ライフサイエンスコーパス: be mimicked by

1 The heat-induced hyperpolarization was mimicked by 10 microM arachidonic acid, an agonist o

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

3 This promigratory effect was mimicked by 2-MeSADP, but not by AMP, and was inhibi

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

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

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

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

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

9 0-c arboxylic acid hexyl ester (KT 5720) and was mimicked by 8-bromo-cGMP and BAY 41-2272.

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

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

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 closure on chain length in a way that cannot be mimicked by a simple wormlike model and accumulating

15 extensive dendritic Ca2+ electrogenesis and being mimicked by a non-specific block of K+ channels wi

16 voltage-sensitive Ca2+ channel blockers and is mimicked by a brief climbing fiber burst.

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

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

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

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

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

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 This effect was mimicked by a peroxisome proliferator-activated rece

26 2 ligation on in vitro macrophage maturation was mimicked by a selective protein kinase A agonist.

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

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

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

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

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

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

33 The effect of wounding on tumor growth can be mimicked by acellular wound fluid, suggesting that T

34 1beta-inducing effect of acidic medium could be mimicked by acidifying the cytosol with bafilomycin A

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

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

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

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

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

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

41 mparison, anti-inflammatory effects of AICAR were mimicked by adenosine but not inosine, the metaboli

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

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

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

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

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

47 ent with PGE(2) induced Id-1, an effect that was mimicked by an EP(4) agonist.

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

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

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

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

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

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

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

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

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

57 These effects were mimicked by antagonism of adenosine receptors with

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

59 The effects of in vivo cocaine could be mimicked by application of cocaine to BNST-containing

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

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

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

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

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

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

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

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

68 ted changes in phosphorylation at both sites were mimicked by cAMP addition and inhibited by protein

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

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

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

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

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

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

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

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

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

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

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

80 Regional ischemia was mimicked by covering the central portion of monolaye

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

82 tagonism of the CRF receptor-1 (CRF-R1), and was mimicked by CRF-R1 agonists.

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

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

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

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

89 a superoxide dismutase mimetic, MnTBAP, and was 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 Chemotaxis induced by PGE2 was mimicked by EP3 agonists, blocked by an EP3 receptor

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

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

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

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

108 This nicotinic effect was mimicked by exogenous administration of acetylcholin

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

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

111 These effects were mimicked by exogenous adenosine administration and

112 yperglycemia on Na(V)1.7 production in vitro was mimicked by exposure to PMA and blocked by the myris

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

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

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

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

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

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

119 ciated vasodilatation, this response pattern is mimicked by general anesthetics, questioning to what

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

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 ion into human NK cells, and this effect can be mimicked by IL-2.

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

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

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

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

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

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

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

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

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

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

135 These effects of lovastatin were mimicked by inhibitors of geranylgeranyl-transferas

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

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

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

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

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

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

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

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

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

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

146 ncreases in dynorphin function, because they are mimicked by kappa-opioid receptor (KOR) agonists and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Phosphorylation of PLB was mimicked by mutations S16E (PKA site) or S16E/T17E (

170 -1 binding to the HR2 in response to glucose are mimicked by N-acetyl glucosamine, an intermediate of

171 We then show that this effect is mimicked by nanoinjections of TNFalpha, which produce

172 The effects of OGD were mimicked by NMDA.

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

174 namics requires Aurora A, and its effect can be mimicked by nondegradable Aurora kinase.

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

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

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

178 These effects were mimicked by overexpressing the mitochondrial MnSOD

179 centrosome overproduction, alterations that are mimicked by overexpression of cyclin B1 and cyclin A

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

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

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

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

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

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

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

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

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

189 ts from ON and OFF pathways, which could not be mimicked by pharmacologically blocking of glycinergic

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

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

192 mutant that associates more tightly with IF is mimicked by PKP2 and PKC alpha knockdown and PKC phar

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

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

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

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

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

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

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

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

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

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

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

204 ayer with a glass coverslip, and reperfusion was mimicked by removing the coverslip.

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

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

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

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

209 require activation of guanylate cyclase but was mimicked by S-nitroso-glutathione (GSNO; an S-nitros

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

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

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

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

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

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

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

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

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

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

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

221 hus, the tissue-protective activities of EPO are mimicked by small, nonerythropoietic peptides that s

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

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

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

225 The effects were mimicked by sulprostone, an agonist to PGE(2) EP(3)

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

227 These effects are mimicked by synthetic CpG oligodeoxynucleotides (ODN

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

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

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

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

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

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

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

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

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

237 strate nicotinamide in the medium, could not be mimicked by the Nampt enzymatic product nicotinamide

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

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

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

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

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

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

244 This phenomenon is mimicked by the acute administration of mitochondrial

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 effects of mid-range concentrations of PGE2 were mimicked by the EP3-selective agent, sulprostone, b

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

271 These effects of MPP+ were mimicked by the injection of an active form of casp

272 These results were mimicked by the JNK inhibitor SP600125, indicating

273 SP responses were mimicked by the NK1 receptor agonist [Sar9,Met(O(2)

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

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

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

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

285 ffect of SWP1 knockout on the root phenotype is mimicked by transgenic expression of LRP1, which bypa

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

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

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

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

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

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

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

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

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

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

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

297 ain tail-dependent transcription in vivo can be mimicked by using the intracellular signaling molecul

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

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

300 This can be mimicked by Wnt/beta-catenin signaling activation wit