ライフサイエンスコーパス: be mimicked by

1 SD to LD transition (increased food intake) was mimicked by 2 weeks of ICV infusion of chemerin into

2 midine (HET0016), an inhibitor of CYP4A, and were mimicked by 20-HETE.

3 OVA contraction was mimicked by 5-HT, and responses to both OVA and 5-HT

4 s persisted in the presence of tetrodotoxin, were mimicked by 5-HT(2C) receptor agonists and reversed

5 The YC-1-induced cell volume decrease was mimicked by 8-Br-cGMP and abolished by the sGC inhib

6 The BAY-58-2667-induced cell volume decrease was mimicked by 8-Br-cGMP and was abolished by the PKG i

7 the SNP's effect on pH(i) recovery was mimicked by 8-pCPT-cGMP but suppressed by ODQ and H-

8 s of caffeine on sleep and circadian rhythms are mimicked by a potent phosphodiesterase inhibitor, IB

9 hat the effect of such a remote coupling can be mimicked by a 3D Frohlich interaction with Thomas-Fer

10 This result could be mimicked by a depletion of cholesterol from cells.

11 ed reduction in mEPSC frequency, which could be mimicked by a GPER agonist and abolished by a GPER an

12 factor GLIS3, a pathogenic pathway that can be mimicked by a high-fat diet.

13 ed by the beta1a subunit and this effect can be mimicked by a peptide (beta1a490-524) corresponding t

14 ated by a general COX blocker and the effect is mimicked by a COX-1, but not COX-2, antagonist, sugge

15 TP) analogues in which the beta,gamma-oxygen is mimicked by a CXY group (beta,gamma-CXY-dNTPs) have p

16 aining peptides binding to the enzyme, which is mimicked by a helical domain mutation (E545K).

17 compounds in which the intramolecular H-bond is mimicked by a methylene linker.

18 ptophan metabolic enzyme kynureninase (KYNU) is mimicked by a portion of the HIV Env gp41 membrane pr

19 This activity is mimicked by a secreted variant of Crumbs2 (CRB2S) whi

20 we show that this deficit in differentiation is mimicked by a single mutation at serine-122, and demo

21 The G6P lowering by metformin was mimicked by a complex 1 inhibitor (rotenone) and an

22 d BTB (POZ) domain containing 2 (Kbtbd2) and was mimicked by a CRISPR/Cas9-targeted null allele of th

23 The latter effect was mimicked by a CXCR7-selective agonist TC14012 and ab

24 firing response of RTN chemoreceptors to ACh was mimicked by a muscarinic receptor agonist (oxotremor

25 2 ligation on in vitro macrophage maturation was mimicked by a selective protein kinase A agonist.

26 These effects were mimicked by a chloride-extruding cotransporter and

27 Moreover, the synaptic effects were mimicked by a combination of clonazepam with FGIN (

28 These results were mimicked by a kinetic model in which BBG binds weak

29 f ethanol on neurosteroid production and LTP were mimicked by a low concentration of NMDA (1 mum), an

30 The effects of NADH and NAD+ were mimicked by a phorbol ester and forskolin, respecti

31 ed by the addition of excess amino acids and is mimicked by AAR activation after selective amino acid

32 These protective effects were mimicked by acetate, but not by butyrate supplement

33 1beta-inducing effect of acidic medium could be mimicked by acidifying the cytosol with bafilomycin A

34 , the selective effect on erythropoiesis can be mimicked by activating p53 with the compound nutlin-3

35 We focus on cytokine receptor signaling that is mimicked by activating lesions in receptor subunits o

36 This effect was mimicked by activating adenylate cyclase (AC) with f

37 This regulation was mimicked by acute desphosphorylation of the GluR1-S8

38 emory deficits in mice lacking translin/trax are mimicked by ACVR1C inhibition.

39 Importantly, the effects of MCTs could be mimicked by adding Pluronic L81 to LCTs, and in vitro

40 for by suppression of OEA biosynthesis, and are mimicked by administration of the selective beta2-ad

41 st revealed that REM sleep abnormalities can be mimicked by administration of cholinomimetic agents.

42 n the absence of external stimuli, which can be mimicked by administration of hallucinogens.

43 imulation of CB1 cannabinoid receptors as it is mimicked by administration of CB1 agonists, blocked b

44 synovial fibroblast growth, and this effect was mimicked by Akt and NF-kappaB inhibitors.

45 olites in IL-4-stimulated macrophages, which was mimicked by ALOX15 knockdown.

46 tic effect of E2, increased mEPSC frequency, was mimicked by an ERalpha agonist in males, whereas in

47 tradiol reduced firing of GnRH neurons; this was mimicked by an ERalpha agonist.

48 ulation after intranasal insulin application was mimicked by an intravenous insulin bolus on placebo

49 amplitude, whereas in females, these effects were mimicked by an agonist of G protein-coupled ER-1.

50 The effects of PGE2 depended on cAMP, were mimicked by an EPAC-selective agonist, and were att

51 These effects were mimicked by an estrogen receptor (ER) beta-specific

52 These effects were mimicked by an inhibitor of c-myc function, implica

53 This effect was mimicked by, and was not additive with, genetic abla

54 tant downstream consequences of mimicking or being mimicked by another person.

55 These effects were mimicked by antagonism of adenosine receptors with

56 rating helminth larvae, which ideally should be mimicked by anti-helminth vaccines.

57 not induced by repeated activation and could be mimicked by application of drugs that increase cAMP c

58 The effect was mimicked by application of the membrane-impermeant B

59 This inhibitory action on fGDPs was mimicked by applying 2 mum glycine or 0.1 mum isoguv

60 This activity is mimicked by association of KIND to Fmn2.

61 This effect was mimicked by ATP and its metabolite, ADP, whereas the

62 n in human coronary artery endothelial cells were mimicked by bilirubin and abolished by incubation w

63 S8 distribution seen in transduction mutants were mimicked by block of transduction channels of cochl

64 This effect can be mimicked by blockade of NMDA-type glutamate receptors

65 This preference can be mimicked by BMP2/4 and suppressed by Noggin.

66 Warning signals displayed by defended prey are mimicked by both mutualistic (Mullerian) and parasit

67 This later action was mimicked by calciseptine, a Cav1 channel blocker.

68 spinal cord slices where C-fiber activation was mimicked by capsaicin challenge.

69 ER dysfunction can be mimicked by cellular stress signals such as disruptio

70 As these effects on DCs can be mimicked by chemical actin disruption, our results pr

71 nd modifying complexes, and this removal can be mimicked by chemical inhibition of histone deacetylas

72 ogenic to chondrogenic, a process that could be mimicked by chemical inhibition of NFAT translocation

73 using on olfactory response and behavior can be mimicked by chronically exposing single-housed males

74 stems can be correlated in a way that cannot be mimicked by classical systems.

75 nulopoiesis during infection, a process that is mimicked by clinical G-CSF use, yet we understand lit

76 tered expression of Fcgamma receptors, could be mimicked by co-culture of WT but not ST2(-/-) MCs wit

77 t of neurons from naive mice, and the change is mimicked by coculturing DRG neurons with the fibrosar

78 The Pten phenotype is mimicked by constitutive activation of PI3 kinase and

79 by overexpression of Stat5a but not Stat5b, was mimicked by constitutively active Stat5a, but did no

80 ing simplification induced by Abeta exposure were mimicked by constitutively active NFAT, and abolish

81 icoid receptor (MR) signaling, given that it was mimicked by corticoids and reversed by an MR inhibit

82 ed by various skin manifestations, which may be mimicked by CRDD.

83 ingly, the suppression phenotype of imgi can be mimicked by crossing im with the starch accumulation

84 CL2 family proteins, and this resistance can be mimicked by culturing CLL cells on CD154(+) stroma ce

85 This was mimicked by cyanide, but not by rotenone or antimyci

86 These effects were mimicked by D(1)-like agonists, blocked by a D(1)-l

87 sequences of ATP binding by E1, one that can be mimicked by D478A and N523A and one which cannot.

88 onsequence of chromosome nondisjunction, but is mimicked by depletion of vesicle fusion machinery.

89 ulating activity of RA on VEGF secretion can be mimicked by direct addition of H2O2.

90 5-HT effects were mimicked by direct activation of PLC, suggesting th

91 heir functional consequences, these variants were mimicked by directed mutagenesis and expressed in H

92 tide-depleting drug hydroxyurea, which could be mimicked by DNA cross-linking agents.

93 further demonstrated that biphasic responses were mimicked by dopamine, that the inhibitory phase dep

94 Such defects are mimicked by downregulation of OSBP, a VAP interactor

95 receptors and its antiepileptic activity can be mimicked by drugs acting on serotonin signalling path

96 east, the effect of eIF2 phosphorylation can be mimicked by eIF5 overexpression, which turns eIF5 int

97 obust, long-lasting hyperthermia effect that was mimicked by either H1 or H3 histamine receptor subty

98 This effect can be mimicked by elevating cAMP and is transcription depen

99 This unique configuration was mimicked by embedding primary hepatocytes in collage

100 seeds, a crowded macromolecular environment was mimicked by encapsulating Abeta40 monomers into reve

101 alysis of the G-protein signaling inhibitor, was mimicked by endogenous release of glutamate by tract

102 activation by endogenous ligands, which can be mimicked by environmental ligands, is an increase in

103 The GLP-1 effects were mimicked by exendin-4 and antagonized by exendin-9-

104 ippocampus-dependent memory, and this effect is mimicked by exogenous administration of stress-respon

105 The effect of strain on IGF-IR is mimicked by exogenous des-(1-3)IGF-I and is blocked b

106 enhancement requires dopamine signalling and is mimicked by exogenous dopamine.

107 This nicotinic effect was mimicked by exogenous administration of acetylcholin

108 This effect was mimicked by exogenous application of the heme degrad

109 pleted of NK cells or lacking IFN-gamma, and was mimicked by exogenous interleukin-15 (IL-15).

110 These effects were mimicked by exogenous adenosine administration and

111 in AMs from challenged mice and this defect was mimicked by exposing normal AMs to cytokines associa

112 This effect was mimicked by expression of a phosphorylated mimetic e

113 Such MN-selective changes were mimicked by expression of a single copy of the muta

114 The metabolic effects of RA or RARbeta are mimicked by FGF21 overexpression and largely abolish

115 Mannosylation patterns were mimicked by FL Ig-derived single-chain Fvs (scFv),

116 evidenced by the fact that the effect of CRH is mimicked by forskolin and 8-bromo-cAMP.

117 These actions were mimicked by forskolin, absent in IELs from Glp1r(-/

118 These effects were mimicked by free arginine or by a modified ZIP in w

119 The effect of proline was mimicked by glutamate, an intermediary of proline me

120 LA effects were mimicked by glycolytic inhibitors and reversed by i

121 of the glycoprotein VI agonist convulxin and was mimicked by glycoprotein VI inhibition or deficiency

122 This inhibition was mimicked by GW405833, another CB(2) receptor agonist

123 s, and sensitization to TRAIL; these effects were mimicked by H(2)O(2).

124 t of dendritic cell-targeted protein vaccine was mimicked by immunization with specific MHC II bindin

125 between cellulose microfibrils, which cannot be mimicked by in vitro binding assays.

126 lament structure and its calcium sensitivity were mimicked by increasing sarcomere length or by delet

127 Both sets of antagomir effects were mimicked by infecting cells with a p220 cDNA-encodi

128 ted inhibition of platelet aggregation could be mimicked by infusing mannitol.

129 systemic and hepatic metabolic fluxes could be mimicked by infusing rats with Intralipid or corticos

130 This can be mimicked by infusion of serum from exercised mice int

131 The reaction can be mimicked by inhalation of mannitol, but it has parado

132 e to adenosine-induced toxicity, which could be mimicked by inhibiting adenosine deaminase in control

133 luding suppression of CDX1 expression, could be mimicked by inhibiting prolyl-hydroxylases that activ

134 This effect is transient and can be mimicked by inhibiting the target-of-rapamycin kinase

135 ation of the antiapoptotic Bcl-2 protein; it was mimicked by inhibition and attenuated by overexpress

136 ts of DHA on cytokine-induced CAM expression were mimicked by inhibition/gene silencing of ASMase and

137 Stimulation by PIP(2) injection was mimicked by injecting IP(3), but inhibited by either

138 scular inflammation Methods: Acute infection was mimicked by injection of a single dose of lipopolysa

139 ased population density on reproductive span was mimicked by ins-6 loss of function that exerted effe

140 These acute cognitive impairments were mimicked by insulin (11.5 IU/kg) and mitigated by g

141 Self-peeling of gecko toes is mimicked by integration of film-terminated fibrillar

142 LPS (250 ug/kg) induced hypoglycemia, which was mimicked by interleukin (IL)-1beta (25 ug/kg) but no

143 The effect of LHb injection of GABA agonists was mimicked by intra-LHb muscarinic cholinergic (mACh)

144 eding-bout duration and reduction in rearing were mimicked by intra-vmPFC blockade of AMPA-type but n

145 zure onset and the reduced seizure frequency were mimicked by intracerebroventricular delivery of the

146 ose-dependent antihyperalgesic action, which was mimicked by intrathecally injected AM 404.

147 panion paper, we show that these defects can be mimicked by introducing conical lipids in a flat lipi

148 plification of Gq-coupled [Ca(2+)]i increase was mimicked by ionomycin and was not affected by inhibi

149 Both effects can be mimicked by iontophoretic application of glycine.

150 This response is mimicked by ISR-inhibiting drugs, providing insight i

151 nti-inflammatory effect could only partially be mimicked by JNJ28307474 and only when the H4R antagon

152 These effects are mimicked by knockdown of Shox2 in C3H10T1/2 cells.

153 -mediated Akt dephosphorylation, which could be mimicked by knockdown of HDAC3.

154 cell adhesion molecule-1 (VCAM-1) and could be mimicked by knockdown of mammalian target of rapamyci

155 This effect is mimicked by knockdown of Sirt3 in cultured myoblasts,

156 The effect of polyQ-htt on mEPSC was mimicked by knockdown of HAP1 and occluded by the do

157 and larger action potential amplitude, which was mimicked by knocking down full length survival motor

158 These patient-specific differences were mimicked by knocking out UBE3A using CRISPR/Cas9 or

159 Laryngeal citric acid-evoked swallowing was mimicked by laryngeal capsaicin challenges, implicat

160 d deficits in BDNF trafficking and signaling are mimicked by LDN (an inhibitor of UCH-L1) and can be

161 observed in patients with prefrontal damage are mimicked by lesions of our network.

162 ency for both isotopes from pH 6 to 8, which was mimicked by less desorption of (238)U, after the (23

163 isplay specific differentiation defects that are mimicked by loss of the transcription factor KLF4.

164 The effect of these mutations can be mimicked by loss of function of BAK1-INTERACTING RECE

165 y SB-269970 (5-HT7 receptor antagonist), and was mimicked by LP-211, a novel selective 5-HT7 receptor

166 and the LTB4:LXA4 ratio in vitro and in vivo was mimicked by macrophages lacking CaMKII or expressing

167 We show that the effects of SLC perturbation are mimicked by manipulation of either external sulfate

168 This effect is mimicked by membrane-impermeable analogs of estradiol

169 This inhibitory effect was mimicked by membrane-impermeable glucocorticoids, in

170 rimitive root and ternary sequence diffusers are mimicked by metadiffusers whose thickness are 1/46 t

171 Partition of the individual microspecies was mimicked by model compounds of the closest possible

172 block efferent-mediated fast excitation, but were mimicked by muscarine and antagonized by atropine,

173 desensitizing responses in NG2 cells, which were mimicked by muscimol and inhibited by bicuculline.

174 g and toxicity in yeast, part of which could be mimicked by mutating aspartic acid at position 2 to a

175 Phosphorylation of PLM was mimicked by mutation S63E (PKC site), S68E (PKA/PKC

176 -1 binding to the HR2 in response to glucose are mimicked by N-acetyl glucosamine, an intermediate of

177 The effects of OGD were mimicked by NMDA.

178 The effects of liver sinusoidal ECs can be mimicked by NO donors and can be reversed by NO inhib

179 are shared by class IA PI3Ks; the activation is mimicked by oncogenic mutations and the inhibition of

180 ticipated in a conditioning task, where they were mimicked by one face and 'anti-mimicked' by another

181 ts in repression of the rh5 promoter and can be mimicked by other Drosophila rhodopsins; it is partly

182 This phenotype is mimicked by other mouse mutants or pharmacological tr

183 These effects were mimicked by overexpressing the mitochondrial MnSOD

184 The latter phenotype is mimicked by overexpression of endocytosis-defective v

185 ot of P2X receptor inhibitors and also could be mimicked by P2Y1 agonist 2MeSADP.

186 Th17 and Th1 immune responses, and this can be mimicked by parasite-derived molecules.

187 show that this overgrowth relative to norms is mimicked by patterns of HC growth age in a large cont

188 ophage phagocytosis induced by palmitic acid were mimicked by PGE2 and PGD2 and were reversed by cycl

189 These effects can be mimicked by pharmacologic inhibition of beta-catenin

190 P on miR-206 expression and RMS tumor growth were mimicked by pharmacologic inhibition of HDAC.

191 The effect of neonatal handling is mimicked by pharmacological modulation of glia in adu

192 eptor-mediated enhancement of Kv7.5 currents was mimicked by pharmacological agents that increase [cA

193 Pulling events and cell spreading were mimicked by pharmacological phospholipase Cgamma1 a

194 This effect is boosted and can be mimicked by physiological concentrations of serotonin

195 eurons, displayed a Hebbian form of LTP that was mimicked by PKC activation.

196 The action of nicotine and NS1738 was mimicked by PNU-282987 (an alpha7 nAChR agonist), an

197 P(3)-mediated signaling, and, conversely, it is mimicked by postsynaptic injection of nonhydrolyzable

198 The actions of OEA are mimicked by PPAR-alpha agonists and abolished in mut

199 rks inhibits telomere replication, which can be mimicked by preventing replication fork restart throu

200 Furthermore, eEF2 phosphorylation was mimicked by prolyl hydroxylase (PHD) inhibition with

201 e, whereas in some others the role of sodium is mimicked by proton.

202 enhancing effects of calorie restriction can be mimicked by rapamycin.

203 Transport inhibition can be mimicked by recombinant beta-glucuronidase and is ass

204 th factor binding protein-5 (IGFBP-5), as it was mimicked by recombinant IGFBP-5 and mitigated by neu

205 ficits were abolished by IL-6 antibodies and were mimicked by recombinant IL-6; IL-1beta was not invo

206 rcapnia on HIF-alpha protein stability could be mimicked by reducing intracellular pH at a constant l

207 These effects were mimicked by repeated treatment with rolipram in wil

208 Contacts from B-DNA to UDG are mimicked by residues of the p56 helix, echoing the r

209 rine (NE) differentiation, a phenomenon that is mimicked by REST inactivation.

210 presynaptic D(2) receptors, and this effect was mimicked by Rp-cAMP, an inhibitor of cAMP-dependent

211 triatal circuit dynamics could be blocked or be mimicked by selective optogenetic manipulation of the

212 astric transit and acid secretion, which can be mimicked by selective sst(2) receptor agonist.

213 receptor 2 and PI3K/AKT signalling, and can be mimicked by selectively inhibiting VEGF-A binding to

214 -threonine residues, which in some cases can be mimicked by serine/threonine --> glutamate or asparta

215 ts of feeding on synaptic transmission could be mimicked by serotonin.

216 These phenotypes were mimicked by SHANK3-edited ES cells and rescued by t

217 Effects of gp130 depletion on growth could be mimicked by short hairpin RNA targeting of ERKs 1 and

218 inhibited neurite outgrowth, an effect that was mimicked by shRNA targeting the N1-Src microexon.

219 This phenotype can be mimicked by silencing G6P neurons and rescued by expe

220 lates with de-repression of let-7 miRNAs and is mimicked by silencing of downstream let-7 target HMGA

221 a synergistic mechanism of cell death, which was mimicked by simultaneous pharmacological inhibition

222 Strikingly, all these phenotypes are mimicked by single-gene RNAi experiments in C. elega

223 opmentally immature prefrontal responses can be mimicked by single microinfusion of the GABA(A) recep

224 tural alterations induced by sialylation can be mimicked by specific amino acid modifications to the

225 site occurred with an EC(50) of 0.8 mum and was mimicked by Sr(2+) but not Ba(2+).

226 or survivin in DC progenitors and conversely is mimicked by STAT3 inhibition.

227 The phenotypes are mimicked by sustained BAF60a or BAF60b expression an

228 These effects are mimicked by synthetic CpG oligodeoxynucleotides (ODN

229 sion and dampening of thalamocortical output was mimicked by tetanic activation of retinogeniculate a

230 ore, the effects of genetic ablation of eNOS are mimicked by the administration of the NOS inhibitor

231 enoceptor-selective antagonist prazosin, and are mimicked by the alpha(1)-adrenoceptor-selective agon

232 the presence of tolerizing autoantigens that are mimicked by the membrane-proximal external region of

233 change during flight, and that these effects are mimicked by the neuromodulator octopamine.

234 This could be mimicked by the actin-depolymerizing drug latrunculin

235 The AA mobilization induced by CMS could be mimicked by the addition of extracellular ATP and was

236 This gene regulation can be mimicked by the administration of normal, but not ADi

237 rease in sGC-beta1 heme content; (iii) could be mimicked by the heme-independent sGC activator BAY 60

238 Hypoxia-induced RNA editing by APOBEC3G can be mimicked by the inhibition of mitochondrial respirati

239 em subsequent to circuit development and can be mimicked by the inhibition of motor network function.

240 alcohol-aversion exhibited by male mice can be mimicked by the local inhibition of ERK signaling wit

241 nerative disorder that can, at least partly, be mimicked by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-

242 and soluble guanylyl cyclase (sGC), and can be mimicked by the nitric oxide (NO) donor sodium nitrop

243 ect of DHA on SOD-1 gene transcription could be mimicked by the peroxisome proliferator-activator rec

244 ges near the heme site in sGC-beta1 that can be mimicked by the pharmacologic sGC activator.

245 intracellular Sb(R)LD replication, which can be mimicked by the presence of Ab to IL-10.

246 The effects of PGD(2) on ILC2s could be mimicked by the supernatant from activated human mast

247 Although HPV is mimicked by the Complex I inhibitor, rotenone, the mo

248 This inhibitory effect is mimicked by the expression of a truncated OPHN1 mutan

249 The inhibitory effect was mimicked by the (kappa)2 receptor agonist GR89696, b

250 This inhibitory 5-HT effect was mimicked by the 5-HT1B receptor agonist CP93129 and

251 by MRS1754 (A2B receptor antagonist), and it was mimicked by the A2A receptor agonist CGS21680.

252 The effect of inosine was mimicked by the adenosine receptor agonist NECA and

253 The FRET response was mimicked by the agonist DHPG, abolished by the compe

254 thetic CB1R agonists induced robust LTD that was mimicked by the endocannabinoid (EC), noladin ether

255 ly enlarged late endosomes, a phenotype that was mimicked by the fusion inhibitor chloroquine in wild

256 This effect was mimicked by the FXR agonist GW4064 and suppressed by

257 Abeta-facilitated LTD was mimicked by the glutamate reuptake inhibitor TBOA, i

258 This asynchronous targeting pattern was mimicked by the injection of free H1 prior to or wit

259 ns followed by a rebound, a time course that was mimicked by the instantaneous silence density.

260 dies against the G protein subunit Gbeta and was mimicked by the myristoylated betagamma-binding/acti

261 This was mimicked by the PAR1-activating peptide TFLLR-NH(2),

262 KA inhibitor H89, whereas the effect of GD1a was mimicked by the PKA activator dibutyryl-cAMP.

263 izing effect of GLP-1 on electrical activity was mimicked by the PKC activator PMA, occurred without

264 This effect was mimicked by the selective CRTH2 agonist 13,14-dihydr

265 The effect of PGD(2) on HA production was mimicked by the selective DP1 agonist BW245C.

266 ons against amyloid toxicity, and its action was mimicked by the selective ERalpha agonist, 1,3,5-tri

267 This effect was mimicked by the selective mGluR2 agonist LY395756 an

268 These actions were mimicked by the A(1) receptor-specific agonist, N(6

269 The effects of PGI2 on stress fibres were mimicked by the adenylyl cyclase activator forskoli

270 Furthermore, these responses were mimicked by the beta-adrenergic receptor (betaAR) a

271 n were observed experimentally; these trends were mimicked by the computational results, which showed

272 s and extrasynaptic responses; these effects were mimicked by the glutamate reuptake inhibitor dl-thr

273 The inhibitory actions of YVAD-cmk were mimicked by the pan-caspase inhibitor zVAD-fmk and

274 These effects were mimicked by the PPAR-alpha synthetic agonists, feno

275 elated alterations in myocyte Ca(2+) cycling were mimicked by the RyR2 agonist, caffeine.

276 The excitatory actions of CCK8S were mimicked by the selective CCK(B) receptor agonist C

277 Effects of DCA were mimicked by the Takeda GPCR 5 agonist, INT-777 (50

278 the relaxation of agonist-contracted airways were mimicked by the thiol-reducing agent dithiothreitol

279 The effects of UCP2 deletion were mimicked by the UCP2 inhibitor genipin on both muri

280 S408/9) in the beta3 subunit, an effect that is mimicked by their mutation to alanines.

281 enerated reactive metabolites of paracetamol was mimicked by their adduct formation with the antioxid

282 This trend was mimicked by thermal insulation which initially impro

283 were enhanced by miR-10b, and these effects were mimicked by TIP30 silencing.

284 chronic inflammatory environment, since they were mimicked by TNF-alpha treatment of differentiated a

285 the spine surface occurred after GI-LTP and was mimicked by transfection with constitutively active

286 This protective effect could be mimicked by transient treatment with alphaIFN-gamma a

287 nted vacuolar phenotype of sac mutants could be mimicked by treating wild-type seedlings with PtdIns(

288 ent of basolateral amygdala neural input and was mimicked by treating isolated NPCs with conditioned

289 Influenza-induced protection was mimicked by treating suckling mice with a glycolipid

290 The conditions of immunocompromised patients were mimicked by treating pigs with an immunosuppressive

291 CD148 deficiency on ASM contractility could be mimicked by treatment of both mouse trachea and human

292 with cholesterol and sphingomyelin, and can be mimicked by treatment with cholesterol and sphingomye

293 The increase was mimicked by treatment with a liver X receptor (LXR)

294 The phenotype of CD81 knockdown cells was mimicked by treatment with a soluble peptide with th

295 These results were mimicked by treatment with the myosin II inhibitor

296 ity of the active site of [FeFe]-Hydrogenase is mimicked by two cyclodextrin molecules which surround

297 numerous ways in which the OEEF effects can be mimicked by use of (designed) local-electric fields (

298 The two detectors are mimicked by using two different distances from the c

299 The action of LY379268 on Gadd45-beta was mimicked by valproate and clozapine but not haloperi

300 ut due to innate immune activation and could be mimicked by virus-associated molecular patterns such