH 7 upon dark adaptation.

19 It is shown that the enzyme is inhibited by a variety of negatively charged phosphol

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

21 D) antibodies that mediate hemolysis in vivo was inhibited by a humanized monoclonal antibody (mAb) t

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

23 cognition of Der p 2 by the first three hIgE was inhibited by a single murine IgG, but the fourth hIg

24 rgdorferi and neutrophil migration to LTB(4) were inhibited by AC.

25 l root ganglion (DRG), native TRPM3 channels were inhibited by activating G(s)-coupled prostaglandin-

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

27 revealed functional activity of Cx43, which was inhibited by administration of Gap19 peptide mimetic

28 Several kinases are known to be inhibited by ADP.

29 Rca is inhibited by ADP, and the extent of ADP sensitivity o

30 At the lysosomal membrane, CMA is inhibited by Akt-dependent phosphorylation of the CMA

31 on, a process requiring farnesylation, which is inhibited by alendronate.

32 d other Mc4r neurons in spinal lamina X that are inhibited by alpha-MSH, which is in line with previo

33 Binding to CHX ImmunoCAP was inhibited by ALX in 1/32 sera, and binding to PHMB w

34 We show that centromere translocation can be inhibited by an evolutionarily conserved pole-localiz

35 BE2N through Ub(Gln40) in a process that can be inhibited by another Legionella effector, Lpg2149.

36 rapid increase in transmembrane current that was inhibited by antagonists of the mechanogated channel

37 metastasis of breast and liver cancer cells are inhibited by anti-Cnx antibodies.

38 ion, cellular activation induced by gp120 V2 is inhibited by anti-alpha(4)beta(7) monoclonal antibodi

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

40 otrophic activity of esophageal cancer cells was inhibited by anti-NGF blocking antibodies.

41 ocyte progenitor cell differentiation, which is inhibited by antibiotics but unaffected by our other

42 -dependent, involves ERK-MAPK-signalling and is inhibited by antibodies against amphiregulin, an EGFR

43 hesion to the PF4-VWF-HIT antibody complexes is inhibited by antibodies that block FcgammaRIIA or the

44 We determined that recall responses were inhibited by antibody feedback, potentially via epi

45 amp recording, we found that THIK-1 currents were inhibited by application of IBMX with an IC(50) of

46 for the facilitated dissociation pathway can be inhibited by applied forces.

47 ion of one or more chemosensory neurons that are inhibited by attractive odors.

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

49 , eggplants, pepper, petunia and tobacco can be inhibited by Avr2 with the exception of tobacco Rcr3.

50 +) T cell-mediated immunity against Brucella is inhibited by B cells.

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

52 In bacteria, Cas12a enzymes can be inhibited by bacteriophage-derived proteins, anti-CRI

53 AT1-B2 receptor aggregation was inhibited by beta-arrestin-mediated downregulation.

54 able to digest penicillin and this activity was inhibited by beta-lactamase inhibitor, i.e. sulbacta

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

56 01-restricted Gag(181-189)CM9 epitope, could be inhibited by blockade of MHC-I presentation.

57 Tumor cell migration to LECs was inhibited by blocking CXCL11 whereas recombinant CXC

58 ucleatum subspecies in vitro; an effect that was inhibited by blocking or mutating the adhesin RadD o

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

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

61 Here we report that OPC differentiation is inhibited by both effector T cells and IFNgamma overe

62 T (Ser473) expression (as a readout of PI3K) was inhibited by both drugs but less markedly so than ph

63 Although the growth of VRE is inhibited by BP(SCSK) and L. lactis in vitro, only BP

64 ssium into the cell, and both KimA and KtrCD are inhibited by c-di-AMP in vivo For KimA, c-di-AMP-dep

65 Platelet SFKs are inhibited by C-terminal Src kinase (Csk), which phos

66 tation and amplified copy numbers, which can be inhibited by c-MET small molecule inhibitors.

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

68 pha-Actinins are major F-actin bundlers that are inhibited by Ca(2+) in nonmuscle cells.

69 In contrast to the mammalian homologs, CALX is inhibited by Ca(2+) binding to CALX-CBD1, whereas CAL

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

71 ly export miR-375-3p to HDL and this process is inhibited by cellular mechanisms that promote insulin

72 had difficulty becoming proficient when MLIs were inhibited by chemogenetic intervention.

73 When protein synthesis was inhibited by CHX, MeHg promoted the degradation rate

74 te that lung and circulating hepcidin levels are inhibited by cigarette smoke.

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

76 gambiense surface glycoproteins can be inhibited by circulating antibodies of gHAT patients

77 form of T-type calcium channels (T-channels) is inhibited by clinically relevant concentrations of vo

78 iation and cue-induced selective translation are inhibited by co-exposure to translation-repressive c

79 on, invasion, and metastasis of cancer cells is inhibited by co-expression of the glycoprotein E-cadh

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

81 isms regulating YAP1 in rhabdomyosarcoma can be inhibited by combinatorial therapy of DNMTi and dasat

82 ed to an inert polymer scaffold, and binding was inhibited by competing dextran sulfate.

83 Neurons in which GCase was inhibited by conduritol beta-epoxide did not increas

84 nhibitors of human and mouse SAMD9&L, it can be inhibited by cowpox virus CP77, indicating that OPXVs

85 Yet, practical usage of these fuels is inhibited by current gas storage technology.

86 ce mutations, T790M and C797S, can no longer be inhibited by currently approved EGFR TKIs.

87 uggesting that the reduction of IMs will not be inhibited by cyclic nitramines, but degradation dynam

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

89 sitively regulated by microRNA-128-3p, which was inhibited by CYP2J2.

90 d with a higher expression of enzymes, which are inhibited by cytotoxic agents.

91 ess of a bladder cancer stem cell population was inhibited by decitabine treatment in mice.

92 r, when endosome translocation or exocytosis was inhibited by depletion of Protrudin or Synaptotagmin

93 to removal by several KDM subfamilies which are inhibited by DFP in cell-free assay.

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

95 Furthermore, when the AKT gene (HdAKT) was inhibited by double-stranded RNA (dsRNA), expression

96 he budding yeast nucleus when cell expansion is inhibited by down-regulating components of the secret

97 ition by E4orf4 earlier during infection but is inhibited by E4orf4 as infection progresses.

98 ream target of mTORC1, ribosomal protein S6, was inhibited by EAD1.

99 ion channel expressed in the wing disc, and are inhibited by EGTA and by the GluR inhibitor NASPM (1

100 The increased membrane current was inhibited by either 2 mM calcium, or 5 uM gadolinium

101 We found that when SIRT1 was inhibited by either chemical or genetic manipulation

102 Both of these systemic signals were inhibited by either disruption of both GLR3.3 and G

103 tinol-isomerase activities of Rpe65 and Des1 are inhibited by emixustat and fenretinide, respectively

104 us Ca(2+) ionophore and malate, was shown to be inhibited by exogenous application of a CaM inhibitor

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

106 ytes, but not in those of the LV base, which is inhibited by expression of the nuclear phospho-ERK1/2

107 These d[Na(+) ](i) /dt increases are inhibited by EZA and blocked by EIPA, a Na-H exchang

108 tion of several proteins TLR4 signal pathway was inhibited by FK866-mediated NAD(+) depletion, specif

109 lines and primary cells ex vivo, CDN uptake is inhibited by folates as well as two medications appro

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

111 tant pathway after the 1st wave of spreading is inhibited by FTY720.

112 YC promoter and DDX5-mediated MYC activation is inhibited by G4-interactive small molecules.

113 and neuronal sensitisation which in turn can be inhibited by gabapentin, suggesting a potential role

114 This pathway was inhibited by Galpha(q)QL and Galpha(13)QL, which als

115 TRPM3) is a nonselective cation channel that is inhibited by Gbetagamma subunits liberated following

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

117 n of structural differences with a Bgl3 that is inhibited by glucose.

118 otoneurons controlling postural muscles that are inhibited by glycinergic transmission during REM sle

119 n' mechanism and suggest that rRNA promoters are inhibited by GreB/DksA because their short-lived RNA

120 tically, attachment, which we anticipated to be inhibited by H84T, was only somewhat decreased by the

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

122 s on Ca(2+) but not on ATP concentration and is inhibited by heparin, caffeine, and 2-aminomethoxydip

123 n cultured under hyperglycemic stress, which was inhibited by heparin.

124 Unexpectedly, L. pneumophila can itself be inhibited by HGA secreted from neighboring, isogenic

125 ns) variants display much lower activity and are inhibited by high concentrations of H(2)O(2) upon ad

126 te to aggregation of PFV intasomes which may be inhibited by high ionic strength buffer or the small

127 HO expression in daughter cells is inhibited by high concentration of Ash1 in daughters.

128 ty is increased through NAA15 tethering, but is inhibited by HYPK through structural alteration of th

129 ntal advances, small molecule identification is inhibited by (i) chemical reference libraries (e.g.,

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

131 enhances insulin binding and signaling which is inhibited by IGF1Ralpha.

132 ltaN exhibited enhanced proliferation, which was inhibited by IGFBP2 short interfering RNA treatment.

133 he important roles of genes whose expression is inhibited by IL-33 in key cellular processes associat

134 worsened airway disease, and this worsening was inhibited by IL-9 neutralization.

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

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

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

138 is supported by the LCN2/SLC22A17 system and is inhibited by iron chelation therapy.

139 pose tissue and increased leptin levels that were inhibited by iron.

140 ally, when the functions of OATP1A2 in cells are inhibited by its substrates or an inhibitor or block

141 crease in [Ca(2+)](i) and PS exposure, which was inhibited by its antagonist Dooku1 and the PIEZO1 in

142 ng phagocytosis, the growth of C. neoformans is inhibited by KCs in an IFN-gamma independent manner.

143 bitors, while expressed IKCa channel current was inhibited by known IKCa channel blockers.

144 opment of treatments for vocal dysphonia has been inhibited by lack of human vocal fold (VF) mucosa m

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

146 d silently, mainly through phagocytosis, and was inhibited by latrunculin A.

147 r factor-activated T-cells 1 (NFATc1), which was inhibited by LDN treatments.

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

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

150 with recombinant DSG1; these IgG1 antibodies were inhibited by LJM17, LJM11, and DSG1 in a dose-depen

151 nd increased vascular hyperpermeability; all were inhibited by losartan.

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

153 neonatal rat ventricular myocyte hypertrophy are inhibited by mAKAPbeta signalosome targeting.

154 HP5 is inhibited by Manduca sexta serpin-4, serpin-1A, and s

155 associated with enhanced tumor growth, which were inhibited by metformin.

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

157 r beta-catenin in the nucleus of SW480 cells was inhibited by methyltransferase inhibition, EIPA, or

158 ATP synthase that activates the MMC/PTP, and were inhibited by Mg(2+) and adenine nucleotides, which

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

160 he adaptor proteins MyD88 and TRIF, and this is inhibited by MK2.

161 We also noted that this aggregation effect was inhibited by MQ and PRIMA-1.

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

163 ulator and the only known ClpXP adaptor that is inhibited by multiple but dissimilar antiadaptors (Ir

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

165 uronal reprogramming when the muscle program is inhibited by Myt1l.

166 lammatory responses in LPS-exposed monocytes were inhibited by NAD(+) depletion with FK866, 3) the in

167 -acetyl-modified Sia; however, while IAV NAs were inhibited by Neu5Gc and O-acetyl modifications, the

168 we show for the first time that MOC neurons are inhibited by neurons of the MNTB, which may suppress

169 kb) deletion fragments of the ITPR3 promoter were inhibited by NF-kappaB subunits.

170 oxidase, which is a major source of NO, also is inhibited by NO, thereby reducing the respiratory rat

171 nd African green monkey kidney (Vero) cells, was inhibited by noncytotoxic concentrations of the lyso

172 r) and Nox5 siRNA, while p53 phosphorylation was inhibited by NoxA1ds (Nox1 inhibitor).

173 eurons innervating the first olfactory relay are inhibited by odorants (Zhang and Gaudry, 2016).

174 CSDn processes in the antennal lobe are inhibited by odors in an identity independent manner

175 BHT scavenging activity was inhibited by organic acids.

176 Since Riplet is known to be inhibited by other RNA viruses, such as such influenz

177 poptosis of HCV-infected hepatocytes and can be inhibited by overexpression of ATM from a clone lacki

178 IL-6-induced VEGFR2 up-regulation was inhibited by overexpression of DNMT1.

179 Phosphatase activity of Siw14 was inhibited by oxidation that was reversible.

180 Additionally, we report that SLO2.1 is inhibited by oxytocin binding to the oxytocin recepto

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

182 elements to NF-kappaB, and promoter activity was inhibited by p65/p50.

183 s lacking defects in DNA repair whose growth is inhibited by PARPi.

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

185 This unfoldase activity is inhibited by Pex3, a membrane protein proposed to reg

186 rts co-substrates (Na(+) and glucose) and it is inhibited by phlorizin in electrophysiological experi

187 .1b, from the flowering plant Papaver rhoeas were inhibited by phosphorylation.

188 ze the otolith circuit until they themselves are inhibited by photoreceptors in response to dimming,

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

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

191 protein expression of p53, and these effects were inhibited by pifithrin-alpha.

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

193 s from healthy volunteers, a phenomenon that was inhibited by platelet P-selectin neutralization or i

194 Anaphylaxis was inhibited by platelet-activating factor receptor or

195 extracts from nocodazole-arrested HeLa cells was inhibited by Polo-like kinase 1 (Plk1), as suggested

196 the presence of a cystogenic activator that is inhibited by polycystins and an independent but relat

197 patient and healthy control sera, and could be inhibited by pre-incubation with IgG1 Fc.

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

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

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

201 CSE is inhibited by propargylglycine (PPG), a widely used me

202 ct cardioprotective effect at the myocardium is inhibited by propofol.

203 3 cell extracts requires methylcobalamin and is inhibited by propyl iodide, a specific inhibitor of c

204 NHE3 is inhibited by protein kinase A.

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

206 eurydendroid neurons (ENs) in teleost fish, are inhibited by Purkinje cells and excited by parallel

207 Herein, we demonstrate that both kinases are inhibited by quercetin and 16 related flavonoids; IP

208 igher eukaryotes), and that this interaction is inhibited by R37Me and K49Ac modification on Cse4.

209 local delivery of both Ag and costimulation, is inhibited by rapamycin treatment during secondary CD8

210 Adenosine-induced NET formation was inhibited by recombinant ADA2, A(1)/A(3) AR antagoni

211 XPR1-mediated Pi efflux was inhibited by reducing cellular InsP(8) synthesis, ei

212 y to treat broad classes of viruses known to be inhibited by Retro-2.

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

214 ased cardiomyocyte binucleation, which could be inhibited by RGD peptide treatment.

215 the developed protocol could be observed and was inhibited by ribavirin.

216 activation and thrombus formation, which can be inhibited by rivaroxaban.

217 ild type phenotype when beta(2)-m expression was inhibited by RNA interference (RNAi).

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

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

220 rbamylation of Fremyella recombinant rubisco was inhibited by RuBP, but this inhibition was not relie

221 t intracellular double-stranded RNA (dsRNA), was inhibited by RV.

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

223 Tumour growth was inhibited by sensory denervation or pharmacological

224 n of STAT3 target genes MUC1 and OSMR, which were inhibited by SFX-01 in patient samples.

225 R-802 by aromatic hydrocarbon receptor (AHR) is inhibited by SHP.

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

227 egarding which specific cyclin/CDK complexes are inhibited by SIM in vivo.

228 neurons whose response to the visual adapter was inhibited by simultaneous photo-stimulation, RS to v

229 sponsiveness to exogenous Wnt ligands, which is inhibited by siRNA-mediated knockdown of Lef1.

230 ng its 3'UTR (untranslated region) and could be inhibited by SIRT1 via histone deacetylation.

231 HF23 recognizes the histone mark H3K4me3 and is inhibited by small molecule compounds, including disu

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

233 lation of Col3a1 and Col1a1 in PTH1R-VKO VSM was inhibited by small interfering RNA targeting Mkl1 an

234 ter (ABCC3pr) revealed that ABCC3pr activity was inhibited by SOX17 expression and SOX2/SOX9 silencin

235 tx2 transcriptional activity and DNA binding is inhibited by Sox2, and this interaction controls gene

236 Rather, adenosine-induced depotentiation is inhibited by specific antagonists of p38 MAPK, but no

237 ne alphaherpesvirus pseudorabies virus (PRV) was inhibited by sphingomyelin-depletion of cells.

238 [PSI+] prion generation/propagation may be inhibited by Ssb1/2/RAC chaperones by ensuring proper

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

240 When the function of OATP1A2 in cells was inhibited by substrates or inhibitors, attachment an

241 oxoglutarate) as an obligate cosubstrate and are inhibited by succinate, fumarate, and 2-hydroxygluta

242 It cleaved penicillin and was inhibited by sulbactam.

243 trogen starvation and osmotic stress and can be inhibited by sulfide.

244 Neurons in different IO subnuclei are inhibited by synapses with wide ranging release kine

245 MAPK signaling can be inhibited by targeting MEK1/2; unfortunately, this ap

246 s injected to express small intestinal GLUTs were inhibited by teas, but SGLT1 was not.

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

248 ect of H(2)O(2) The H(2)O(2)-induced current was inhibited by tetrodotoxin as well as the cation chan

249 endogenous brakes for GLS1 expression, which are inhibited by TGF-beta.

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

251 at GSK3alpha and to a lesser extent GSK3beta are inhibited by the advanced clinical candidate tivanti

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

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

254 e microbial degradation of one pollutant may be inhibited by the toxicity of another.

255 lask, preventing the palladium catalyst from being inhibited by the high concentrations of ammonia, s

256 bosome remains active, while its hibernation is inhibited by the caseinolytic protease (Clp) system i

257 media increases macrophage migration, which is inhibited by the CCL5/CCR5 antagonist maraviroc.

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

259 This process is inhibited by the cytokine IL-37.

260 pen fullerene, was completed, even though it is inhibited by the endohedral molecule.

261 ic stellate cells (PSCs) into myofibroblasts is inhibited by the estrogen-receptor modulator, tamoxif

262 e that the Drosophila PLK Polo kinase (Polo) is inhibited by the female meiosis-specific protein Matr

263 nd displacements with ever greater precision is inhibited by the Heisenberg uncertainty principle, wh

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

265 tion of conjugation genes from promoter P(Q) is inhibited by the master regulator PrgX, further repre

266 ositol 4,5 bisphosphate but this interaction is inhibited by the N-terminal segment of RIAM.

267 We found that this effect is inhibited by the potent human TAS2R46 (hTAS2R46) anta

268 f in regards to the catalytic subunit, which is inhibited by the regulatory subunits in the absence o

269 kinase-activated protein kinase 2 (MK2) but is inhibited by the RNA-binding protein tristetraprolin

270 guinis imports 5-HT through a mechanism that is inhibited by the selective 5-HT reuptake inhibitor fl

271 cal to their increased commercialization but is inhibited by the slow oxygen exchange kinetics at the

272 The hypersensitivity of PUT3OE is inhibited by the sos1 and sos2 mutations, which indic

273 MMP enzymatic activity is inhibited by the tissue inhibitor of metalloproteinas

274 pioglitazone, but this trans-differentiation is inhibited by the transcription factor NK2 homeobox 1

275 tracellular TGF-beta signaling in adipocytes is inhibited by the transcriptional factor PPARgamma, sp

276 e to drive signaling and that this structure is inhibited by the unliganded ectodomain.

277 made within the peptide, and this conversion was inhibited by the anti-amyloid compound epigallocatec

278 Wnt-induced endolysosomes within 30 minutes was inhibited by the depletion of methionine, an essenti

279 The HPK1-mediated AXL degradation was inhibited by the endocytic pathway inhibitors leupep

280 to mouse AtoMs, and human osteoclastogenesis was inhibited by the FoxM1 inhibitor thiostrepton, const

281 RHV-rn1 replication was inhibited by the HCV polymerase inhibitor sofosbuvir

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

283 ytic activity of the Ser/Thr kinase Aurora A was inhibited by the oxidation of a conserved cysteine r

284 ease induced by 12(S)-HETE-lysophospholipids was inhibited by the TNFalpha converting enzyme inhibito

285 These effects were inhibited by the 5-HT(2C) receptor-specific inverse

286 The effects of T were inhibited by the ER antagonist tamoxifen and aromat

287 agate independently of extracellular ATP and were inhibited by the gap junction blockers 1-octanol an

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

289 Both mutants were inhibited by the TRPM3 antagonist primidone, sugges

290 y, tumour growth and abnormal bone formation are inhibited by these direct effects and by the disrupt

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

292 ptotic cell death and lipid peroxidation can be inhibited by treatments that induce or mimic energy s

293 While the Chinese hamster SAMD9L could not be inhibited by two previously identified OPXV inhibitor

294 ScPpz1 is inhibited by two regulatory proteins, Hal3 and Vhs3,

295 K2 recycling to synaptic membranes after TBS is inhibited by Ube3a.

296 technique for nanoscale chemical imaging has been inhibited by various experimental challenges, such

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

298 , was independent of nucleotide primers, and was inhibited by viral Z protein.

299 of USP7 interaction, while lytic replication was inhibited by vIRF-2, in part or in whole via USP7 in

300 Yoda1 evoked Ca(2+) entry was inhibited by Yoda1 antagonist Dooku1 as well as othe