ライフサイエンスコーパス: reverse @3 effect

1 vivo, whereas knockdown of GPC5 was able to reverse the effect.

2 of the Notch Intracellular Domain (NICD) can reverse the effect.

3 dition of high molecular weight HA failed to reverse this effect.

4 Adenotonsillectomy appears to reverse this effect.

5 is the potential for antiviral treatment to reverse this effect.

6 cocaine-seeking behavior induced by OrxA but reversed DynA effect.

7 t, whereas supplementation with testosterone reversed that effect.

8 reas short-term deletion of PCSK9 expression reversed this effect.

9 nished xenograft growth and Brk reexpression reversed this effect.

10 owing BDNF treatment, and calpain inhibition reversed this effect.

11 n fluvastatin sensitivity; knocking out ZEB1 reversed this effect.

12 mice compared with WT, and exogenous ghrelin reversed this effect.

13 bsequent addition of ketotifen significantly reversed this effect.

14 ial function, as inhibition of NOS partially reverses this effect.

15 in associated with formin homology 1 domains reverses this effect.

16 on of VAC14 in postsynaptic Vac14(-/-) cells reverses this effect.

17 le's growth; interfering with Yap's activity reverses this effect.

18 beta-Carotene can upregulate BCMO1 and reverse these effects.

19 emia and identify dietary interventions that reverse these effects.

20 85.9%), accounting for more than half of the reverse triage effect.

21 uated, and anti-heparanase or PI3K activator reversed these effects.

22 at 22d after HI, while wortmannin partially reversed these effects.

23 le expression of constitutively active STAT5 reversed these effects.

24 in UM-UC-3 or ASS1 silencing in RT112 cells reversed these effects.

25 caveolin-1 scaffolding domain peptide (CSP) reversed these effects.

26 tests, and genetic deletion of hepatic FoxO1 reverses these effects.

27 nous source of processed HH or a SMO agonist reverses these effects.

28 saggregases, or overexpression of kinesin-1, reverses these effects.

29 ond NMR coupling constants in ethers and the reverse anomeric effect.

30 Yops reported to inhibit translocation could reverse the CNF-Y effect.

31 th reduction is normally expected due to the reverse Hall-Petch effect.

32 , whereas damage to structure B produces the reverse pattern of effects.

33 t with mannitol after traumatic brain injury reversed all these effects.

34 f the active vitamin D metabolite calcitriol reversed all these effects.

35 a well-described KLF4 target, did not fully reverse KLF4-mediated effects.

36 f anti-B7-H1 blocking antibody significantly reversed the inhibitory effect.

37 crophage parasite burden and, given in vivo, reversed their protective effects.

38 h VKAs and LMWH, there are no antidotes that reverse their anticoagulant effect.

39 ht loss via dietary modification effectively reverses these deleterious effects.

40 Knockdown of Nrf2 expression reversed these IER3-dependent effects.

41 artificial photonic material mimicking this reverse color-order diffraction effect.

42 neutralising anti-Anx-A1 monoclonal antibody reversed the cromone inhibitory effect.

43 al dementia rating (CDR) is not because of a reverse causation or confounding effect.

44 de of GLT1 in NAc core, but not shell, would reverse the ceftriaxone-mediated effect.

45 ic regional perfusion (NRP) in the donor may reverse these effects and improve organ function.

46 The phosphomimetic mutants reverse these effects and reduce K0.5Na below control K0

47 n immunosuppressive cytokine, TGFbeta, might reverse these effects and thereby potentiate oHSV effica

48 Inactivating mutations in ANK3/unc-44 reverse this effect and cause detrimental effects in you

49 In contrast, interferon gamma (IFN-gamma) reversed these effects and medroxyprogesterone acetate e

50 at the naturally occurring statin mevastatin reverses FPP's effects and promotes healing by using in

51 This can be called "reverse fluorine Perlin-like effect", and it is shown to

52 lipoxin A4 receptor with the antagonist Boc2 reversed this effect, and treatments were ineffective in

53 expression in the NAc shell (NAcsh) not only reversed these cocaine-induced effects but also downregu

54 DOT1L inhibitors reverse these effects, but their clinical use is potenti

55 The mGlu2/3 antagonist LY341495 reversed the LY354740 effect, but not the XA effect.

56 ptor or the nicotinic acetylcholine receptor reversed the protective nutritional effects compared wit

57 The reverse fluorine Perlin-like effect does not have a gene

58 ISRIB substantially reversed the translational effects elicited by phosphory

59 Here, we documented that methylene blue (MB) reverses the Warburg effect evidenced by the increasing

60 ntly marketed KV 7 channel opener, partially reversed these effects for the majority of analyzed muta

61 y is suppressed, and this inhibition must be reversed to engender tissue effects; however, the mechan

62 er than hyphen-insert priming and produced a reversed priming effect in the N400 time-window compared

63 overexpression in the PFC of these HET mice reversed the antidepressant-like effect in SPT and TST.

64 ade of the synthesis of 20-HETE with HET0016 reversed the renoprotective effects in SS.5(BN) rats.

65 toma neurospheres, whereas a STAT3 inhibitor reversed this effect in vitro and in vivo.

66 CBR703 partially reverses these effects in CBR-resistant RNAPs while inhi

67 ersely proportional, whereas NOS1 deficiency reverses this effect, increasing leak and elevating reac

68 oncogenic kinase that stimulates glycolysis, reversed these effects, indicating that metabolism of py

69 rial treatment using BRAF and MEK inhibitors reversed the developmental effects induced by BRAF(V600E

70 Inhibition of GSK-3beta activity reversed the effects induced by mAb16D10 in SOJ-6 cells,

71 The ability to reverse their anticoagulant effects is important when se

72 t for latency considerations and to minimize reverse causality, and considering effect modification b

73 Indeed, addition of an EP4 antagonist could reverse the effects observed on cytokine production afte

74 Reducing E2 expression by doxycycline reversed the inhibitory effects observed in the E2-expre

75 This partially reversed the protective effects observed in the linezoli

76 was confirmed by depletion experiments that reversed the tumor inhibitory effects observed in C3aR-d

77 at a single session of atDCS can temporarily reverse nonbeneficial effects of aging on cognition and

78 ith the alpha2delta-1 receptor, and thus may reverse or ameliorate the effects of AIE on hippocampal

79 ged animal to young blood can counteract and reverse pre-existing effects of brain aging at the molec

80 of intravenous idarucizumab would be able to reverse the anticoagulant effect of dabigatran in patien

81 noclonal antibody fragment, was developed to reverse the anticoagulant effect of dabigatran.

82 med to using vitamin K if there is a need to reverse the anticoagulant effect of vitamin K antagonist

83 intravenous idarucizumab and its capacity to reverse the anticoagulant effects of dabigatran in patie

84 umab, an antibody fragment, was developed to reverse the anticoagulant effects of dabigatran.

85 Andexanet is designed to reverse the anticoagulant effects of factor Xa inhibitor

86 The ability of FXa(I16L) to reverse the anticoagulant effects of FXa inhibitor depen

87 onclusion of carotid endarterectomy (CEA) to reverse the anticoagulant effects of heparin and to limi

88 h is routinely used after cardiac surgery to reverse the anticoagulant effects of heparin, is known t

89 Acute antagonist treatment did not reverse the beneficial effects of chronic drug treatment

90 at cranial transplantation of stem cells can reverse the deleterious effects of chemobrain, through a

91 udy, we determined ifmaternal exercise could reverse the detrimental effects of maternal high-fat fee

92 receptor antagonists can partially or fully reverse the detrimental effects of Tat, glutamate recept

93 beta-catenin to truncated APC and thereby to reverse the effect of APC truncation.

94 r, these agents inhibit exon 10 splicing and reverse the effect of destabilizing disease-causing muta

95 RNA-induced cell-cell adhesion but failed to reverse the effect of Galpha13 siRNA on proteolytic inva

96 f S-nitroso-N-acetylpenicillamine (SNAP) can reverse the effect of l-NAME in partial restore IkappaB

97 s and recombinant factor VIIa can be used to reverse the effect of NOACs.

98 had no effect on BOLD responses and did not reverse the effect of TMPAP.

99 macologically repressed in ETPs to partially reverse the effects of aging.

100 zumab is available as an antidote to rapidly reverse the effects of dabigatran.

101 ceptor antagonist methoctramine was found to reverse the effects of EDR.

102 contrast, medical professionals can quickly reverse the effects of heparin using protamine.

103 ated platelets was sufficient to efficiently reverse the effects of ibrutinib, and platelet functions

104 ully antiquated and have failed to arrest or reverse the effects of kidney-related diseases.

105 and forced expression of either of them can reverse the effects of miR-495 overexpression on inhibit

106 al need for a rapid, pro-hemostatic agent to reverse the effects of several new anticoagulants.

107 hrine uptake inhibitor desipramine failed to reverse the effects of TBZ, and higher doses of these dr

108 on of various monoamine uptake inhibitors to reverse the effects of TBZ.

109 xanet and ciraparantag have been reported to reverse the effects of the anti-Xa NOACs (rivaroxaban, a

110 Diazoxide did not reverse the glucagonostatic effect of glucose.

111 The data suggest that S107 can reverse the harmful effects of redox active species on S

112 iments further showed that exogenous ATP can reverse the inhibitive effects of carbenoxolone and that

113 We show that these oxysterols reverse the inhibitory effect of an RORgammat antagonist

114 Co-overexpression of EPI64B with Rab27B can reverse the inhibitory effect of Rab27B on amylase relea

115 that L-amino acids were able to specifically reverse the inhibitory effects of their cognate D-amino

116 natives during invasion could weaken or even reverse the negative effects of exotic-native phylogenet

117 deficiency in IL-4 and IL-10 was required to reverse the negative effects of helminth coinfection on

118 ht be an interesting therapeutic approach to reverse the pathogenic effect of such mutants.

119 g SMCs with rexinoids would more effectively reverse the pathophysiologic effects of angiotensin II t

120 leeding when it does occur with NOACs and to reverse the pharmacological effect of these agents if ne

121 IL-6, IL-8, and CXCR1 signaling pathways to reverse the proapoptotic effect of the IL-32gamma isofor

122 important given the potential to mitigate or reverse the side effects of immunosuppressive medication

123 d activation of mPT were found to mirror and reverse, respectively, the antiseizure effects of the KD

124 Knockdown of phb2 partially reversed beneficial effects of SPL overexpression.

125 y, we also determined that PLN-alen not only reversed protumoral effects of the PLN carrier, but also

126 Importantly, maternal ADN supplementation reversed the adverse effects of maternal obesity on plac

127 neutralization of TGF-beta1, but not IL-10, reversed the analgesic effect of BMSCs.

128 macological inhibition of PI3K/Akt signaling reversed the anti-apoptotic effects of NRG4, confirming

129 Mevalonate reversed the anti-fibrogenic effect of CSA13.

130 atus, and that suppression of AhR expression reversed the anti-proliferative effects of flutamide.

131 Idarucizumab completely reversed the anticoagulant effect of dabigatran within m

132 s, idarucizumab rapidly, durably, and safely reversed the anticoagulant effect of dabigatran.

133 T-737 promoted mixed chimerism induction and reversed the antitolerogenic effect of calcineurin inhib

134 Knockdown of GRP78 reversed the attenuating effect of ECD overexpression on

135 rs of phagosome and autophagosome maturation reversed the beneficial effect of statins on bacterial g

136 ic oxide synthase inhibitor to FoxO4 KO mice reversed the beneficial effects of FoxO4 deletion on pos

137 Additionally, cell-autonomous PDF signaling reversed the circadian behavioral effects of lowered Ral

138 cetyl cysteine attenuated ROS production and reversed the cytotoxic effects of K-Ras(G12V) in the TKO

139 trate/nitrite restored intestinal perfusion, reversed the deleterious effects of endothelial TLR4 sig

140 Strikingly, a single insulin injection reversed the deleterious effects of HFD on memory and so

141 malized monocyte/macrophage polarization and reversed the detrimental effects of hyperglycemia, sugge

142 -treatment with the KMO inhibitor Ro 61-8048 reversed the detrimental effects of IL-1beta on neurogen

143 Blocking cell cycle progression reversed the effect of Atm loss on tumor endothelial cel

144 In vivo, EP3 receptor antagonism reversed the effect of cancer-induced thrombosis in WT m

145 In contrast, anti-IFN-gamma antibody reversed the effect of epithelial mediators on RANKL exp

146 nhibitors of ERK and AKT pathways completely reversed the effect of GHRH-R agonists on CSC proliferat

147 COL2A1 and aggrecan mRNA expression), which reversed the effect of IL-1beta.

148 In addition, anti-C1q reversed the effect of imC1q alone, shifting the LPS-ind

149 but not beta2, subunit knockdown effectively reversed the effect of increased ACh signaling in a mous

150 sion of a catalytically inactive Shp2 mutant reversed the effect of ITSN1 on Spry2 dephosphorylation

151 ogical blockade of CRF1 receptors in the VTA reversed the effect of nicotine on GABAergic input to do

152 d dominant negative mutants of Arf6 and Rac1 reversed the effect of reduced ARAP2 expression.

153 7a, and activation by the agonist quinpirole reversed the effect of the D2R.

154 verexpression of several proteasome subunits reversed the effect of UBE3A(T485A) on Wnt signaling.

155 effect of AC whereas remethylation of AC DNA reversed the effects of activation and restored the abil

156 of MCK-betaAPP muscle cells with glutathione reversed the effects of beta-amyloid accumulation on Ca(

157 s Tap1 and Tap2 The PSMB8 inhibitor ONX-0914 reversed the effects of BPTF ablation, consistent with a

158 Tetracaine reversed the effects of caffeine but not of ryanodine.

159 ration of a 20-HETE antagonist prevented and reversed the effects of dihydrotestosterone on BP.

160 The 4F-PCC dose-dependently reversed the effects of edoxaban (60 mg), with complete

161 which can function downstream of DDR1, also reversed the effects of Galpha13 knockdown on cell-cell

162 at also co-localizes to cell-cell junctions, reversed the effects of Galpha13 knockdown on cell-cell

163 nd the SK2 specific blocker apamin partially reversed the effects of increased NeuroD2 expression on

164 tumor formation, and ectopic MYCN partially reversed the effects of MDM2 depletion, indicating that

165 Inhibition of Shh signaling reversed the effects of miR-219 depletion and forced exp

166 Forced expression of EphA4 reversed the effects of miR-519d overexpression, whereas

167 ced gene expression for galectin-1, and they reversed the effects of morphine on galectin-1 expressio

168 Restoring serum adiponectin levels reversed the effects of obesity on the lung endothelium

169 sterone receptor antagonist RU-486 partially reversed the effects of P4 on NF-kappaB pathway.

170 Mating reversed the effects of pheromone perception; therefore,

171 analyses demonstrated that dephosphorylation reversed the effects of phosphorylation on the magnitude

172 Conversely, a TGFbetaR1 inhibitor reversed the effects of PKCalpha loss in LSL-Kras/Prkca(

173 res induced expression of ductal markers and reversed the effects of Slug by inducing ductal structur

174 Intranasal OT largely reversed the effects of stress on behavior in male mice,

175 Inhibition of STAT3 or AKT reversed the effects of TC-PTP deficiency on apoptosis a

176 ated with pharmacologic interventions, which reversed the effects of the extravasated vasopressors: i

177 Interestingly, TCF4 knockdown reversed the effects of Wnt3a activation on BACE1 transc

178 Indeed, two different JNK inhibitors reversed the enhanced analgesic effect of morphine, a kn

179 that both IFNalpha and IFNbeta (type I IFNs) reversed the immunosuppressive effect of MSCs on splenoc

180 oups in p65, whereas the thiol reductant DTT reversed the inhibiting effect of H2S on the p65 DNA bin

181 nted 5-HT-induced phosphorylation of Mypt-1, reversed the inhibitory effect of 5-HT on efferocytosis,

182 siRNA-mediated VDR knock-down reversed the inhibitory effect of calcitriol on LEC tube

183 analogue 1-oleoyl-2-acetyl-sn-glycerol (OAG) reversed the inhibitory effect of candesartan, while thi

184 These compounds potently reversed the inhibitory effect of GKRP on GK activity an

185 We also found that IR415 reversed the inhibitory effect of HBx protein on activit

186 IRF3 siRNA, but not MyD88 siRNA, reversed the inhibitory effect of HMGB1 on HPAEC migrati

187 Likewise, TLR4 siRNA but not control siRNA reversed the inhibitory effect of hypoxia in HPAECs.

188 In addition, siRNA interference of FBXW7 reversed the inhibitory effect of MAGEA1 on migration an

189 ly, acetylation at K6, but not at K9 or K15, reversed the inhibitory effect of T3 phosphorylation.

190 Transfection of anti-miR-146a nucleotides reversed the inhibitory effect of Tbeta4 on IRAK1 and TR

191 cytes, and the addition of a STAT5 inhibitor reversed the inhibitory effect of the CB2 agonist on IL-

192 tat-treated cells with recombinant sAPPalpha reversed the inhibitory effect of the drug thereby indic

193 luc cells delivered with miR-135 and miR-203 reversed the inhibitory effect of the miRNAs on tumor gr

194 rofen arginate but not ibuprofen sodium also reversed the inhibitory effects of ADMA and N(G)-nitro-l

195 not CD8(+) T cells in tumor-bearing subjects reversed the inhibitory effects of C3 deletion.

196 -monomethyl l-arginine [l-NMMA] monoacetate) reversed the inhibitory effects of DCP on intracellular

197 diate alpha-ketoglutarate to the Rb TKO MEFs reversed the inhibitory effects of glutamine deprivation

198 ceptors nor an inhibitor of protein kinase A reversed the inhibitory effects of propofol.

199 OCK1/2 activity in Slug-expressing Kras mice reversed the inhibitory effects of Slug on ADM, ERK1/2 p

200 ed drug delivery in various tumor models and reversed the negative effect of VEGF ablation on drug de

201 or blockers A779 and D-Pro-angiotensin-(1-7) reversed the normalizing effects of angiotensin-(1-7) on

202 by ICG-001, a beta-Catenin inhibitor, which reversed the promoting effect of miR-101.

203 with a CD39 or CD73 inhibitor significantly reversed the protective effect of G-MSCs on CIA.

204 4, a LXA4 receptor antagonist, significantly reversed the protective effect of MSCs on both survival

205 Targeting the ErbB3/ErbB2 pathway partially reversed the protective effects of fibroblast/CAF-derive

206 rmacological and genetic inhibition of STAT3 reversed the protective effects of IL-10, whereas ectopi

207 itor or Zileuton, a 5-LOX inhibitor with VPC reversed the protective effects of VPC against neuroinfl

208 expression in vivo by small interfering RNA reversed the renoprotective effects of AG.

209 Moreover, TNPO1 overexpression partially reversed the repressive effect of miR-128 on L1 retrotra

210 ROCK target, and inhibitors of RhoA and ROCK reversed the suppressive effect of 5-HT on efferocytosis

211 minals in nucleus accumbens (NAc) completely reversed the suppressive effect of BDNF on morphine rewa

212 Sialidase treatment of fibrinogen reversed the suppressive effect of siglec-E on CD11b sig

213 Neutralization of IL-27 completely reversed the therapeutic effect of R848 in the experimen

214 cking defect, and restoring full-length RILP reversed the trafficking effects of virus.

215 ut not suppression of intestinal microbiota, reversed these protective effects of CSA13.

216 enzyme transketolase-like 1 (TKTL1) by siRNA reversed theses effects of TIGAR.

217 , and increasing the extracellular viscosity reversed, the effect of suppressed glial buffering on th

218 of GLUD2 into murine glioma progenitor cells reverses deleterious effects of IDH1 mutation on metabol

219 Cardiolipin reverses destabilizing effects of ADP and bongkrekic aci

220 We find that AF reverses negative effects of nestedness and positive eff

221 n of CD47 by TSP1 or loss of CD47 expression reverses some inhibitory effects of VEGF on proliferatio

222 he development of a monoclonal antibody that reverses the anticoagulant effect of the direct thrombin

223 Overexpression of PIM2 or eIF4E partially reverses the antiproliferative effect of CHES1, indicati

224 ippocampus, with the antagonist bicuculline, reverses the anxiolytic effect of running.

225 ction and young blood-induced revitalization reverses the behavioral effects of aging.

226 CV, either from late relapse or reinfection, reverses the beneficial effects of SVR.

227 Critically, a claudin-5 peptide mimetic reverses the deleterious effects of alcohol on alveolar

228 ild-type and ob/ob mice, and also completely reverses the deleterious effects of the Cdk5 ablation.

229 A G-quadruplex stabilizer partially reverses the effect of ATRX, inferring ATRX may normally

230 of H3K9M, a histone H3 mutant transgene that reverses the effect of Kdm4d on H3K9 methylation.

231 , has identified mechanisms whereby ketamine reverses the effect of stress, but little is known regar

232 s susceptibility, whereas its overexpression reverses the effects of early life stress.

233 le, named ISRIB, that potently (IC50 = 5 nM) reverses the effects of eIF2alpha phosphorylation.

234 s, whereas warming to 39 degrees C partially reverses the effects of hypothermia on monocyte function

235 Suppression of PGC-1beta and PRC with siRNA reverses the effects of IGF-1 and disrupts mitochondrial

236 s a naturally occurring NMDAR modulator that reverses the effects of NMDAR antagonists in animal mode

237 (1)-pyrroline-5-carboxylate (P5C) or proline reverses the effects of P5C synthase knockdown but not P

238 Additionally, we demonstrate that SFN reverses the effects of PMI in co-treated cells by reduc

239 PA1 reverses the effects of the coactivator TIF2 on GR-media

240 Accordingly, knockdown of SIP1 reverses the inductive effects of DM/SB on mDA different

241 Inhibition of AKT also effectively reverses the protective effect of NRG1 and HGF in tramet

242 R-induced phosphorylation of STAT3, and also reverses the protective effect of OSM and IL-6/R on NMDA

243 Blocking these changes reverses the protective effect of V3 on monocyte adhesio

244 upplementation of iron-deficient individuals reverses the protective effects of iron deficiency.

245 Blockade or loss of IL-6 signaling reverses the protective effects of p53 deficiency.

246 15 mg/kg dose of ACET was also effective in reversing behavioral effects of the selective kainate ag

247 mprove vagal neuronal health in the brain by reversing some effects of chronic high-fat diet as well

248 bserved that notch signaling was involved in reversing the adverse effects of BEV.

249 part human disorder but more importantly for reversing the adverse effects of the mutant gene using g

250 n glucocorticoid-treated macrophages without reversing the anti-inflammatory effects of glucocorticoi

251 changes in neurons, a potential strategy for reversing the deleterious effects of DOX treatment.

252 zed that this approach would be effective in reversing the detrimental effects of apolipoprotein (apo

253 tatory neurostimulation protocols capable of reversing the disruptive effects of focal cortical inhib

254 For example, reversing the effect of climate-related stress on macroa

255 of EPs and present an innovative method for reversing the effect of loss.

256 Compound 7z was active in reversing the effect of scopolamine in the novel object

257 onoclonal antibody fragment idarucizumab for reversing the effects of dabigatran, the investigational

258 1A and provide an important new approach for reversing the effects of human disease.

259 induced a proinflammatory phenotype in HMDMs reversing the effects of imC1q alone.

260 Controlling and reversing the effects of loss are major challenges in op

261 rformance in humans, perhaps forestalling or reversing the effects of neurodegeneration in aging.

262 y in C. difficile-infected mice by partially reversing the effects of TcdB on enterocyte proliferatio

263 ine transmission are relatively effective at reversing the effort-related effects of TBZ, and are con

264 d PMEPs bilaterally (F1,14 = 7.4, P = 0.017) reversing the inhibitory effects of 1 Hz rTMS in the pre

265 parasitoid species, drought stress partially reversing the negative effect of root herbivory on perce

266 LL4 in interacting with the HDAC complex and reverse its effect on PTEN repression.

267 CRT exerts pronounced reverse remodeling effects on the left atrium that indep

268 recurrent mitral regurgitation, and improved reverse remodeling without adverse effect on left ventri

269 Finally, 5377051 can reverse SGK1's effects on NaV1.5 and shorten the action

270 o the direct activator of AMPK, ZMP, did not reverse the effects on TNF-alpha-induced CFB expression,

271 inhibiting matrix metalloproteinases in ACM reversed ACM's effect on tumor cells.

272 to the rVLM of EA-treated CIH rats partially reversed EA's effect on elevated BP (n = 4).

273 tration of edoxaban (60 mg) dose-dependently reversed edoxaban's effects on bleeding duration and end

274 hibition against Activin A signaling and was reversed for effects on calcium handling in HL-1 cells.

275 bitors diminished nascent HSC production and reversed glucose-mediated effects on HSCs.

276 d mammalian cells for somatic mutations that reversed its effect on the ISR.

277 nduced death of immature OLs, but only MK801 reversed Tat effects on myelin-like membranes.

278 Ab-mediated blockade of hepcidin partially reversed the effects on iron biology caused by IL-22R st

279 ed by peripheral stimulation and LHb lesions reversed the inhibitory effects on cocaine locomotion pr

280 Inhibition of this pathway reversed the observed effects on cancer stem cell (CSC)

281 Inhibition of NKCC1 with bumetanide reversed the paclitaxel effect on GABA-mediated hyperpol

282 Anti-CTGF reversed the SCM-mediated effects on myelination.

283 Encapsulating alendronate in PLN reversed these effects on myeloid cells and shifted the

284 indicated that TGF-beta pathway attenuation reverses carbofuran's inhibitory effects on neurogenesis

285 al administration of ketamine (2.5-20 mg/kg) reverses CSDS-induced effects on reward or, in separate

286 XE991 or the KCNQ channel opener retigabine reverses the effects on consolidation caused by manipula

287 Both priming and following cTBS150 reversed the LTD-like effect produced by PAS10 with litt

288 d viability of Huh7.5A2 cells, PD-1 blockade reversed this effect, producing enhanced cytolytic elimi

289 trophils, whereas the presence of tryptophan reversed this effect, providing a possible mechanism for

290 antagonist, or the mTOR inhibitor rapamycin reversed LIF-mediated effects, resulting in growth arres

291 Supplementation with AA failed to reverse this effect, suggesting that the sites of action

292 the histone H3K4 methyltransferase Trithorax reverses these effects, suggesting that an Lsd1/CoRest c

293 with bevacizumab (BEV, anti-VEGF), it could reverse the adverse effects that precipitate fibrotic ch

294 nhibition of the protein kinases Akt or mTOR reversed the IL-7 effect, thereby restoring the function

295 knockdown of OGT by RNA interference (RNAi) reverses this effect, thereby opening up the opportunity

296 n and to determine whether it is possible to reverse these effects through nutritional interventions

297 sport in vitro, the potential mechanisms for reversing this detrimental effect to maintain healthy tr

298 A similar effect to the well-known reverse Perlin effect was observed on the (1)JC-F coupli

299 tentially toxic chemosensitizing agents that reverse MDR effects, which has raised expectations in th

300 istance of breast cancer and the avenues for reversing such effects with aspirin.