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

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

6 bsequent addition of ketotifen significantly reversed this effect.

7 irus production, while CCL2 immuno-depletion reversed this effect.

8 erior Insular Cortex, while deep hypothermia reversed this effect.

9 e, whereas inhibition of miR-301a completely reverses the effects.

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

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

12 T1AR internalization and that MDM2 knockdown reverses this effect.

13 in phosphatases PP-1 and PP-2B (calcineurin) reverses this effect.

14 emia and identify dietary interventions that reverse these effects.

15 that treatment of edema has the potential to reverse these effects.

16 85.9%), accounting for more than half of the reverse triage effect.

17 be blocked by a small molecule predicted to reverse the tau effect.

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

19 ChemR23 downregulation reversed these effects.

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

21 AGEs or RAGE deletion in hepatocytes in vivo reversed these effects.

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

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

24 K27 methylation homeostasis in hypoxic cells reversed these effects.

25 on of Plin5 in the livers of Plin5(LKO) mice reversed these effects.

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

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

28 COS women and oestradiol (EE) administration reverses these effects.

29 s, and restoration of mitochondrial function reverses these effects.

30 ond NMR coupling constants in ethers and the reverse anomeric 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 f the active vitamin D metabolite calcitriol reversed all these effects.

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

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

36 her pharmacological upregulation of KLF2 can reverse the radiation effects.

37 All of these changes were reversed by blocking TSP1 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 o identify brain changes that do not reflect reverse causation or treatment effects.

42 es and trial lenses induce indistinguishable reverse Pulfrich effects, (2) anti-Pulfrich corrections

43 drenoceptor antagonist (BRL 44408) partially reversed the oxytocin effect, a descending noradrenergic

44 However, the reverse Pulfrich effect and the efficacy of anti-Pulfric

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 and programmed cell death 1 (PD-1) partially reverse this effect and are becoming standard of care in

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

50 SH-6 restored splicing factor expression and reversed both hormone staining effects and patterns of g

51 lenishing infected cells with exogenous heme reversed these effects and restored NAD(P)H oxidase acti

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

53 n of RASSF1A or inhibition of P4HA2 activity reverses these effects and increases markers of lung dif

54 netic inactivation of IMPDH2 in glioblastoma reverses these effects and inhibits cell proliferation,

55 In mice, the CD diet reverses these effects and promotes regression of HCCs t

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

57 The motion illusion-the reverse Pulfrich effect-and the paradigm we use to measu

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

59 Antidepressant-dose ketamine reversed these effects by selectively rescuing eliminate

60 oline dehydrogenase (PDH) activity, while Si reversed these effects caused by Buta.

61 of the quantum anomalous Hall effect can be reversed via field-effect control of the chemical potent

62 o fluorite-structure binary oxides-in which 'reverse' size effects counterintuitively stabilize polar

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

64 ISRIB substantially reversed the translational effects elicited by phosphory

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

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

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

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

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

70 d chains on the islands, adding both species reversed this effect-in part because the apex predators

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

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

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

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

75 emia, but whether inhibition of IL-1beta can reverse these effects is unclear.

76 This recently discovered illusion-the reverse Pulfrich effect-is caused by optical conditions

77 To test for a potential reverse causal effect, MR analysis with genetic instrume

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

79 mpact of these other factors likely reflects reverse causation-namely, downstream effects of early ad

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

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

82 nt to alleviate depression-like behavior and reverse the adverse effects of unpredictable chronic mil

83 as mDia1-interacting domains of Prohibitin2 reverse the anti-myogenic effects of mDia1DeltaN3, while

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

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

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

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

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

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

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

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

92 aspartate supplementation was sufficient to reverse the antihypertrophic effect of ACC2 deletion dem

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

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

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

96 Cerebellar rTMS was able to reverse the disruptive effects of a 'virtual lesion'.

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

98 tricted oxytocin receptor antagonist did not reverse the effect of intranasal oxytocin on alcohol dri

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

100 -kappaB inhibition in chondrocytes failed to reverse the effect of T1D.

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

102 contra-lesional and sham cerebellar rTMS to reverse the effects of a 'virtual-lesion' in health.

103 icated on identifying molecular targets that reverse the effects of aging in vulnerable regions of th

104 ly, irrigation can regionally cancel or even reverse the effects of all other forcings combined.

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

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

107 witching offspring to a healthy diet did not reverse the effects of maternal WSD on muscle insulin ac

108 afe and effective opiate antagonist that can reverse the effects of overdose and minimizing the delay

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

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

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

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

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

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

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

116 LP diets with branched-chain AA (BCAA) would reverse the negative effects of these diets on growth an

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

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

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

120 ilisation and subcutaneous injection did not reverse the positive effects of tunnel handling.

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 Mevalonate reversed the anti-fibrogenic effect of CSA13.

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

130 Idarucizumab completely reversed the anticoagulant effect of dabigatran within m

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

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

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

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

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

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

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

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

139 Finally, fenugreek specifically reversed the dysbiotic effects of HFD on numerous taxa i

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

141 ASHW treatment significantly reversed the effect of C-Ab with reduced pedal edema, ar

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

143 Deleting one copy of Fgf8 reversed the effect of deleting one copy of Spry1, which

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

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

146 Growth of osteoclasts in 3D gels reversed the effect of HIF-2alpha knockdown; HIF-2alpha

147 Addition of heme largely reversed the effect of HSPs on tumorigenic functions.

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

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

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

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

152 cells expressing mutant NRas with trametinib reversed the effect of mutant NRas expression by restori

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

154 7a, and activation by the agonist quinpirole reversed the effect of the D2R.

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

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

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 complex or inhibition of Fyn only partially reversed the effects of CD36 on hepatic insulin signalin

160 Moreover, we showed that a CD27 agonist Ab reversed the effects of CD70 ablation, indicating that t

161 Importantly, nebulized A967079 reversed the effects of e-cig liquid on sheep tracheal m

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

163 ion with alpha2delta-1Tat peptide completely reversed the effects of FK506.

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

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

166 pharmacologic manipulation of AC reduced or reversed the effects of HC on AC activity (THAM 103%, HC

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

168 ion of KCNQ channels altered cell firing and reversed the effects of M1R compounds, suggesting that K

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

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

171 Forced expression of RARbeta reversed the effects of miR-29b overexpression in prolif

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

173 of ULK1 (by MRT68921) or autophagy (by 3-MA) reversed the effects of mTOR inhibition, leading to incr

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

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

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

177 An IL6-blocking antibody reversed the effects of PTPN2-deficient macrophages, red

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

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

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

181 Inhibition of STAT1, STAT3, STAT5, or AKT reversed the effects of TC-PTP overexpression on epiderm

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

183 of an oncogenic Kras p.G12D mutation in mice reversed the effects of the MSC2504877/palbociclib combi

184 e-operated Ca(2+) entry blocker (GSK 7975 A) reversed the effects of TTX, L-NNA and ODQ.

185 ynthesis because inhibiting purine synthesis reversed the effects of UHMK1 overexpression.

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

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

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

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

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

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

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

193 tative KChIP2-interacting residues of DPP6-L reversed the inhibitory effect of NS5806 into potentiati

194 ns, increased Fos in CeM output neurons, and reversed the inhibitory effect of social choice-induced

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

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

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

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

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

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

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

202 P = 0.011) or contra-lesionally (P = 0.005), reversed the inhibitory effects of the cortical 'virtual

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

204 sion in the brain through carbogen breathing reversed the neuroprotective effects of FLASH, while rad

205 The use of NAC, a potent antioxidant, reversed the neurotoxic effects of HIV and methamphetami

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

207 4, a LXA4 receptor antagonist, significantly reversed the protective effect of MSCs on both survival

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

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

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

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

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

213 all molecule agonist directed against TRPML1 reversed the toxic effects of VacA on endolysosomal traf

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

215 Forced ASCL1 expression reversed the tumor-suppressive effects of Norrin in ASCL

216 ip loss, whereas, 10.0 g TRP supplementation reversed these negative effects of FSM.

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

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 Here, we show that estrogen replacement reverses some of the effects of surgical removal of the

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

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

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

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

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

228 Addition of heme to NSCLC cells partially reverses the effect of CycT on oxygen consumption, proli

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

230 This latter activity reverses the effect of melanoma cell-conditioned macroph

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

232 g (RGS) 16, and genetic RGS16 reconstitution reverses the effects of Arg2 overexpression.

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

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 Moreover, weight loss reverses the effects of obesity on MMe macrophage inflam

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

239 inhibition of calcineurin and NFAT signaling reverses the effects of phenformin on keratinocyte diffe

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

241 -1 receptor (Sig-1R), a molecular chaperone, reverses the pathological effects of (G4C2)-RNA repeats

242 JAK/STAT3 pathway by a JAK inhibitor AZD1480 reverses the pro-metastatic effect of sevoflurane and th

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

244 tically inhibiting EE-engaged neurons in CA1 reverses the rescue effect of EE on memory recall.

245 ls and promotes goblet cell differentiation, reversing an effect of aging.

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

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

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

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

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

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

252 1A and provide an important new approach for reversing the effects of human disease.

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

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

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

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

257 obin, improving systemic oxygen delivery and reversing the inhibitory effects of CO on mitochondria.

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

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

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

261 ter in development, CD40-Fc, which activates reverse signalling, had no effect on early sensory axon

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

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

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

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

266 Dihydrotestosterone (30 nM) reversed enzalutamide electrophysiological effects on in

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

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

269 pretreatment with clopidogrel (n = 3) partly reversed the detrimental effects on SEC injury and there

270 Blockade of interferon signaling reversed the effects on HBV replication.

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

272 full leptin-receptor antagonist, completely reversed the leptin-mediated effects on cell growth and

273 vation of PPARgamma by Rosiglitazone (10 uM) reversed the LPS-mediated effects on inflammatory cytoki

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

275 olinesterase inhibitor, donepezil (Aricept), reverses AIE effects on dendritic spines, possibly by in

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

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

278 e in Ras GTPase activating protein activity, reverses miR-431's effect on promoting invasion, Erk pho

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

280 tophagy and induces neuronal damage, and NAC reverses these deleterious effects on mitochondrial func

281 nduces candidal resistance to fluconazole by reversing the antifungal's effect on the ergosterol bios

282 even 24 h after acute stress, is capable of reversing the delayed enhancing effects on BLA synaptic

283 Reversing these effects on MBNL1 may therefore, yield po

284 sion; however, this treatment demonstrated a Reverse Warburg effect phenotype observed in cancer-asso

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

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

287 ly, combining antioxidant treatment and LDIR reverses this effect, promoting wild-type cell prolifera

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

289 c, if not controversial, theory known as the reverse anomeric effect (RAE).

290 ve, and enhancing B cell Ab responses, could reverse the immunosuppressive effects resulting from tob

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 To confidently attribute the reverse Pulfrich effect to interocular optical blur diff

298 Pharmacological inhibition of HSP90 reversed these effects to recapitulate the phenotype of

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.