ライフサイエンスコーパス: inhibition by

1 s in HeLa cells, which are more sensitive to inhibition by 1 in the presence of the glycolysis inhibi

2 acosamide block was very weak at -120 mV (3% inhibition by 100 microM lacosamide) but greatly enhance

3 osamide) but greatly enhanced at -80 mV (43% inhibition by 100 microM lacosamide), where there is par

4 agnitude), and pharmacology (enhancement and inhibition by 2-aminoethoxydiphenyl borate).

5 CatS inhibition by a cell-permeable inhibitor abrogated the r

6 rate specificity, allosteric regulation, and inhibition by a class of small molecules that are curren

7 Differential inhibition by a common inhibitor revealed that all three

8 we examined the adaptive response to VEGF-A inhibition by a loss-of-function analysis using plasmid-

9 rine-aspartate repeat protein SdrC and their inhibition by a peptide.

10 al vector injection with chronic 4 week PREP inhibition by a potent small-molecule PREP inhibitor, 4-

11 , we investigated the impact of chronic PREP inhibition by a small molecule inhibitor, 4-phenylbutano

12 ed for both the MDM2-p53 interaction and its inhibition by a small-molecule Nutlin-3 drug analogue kn

13 Notably, PIP4Ks inhibition by a131 causes reversible growth arrest in no

14 copy of the pharmacological effects of PIP4K inhibition by a131.

15 thaliana seedling roots is more sensitive to inhibition by A2C than is cotyledon growth.

16 rin interactions were also less sensitive to inhibition by abciximab and eptifibatide.

17 Inhibition by acetylene of reductive dechlorination and

18 contributing to their relative resistance to inhibition by AE.

19 and decreased with leptin receptor signaling inhibition by AG490, a JAK2/STAT3 inhibitor.

20 Exoelectrogenesis recovery from inhibition by all compounds was observed at different ra

21 ons showed significant differences in pSTAT6 inhibition by all concentrations of indomethacin and asp

22 caused reduced inhibition or highly reduced inhibition by all NA inhibitors.

23 latively insensitive to activation by FAs or inhibition by allosteric inhibitors.

24 ble aggregate-bound plasmin is shielded from inhibition by alpha2-antiplasmin and degrades amorphous

25 form of the complex, allowing more efficient inhibition by an inhibitor whose quantity is limited.

26 This inhibition by anionic membranes could be a potential mec

27 lity, and biosynthesis potential and reduced inhibition by anti-drug antibodies.

28 for exploring mechanisms of virus infection inhibition by antibodies.

29 ibutes to clot stability and is resistant to inhibition by antithrombin/heparin while still susceptib

30 m proliferation was successfully tested with inhibition by aphidicolin.

31 This study demonstrated that dual PI3K/mTOR inhibition by apitolisib was less effective than was eve

32 Significant inhibition by apple phenolics was found as compared to t

33 ts on the dynamics of HIV-1 protease and the inhibition by APV and DRV, providing useful information

34 ral basis of the mechanism underlying fusion inhibition by Arbidol has remained obscure, thereby hind

35 We show that PKA inhibition by ARHGAP36 promotes derepression of the Hedg

36 Here we report beta5i-selective inhibition by asparagine-ethylenediamine (AsnEDA)-based

37 donate during physiological activation, with inhibition by aspirin in vitro or in vivo, implicating c

38 atelets by anti-CD41 mAb treatment, platelet inhibition by aspirin, and adoptive transfer of wild-typ

39 s conferred either reduced or highly reduced inhibition by at least 1 NA inhibitor; half of them caus

40 These benign tumors are sensitive to inhibition by ATP-competitive Akt inhibitors, including

41 II in isolated mitochondria: (a) complex II inhibition by atpenin A5 or complex III inhibition by st

42 ost completely ameliorated the disease (>97% inhibition) by augmenting nitric oxide generation and sh

43 o-culture challenge assays, we quantified Bd inhibition by bacterial isolates collected from the skin

44 This discrepancy in SOAT inhibition by BeauIII was investigated.

45 SOAT1-selective inhibition by BeauIII was reproduced in intact ER fracti

46 However, chemical inhibition by BEL is subject to off-target pharmacologic

47 PLK1 inhibition by BI-2536 or siRNA-mediated knockdown suppre

48 rolases are susceptible to potent reversible inhibition by boronic acids.

49 and [(3)H]C2 transport and decreased growth inhibition by C1 and C2, and to a lesser extent by PMX.

50 on of either the eagD or cNBHD abolished the inhibition by Ca(2+) i However, deletion of just the PAS

51 Feedback potentiation of distal dendritic inhibition by CA1 place cells attenuated the excitatory

52 us cell-based models by short hairpin RNA or inhibition by cabozantinib, the multi-tyrosine kinases i

53 may explain the stronger CaM-dependent RyR2 inhibition by CaM-F142L, despite its reduced Ca(2+) bind

54 basis of tissue-specific enzyme activity and inhibition by catalytic products, Hans Krebs first demon

55 s of RECON activity, via genetic ablation or inhibition by cdNs, increased NF-kappaB activation and r

56 ction of endomesoderm, as indicated by their inhibition by Cerberus overexpression.

57 Specific inhibition by chemical genetics in MEFs confirmed the in

58 Translational inhibition by chemicals abolishes the OCTR-1-controlled

59 The inhibition by ciproxifan was reversible for both human i

60 e provides an insight into RNA targeting and inhibition by cisplatin, which can help predict cisplati

61 PAD4 inhibition by Cl-amidine reduced NETting neutrophils and

62 at AdoMet binding significantly enhances CBS inhibition by CO.

63 tal and subcortical brain areas for response inhibition, by comparing 20 dynamic causal models of the

64 e, Q77 and T86, may also play a role in NaCT inhibition by compounds 2: and 4: Our results provide ne

65 mutant cancer cells in the presence of PI3K inhibition by conducting a genome scale shRNA-based apop

66 cologic 5-LO inhibition by zileuton and LTB4 inhibition by CP-105,696.

67 ented AML cell death in response to FLT3-ITD inhibition by crenolanib, which was restored by wild-typ

68 FoxQ1 using small hairpin RNA augmented bCSC inhibition by DATS.

69 ndicate that FoxQ1 is a novel target of bCSC inhibition by DATS.

70 ding, suggestive of a cycle of unwinding and inhibition by Dbp2.

71 give insight into transposase overproduction inhibition by demonstrating that the appearance of trans

72 this lipid is a major determinant of channel inhibition by depletion of PI(4,5)P2 upon phospholipase

73 susceptible and resistant strains with their inhibition by different beta-lactams.

74 In this study, we revisited the mechanism of inhibition by diminazene and its binding site on ASIC1a,

75 argeting mIDH demonstrated common allosteric inhibition by distinct chemotypes.

76 To investigate whether inhibition by divalent cations is conserved in an invert

77 R1 from Tric-a KO mice are more sensitive to inhibition by divalent cations, although they respond no

78 e residue (His-347) downstream of S6 reduces inhibition by divalent cations.

79 e recently defined by two other groups using inhibition by Dkk1 mRNA or Wnt8 morpholinos, which indic

80 Despite inhibition by dominant-negative TonEBP, IL6 and NOS2 pro

81 Piezo2 inhibition by drugs or molecular knockdown decreases mec

82 0 mV the net effect of the co-application is inhibition by dynorphin-A, whereas at -70 mV the excitat

83 0 mV the net effect of the co-application is inhibition by dynorphin-A, whereas at -70 mV the excitat

84 TG2 inhibition by either a viral particle or pharmacological

85 NMDAR inhibition was not responsible for LTP inhibition by either agent when applied for only 20 minu

86 Mechanistic target of rapamycin inhibition by either nutrient starvation or use of an ac

87 subset of MCLs is addicted to MALT1, as its inhibition by either RNA or pharmacologic interference i

88 centrations, and 3) alleviation of metformin inhibition by elevated glucose concentrations.

89 RAAS inhibition by enalapril (angiotensin-converting enzyme i

90 luR1 increases the strength of this efferent inhibition by enhancing the presynaptic release of acety

91 CSAR inhibition by epicardial lidocaine decreased cardiac con

92 Following CSAR inhibition by epicardial lidocaine, blood pressure, HR,

93 ress Klf1, suggesting a model of cooperative inhibition by epigenetic modifiers.

94 he evaluation of the potential for metabolic inhibition by every new chemical entity.

95 oMet puzzlingly sensitizes the enzyme toward inhibition by exogenous ligands, like CO and NO(*).

96 In contrast, CaMKII inhibition by expression of AC3-I has been shown to slow

97 mplexes but became refractory to biochemical inhibition by EZH2 inhibitors.

98 rtase in amplifying complement cascades, its inhibition by FACIN results in a very potent downregulat

99 Inhibition by (-)-fenchone and six structurally related

100 Apparent negative-feedback inhibition by ferrous ions is documented at nanomolar co

101 basis of the observation of selective DYRK1A inhibition by firefly d-luciferin, we have explored stat

102 eaminase activity protect plants from growth inhibition by flooding and anoxia, drought, high salt, t

103 mechanistic component of substrate-selective inhibition by flufenamic acid, mefenamic acid, and tolfe

104 These results suggest that SERT inhibition by FLX may hinder survival in hypoxia.

105 chol/Ca(2+) ionophore), but there was normal inhibition by forskolin and hyperosmolarity.

106 We present causal evidence that Mef2c inhibition by Foxp2 in neonatal mouse striatum controls

107 despite high levels of exhaustion and likely inhibition by Foxp3(+) cells, a subset of follicular SIV

108 Notably, systemic pharmacologic Gbetagamma inhibition by gallein, which we previously showed allevi

109 pression, were sensitive to hedgehog pathway inhibition by GANT61 or GDC-0449 (vismodegib) using ex v

110 l subtype of triple-negative tumors, and its inhibition by genetic or pharmacological methods suppres

111 itus, 14 days of ileal bile acid transporter inhibition by GSK2330672 was generally well tolerated wi

112 e" complex formation and overcomes catalytic inhibition by halide ions.

113 Inhibition by high CD45 on CD8(+) T cells may protect ag

114 (-) and 3DS1(+) NK cells were insensitive to inhibition by HLA-Bw4-expressing NB targets.

115 fect was non-additive with respect to Kv 1.5 inhibition by hypoxia and mitochondrial poisons.

116 We conclude that AMPK mediates Kv channel inhibition by hypoxia in pulmonary arterial myocytes, at

117 ich is insensitive to Bruton tyrosine kinase inhibition by ibrutinib, and the activated B-cell (ABC)

118 n contrast to NP mRNA, remained sensitive to inhibition by IFIT1 following in vitro 2'O methylation,

119 nzymes, we show biochemically that efficient inhibition by IFIT1 is dependent upon a 5' guanosine nuc

120 ulaviruses do not protect these viruses from inhibition by IFIT1.

121 iral replication, sensitivity to mutagen, or inhibition by IFN-beta compared to WT MHV.

122 Consistent with increased inhibition by IGCs, MCs responded to sensory input stimu

123 dr1 gene activation and multidrug resistance inhibition by iKIX1.

124 However, Abl kinase inhibition by imatinib reduces rapid redistribution of t

125 strains conferred partial resistance to GBP5 inhibition by increasing Env expression.

126 reviously reported that cyclooxygenase (COX) inhibition by indomethacin augmented allergic airway inf

127 line PANC-1 and exhibited cell proliferation inhibition by inducing cells to undergo G2/M arrest.

128 on the ICP0 gene (0DeltaNLS) is sensitive to inhibition by interferon beta (IFN-beta) in vitro and fu

129 1 (hEAG1) channel is remarkably sensitive to inhibition by intracellular calcium (Ca(2+) i) through b

130 rTRPM7 has two protein domains that regulate inhibition by intracellular magnesium and nucleotides, a

131 th systemic NBQX, or selective AMPA receptor inhibition by intramuscular perampanel restored myelinat

132 Moreover, NF-kappaB inhibition by IT-901 resulted in reduced stimulation of

133 of the cellular metabolome showed that FLT3 inhibition by itself causes profound alterations in cent

134 Depletion of BRD4 by shRNA and inhibition by (+)-JQ1, an inhibitor of BET family protei

135 e G9a as a model to explore the mechanism of inhibition by K-to-M oncohistones.

136 Conversely, presynaptic inhibition by KORs of inhibitory synapses on D2 MSNs enh

137 ve homologues, the MtDapE was insensitive to inhibition by L-captopril which we show is consistent wi

138 Furthermore, inhibition by lacosamide was greatly reduced by pretreat

139 esidue of A(H7N9) viruses, conferred reduced inhibition by laninamivir.

140 XIAP inhibition by lentivirus mediated RNA interference enhan

141 We further show that inhibition by light-gated chloride channels is mediated

142 Neointimal inhibition by limus-coated balloons has been shown in fe

143 activation is persistently enhanced, and its inhibition by low-dose aspirin is impaired in type 2 dia

144 mains (VSD2) encodes voltage sensitivity and inhibition by luminal Ca(2+) and adopts a conformation d

145 ability of dbcAMP and putrescine to overcome inhibition by MAG is abolished in the presence of roscov

146 cessary for putrescine's ability to overcome inhibition by MAG.

147 ced with HSV overexpressing p35 can overcome inhibition by MAG.

148 period, reducing its sensitivity to feedback inhibition by malate and thus enhancing nocturnal CO2 fi

149 re and on the pharmacophore for ASIC channel inhibition by mambalgins that could have therapeutic val

150 Therefore, urease inhibition by manuka honey is mainly due to MGO and DHA.

151 contribute to the understanding of bacterial inhibition by manuka honey.

152 nstitution, we show that Mps1 promotes APC/C inhibition by MCC components through phosphorylating Bub

153 TRIP13 and p31(comet) prevent APC/C inhibition by MCC components, but cannot reactivate APC/

154 Therefore, differential inhibition by memantine and ketamine based on NMDAR loca

155 repancy has been hypothesized to result from inhibition by memantine and ketamine of overlapping but

156 As a result, inhibition by memantine of GluN1/2A receptors in tsA201

157 ts showed mechanical activation of NMDAR and inhibition by MK-801.

158 Heat shock protein 90 (Hsp90) inhibition by modulation of its N- or C-terminal binding

159 cted enzymes also showed different levels of inhibition by monochloramine when tested.

160 However, a reduction in the inhibition by morphine for DOP-/- c.f. WT neurons and a

161 nt of MOPs, DOPs, beta-arr2 and c-Src in the inhibition by morphine of GABAergic inhibitory postsynap

162 c inhibitor, PP2, to WT neurons also reduced inhibition by morphine, while the inactive PP3, and the

163 In support of this notion, we find that sAHP inhibition by muscarinic receptors that increase phospho

164 Conversely, CeA inhibition by muscimol/baclofen microinjections prevente

165 D and A105T, both of which allow escape from inhibition by MX2 and the truncated version of cleavage

166 NADH and therefore cannot be used to measure inhibition by NADH.

167 report a remarkable stereoselectivity of NKA inhibition by native 3beta-hydroxy bufalin over the 3alp

168 Phase 2 was less sensitive to inhibition by NBQX but more sensitive to block by pentob

169 Here, we show that AMPA-kainate receptor inhibition by NBQX suppresses inflammation, attenuates a

170 a metabolic liability of NSCLC and that ACC inhibition by ND-646 is detrimental to NSCLC growth, sup

171 ac1 deletion in SMCs or pharmacological Rac1 inhibition by nebulization of NSC23766 prevented AHR in

172 ght to subvert CTLs while preserving NK cell inhibition by Nef-mediated downregulation of HLA-A and -

173 eterotrophic perchlorate reducers and direct inhibition by nitrite produced from heterotrophic nitrat

174 nd neither TNF-alpha nor IL-6 secretion, nor inhibition by NO-np was found to be dependent on this pa

175 echanisms accounting for NF-kappaB signaling inhibition by NO2-OA in TNBC cells were multifaceted, as

176 nesis of GluN1-Glu781 reduced the potency of inhibition by NVP-AAM077, thus confirming the involvemen

177 determined the structural basis for receptor inhibition by obtaining the first co-crystal structure o

178 The IC50 values for ACE inhibition by OD-FPH and FD-FPH samples were found to be

179 nistration and laser preference, whereas CeA inhibition by optogenetic halorhodopsin suppressed cocai

180 Nuclear export inhibition by ORF10 requires an interaction with an RNA

181 r group 2NA), H274Y conferred highly reduced inhibition by oseltamivir.

182 conversely biasing the circuit toward local inhibition by overexpression of neuregulin-1 type 1 resu

183 its selectivity for anterograde DCVs and its inhibition by overexpression of the fragile X retardatio

184 f down-regulation of AHAS activity involving inhibition by oxidized redox-signaling molecules.

185 no shift in the voltage dependency under the inhibition by oxo-M.

186 al repressor, suppresses the effects of EGFR inhibition by partially restoring the EGFR-promoted gene

187 Smoothened (Smo) inhibition by Patched (Ptch) is central to Hedgehog (Hh)

188 ential sensitivity of phase 1 and phase 2 to inhibition by pentobarbital and NBQX mirrors the differe

189 ls, confirming its activity at acidic pH and inhibition by pepstatin.

190 Unexpectedly, inhibition by peptide aldehydes is non-competitive, reve

191 MARCKS inhibition by peptide significantly decreased proplatele

192 Here we disrupted this inhibition by perturbing distinct sets of GABAergic inpu

193 ction of both noncooperative and cooperative inhibition by PF74 is regulated by interactions of cellu

194 We now show that MR inhibition by phosphorylation occurs even at high agonis

195 t as repressors of photomorphogenesis; their inhibition by PHYs leads to substantial changes in gene

196 for PI(4,5)P2, and were largely resistant to inhibition by PI(4,5)P2 depletion.

197 t genetic deficiency of p53 or pharmacologic inhibition by pifithrin impairs thrombus resolution and

198 rthered our understanding of how HCMV evades inhibition by PKR and identified new strategies for how

199 xclusively be attributed to Ile-Trp, the ACE inhibition by plant protein hydrolysates is caused by a

200 ve studies included analysis of in vivo FLT3 inhibition by plasma inhibitory activity assay and indic

201 we investigated the molecular basis of PME3 inhibition by PMEI7 in Arabidopsis thaliana Our compleme

202 r growth in vivo, and prevented tumor growth inhibition by PMPs.

203 Puma then overcomes inhibition by pro-survival Bcl-xL and Bcl-w and initiate

204 Depletion of PNX1 by siRNA or inhibition by probenecid resulted in significant blockin

205 which presented autoproteolytic activity and inhibition by protease inhibitors.

206 er that the enhancement of TFPI-mediated FXa inhibition by protein S and FV depends on a direct prote

207 s SET, we investigated a role for SET in DDR inhibition by protein VII.

208 utations render PSS1 insensitive to feedback inhibition by PS levels.

209 mportant for activation by PtdIns(3,5)P2 and inhibition by PtdIns(4,5)P2.

210 pTRS1 binding and rendered PKR resistant to inhibition by pTRS1.

211 However, the mechanism of pol II inhibition by Py-Im polyamides is unclear.

212 itical role for 3'-processing efficiency and inhibition by RAL and DTG.

213 mTOR inhibition by rapamycin restores corticosteroid sensitiv

214 uction of DNA double-strand breaks or mTORC1 inhibition by rapamycin results in reduced levels of HMO

215 mTOR inhibition by rapamycin significantly preserves neuronal

216 e to mammalian Target of Rapamycin Complex 1 inhibition by rapamycin.

217 m contributes to the homeostasis of synaptic inhibition by rapidly adjusting neuronal [Cl(-)]i to GAB

218 substitution makes RetGC1 less sensitive to inhibition by retinal degeneration-3 protein (RD3).

219 cifically to the mitochondria and ensure Bax inhibition by retrotranslocation into the cytosol.

220 also rendered the virus more susceptible to inhibition by ribavirin, coincident with the accumulatio

221 Calpain inhibition by ritonavir may be a powerful tool for prese

222 csin C-insensitive pathway and the increased inhibition by rosiglitazone G confirmed the sensitivity

223 that PHF11 stimulates EXO1 by overcoming its inhibition by RPA, suggesting that PHF11 acts (in part)

224 lude cytoreduction by hydroxyurea and JAK1/2 inhibition by ruxolitinib, both of which are not curativ

225 However, the mechanism of Sirt1 inhibition by S-nitrosation was unknown.

226 leavage by separase and suggests competitive inhibition by securin.

227 logical and molecular effects of correlative inhibition by seeds on Arabidopsis (Arabidopsis thaliana

228 s is counterbalanced by their sensitivity to inhibition by "self" MHC class I molecules in a process

229 Fast inhibition by Semapimod is consistent with gp96 particip

230 network dynamics of the recruitment of local inhibition by sensory input.

231 Their functional inhibition by sequence-specific antisense oligonucleotid

232 , although both IC50 titers and percent C179 inhibition by sera diluted 1:5 or 1:10 correlated with h

233 porcine surfactant made it more resistant to inhibition by serum than the addition of equivalent amou

234 We show that transient apoptosis inhibition by short-term overexpression of prosurvival B

235 These results indicate that MEV cascade inhibition by simvastatin induced the intrinsic apoptosi

236 We propose that catastrophe inhibition by SLAIN2 and CLASP1 supports mesenchymal cel

237 The assays were employed to measure enzyme inhibition by small molecules and activity in cell lysat

238 enes is commonly observed in cancer, and its inhibition by small molecules is promising for their rea

239 GSK-3 siRNA downregulation, or inhibition by small molecules, blocked PD-1 expression,

240 apeutic targets through either activation or inhibition by small molecules.

241 alidated by site-directed mutagenesis and by inhibition by small peptides that mimic the loop residue

242 ating kinetics influenced the sensitivity to inhibition by SMase.

243 HO-1 inhibition by SnPP reduced growth and vascularization of

244 hibition with the susceptibility of HIV-1 to inhibition by soluble CD4 and the 17b antibody that reco

245 Here, we demonstrate that RAF inhibition by sorafenib rapidly leads to RAF dimerizatio

246 Not only subjected to growth inhibition by spermine, the pauA2 mutant became more sen

247 to quantify because the degree of isoprenoid inhibition by statins correlates to some extent with the

248 x II inhibition by atpenin A5 or complex III inhibition by stigmatellin that results in succinate-dep

249 ession can remain inhibited and sensitive to inhibition by strigolactone.

250 d shoot Se accumulation and less competitive inhibition by sulfate or by high-S pretreatment.

251 ion, we hypothesized that PIN1 relieves CDK2 inhibition by suppressing the CDK inhibitory activity of

252 VAMP8(-/-) acini are resistant to secretory inhibition by supramaximal CCK-8, and despite a 4.5-fold

253 nd in solution conditions; while the mode of inhibition by tannic acid was found to be purely non-com

254 validate the viability of locus-specific DDR inhibition by targeting DDRNAs.

255 bined results reveal the potential for KDM5B inhibition by TCA cycle intermediates, but suggest that

256 ntly escape the slow kinetics of Kunitz-type inhibition by TF pathway inhibitor and preferentially ac

257 , TEM can be maintained in the face of IL-15 inhibition by the activity of other homeostatic regulato

258 thovanadate and is particularly sensitive to inhibition by the adenylates, ATP and ADP.

259 Nrf2 inhibition by the chemical brusatol also induces lytic g

260 aturable process that is highly sensitive to inhibition by the classic nucleoside transporter inhibit

261 ts to a mechanistic difference in ice growth inhibition by the different classes of AFPs: blocking fa

262 Importantly, AMPA-specific inhibition by the FDA-approved perampanel, which unlike

263 e most comprehensive analysis to date of KAT inhibition by the feedback metabolite CoA.

264 n by phosphatidylserine, and pharmacological inhibition by the lipid-competitive inhibitor GW4869.

265 mutants that undergo self-reactivation after inhibition by the organophosphorus agent paraoxon.

266 lammatory mechanism of action, through COX-2 inhibition by the phenolic acids identified.

267 higher level of ALPs are more susceptible to inhibition by the phosphorylated D-tetrapeptides; the pr

268 and indicate that the catalyst is subject to inhibition by the product of the chloroacylation reactio

269 r cellular entry and are thus susceptible to inhibition by the same antivirals and cellular defenses.

270 f KCNQ1 was limited to 40% at +40 mV vs. 80% inhibition by the shorter form, and augmentation of KCNQ

271 Furthermore, the abrogation of LoxP inhibition by the simple addition of an extra generation

272 investigated the mechanism of Kif18A and its inhibition by the small molecule BTB-1.

273 he immune system with the combination of IDO inhibition by the small-molecule immunotherapy agent and

274 d the responses of these channel variants to inhibition by the sulfonylurea drug glibenclamide, a pot

275 ated rare variant (M2145T) in TGEF2 impaired inhibition by the TGEF2 pleckstrin-homology domain, resu

276 tablish the structural basis of differential inhibition by the widely used Wee1 inhibitor MK-1775.

277 We demonstrate TRPV4 inhibition by these compounds in primary cells with know

278 find that Mtb's ETC rapidly reroutes around inhibition by these drugs and increases total respiratio

279 oresis and analyzed acceleration of protease inhibition by these molecules.

280 ght on the mechanism of thrombin binding and inhibition by this family of salivary anticoagulants fro

281 Rubisco is prone to inhibition by tight-binding sugar phosphates, whose remo

282 a structural basis for the mechanism of PCNA inhibition by TIP.

283 The inhibition by trans addition of alcohols implies that th

284 Here we show ZIKV inhibition by two different Wolbachia strains: wAlbB (is

285 n viral replication, sensitivity to mutagen, inhibition by type I interferon (IFN), and translation e

286 We go on to determine that this channel inhibition by Ucn1 is mediated initially by an increase

287 nism through which pCPI-17 and MLCP interact inhibition by unfair competition: MLCP protects pCPI-17

288 extending previous results that demonstrated inhibition by uracil.

289 to investigate the effect of single TLR4-MD2 inhibition by using eritoran, compared with the effect o

290 Also, Wnt inhibition by using small molecules along with TrkC-miR2

291 nhibition of Bcl-xL with ABT737 or molecular inhibition by using the D61A and D76A Bcl-xL mutant lead

292 Importantly, neddylation inhibition, by using the pharmacological inhibitor, MLN4

293 Metabolic inhibition by V-58 was carbon source dependent in Mtb an

294 Their dominant response was inhibition by valueless objects, which generated disinhi

295 h at a level on par with the level of growth inhibition by vancomycin.

296 We found that the probability of ribosome inhibition by viomycin depends on competition between vi

297 ApoC-III inhibition by volanesorsen reduced plasma levels of apoC

298 posite roles in GSK3beta phosphorylation and inhibition, by which mTORC2 and pAKT-S473 negatively reg

299 kinase M zeta (PKMzeta), mainly because its inhibition by zeta inhibitory peptide (ZIP) interferes w

300 nvestigated the effect of pharmacologic 5-LO inhibition by zileuton and LTB4 inhibition by CP-105,696