ライフサイエンスコーパス: be abrogated in

1 reduced, and catecholamine histofluorescence was abrogated in 15-day-old TH-null mice.

2 ikingly, these electroretinographic deficits are abrogated in a dose-dependent manner by systemic adm

3 antigen specificity, its therapeutic effect is abrogated in a mouse model requiring pertussis toxin.

4 This phenotype was abrogated in a Deltacln3 or Deltacln2 background.

5 glia following TNF-alpha stimulation, which was abrogated in a dose-dependent manner by acetylcholin

6 To accomplish this, E-cadherin function was abrogated in a human cell line representing an early

7 specific antagonist AMD3100, and replication was abrogated in a novel CXCR4(-) SupT1 line.

8 sages was not altered, but their translation was abrogated in a selective manner.

9 Serum resistance was abrogated in A. baumannii treated with protease inhi

10 LMP1-mediated NF-kappaB and AP-1 activation were abrogated in a dose-dependent manner, with a concom

11 ed Akt phosphorylation or cell proliferation was abrogated in A7r5 cells overexpressing a dominant-ne

12 2-mediated resistance to SN-38 and topotecan was abrogated in ABCG2-transfected HEK-293 cells treated

13 broblasts (MEFs) exposed to serum starvation was abrogated in AKBI MEFs.

14 CXCL16-induced platelet activation was abrogated in Akt1- or Akt2-deficient platelets.

15 mAChR-induced inhibition of proliferation is abrogated in all cell lines when Galpha(q/11) signali

16 ractions between beta-catenin and E-cadherin were abrogated in all three immortalized MMECLs and the

17 type (OPN(+/+)) mice, but pro-MMP9 induction was abrogated in AMFs from OPN(-/-) mice.

18 UV- and Bax-induced apoptosis is abrogated in AR-positive cells that express small int

19 Catecholamine-induced DNA damage is abrogated in Arrb1-knockout (Arrb1(-/-)) mice, which

20 MAPK activation by pathogen was abrogated in Asc(-/-) but not Nlrp3(-/-), Nlrc4(-/-)

21 Induction of gamma-H2AX was abrogated in ATF4 knockdown cells.

22 NF-kappaB2/p100 cleavage was abrogated in B cells from A/WySnJ mice possessing a

23 zation and the ensuing MAP kinase activation was abrogated in B-lymphocytes and fibroblasts derived f

24 demonstrate that the protective effect of E2 is abrogated in B6.129-Esr1(tm1Unc) mice (Esr1-/-) but n

25 xpression in response to T. gondii infection was abrogated in B6 IFNAR-/- mice, which lack a function

26 a caspase 3-defective cell line (MCF-7) and was abrogated in Bak-sensitive tumors after administrati

27 ly transferred tumor-specific CD8(+) T cells were abrogated in Batf3(-/-) mice.

28 vation in Bax-proficient cells, these events were abrogated in Bax-deficient cells.

29 by the mitochondria-initiated apoptosis that was abrogated in Bcl-x(L)-transgenic T cells.

30 r, the inhibitory effects of epsilon subunit are abrogated in both purified F(1) and membranous F(o)F

31 he spinal cord associated with classical EAE is abrogated in both IFN-gamma-deficient systems.

32 B-cell reconstitution is abrogated in both syngeneic and allogeneic transplant

33 ATP hydrolysis and drug transport activities were abrogated in both E556Q and E1201Q mutant Pgps, [al

34 , we show that activation of caspase-3 by UV is abrogated in BRCA1-mutated SNU251 and HCC1937 cells b

35 on of DJ-1 and protection against cell death were abrogated in C106A but not C53A or C46A.

36 and endothelial NO synthase phosphorylation were abrogated in C451A-ERalpha mice.

37 Several long noncoding RNAs (lncRNA) are abrogated in cancer but their precise contributions

38 Accordingly, the inotropic effects of Hsp20 were abrogated in cardiomyocytes expressing nonphosphory

39 + macrophage infiltration into the heart and was abrogated in CCR2(-/)(-) mice, demonstrating target

40 phospholipid-induced macrophage accumulation was abrogated in CCR2-/- mice.

41 acteria, although the response to GBS factor was abrogated in CD14-null cells.

42 Activation of iNKT cells is abrogated in Cd169(-/-) mice and is macrophage-depend

43 ony-stimulating factor-secreting tumor cells was abrogated in CD1d- and J alpha 281-deficient mice, r

44 -gamma and lesional T cell infiltration, and was abrogated in CD4(+) T cell-depleted animals.

45 P-gp activity was abrogated in CD71 cycling cells but remained high in

46 Rescue is abrogated in CD8(+) T cells lacking NKG2D.

47 inally, we demonstrate that these structures are abrogated in cells derived from incontinentia pigmen

48 These effects are abrogated in cells transfected with the ANG inhibito

49 cytokine responses by a pathogen product can be abrogated in cells derived from TLR4 knockout, but no

50 Iron inhibition of Aft1/Aft2 is abrogated in cells defective for Fe-S cluster biogene

51 of the downstream transcription factor, CSL, is abrogated in cells deficient in presenilins or treate

52 f MMP-9 in response to NGF, as this response is abrogated in cells expressing a mutant TrkA receptor

53 This process is abrogated in cells expressing Pak1 kinase mutants.

54 nucleolar localization during this response is abrogated in cells lacking functional p53.

55 teocalcin production, and that this response is abrogated in cells that overexpress CrmA.

56 tion of movement by the FKBP52 PPIase domain is abrogated in cells treated with colcemid to eliminate

57 n the host we asked whether the AID response was abrogated in cells deficient in the interferon pathw

58 n-induced inhibition of centrosome splitting was abrogated in cells expressing Nek2 mutated in the PP

59 This effect was abrogated in cells lacking Bak/Bax-two pro-apoptotic

60 egradation of its downstream target, CDC25A, was abrogated in cells lacking mismatch repair.

61 aggregation of A. oris with PRP-coated beads was abrogated in cells lacking srtC1 or fimP.

62 Intracellular expression of Hsp72 was abrogated in cells stably transfected with a mutant

63 Tachpyridine-induced cell-cycle arrest was abrogated in cells treated with caffeine, an inhibit

64 These changes were abrogated in cells deficient for the essential auto

65 Similarly, effects of hyperoxia were abrogated in cells depleted of focal adhesion kinas

66 at serine 133 and CREB DNA binding activity were abrogated in cells treated with inhibitors of eithe

67 in alphaIIbbeta3 activation, and aggregation were abrogated in ck2beta(-/-) platelets.

68 t cells, execution of PUMA-induced apoptosis is abrogated, in company with decreases in caspase activ

69 This enhancement in TSHR-/- and TSHR+/- mice is abrogated in compound TSHR-/-/TNFalpha-/- and TSHR+/-

70 dic device, we found that the effects of ACM were abrogated in confinement.

71 ection against I/R-induced intestinal injury is abrogated in conventionally derived Nod2(-/-) mice an

72 bilization by G-CSF or the chemokine Grobeta was abrogated in CXCR4(-/-) bone marrow chimeras.

73 n in spinal astrocytes, and neuropathic pain was abrogated in Cxcr5-/- mice.

74 These pathologic responses were abrogated in cyclophilin D-knockout mice.

75 association of heterologous MHC II molecules was abrogated in DCs from CD9(-/-) mice.

76 -fold increase in the rpoEP3 activity, which was abrogated in Delta(waaC rcsB).

77 Accordingly, SnRK1 repression is abrogated in double and quadruple pp2c knockout mutan

78 ced by platelet-derived growth factor (PDGF) are abrogated in EDG-1 null fibroblasts.

79 lpha, IL-1 beta, MCP-1, IL-8, and MIP-1 beta was abrogated in Egr-1 small inhibitory RNA-transfected

80 All of these changes were abrogated in eNOS-/- mice.

81 ly, the atheroprotective action of tamoxifen is abrogated in ERalpha(-/-)LDL-r(-/-) mice and in LDL-r

82 ast majority of E2-dependent gene regulation was abrogated in ERalpha-AF2(0), whereas in C451A-ERalph

83 lpha-replete CD4+ T cells, while this effect was abrogated in ERalpha-deficient CD4+ T cells.

84 nges elicited by tamoxifen in wild-type mice were abrogated in ERalpha-AF1-deficient mice.

85 ranasal infection with ST3, but its efficacy was abrogated in FcgammaR (F common gamma receptor)-defi

86 -infected wild-type (Wt [C57BL/6]) mice that was abrogated in FcgammaRIII(-/-) mice.

87 In contrast, disease development was abrogated in FcRgamma chain-deficient mice and marke

88 fic marker genes, and miR-30b and 378, which were abrogated in Ffar4-silenced cells.

89 The IFN pathway is abrogated in fibroblasts from Li-Fraumeni syndrome (L

90 ibodies in placebo recipients, this increase was abrogated in FMT recipients.

91 reveal that beta1-mediated neurite outgrowth is abrogated in Fyn and contactin (Cntn) null CGNs.

92 ve effects of dietary tryptophan restriction are abrogated in germ-free mice, but are independent of

93 ed NF-kappaB activation in enteric glia that was abrogated in glia from TLR4 knockout mice and by kno

94 ia and subsequent Parkin-dependent mitophagy is abrogated in glucose-free medium or in the presence o

95 Neutrophil-mediated inflammation was abrogated in group 3.

96 this model, we have shown that cell widening is abrogated in growth conditions that promote higher su

97 All effects of GRP were abrogated in GRPR-null mice.

98 nishing inflammatory symptoms and the effect was abrogated in HCA2(-/-) mice.

99 , and ApoB in response to cytokine treatment were abrogated in HepG2 cells with dramatically reduced

100 MPK) dependent since all the effects studied were abrogated in HFD apelin-treated mice with muscle-sp

101 Here, we found miR-206 to be abrogated in human pancreatic ductal adenocarcinoma (

102 KLF6 function is abrogated in human cancers owing to increased alterna

103 We also show that Fas antagonism by Met is abrogated in human fatty liver disease (FLD).

104 fects of radiotherapy and STING agonists can be abrogated in humans by a translational strategy invol

105 DNA damage-induced germ cell death is abrogated in hus-1 mutants, in part, due to the inabi

106 growth inhibition observed in LPS-B16 tumors was abrogated in IFNAR1-deficient mice lacking a functio

107 nding Notch target gene activator RBP-Jkappa was abrogated in Ik(-/-) double-positive thymocytes.

108 flammasome activation and IL-1beta secretion was abrogated in IL-10R-deficient macrophages.

109 aster in ST2-deficient perinates, whereas it was abrogated in IL-33-treated mice.

110 IL-4-mediated suppression of L-CNV was abrogated in IL-4R-deficient mice and in bone marrow

111 RXDX-106 was observed in wild-type mice and was abrogated in immunodeficient mice, suggesting that t

112 n Deltaarg or control intracellular survival was abrogated in iNOS-deficient macrophages, suggesting

113 ng hepatic steatosis and glucose intolerance-were abrogated in Insp3r1 (also known as Itpr1)-knockout

114 Reporter activity was abrogated in isolated mutant proximal or distal miR-

115 contrast, CAF16, a potential ligand of CCR4, was abrogated in its binding to the LRR by mutations in

116 n-E production and dermatitis by delta-toxin was abrogated in Kit(W-sh/W-sh) mast-cell-deficient mice

117 Oral anaphylaxis was abrogated in Kit(W-sh/W-sh) mice and restored by mea

118 These functions are abrogated in lamin A/C-deficient mouse embryonic fib

119 ortantly, the membrane translocation of Vav3 was abrogated in Lck, ZAP-70, LAT, and SLP-76-deficient

120 be not cell type specific as its expression was abrogated in leukemic, skin, kidney, lung, and pancr

121 oth insulin receptor and Akt phosphorylation were abrogated in liver, but not in adipose tissue or in

122 n dermal alpha-SMA+ and phospho-Smad2+ cells were abrogated in LPA(1)-KO mice.

123 Stimulated p75NTR shedding is abrogated in M2 mutant Chinese hamster ovary cells th

124 triggered by poly(I:C), dsRNA, and viral RNA was abrogated in macrophages lacking cryopyrin or the ad

125 Indeed, caspase-1 activation was abrogated in macrophages lacking the NOD-like (NLR)

126 Induction of Cox-2 was abrogated in macrophages that lack IFN regulatory fa

127 regulation of mTORC1 signaling by DNA damage is abrogated in many cancer cells, thus mTORC1 signaling

128 IV-1 replication and BAFF induction, as both were abrogated in MDMs displaying a M1 phenotype.

129 This effect was abrogated in MDSCs treated with a PNT inhibitor.

130 xpression and prostaglandin E2 release could be abrogated in metastatic breast cancer cells by inhibi

131 n volume fraction in MHCsTNF/c-kit(+/-) mice was abrogated in MHCsTNF/c-kit(-/-) mice, and that the l

132 very that NAS neuroprotective effects in EAE are abrogated in mice lacking IDO1 expression, we invest

133 the adenoma-preventive activity of celecoxib is abrogated in mice genetically lacking 15-PGDH.

134 The pathogenesis of VEEV infection is abrogated in mice with deletions in Ldlrad3, and admi

135 The protective effect of hydroxyurea was abrogated in mice deficient in E-selectin.

136 han in CD4-replete mice, and this difference was abrogated in mice depleted of neutrophils before UVB

137 of the endothelial barrier, and this effect was abrogated in mice exposed to PDGF-BB neutralizing an

138 responsiveness of the endogenous RANKL gene was abrogated in mice from which we deleted this conserv

139 2 detoxication and antioxidant enzymes, and was abrogated in mice lacking the nrf2 gene, which regul

140 In fact, islet-specific homing was abrogated in mice that lack MHC class I expression,

141 betes protection conferred by the NOR allele was abrogated in mice treated with exogenous type 1 IFN-

142 ation, tubular damage, and renal dysfunction were abrogated in mice deficient in MyD88; NLRP3, ASC, a

143 ronal glutathione content, and these effects were abrogated in mice genetically deficient in either N

144 CD4-dependent Ab responses were abrogated in mice immunized with TPCS2a-containing

145 atic expression of proinflammatory cytokines were abrogated in mice lacking NPY.

146 These protective effects were abrogated in mice that were deficient in MyD88 and

147 found that TNF-induced NF-kappaB activation was abrogated in MKK4 gene-deleted cells, as determined

148 , colony forming ability and leukemogenicity are abrogated in MLL-AF9 containing either the CGBP or M

149 ATM-proficient cells, whereas this response is abrogated in MMR-deficient cells and attenuated in AT

150 y mTORC1 inhibition subsequent to DNA damage is abrogated in most human cancers.

151 rome c-mediated apoptotic pathway because it was abrogated in mouse embryonic fibroblasts with knocko

152 These effects were abrogated in MT-TG mice, MT-TG cardiomyocytes, and

153 el in which multi-isoform TGF-beta signaling is abrogated in multiple leukocyte lineages while leavin

154 The hemolytic activity is abrogated in mutants that disrupt these intermolecula

155 Induced endoreduplication was abrogated in myb3r4 mutants, and G. orontii growth a

156 roduction by macrophages and dendritic cells is abrogated in MyD88 and TLR4, but not TLR2, knockout,

157 tive advantage conferred by the mutant Csf3r was abrogated in myeloid progenitors lacking both Stat5A

158 This effect was abrogated in never-smoking and accentuated in ever-s

159 Colitis was abrogated in Nfil3/Il12b double-deficient mice, iden

160 rejection of Clr-b(-/-) hematopoietic cells was abrogated in Nkrp1b-deficient recipients, which lack

161 induced IL-1beta production in serum, which was abrogated in Nlrp3-null mice but was unaffected in P

162 ilar, long timescales, these long timescales are abrogated in non-REM sleep.

163 costimulatory molecules, and Ag degradation were abrogated in NOTAM DCs in response to FcgammaR liga

164 d-Serine responses were abrogated in NR3A-deficient mice.

165 sponse and suppression of the iNOS induction was abrogated in nrf2(-/-) and keap1(-/-) mouse embryoni

166 The anti-tumor activity of IL-1H4 was abrogated in nude and SCID mice and in IL-12-, IFN-g

167 h transcription across the Zac1/Plagl1 locus is abrogated in oocytes, resulting in failure of DNA met

168 on and potentiation of primary sensory input were abrogated in Oprm1-cKO mice.

169 10-mediated inhibition of liver regeneration is abrogated in p21-deficient animals.

170 a in the kidneys, and the inductive response was abrogated in p53-deficient animals.

171 cted mutagenesis study, antioxidant activity was abrogated in p53R2 mutants Y331F, Y285F, Y49F, and Y

172 The interaction between BRCA1 and BRCA2 is abrogated in PALB2-deficient Fanconi anemia cells and

173 inducible expression of all RARbeta isoforms is abrogated in PARP-1(-/-) cells in vivo.

174 Cell-trafficking impairments are abrogated in part by pharmacological chaperones that

175 PCARE module and actin colocalize, but which is abrogated in Pcare (-/-) mice.

176 lowered LDL-C levels, whereas this response was abrogated in Pcsk9(-/-) and Ldlr(-/-) mice.

177 BCG-mediated protection was abrogated in PEM derived from A1-a(-/-) mice, indica

178 ck protein (HSP70) to which antibody binding was abrogated in peptide competition experiments.

179 mediated by killer cytotoxic lymphocytes: it is abrogated in perforin-deficient mice or mice depleted

180 d by PERK activation in oligodendrocytes and were abrogated in PERK-deficient animals.

181 Surprisingly, feedback inhibition is abrogated in phagocytic cells.

182 ed by raising pulmonary microvessel pressure were abrogated in Piezo1 (iDeltaEC) mice.

183 01), the protective effects of second window were abrogated in pigs with CD resulting in an infarct s

184 As a consequence, dendritic cell trafficking is abrogated in polysialyltransferase-deficient mice, ma

185 Ad5.FX transduction was abrogated in primary hepatocytes from Ext1(HEP) mice

186 th this, Akt-induced mammary differentiation was abrogated in Prl(-/-), Prlr(-/-), and Stat5(-/-) mic

187 ivity, and how their antagonist activity may be abrogated in prostate cancer that progresses after an

188 d Akr1b7 gene expression, whereas the effect was abrogated in PXR(-/-) mice.

189 ocation: the latter response to all agonists was abrogated in R1B cells or by pretreatment of Mv1Lu c

190 chological stress and whether such responses are abrogated in RA patients taking TNFalpha antagonists

191 ing that the maturation process of caspase 4 is abrogated in RAS-transformed T29H cells.

192 erved during the early phases of disease and were abrogated in recombination-activating gene 1-defici

193 Cardioprotective effects of propionate were abrogated in regulatory T cell-depleted angiotensin

194 ECFC-derived ECM is abrogated in response to TGFbeta signaling inhibition

195 x metalloproteinase 9 secretion and activity were abrogated in response to ADAM15 reduction.

196 changes in ER-alpha expression and activity were abrogated in response to estradiol by an arginine t

197 7, caspase-1 activation and IL-1beta release were abrogated in response to signals that activate NLRP

198 mycobacteria-induced phosphorylation of Akt was abrogated in RP105(-/-) macrophages.

199 esponses following isoproterenol stimulation were abrogated in RyR1-S2844A mice in which the serine i

200 This defect was abrogated in SCID mice, suggesting that BatB functio

201 regulation of p21(WAF1/cip1) (CDKN1A), which is abrogated in several tumor-derived mutants.

202 IVIG on leukocyte recruitment and activation was abrogated in SHP-1-mutant mice.

203 The dephosphorylation of phospho-Lyn Tyr507 was abrogated in Shp2-deficient cells transfected with t

204 This increase was abrogated in Slc26a6 (-/-) mice associated with a si

205 n of several of the biogenic amine receptors is abrogated in specific cell types in Lhx gene mutants,

206 d architecture of Srb5/Med18-dependent genes was abrogated in srb5(-) cells.

207 mportant, because many IFN-induced responses are abrogated in Stat-1-deficient mice.

208 gnals mediated by the IL-21R and the FcR and was abrogated in STAT1-deficient NK cells.

209 lymphopoietin in WT mice with colitis, which was abrogated in STAT6(-/-) mice.

210 al effects of exogenous histamine injections were abrogated in STAT6(-/-) mice.

211 tivity of the cHS4 element was also found to be abrogated in studies using bone marrow from Parp1-nul

212 The negative effects of PM(2.5) were abrogated in subjects with higher intakes (above me

213 that HCV as well as HIV-1 infectivity could be abrogated in syringes and filters.

214 The stimulatory effect is abrogated in T cells lacking the IFNgamma receptor, i

215 Th2 differentiation induced by APC is abrogated in T cells lacking the Notch effector RBPJk

216 peutic effects of anti-CD47 antibody therapy were abrogated in T cell-deficient mice.

217 lation and degradation of RNA polymerase II) are abrogated in T714A and T734A mutants.

218 This increase in PPI was abrogated in TAAR1 knockout mice, implicating TAAR1

219 of normal thymocyte differentiation, but it is abrogated in TCR-transgenic mice, which prematurely e

220 tion and nondeletion components of tolerance were abrogated in TCR transgenic H-Y-specific lpr (Fas-d

221 on (P<0.01) in wild-type mice, both of which were abrogated in Tcrdelta(-/-) mice (P<0.01).

222 lopment from round into elongated spermatids is abrogated in Tdrd6(-/-) mice.

223 plication stress or telomere dysfunction and is abrogated in ter2 mutants.

224 This regulation was abrogated in TGF-beta-defective mice and BWS, result

225 Type I IFN-inducible genes are abrogated in the absence of IFN-gamma signaling and

226 , leukocyte adhesion and integrin activation are abrogated in the absence of receptor Notch3.

227 ility of these fibrils to increase infection are abrogated in the presence of various polyanionic com

228 -5, IL-13, eotaxin, and eotaxin-2 production are abrogated in the RAGE knockouts.

229 ddition, the cystine addiction phenotype can be abrogated in the cystine-addictive cells by miR-200c,

230 atidylserine-exposing oligodendroglial cells is abrogated in the absence of ATG5.

231 ow that TNFalpha-induced RIP1 ubiquitination is abrogated in the absence of c-IAPs.

232 rate conclusively that viral DNA replication is abrogated in the absence of H5.

233 d its ability to induce Th17 differentiation is abrogated in the absence of Stat3.

234 Mammary alveologenesis is abrogated in the absence of the transcription factors

235 hibited the overall currents, an effect that is abrogated in the almt12(-/-) and (2) reduced the curr

236 P1 complex-mediated inhibition of telomerase is abrogated in the context of the POT1 H266L mutation,

237 Cell wall attachment of CP5 is abrogated in the Deltalcp variant, a defect that is b

238 Although DNA-damage-induced apoptosis is abrogated in the mrt-2, hus-1, and clk-2 mutant backg

239 ted 185 amino acid protein, whose expression is abrogated in the mu allele which contains an insertio

240 In H. polygyrus infection, ST2 detection is abrogated in the peritoneal cavity and lung, consiste

241 This process is abrogated in the presence of an inhibitor which parti

242 The stimulatory effect of NE on ERK is abrogated in the presence of anti-EGF-neutralizing an

243 2H) exhibits a growth-inhibitory effect that is abrogated in the presence of glutamate dehydrogenase

244 Destabilization of p53 by aurora kinase A is abrogated in the presence of mutant Mdm2 that is unab

245 Rho kinase, and Arc/Arg3.1 mRNA localization is abrogated in the region of Rho kinase blockade.

246 ry between control and TRPM5 knockdown cells was abrogated in the absence of extracellular Ca(2+) and

247 and the antiapoptotic effect of GSK-3beta-DN was abrogated in the absence of myeloid cell leukemia-1.

248 ASC oligomerization and ASC speck formation, was abrogated in the absence of NEK7.

249 the increased susceptibility to phagocytosis was abrogated in the absence of opsonins.

250 Self-renewal was abrogated in the absence of STAT5a/b, and in the pre

251 bility of SCF to promote cytokine production was abrogated in the Btk-/- BMMCs.

252 els; however, this inhibitory action of CLE3 was abrogated in the clv1 mutant background.

253 ene than in the wild type and that apoptosis was abrogated in the Delta yca1 strain, whereas wild typ

254 Accordingly, VEGF-induced vascular leakage was abrogated in the DEP-1-deficient mice.

255 ylation of WNK4 at Ser(1196), an effect that was abrogated in the double mutant.

256 pithelial cells and to induce IL-8 synthesis was abrogated in the presence of a specific NK-1 recepto

257 manner because the protective effect of IL-6 was abrogated in the presence of a STAT3 inhibitor and u

258 n of some of NRF2's antioxidant target genes was abrogated in the presence of ACA11 overexpression.

259 creting INS-1E cells, respectively, and this was abrogated in the presence of an irisin-neutralizing

260 ause priming of macrophages by anti-CD40 mAb was abrogated in the presence of anti-IFN-gamma mAb, as

261 ITC-induced activation of p38 protein kinase was abrogated in the presence of its specific inhibitor

262 led to enhanced PDGFRalpha expression, which was abrogated in the presence of nuclear factor kappaB (

263 P2X7R-dependent blebbing was abrogated in the presence of Rho-effector kinase inh

264 iation of both fibroblasts and preadipocytes was abrogated in the presence of TGF-beta; this effect w

265 of CGRP to stimulate cAMP and IL-8 synthesis was abrogated in the presence of the CGRP receptor antag

266 se arrest, HU- and UV-induced S-phase arrest was abrogated in the Rad9 phosphorylation mutants.

267 ArcABC), histidine (HutI), and serine (SdhA) was abrogated in the rgg mutant strain, which synthesize

268 But EMT was abrogated in the Tyr to Phe mutant.

269 it-H2B immunoreactivity of selected RA-rmAbs was abrogated in the VH and VL GL counterpart.

270 d and observed that the effects of RELMalpha were abrogated in the absence of adaptive immunity.

271 found that the effects of the fibrate drugs were abrogated in the absence of retinoid X receptor-alp

272 -regulated differences in protein expression were abrogated in the mutant, indicating that the mening

273 ts in endothelial function in eNOS(-/-) mice were abrogated in the presence of 25 mm KCl, implicating

274 The enhanced antiviral effects were abrogated in the presence of a potent and specific

275 tochondrial and Fas receptor pathways, which were abrogated in the presence of mutant p53.

276 hat the fumarate-stimulating ULBP2/5 pathway is abrogated in these cells as an immune-evasive strateg

277 her, leptin action on euglycemia restoration was abrogated in these mice, which was associated with r

278 type that is induced by IL-10 overexpression was abrogated in this model.

279 , genes critical for DC differentiation, and are abrogated in thymectomized mice.

280 , and diabetic neuropathy, but this blockade is abrogated in Tlr5-deficient mice.

281 CpG-ODN-induced intraocular inflammation was abrogated in TLR9(-/-) and macrophage-depleted mice.

282 the elevated corticosterone response to SEA was abrogated in TNF-/- mice and was shown to be cortico

283 eneficial effects of NF-kappaB up-regulation were abrogated in TNF-alpha-deficient mice.

284 mycin-induced down-regulation of peroxisomes was abrogated in transforming growth factor beta (TGF-be

285 lopment of anti-beta-cell surface antibodies was abrogated in treated mice compared with controls.

286 PAF production could be abrogated in triple-negative breast cancer cells by i

287 ped mRNAs in wild-type plants, this increase was abrogated in TSN knockout plants.

288 directly correlated with p63 expression and is abrogated in tumor cells that overexpress endogenous

289 which was not seen when TGF-beta1 expression was abrogated in tumor cells.

290 relative protection afforded by PR8 priming was abrogated in tumor necrosis factor-deficient (TNF(-/

291 ncreases in COX-2 message and protein levels were abrogated in UVA-irradiated cells.

292 urthermore, the upregulation of PG0893 (hcp) was abrogated in V2807 exposed to nitrosative stress.

293 tection of needle-challenged vaccinated mice was abrogated in vector-initiated cutaneous leishmaniasi

294 tion and peripheral tolerance, both of which are abrogated in vitro by mediators of T cell help.

295 M3 inhibitory effect on EGFR tyrosine kinase was abrogated in vitro by coincubation with glycan havin

296 e regulatory function of CD25(-)LAP(+) cells was abrogated in vivo by anti-TGF-beta mAb.

297 Remarkably, when CCR7 function was abrogated in vivo by treatment of WT recipients with

298 fection with ST3 and found that its efficacy was abrogated in Wt mice depleted of macrophages intrana

299 nhanced barrier integrity and cell migration were abrogated in ZO-1 knockdown cells, indicating ZO-1

300 cement coincides with zyxin mobilization and is abrogated in zyxin-null cells.