ライフサイエンスコーパス: inhibition of

1 The inhibition of 5-HT(3A)Rs and 5-HT(3AB)Rs was non-use dep

2 centrolateral amygdala is necessary for the inhibition of a conditioned response to a safety cue.

3 e essence of the model is that intracortical inhibition of a direction-selective cell is spatially in

4 o the molecular mechanism of drug export and inhibition of a major multidrug efflux pump and the dire

5 In addition, we show inhibition of a non-enveloped adenovirus.

6 riven by significantly selective (>100-fold) inhibition of a subset of the eight bromodomains is enti

7 SNI-1 enhances chemotherapy-dependent growth inhibition of a variety of cancer cells, including human

8 Here, we find that inhibition of ABC transporter activity reduces migration

9 on of an actin regulator, by pharmacological inhibition of actin polymerization, and by the expressio

10 ty in migrating cells rapidly decreases upon inhibition of actomyosin contractility (specifically, of

11 The inhibition of CD73 or the inhibition of adenosine receptors abrogated the ATP effe

12 Inhibition of adenylyl cyclase with SQ 22,536 restored B

13 se activity, but rather as increased passive inhibition of aggregation of specific substrates.

14 Chemogenetic inhibition of all GABA interneurons (Gad1+), as well as

15 Here we have systematically studied Zn(2+) inhibition of AMPARs by varying calcium permeability, au

16 hondrial content that is restored by genetic inhibition of AMPK and autophagy.

17 However, greater hippocampal inhibition of amygdala, thalamus, IFG and dmPFC correlat

18 lin-dependent kinase 12 (CDK12) or selective inhibition of an analog-sensitive CDK12 reduces DNA dama

19 Genetic deletion or chemical inhibition of AP-1 suppresses growth of YAP-driven cance

20 trate that RUNX3 plays a pivotal role in the inhibition of apoptosis found in the beta-catenin S45F m

21 n liver injury, and provide evidence for mAb inhibition of AQP3-mediated H(2)O(2) transport as therap

22 e term "pull-away" and "search-and-capture." Inhibition of Arp2/3 complex inhibits TMT assembly by bo

23 ion murine model, T1317-sHDL showed superior inhibition of atherogenesis and reduced hypertriglycerid

24 the intestinal epithelium or pharmacological inhibition of ATM, YAP1, or caspase-1 as well as antibio

25 nic phenotypes, which are all abolished upon inhibition of AXL.

26 revealed 9-dechlorochrysophaentins leads to inhibition of bacterial cell wall biosynthesis by disass

27 nteraction provide a mechanism for efficient inhibition of beta-catenin phosphorylation upon Axin rec

28 Importantly, genetic and chemical inhibition of beta-catenin-TCF/LEF signaling in human CD

29 re resensitized to BBR after pharmacological inhibition of beta-catenin.

30 Conversely, tonic optogenetic inhibition of BF-PV neurons partially rescued the elevat

31 Conversely, inhibition of BLC mir-135b-5p in stress-susceptible anim

32 sibly through NADPH depletion and subsequent inhibition of BMI1, an integral component of polycomb-re

33 In mouse models of SS, inhibition of BMP6 signaling reduced phosphorylation of

34 Inhibition of both cyclin-dependent kinase 9 activity an

35 uice provoked induction of several genes and inhibition of both CYP3A4 and CYP1A2, matching effects o

36 Furthermore, the study shows that combined inhibition of both EGFR and STAT3 might overcome drug re

37 ibits Herpes simplex virus type 1 (HSV-1) by inhibition of both fusion and viral protein synthesis.

38 The balanced synchronous inhibition of both RET and VEGFR2, as well the resistanc

39 Targeting the MAPK pathway by combined inhibition of BRAF and MEK has increased overall surviva

40 Pharmacological inhibition of BRD4 decreased NRP1 expression and ablated

41 These findings demonstrate that inhibition of BRD4 induces transcription-replication con

42 CRISPR/Cas9) and pharmacologic (crizotinib) inhibition of c-MET.

43 ch in Orai1-STIM stoichiometry, resulting in inhibition of Ca2+ entry and Ca2+-dependent gene express

44 Inhibition of CaMKII may be useful for prevention or tre

45 ial) decrease sensitivity to opioid-mediated inhibition of cAMP and promote hyperactivity of nocicept

46 To define the physical basis for EapH1's inhibition of cathepsin-G, we crystallized EapH1 bound t

47 sion, this approach based on the concomitant inhibition of CB1R and iNOS represents a promising thera

48 Inhibition of CD73 eliminates a major pathway of ADO pro

49 The inhibition of CD73 or the inhibition of adenosine recept

50 Our results demonstrate that targeted inhibition of cell cycle checkpoint activation following

51 Methods: Inhibition of cell proliferation after incubation of the

52 ntriguingly, both optogenetic excitation and inhibition of cerebellar cortical output neurons, Purkin

53 e hypothesis that genetic or pharmacological inhibition of CETP would preserve high-density lipoprote

54 lines of research that demonstrate chemical inhibition of cholesterol biosynthesis compromises neuro

55 are necessary and sufficient for binding and inhibition of CK1alpha.

56 Here, we report that inhibition of class I PI3K or PDPK1 activates CMA.

57 h AB1 show that the irreversible competitive inhibition of CLK1 is dependent on a Michael acceptor fo

58 pendent proliferation and countered butyrate inhibition of colonic growth.

59 pe VGCC isoform was required for ACh-induced inhibition of contraction, a mechanism by which those ch

60 stablished the eicosanoid profiles linked to inhibition of COX-1 in platelets and in the remainder of

61 ic mediators in asthmatic patients; however, inhibition of CysLT receptor 1 is not a consistently eff

62 Dysregulation of hydrogen sulfide (H(2)S) by inhibition of cystathionine gamma-lyase (CSE) increases

63 Our studies demonstrated that the inhibition of de novo lipid biosynthesis by interfering

64 Deletion of DNA-PK or PTEN, or inhibition of DNA-PK sensitized recovering BLBCs to AZD1

65 mmetry recordings confirmed that presynaptic inhibition of dopamine release by the KOR agonist U69,59

66 ns of agonist were required for half-maximum inhibition of dopamine-induced cAMP accumulation in cell

67 We further found that pharmacological inhibition of downstream effectors of the PI3K/GSK3 path

68 The inhibition of DPPH radicals accelerated with an increase

69 The mechanistic study showed the inhibition of EGFR caused nuclear translocation of S6K1

70 damage repair gene expression, but selective inhibition of endogenous CDK12 is difficult.

71 y human behavior requires the suppression or inhibition of errant or maladaptive motor responses, oft

72 ular vesicles in the vascular lumen and that inhibition of extracellular vesicle release blocks LTB4-

73 Recent studies also suggest that inhibition of EZH2 enhances the response to tumor immuno

74 enetic ablation or selective pharmacological inhibition of FAAH bidirectionally dysregulates intracel

75 cy (SAI) but not long-latency (LAI) afferent inhibition of face M1, while facial nerve stimulation ev

76 regulates ITGA5/FN1 expression, resulting in inhibition of FAK/Src signaling, induction of apoptosis

77 In sum, mutation and chemical inhibition of Fech reduces retinal neovascularization an

78 Consistent with this, inhibition of FGFR1 function by the selective small-mole

79 hia in the bacterial biofilm can cause local inhibition of fibrinolysis, which could have possible de

80 n of p38 MAPK, decrease in Erk signaling and inhibition of FOXM1 expression.

81 More importantly, inhibition of FOXM1 markedly suppresses leukemogenic pot

82 ard has long been believed to be mediated by inhibition of GABA interneurons in the VTA that subseque

83 rapid-acting drugs are thought to occur via inhibition of GABA interneurons.

84 In the presence of BFT, pharmacological inhibition of GCS caused levels of tight junction protei

85 aining the intercalated cells, we found that inhibition of glutamate release by a submaximal concentr

86 Using inhibition of glutamate release onto the intercalated ce

87 aptation in glutamine metabolism and how the inhibition of glutaminase 1 (GLS1) reverses pulmonary fi

88 Notably, in vivo inhibition of glycolysis enhanced the competitive repopu

89 In line with this, inhibition of GSH reductase (GR), the enzyme responsible

90 Pharmacological inhibition of GSK3 enhanced Nrf2 activity and prevented

91 Pharmacological inhibition of GT1b synthesis attenuates nerve injury-ind

92 Strikingly, combined inhibition of Haspin and AURKB had a better efficacy tha

93 pin depletion and VX-680 was mediated by the inhibition of Haspin with Aurora kinase B (AURKB), but n

94 n solution demonstrated an isoform-dependent inhibition of hemolysis and complement deposition at the

95 Preliminary mechanistic studies suggest inhibition of hemozoin formation as a contributing mode

96 ongly in females than males, perhaps because inhibition of hepatic mTORC2 (mTOR Complex 2) specifical

97 Of particular interest, pharmacological inhibition of histone deacetylase 11 (HDAC11) and suppre

98 Overall, our data show that inhibition of HIV-1 maturation by BVM involves changes i

99 Genetically proxied inhibition of HMG-CoA reductase was significantly associ

100 equences of such binding are suggested to be inhibition of HS cleavage in MDA-MB-231 triple-negative

101 A with short incubation time whereas maximum inhibition of HSA and PPA by EC was reached only after 4

102 EGCG reached maximum inhibition of HSA and PPA with short incubation time whe

103 Small molecule inhibition of HSL activity and siRNA-mediated knock down

104 ting the blocker molecule for more effective inhibition of Hv1.

105 roliferation in vitro, whereas pharmacologic inhibition of hyaluronidase activity prevented hypoxia-

106 ed the effects of genetic or pharmacological inhibition of IFN-beta, a key component of type I IFN me

107 Inhibition of IgE binding and displacement of receptor-b

108 Inhibition of IL-6 by its blocking antibody in BMM-OB co

109 tro capillary sprouting assays revealed that inhibition of IL-6 or STAT3 signaling decreases the vasc

110 L2RA expression as well as antibody-mediated inhibition of IL2RA in human cell lines, mouse models, a

111 We suggest that inhibition of in vitro platelet phagocytosis may prove t

112 anisms of abstinence-dependent expression or inhibition of incubation of craving.

113 Finally, inhibition of inflammasome prevented P. aeruginosa-induc

114 OXTR-induced excitation is mediated by inhibition of inwardly rectifying K(+) (Kir) channels.

115 In the pristane-induced lupus mouse model, inhibition of IRAK4 reduced the expression of IRGs durin

116 hat heme protects S. aureus from CP-mediated inhibition of iron uptake and iron-starvation responses.

117 SOD1 was highly resistant to inhibition of its activity, and therefore, did not have

118 These findings suggest that inhibition of JNK2 may improve diminished BSM contractil

119 Pharmacological inhibition of KDM6A also impairs chemotherapy-induced BC

120 Surprisingly, inhibition of L-type VGCCs, but not GluA2-lacking AMPARs

121 Moreover, inhibition of LAT1 blocks expansion of human gammadelta

122 es tumorigenesis, at least, in part, through inhibition of let-7 microRNA biogenesis.

123 cross-processing seems a promising tool for inhibition of lipid oxidation during pH-shift processing

124 vitro, including: antitumor effects through inhibition of lipogenesis; decreased expression of invas

125 Inhibition of LncRNA MALAT1 has potential to protect the

126 The inhibition of Lp-PLA(2) by darapladib is dependent on ma

127 Inhibition of macrophage IL-1beta production by colchici

128 fects, as antisense oligonucleotide-mediated inhibition of Malat1 also suppresses Maf and IL-10 level

129 To achieve robust inhibition of MAOA/B, the clinically used antidepressant

130 metastasizers had higher levels of MCT1, and inhibition of MCT1 reduced lactate uptake.

131 Pharmaco- and optogenetic inhibition of MEC led to a disruption of border coding i

132 Inhibition of mechanotransduction pathways prevented myo

133 Combined inhibition of MEK and SHP2 is effective in models of NF1

134 Chemical screening revealed that inhibition of MEK/ERK signaling overcame the HIF1a-media

135 oplasmic reticulum, which contributes toward inhibition of MHC class I:beta2M:peptide complex formati

136 Selective in vivo inhibition of miR-128-3p in FMRP-deficient astroglia suf

137 Inhibition of miR-15a/16-1 function in cerebrovascular e

138 Like nitric oxide, pharmacological inhibition of mitochondrial oxidative metabolism attenua

139 ng that IRGM regulates mitophagy through the inhibition of Mitofilin.

140 nk1-deficient bone marrow or pharmacological inhibition of mitophagy promoted macrophage activation,

141 Mechanistically, loss or inhibition of MLK3 down-regulates expression of a prolyl

142 Additionally, pharmacological and genetic inhibition of MNK-eIF4E signaling completely blocked and

143 We show that this is due to acid inhibition of monocarboxylate transporters (MCTs), resul

144 Inhibition of more than one cancer-related pathway by mu

145 Volitional inhibition of motor output could be increased to prevent

146 channel of the ribosome and leads to global inhibition of mRNA translation upon infection.

147 Inhibition of mTOR (mechanistic Target Of Rapamycin) sig

148 However, the inhibition of MTOR has modulatory effects beyond autopha

149 Importantly, inhibition of mTOR, or Rheb, rescues HSC defects in Sel1

150 MP content, which activates AMPK, leading to inhibition of mTORC1.

151 Inhibition of multiple growth factor pathways may postpo

152 ric retention may result from the concurrent inhibition of multiple PDE4s.

153 SNI-1 also enhanced ADR or cisplatin inhibition of murine TNBC tumors in vivo and reduced sys

154 Here we report that the inhibition of mutated EGFR promotes the secretion of a p

155 Prevention of Na(i) overload or inhibition of Na/Ca(mito) may be a new approach to ameli

156 at lidocaine enhances the degree and rate of inhibition of Nav1.7 channels by the aryl sulfonamide co

157 ted it through overexpression, knockout, and inhibition of NCAM1 in Vero cells and human glioblastoma

158 Inhibition of neddylation, the conjugation of the small

159 sistent with this mechanism, pharmacological inhibition of NER using spironolactone abolished SIRT2-m

160 sition of NETs along the arterial lumen, and inhibition of NET release annulled lesion expansion duri

161 Therefore, the inhibition of NETs represents a potential therapeutic ta

162 tion of the eIF4G1 function and chemogenetic inhibition of neuronal activity.

163 nd sufficient for counteracting MOR-mediated inhibition of neuronal firing.

164 minobutyric acid (GABA) results in prolonged inhibition of neurotransmission, which is central to bra

165 ent tumor suppression, and more importantly, inhibition of neutrophil-mediated lung metastasis via th

166 Inhibition of NF-kappaB enhances, whereas activation sup

167 Chemical inhibition of NF-kappaB with BAY11-7082 reduced Wnt5a ex

168 In vivo inhibition of NFAT may represent a novel therapeutic mod

169 3085-3p and may be responsible for the early inhibition of NFkappaB signaling.

170 Inhibition of NFkB activity results in nearly complete l

171 lpha-cobratoxin (alpha-Cbtx) and prevent its inhibition of nicotinic acetylcholine receptors (nAChRs)

172 hat EBV peptides can bind to HLA-E and block inhibition of NK cell effector function.

173 We used genetic and pharmacological inhibition of NMT1 to further dissect the role of this e

174 Inhibition of NOX4 increased CD8(+) T cells and restored

175 activation of EGFR, PARP1, and caspases and inhibition of p53 and NFkappaB.

176 Although inhibition of PDE3A catalytic activity did not account f

177 romoted myogenic differentiation through the inhibition of PEPCK-M.

178 Pharmacological inhibition of phosphatidylinositol kinases and cholester

179 Inhibition of phospholipase A2 (PLA2) has long been cons

180 macodynamic studies demonstrated substantial inhibition of phosphorylation of CHK1, the downstream AT

181 Inhibition of PIM sensitized NSCLC cells to chemotherapy

182 nd xenografts of HCC tumors, suggesting that inhibition of PJA1 may be beneficial in treating HCC or

183 s potential pathological properties, such as inhibition of plasmin generation, have been attributed t

184 se exert an anti-atherothrombotic effect via inhibition of platelet activation.

185 Abeta-induced impairments, and suggest that inhibition of PME-1 may constitute a viable therapeutic

186 modeling induced by pressure overload, while inhibition of PP2A signaling prevents eccentric cardiac

187 E efflux was not affected by pharmacological inhibition of PPARgamma activity, and specific activatio

188 etained both potency and selectivity for the inhibition of prokaryotic translation.

189 t local nutrient depletion and the resulting inhibition of proliferation and motility of bacteria and

190 of gene transcription and the enhancement or inhibition of protein activity.

191 Purkinje cell-specific inhibition of protein kinase C decreased and phase-shift

192 oli that cyclically interact through (i) the inhibition of protein production, (ii) the digestion of

193 iety of applications, including the covalent inhibition of protein targets and dynamic combinatorial

194 disease progression could be ameliorated by inhibition of PTP1B.

195 nd pppGpp interact with proteins involved in inhibition of purine nucleotide biosynthesis and with GT

196 ithin the BC network to generate synchronous inhibition of Purkinje cells, which can entrain cerebell

197 Remarkably, acute chemogenetic inhibition of pyramidal cells successfully corrected mem

198 Specifically, tension-mediated inhibition of Rac activation, which has been experimenta

199 tion of wound repair is mediated through the inhibition of Rac family small GTPase 1 and cell divisio

200 Inhibition of RAGE but not TLR4 signalling may protect a

201 In animal models of HF, central inhibition of RAS and pro-inflammatory cytokines normali

202 xide decreases spermathecal contractility by inhibition of RHO-1, which depends on a conserved cystei

203 Inhibition of RIPK1 or MLKL attenuated RSV-induced HMGB1

204 RMS models in vitro and in vivo resulted in inhibition of RMS development and progression.

205 Inhibition of ROS blocked minority MOMP and Mcl-1 upregu

206 ion and tight junction breakdown, and led to inhibition of RPE65 expression, diminishment of RPE pigm

207 Inhibition of RSK3 signaling prevents concentric cardiac

208 The inhibition of RUNX1 reduced proliferation of human C-PVR

209 signaling, IL-6 signaling, LPS/IL-1-mediated inhibition of RXR Function, PI3K in B lymphocytes, iCOS-

210 ong evidence to show that template-dependent inhibition of SARS-CoV-2 RdRp by RDV is biologically rel

211 We also describe potent inhibition of SARS-CoV-2 strain 2019-nCoV/USA-WA1/2020 b

212 reduced, which was partly attributed to the inhibition of SCD1 expression.

213 , little is known about how the ABA-mediated inhibition of seed germination and seedling establishmen

214 rs orchestrate multiple tasks, including the inhibition of self-generated sensory signals.

215 the structure of the headpiece underlie PLB inhibition of SERCA, and binding of a single Ca(2+) ion

216 OP toxicity is thought to involve off-target inhibition of serine proteases, although the precise mol

217 Finally, VZHE-039 showed no significant inhibition of several CYPs, demonstrated efficient RBC p

218 Inhibition of SHIP1/SHIP2 reduced cellular survival and

219 transcriptional repression that leads to an inhibition of shoot growth in response to ethylene.

220 erfering RNA and Vivo-Morpholino, as well as inhibition of Smyd2 by its specific inhibitor, AZ505, le

221 nstatement of drug-seeking behavior, whereas inhibition of SNr GABA neurons produced optical intracra

222 Pharmacological inhibition of Src or overexpression of a kinase-dead Src

223 inhibitor, compound 15a exhibited sustained inhibition of SRC signaling both in vitro and in vivo.

224 rgeting of uncontrolled self-renewal through inhibition of stem cell-related signaling pathways has p

225 Conversely, inhibition of SubM potentiated laryngeal reflex response

226 l blockers, with possible application to the inhibition of subthreshold membrane depolarizations.

227 san to determine the effect of pharmacologic inhibition of SULT1E1 on AKI.

228 uce suppression of graft rejection relies on inhibition of T-cell activation.

229 roid enhancer and TAL1 promoter-1 leading to inhibition of TAL1 expression in erythroid cells, but no

230 ivator of transciription-6 (STAT6)-dependent inhibition of Tgfb1 transcription.

231 08348 engages alphavbeta6, induces prolonged inhibition of TGFbeta signaling and reduces lung collage

232 lexible N-terminal region and the associated inhibition of the activity is a novel mechanism of regul

233 The inhibition of the alpha-amylase and alpha-glucosidase ac

234 Inhibition of the alternative pathway (AP) of complement

235 Constitutive loss or acute inhibition of the Arp2/3 regulator, N-WASP, which is ass

236 ed with the human P2X1 receptor by measuring inhibition of the ATP-induced calcium influx.

237 Inhibition of the B-cell receptor pathway, and specifica

238 These data implicate inhibition of the cmA as a common denominator of anxioly

239 Remarkably, the inhibition of the competing HER from water reduction wit

240 These phenotypes correlated with inhibition of the CSCs signature, which consists of elev

241 ture-induced chemoresistance is abrogated by inhibition of the CXCR4 and hedgehog pathways.

242 deficits could be rescued by pharmacological inhibition of the eIF4G1 function and chemogenetic inhib

243 We found that type-2 cytokine-mediated inhibition of the expression of genes involved in early

244 These various strategies include the inhibition of the function of individual PRC2 core prote

245 carbapenem efficacy in CRE E. coli, whereas inhibition of the genes flhC and ygaC conferred added re

246 Inhibition of the genes hycA, dsrB, and bolA potentiated

247 Moreover, in several cases, specific inhibition of the IAV-induced splicing pattern also atte

248 ving the survival of PV(+) neurons, and that inhibition of the impairment of NR2B/PSD-95/MAP1A pathwa

249 ion of cystine to cysteine precludes product inhibition of the importer, so cystine import continues

250 Inhibition of the inflammasome effector caspase-1 or IL-

251 Finally, we show that inhibition of the insular cortex using GABA agonists imp

252 note, we identified that in addition to the inhibition of the intracellular replication of HIV by au

253 ncy recorded from neurons in this region via inhibition of the inwardly rectifying K(+) channels.

254 gested that treatment decreased left frontal inhibition of the left amygdala, and larger decreases we

255 We show that oncometabolite-induced inhibition of the lysine demethylase KDM4B results in ab

256 We also show the direct competitive inhibition of the M. abscessus beta-lactamase, Bla(Mab),

257 fting task while genetic and pharmacological inhibition of the MNK-eIF4E signaling axis protected aga

258 of the oncometabolite 2-hydroxyglutarate via inhibition of the mutant isocitrate dehydrogenase 1 (IDH

259 effect was attributable to the chemogenetic inhibition of the NAcC-projecting BLA neurons, as it was

260 We found pharmacologic inhibition of the p38, CK2, CDK, AXL, and PIKFYVE kinase

261 of prodynorphin in the BNST and chemogenetic inhibition of the PFC-BNST pathway restored abnormal res

262 Withdrawal of GABA(A) receptor-mediated inhibition of the RVLM increases sympathetic outflow and

263 Inhibition of the sodium-glucose cotransporter-2 (SGLT2i

264 Inhibition of the system A reduced the uptake of D-serin

265 o- and Ala-stimulated R(N) were mitigated by inhibition of the Target of Rapamycin (TOR) kinase signa

266 Genetic or pharmacological inhibition of the TMEM173-GSDMD-F3 pathway blocks system

267 c response is orchestrated by the reversible inhibition of the TMK1 signaling pathway at the cell sur

268 en projection neurons, feedback, and lateral inhibition of these axons by a large population of neuro

269 Together, inhibition of these two arms of the neutrophil response

270 t the infectivity potential of the virus and inhibition of this process.

271 nly provides insights into the mechanism and inhibition of this transglutaminase-induced ubiquitinati

272 Herein, we demonstrate that inhibition of tissue factor (TF) and the downstream coag

273 Inhibition of Tn-Tx potentially offers a new therapeutic

274 Chemical inhibition of TP53 protein combined with TP53 and RB1 tr

275 underlying this process was found to be the inhibition of TPPP1 by EBV-miRNA-BART12, which, in turn,

276 ation and, accordingly, it was blocked by an inhibition of translation.

277 f treatment effect modification resulting in inhibition of treatment effect in patients receiving alt

278 ing a prometastatic transcriptional program; inhibition of TRIM37 increases chemotherapy efficacy and

279 haracteristic of a metastatic phenotype, and inhibition of TRIM37 substantially reduced the in vivo p

280 Inhibition of TRPCs by small molecules was shown to be p

281 Finally, pharmacological inhibition of TRPM3 dampened TRPV1- and TRPA1-mediated r

282 Deletion of Trpm7 and inhibition of TRPM7 channel activity by the FDA-approved

283 eters and intracellular Ca2+ flux in CMs and inhibition of tubulogenesis in ECs.

284 ombined with focal irradiation causes strong inhibition of tumor growth in mouse xenografts, compared

285 on of (212)Pb-L2 demonstrated dose-dependent inhibition of tumor growth in the PSMA(+) flank tumor mo

286 L1 demonstrated activity-dependent, specific inhibition of tumor growth in the PSMA+ flank tumor mode

287 erate breast cancer metastasis, and targeted inhibition of tumor-derived vesicles may be a promising

288 Inhibition of TWEAK/Fn14 interaction could be efficaciou

289 Inhibition of Ube2v1 decreases CryAB(R120G)-induced aggr

290 Inhibition of USP7 and USP10 by chemical inhibitors or k

291 gene on one allele, with subsequent feedback inhibition of V(D)J recombination on the other allele.

292 A prevailing dogma is that inhibition of vascular thrombosis by antagonizing platel

293 As such, bevacizumab-based inhibition of VEGF has been the clinically adopted strat

294 Inhibition of VTA-core-projecting neurons disrupted Pavl

295 The gain in affinity led to almost equal inhibition of wildtype PfFNT and the Gly107Ser mutation.

296 d the set of genes that are upregulated upon inhibition of Wnt signaling in Wnt-addicted pancreatic a

297 We show that WDR26-mediated inhibition of wound repair is mediated through the inhib

298 26a was able to induce an 80% tumor growth inhibition of xenografts derived from the enzalutamide-r

299 Pharmacological co-inhibition of YAP and TEAD, or genetic deletion of YAP1,

300 This suggests that inhibition of ZNF529 or its gene product should be prior