ライフサイエンスコーパス: be suppressed by

1 tem cells (BMSCs) into the adipocyte lineage was suppressed by 17-beta-estradiol (E2) in WT female mi

2 a) activation in ovarian cancer cells, which was suppressed by 1alpha,25-dihydroxyvitamin D3 [1,25(OH

3 ersely, in tumor cells, C/EBPbeta activation is suppressed by 3'UTR-mediated localization of Cebpb tr

4 meostasis, calbindinD28k, Klotho, and Napi2a were suppressed by 30-40%.

5 resence of Z. rouxii, while Z. rouxii growth was suppressed by 4 log in concurrence with pH increase

6 de in sediments containing 8-18% gas (Da,YE) were suppressed by 7-39% compared to the control (no gas

7 s, the response of wild-type AvLOx electrode was suppressed by 9-12% due to oxygen interference.

8 a phase diagram showing how the excitations are suppressed by a magnetic field.

9 Hypomorph mutations in sld3 are suppressed by a mcm4 regulatory domain mutation.

10 Eosinophils are suppressed by a new class of drugs targeting Interle

11 rtantly, the enhanced SnRK1 levels in sr45-1 are suppressed by a proteasome inhibitor, indicating tha

12 d IFIT1B proteins differ in their ability to be suppressed by a cap 2'O-methyltransferase.

13 n which we confirmed that tumor growth could be suppressed by a carbohydrate-restricted ketogenic die

14 ed dark currents by intense blue light could be suppressed by a following intense green light, sugges

15 y reveals how inflammatory ILC responses can be suppressed by a newly defined subset of ILCs with reg

16 onses to a low-intensity probe sound tend to be suppressed by a preceding high-intensity adaptor soun

17 This process is suppressed by a key regulator of mtDNA-the transcript

18 uated in B6 mice in which Mc3r transcription is suppressed by a lox-stop-lox sequence in the 5'UTR (M

19 ing KCNQ1 channel opening, the ionic current is suppressed by a rapid process called inactivation.

20 This burst firing was suppressed by a cannabinoid receptor antagonist.

21 -smooth muscle actin, and collagen 1(alpha1) were suppressed by a miR-199a-5p mimic, whereas in quies

22 PROLIFERATING CELL NUCLEAR ANTIGEN1 in buds was suppressed by ABA, suggesting that it may inhibit bu

23 xes of HONO from agricultural and urban soil were suppressed by addition of a nitrification inhibitor

24 of C. elegans mitochondrial responses could be suppressed by additional mutations in E. coli, sugges

25 uced mucosal injury in wild-type mice, which was suppressed by administration of a TLR2 ligand, prese

26 icantly suppressed by PI3K inhibition; fewer were suppressed by Akt or mTOR inhibition, and none were

27 sy characteristic of CAE patients, which can be suppressed by AMPA-R and NMDA-R antagonists but not T

28 Both defects are suppressed by an Ssu(-) substitution in eIF1A that s

29 ctive oxygen species, but the elevations can be suppressed by an OGT inhibitor.

30 Fourth, the dynamics were suppressed by an engineered interstrand cross-link

31 of prostate cancer (PCa), and PCa growth can be suppressed by androgen deprivation therapy.

32 NA damage correlated with ROS production and was suppressed by antioxidants (P < 0.001).

33 d non-ATG (RAN) translated dipeptides, which were suppressed by antisense oligonucleotides targeting

34 We show here that TFL1 expression is suppressed by AP1 but promoted by LFY.

35 nsulin-stimulated hepatic glucose production was suppressed by approximately 50% in HF-fed itga1(+/+)

36 rage turbulent kinetic energy during the CAP was suppressed by approximately 80%.

37 -6 messenger RNA expression within the liver was suppressed by ARA 290 treatment.

38 V-infected individuals in whom the infection is suppressed by ART.

39 naive individuals were enrolled, and viremia was suppressed by ART prior to delivery of 4 doses of DC

40 ithout ART, and in individuals whose viremia was suppressed by ART.

41 Sensory-projecting neurons are suppressed by attentional states, demonstrating that

42 cancer cell proliferation mediated by IGF-I was suppressed by attenuating xCT expression or blocking

43 asses of lipids involved in inflammation, as being suppressed by B. anthracis.

44 ed by the proteasome inhibitor MG132, but it was suppressed by bafilomycin A1, which led to the assoc

45 o increased voiding frequency; these effects were suppressed by BB-FCF.

46 BRD4 that supports leukemia maintenance and is suppressed by BET bromodomain inhibition.

47 Finally, these dynamics were suppressed by binding of a specific non-hydrolyzabl

48 ATAF2 expression is suppressed by both BRs and light, which demonstrates

49 Complementation among muscle mitochondria was suppressed by both in vivo genetic perturbations and

50 Energy intake was suppressed by both L and H drinks compared with cont

51 cted embryos, we found that the fluctuations were suppressed by both cortical actin and microtubules.

52 -citronellene etherification on zeolite beta is suppressed by bulky base molecules (2,4,6-collidine a

53 While MMEJ is suppressed by C-NHEJ, the relationship between HR and

54 ctivity requires Ca(2+), basal SACY activity is suppressed by Ca(2+).

55 Cav1.4FL The robust CDI of Cav1.4Deltaex 47 is suppressed by CaBP4, a regulator of Cav1.4 channels i

56 NA polymerase (Pol )-dependent MMR reactions is suppressed by CAF-1- and ASF1A-H3-H4-dependent deposi

57 sion required activation of ERKs and p38 but was suppressed by cAMP.

58 ed with CPVT and AF, which could potentially be suppressed by carvedilol or (R)-carvedilol.

59 n the [Ca(2+)]c and cell death, all of which were suppressed by chelerythrine, a protein kinase C inh

60 Consistently, food intake is suppressed by chemogenetic activation of glutamatergi

61 PKalpha2 knockout mouse aortas, all of which were suppressed by chronic administration of fludarabine

62 ine-5'-diphosphate-hexose cell content which was suppressed by co-treatment with glycogen synthase ki

63 e, another natural product DYRK1A inhibitor, was suppressed by coincubation with the calcineurin inhi

64 veral major events of the metastatic process were suppressed by Col3, including adhesion, invasion, a

65 ormation in xenograft nude mice, which could be suppressed by combined treatment with rapamycin and a

66 When these activities were suppressed by conditional deletion of wntless (Le-c

67 neural crest defects in CAPE-treated embryos are suppressed by constitutively active Akt1.

68 This phenotype is suppressed by constitutively active arl-8 or unc-104

69 However, nucleoid partitioning errors are suppressed by control at two levels: Mitochondrial v

70 t is shown that the VI diffusion process can be suppressed by controlling the affinity of the contact

71 However, this spontaneous activity is suppressed by coupling to an overlying membrane, whic

72 th defects from knockdown of 14-3-3 and Tctp are suppressed by CycE overexpression.

73 Furthermore, PGC-1alpha expression was suppressed by decreased intracellular Ca(2+) levels

74 This low iron transcriptional response was suppressed by deletion of CCC1, the gene that encode

75 charged osmolytes (myo-inositol and taurine) was suppressed by deletion of LRRC8A or LRRC8D, but not

76 These events are suppressed by depletion of internal stores or inhibi

77 These myt1 defects can be suppressed by depletion of Cyclin A activity or ectop

78 e at tDNAs in the absence of these helicases is suppressed by destabilizing R-loops while Pif1 and Rr

79 n the absence of microbes, BAK1 activity may be suppressed by different mechanisms, like interaction

80 AtSAL1 phosphatase activity is suppressed by dimerization, intramolecular disulfide

81 emperature for the supersolid phase tends to be suppressed by disorder.

82 The accumulation of PC in pah1 pah2 is suppressed by disruption of CTP:PHOSPHOCHOLINE CYTIDY

83 in patients with Parkinson's disease and can be suppressed by dopaminergic medication, with the degre

84 es when stripe spin density wave (SDW) order is suppressed by doping, pressure or atomic disorder.

85 ective (OS/DS) cells with a firing rate that is suppressed by drifting sinusoidal gratings (negative

86 a diversity of roles during development and are suppressed by E2F1.

87 to highly energetic food cues are robust and are suppressed by eating.

88 beta (IFN-alpha/beta) innate immune response is suppressed by EBOV viral protein 35 (VP35), a validat

89 he asymmetric DNA synthesis in rad53-1 cells is suppressed by elevated levels of dNTPs in vivo, and t

90 This crosstalk effect can only be suppressed by employing sufficient randomness in the

91 inflammatory cytokines, IL-6 and TNF, and NO was suppressed by EP in macrophages and microglia.

92 Immune detection is suppressed by equally complex pathogen mechanisms.

93 ed expression of Mmp13 and cell invasiveness were suppressed by Etv4 and Etv5 siRNAs, which were acco

94 that this so-called coffee stain effect can be suppressed by exciting evaporating complex fluids thr

95 nd increased double-strand breaks that could be suppressed by exogenously expressed replication prote

96 ate that the growth of lithium dendrites can be suppressed by exploiting the reaction between lithium

97 h all stress defects of Sty1-deficient cells being suppressed by expression of the Atf1 mutant.

98 risingly, we found that p53 mRNA translation was suppressed by FDXR deficiency via IRP2.

99 transcripts in germ cells, a phenotype that is suppressed by feminization of the germline.

100 ffects of spatial confinement in D1CT-7 mice were suppressed by finasteride (25-50 mg/kg, IP), an inh

101 hat pro-cell death lipid ceramide generation is suppressed by FLT3-ITD signaling.

102 ON bipolar cells in which synaptic activity was suppressed by fluctuations at frequencies above appr

103 ay, we discovered that tau prion replication is suppressed by forebrain-derived inhibitors, one of wh

104 The late asthmatic response (LAR) was suppressed by FP in smokers and non-smokers; with pl

105 The Early AR was suppressed by FP treatment in non-smokers, but was n

106 Lysosomal phenotypes are suppressed by genetic inhibition of Rab7 or the HOPS

107 , and a profound inflammatory phenotype that was suppressed by genetic ablation of lymphocytes.

108 eover, these synaptic development phenotypes are suppressed by genetically correcting Wg levels in No

109 These sensitivities are suppressed by genetically eliminating Ku nonhomologo

110 ntly, oxidative stress caused by loss of SMS is suppressed by genetically or pharmacologically enhanc

111 strongly respond to local motion signals but are suppressed by global image motion.

112 amino acid metabolism, and cell death, which is suppressed by glutamate and alpha-ketoglutarate suppl

113 ransplantation, and the expression of Cyp7a1 was suppressed by glycerol administration in wild-type l

114 responds to the leading edge of a figure and is suppressed by ground motion.

115 ently with this, MTP protein and mRNA levels were suppressed by HCV infection.

116 ed by circulating beta-alanine levels, which are suppressed by hepatic and renal beta-alanine transam

117 Caspase-2, an apoptotic initiator, can be suppressed by high levels of nutrient flux through th

118 The anomalous current is suppressed by high intracellular Ca(2+) , suggesting

119 r form (which we estimated to be 75 kDa [2]) were suppressed by high concentrations of inhibitors tha

120 activated receptor gamma (PPAR-gamma), which is suppressed by HIV-1 replication.

121 mobilization of transposable elements (TEs) is suppressed by host genome defense mechanisms.

122 study suggests that the activity of tPA can be suppressed by HSA and regenerated by thrombin present

123 C-C bond formation by the cis-isomer is suppressed by hydrogen bonding of the cis-aldehyde ca

124 n vivo was not decreased when dNTP synthesis was suppressed by hydroxyurea, indicating that Polzeta f

125 This germline defect is suppressed by hyperactivation of glp-1 or disruption

126 n at rest, but not when inspiratory activity was suppressed by hyperpolarizing preBotC neurons.

127 We show that DICER expression is suppressed by hypoxia through an epigenetic mechanism

128 egative regulator of osteoclastogenesis that is suppressed by hypoxia.

129 tor-activated receptor alpha target proteins were suppressed by hypoxia, but activated by diabetes.

130 While PGE2 production was suppressed by ibuprofen, PGD2 production was not.

131 esearch reveals that neither X4 nor R5 HIV-1 is suppressed by IFITM2 and IFITM3.

132 ulates the macrophage enhancer landscape and is suppressed by IFN-gamma to augment macrophage activat

133 ivation of canonical NF-kappaB signaling and was suppressed by IkappaBalpha and a dominant negative f

134 clei, a marker of genomic instability, which is suppressed by IL6 blockade.

135 ciated with increased TERT expression, which was suppressed by imetelstat treatment.

136 cell death, and its effect on HIV-1 release was suppressed by Imipramine (an antidepressant agent kn

137 fluenza A virus (IAV) ribogenesis and growth are suppressed by impaired RNA exosome activity.

138 Degeneration was suppressed by improving mitochondrial Ca(2+) uptake,

139 ng, but this defect in srs2Delta mutants can be suppressed by inactivation of the resection nuclease

140 that the essentiality of DeltagpsB mutations is suppressed by inactivation of PhpP protein phosphatas

141 the expression of floral repressors in tulip is suppressed by increased ambient temperatures, leading

142 Accordingly, this synthetic lethality is suppressed by increasing RRM2 expression or inhibitin

143 cluding ATM, Chk1, or Chk2, and additionally was suppressed by inducers of DNA single-strand breaks (

144 activation-triggered fusion and vacuolation were suppressed by inhibiting CaM.

145 phenotype of an "RNP assembly disease" might be suppressed by inhibition of a competing RNA quality c

146 and the growth advantage of these cells can be suppressed by inhibition of mitochondrial respiration

147 physiomimetic organotypic assays; which can be suppressed by inhibition of PI3K.

148 -independent cell growth, and cell migration were suppressed by inhibition of MEK1/2/ERK1/2 signaling

149 Migration was suppressed by inhibitors of the prolyl isomerase Pin

150 These translational responses were suppressed by inhibitors of BTK (ibrutinib) and SYK

151 Visual signals during blinks are suppressed by inhibitory mechanisms [3-6], so that s

152 liorated on an Asc (-/-) background, and can be suppressed by injections of anti-IL-1 receptor antibo

153 We show that FMO3 is suppressed by insulin in vitro, increased in obese/in

154 It was suppressed by intracellular Ca(2+) buffering at a fi

155 The inhibitory effect of a long 5'-flap can be suppressed by its interaction with single-stranded DN

156 n pulmonary artery endothelial cells (PAECs) was suppressed by knockdown of either p38 MAPK or GPR40.

157 ne activation in response to USP9X knockdown was suppressed by knockdown of YAP, TAZ, and TEAD2.

158 ression of the microRNA 200 (mir-200) family was suppressed by KRAS activation and that this suppress

159 y, IL-33 effects on primary human mast cells were suppressed by LA in an MCT-dependent manner.

160 increased nuclear exclusion of FOXO3, which was suppressed by LA1-dependent activation of CD11b.

161 expressing LHA neurons projecting to the VTA were suppressed by leptin, a peptide hormone derived fro

162 reinitiation complex during EXT2 translation is suppressed by let-7b, a member of the let-7 microRNA

163 actice because the basicity of an added base is suppressed by Lewis acid/base adduct formation.

164 These responses were suppressed by limiting damaging ROS but enhanced by

165 Transcription of CPS1 is suppressed by LKB1 through AMPK, and CPS1 expression

166 Increases in telomeric DNA are suppressed by loss of BLM but not RAD51, occur witho

167 These phenotypes are suppressed by loss-of-function mutations that arise

168 Here, we found that this phenotype was suppressed by loss of function mutations in the feoA

169 is iron sensitive, and this sensitivity can be suppressed by low levels of Mn(II).

170 These effects were suppressed by lysine or rapamycin treatment, sugges

171 nal autophagy enhances BACE1 turnover, which is suppressed by lysosomal inhibition.

172 ver, transcription directed by RNAP I to III was suppressed by M.

173 a new concept by which tumor progression can be suppressed by manipulating tumor cell identity.

174 ased in the myoblasts in which Mb expression was suppressed by Mb-siRNA transfection (Mb vector trans

175 Remarkably, the augmented p38 signalling is suppressed by MEC17 inactivation.

176 ppressed by Akt or mTOR inhibition, and none were suppressed by MEK inhibition.

177 ate that an "autocrine drug resistance loop" is suppressed by melanocyte lineage signal(s), such as M

178 served in uncontaminated control microbiomes are suppressed by metal/metalloid field exposure, includ

179 nectin, and connective tissue growth factor, was suppressed by metformin in a LKB1-dependent fashion.

180 nf4a activates nearly half of the genes that are suppressed by microbiota, suggesting microbiota nega

181 spin-triplet states due to hyperfine fields is suppressed by microwave driving.

182 Interestingly, CXCL13 expression was suppressed by miR-186-5p, a microRNA that colocalize

183 n energy below 1.3 eV (above 950 nm), the PL is suppressed by more than two orders of magnitude.

184 e, but its heterochromatin-inducing activity is suppressed by mTOR-mediated phosphorylation.

185 growth phenotypes of DCDC-deficient strains are suppressed by mutation of embryonic ectoderm develop

186 nversely, sensitivity in the ytpB background is suppressed by mutation of hepT or by supplementation

187 ying-back of NMJs and axons, which could not be suppressed by mutations that block Wallerian degenera

188 ct of proteasome inhibition on Gcn4 activity is suppressed by mutations in the ubiquitin-selective ch

189 These phenotypes were suppressed by mutations within the coiled-coil and

190 our compiled dataset, free-living N fixation is suppressed by N fertilization and stimulated by Mo fe

191 s Il1b, Il6, Tnf and Il10 in fetal membranes was suppressed by (+)-naloxone, and cytokine expression

192 ociated with a decline in ATP levels and can be suppressed by Necrostatin 7.

193 ammation and autoimmunity; however, how IRF7 is suppressed by negative regulators remains poorly unde

194 nd defects in cell morphology, both of which were suppressed by overexpressing the LPS flippase MsbA

195 icient defects in cardiomyocyte number could be suppressed by overexpression of dickkopf 1 (DKK1), an

196 roduction, which resulted in LRP6 stability, was suppressed by overexpression of PPARalpha and dramat

197 Disintegration can be suppressed by paclitaxel treatment.

198 al chromosomal DNA and its effects on growth were suppressed by pairwise combination with the DNA bin

199 P14 induces ADP-ribosylation of STAT1, which is suppressed by PARP9.

200 EMT is suppressed by partial silencing of p63RhoGEF and GEF-

201 cryptochrome) genes by BMAL1-CLOCK complexes is suppressed by PER-CRY complexes.

202 Expression of AtANN1 in roots was suppressed by peroxide, consistent with the need to

203 ing that TP53 mutant breast tumor growth can be suppressed by pharmacologic TLR4 inhibition, whereas

204 These effects were suppressed by pharmacologic autophagy inhibitors an

205 t proceed in Nlrp3(-/-) or Asc(-/-) BMDC and are suppressed by pharmacological inhibition of caspase-

206 s, PARP activation, and tissue injury, which are suppressed by pharmacological inhibitors of ROS/RNS

207 The latter two phenotypes can be suppressed by pharmacological inhibition of S6K1 duri

208 n-1beta release, though this phenotype could be suppressed by pharmacological neutralization of the p

209 Here, we show that vesicle fusion can be suppressed by phosphorylation of core conserved resid

210 nce was elevated in ECSHIP2(Delta/+) ECs and was suppressed by PI3K and NADPH oxidase 2 inhibitors.

211 Cellular LTC4S activity is suppressed by PKC-mediated phosphorylation, and recen

212 es required cell-cell contact, and induction was suppressed by plasmacytoid dendritic cell depletion.

213 own that fracture due to cutting and folding is suppressed by plastic rolling, which provides kirigam

214 SMARCA2 is suppressed by PRC2 in sensitive models, and induced S

215 ect other types of fibers, and this response was suppressed by pre-administration of the GLP-1R antag

216 h cortical and hippocampal pyramidal neurons were suppressed by preceding APs in an SK-dependent mann

217 LPS-triggered ENO-1 exteriorization was suppressed by pretreatment of MDA-MB-231 cells with

218 The tPTPs were suppressed by preventing mitochondrial Ca(2+) influ

219 a-3p) or repression (miR-26b-5p) by estrogen was suppressed by progesterone plus PR-A were critical f

220 demonstrate that glucocorticoid biosynthesis is suppressed by proinflammatory cytokines and that gluc

221 totic kinases (Aurora B, Mps1, and Plx1) and is suppressed by protein phosphatase 1.

222 duced at hypoxic conditions, a response that is suppressed by RAP2.12 overexpression, suggesting anta

223 0.66%, HC: 2.29 +/- 0.27%; p = 0.019), which was suppressed by rapamycin (control: 3.91 +/- 0.79%, ra

224 tients after 3-d in vitro stimulation, which was suppressed by rapamycin (control: 9.26 +/- 1.48%, ra

225 ian origins can form at any DNA sequence but are suppressed by read-through transcription or that the

226 Here, we find that filopodia initiation is suppressed by recruitment of ArhGAP44 to actin-patche

227 factory attraction - the latter of which can be suppressed by reducing presynaptic GABAB receptors.

228 al targeting of the dendrites, a defect that is suppressed by reduction in Wnt5 gene dosage.

229 inositol (PI) 5-kinase Its3, but this defect was suppressed by removal of eisosomes.

230 Dimerization was suppressed by removing a TERT domain linker with aty

231 hat when activity in the superior colliculus is suppressed by reversible inactivation, animals should

232 ndrome (SIRS) induced by TNFalpha, which can be suppressed by RIPK1 inhibitor Nec-1s.

233 mic instability and replication defects that were suppressed by RNase H1 overexpression.

234 Axon truncation in kbp(st23) mutants can be suppressed by SCG10 overexpression, confirming the di

235 NA crosslinking agents, but this sensitivity is suppressed by simultaneous depletion of Ube2w.

236 Actin catch-slip bonds are suppressed by single residue replacements K113E and

237 92593 as well as when its protein expression was suppressed by siRNA in both Melan-a and B16-F10 cell

238 Induction of IL-6 by ADRB3 activation was suppressed by siRNA knockdown of Sphk1 in cultured a

239 olve alterations in ZIP7 phosphorylation and were suppressed by small interfering RNA-mediated silenc

240 26% incidence of cardiac outlet defects that were suppressed by SOD1 overexpression.

241 vasoactive intestinal peptide (VIP) neurons were suppressed by sound, both preferentially at the cel

242 JNK was suppressed by SP600125 or Jnk siRNA.

243 is gain of function meiotic arrest phenotype is suppressed by spo11Delta, suggesting that it is due t

244 Loss of GpsB can be suppressed by spontaneous mutations, including within

245 Later in life, clonal evolution was suppressed by stabilizing selection in the larger yo

246 e for a (Z)-configuration, although this can be suppressed by steric interactions due to a catalyst.

247 However, when activity is suppressed by stimuli outside the RF, slow LIP dynami

248 ing that the oncogenic function of c-Myc can be suppressed by suitable inhibitors of 5-Lox.

249 anowire, and found that these variations can be suppressed by switching to growth conditions with a l

250 pbPPARG-mediated luciferase activity was suppressed by synthetic contaminant mixtures reflect

251 ung cancer (NSCLC) cells, an effect that can be suppressed by targeting MUC1-C via shRNA silencing, C

252 l cells (HUVECs) developed a SASP that could be suppressed by targeting the JAK pathway using RNAi or

253 imal pyroptosis but secreted IL-1beta, which was suppressed by TcpB.

254 type is induced by loss of p53 function, and is suppressed by telomerase overexpression.

255 This phenotype appears to be suppressed by testicular hormones in male Prkca(-/-)

256 y into virus particles, and several of these are suppressed by the 62QR mutation at the hubs of trime

257 orts have shown that innate immune responses are suppressed by the adaptive immune system.

258 eta5 loop in the FK1 domain of FKBP51, which are suppressed by the FKBP52-like L119P substitution.

259 Most nucleosomal changes are suppressed by the inhibition of RNA polymerase II (P

260 Ca(2+) transients in ICC-DMP are suppressed by the ongoing release of inhibitory neur

261 ons, myocardial fibrosis and metabolic could be suppressed by the different extents of twice weekly a

262 Malignancy can be suppressed by the immune system in a process termed i

263 ark-grown seedlings, photomorphogenic growth is suppressed by the action of the CONSTITUTIVELY PHOTOM

264 transient period of hyperproliferation that is suppressed by the activation of the DNA damage respon

265 FNR-dependent transcription is suppressed by the binding of two nucleoid associated

266 scopy (TEM) results show that the lithiation is suppressed by the compressive interfacial strain.

267 However, this process is suppressed by the disc-specific protein peripherin, w

268 g phenotype of the FOF2 overexpression lines is suppressed by the flc-3 loss-of-function mutation.

269 the HO phase reenters after the LMAFM phase is suppressed by the magnetic field, similar to the beha

270 ionize as well as PCs, and their ionization is suppressed by the PCs.

271 at cortactin phosphorylation at tyrosine 421 is suppressed by the phosphatase PTP1B, and that PTP1B l

272 ns in parallel to RHO-1 and CRMP/UNC-33, but is suppressed by the Rac isoform MIG-2; (2) RPM-1 oppose

273 meric DNA-binding proteins TRF1 and TRF2 and is suppressed by the RecQ helicase BLM in vitro.

274 way that involves mitochondrial homeostasis, is suppressed by the RIP1/RIP3/MLKL signaling in TSC-def

275 tion of the photoexcited electrons and holes is suppressed by the screening, leading to the formation

276 ha/betaR-/- mice, while growth on Vero cells was suppressed by the addition of alpha interferon (IFN-

277 strong thermodynamic non-ideality, but this was suppressed by the addition of salt.

278 Such an induction was suppressed by the concomitant presence of S. aureus

279 es and hypersensitivity to hydrogen peroxide was suppressed by the loss of Dgk1 diacylglycerol kinase

280 nd an increase in MCPH1-deficient cells that was suppressed by the loss of pericentrin.

281 rium tuberculosis-induced matrix degradation was suppressed by the MMP inhibitor doxycycline in vitro

282 in BAX induced by a triggering BIM BH3 helix were suppressed by the BCL-2 BH4 helix.

283 These effects were suppressed by the gamma-secretase inhibitor LY45013

284 Both Lyme and K/BxN-associated arthritis were suppressed by this treatment concurrent with reduce

285 cessary and sufficient for self-renewal, and is suppressed by TLR4 overexpression in CSCs.

286 pyrin-associated periodic syndrome patients, was suppressed by Tr1 cells but not Foxp3(+) Tregs.

287 ICL damage in human cells, with accumulation being suppressed by transcription inhibition.

288 P2C9 and the endogenous expression of CYP2C9 were suppressed by transfection of hsa-miR-128-3p.

289 severe motor neuron degeneration, which can be suppressed by transgenic restoration of Zfp106 specif

290 confirmed in vivo when the protective effect was suppressed by treating glutathione peroxidase 1 mice

291 dapk-1 epidermal phenotypes are suppressed by treatment with microtubule-destabilizi

292 f ATAF2 loss- and gain-of-function seedlings are suppressed by treatment with the BR biosynthesis inh

293 ress, glycolysis, and mitochondrial function was suppressed by TRPM2 depletion.

294 Toxicity is suppressed by truncation of Uso1, a vesicle tether re

295 uced by either vacuolin-1 or P2X4 activation are suppressed by up-regulating the lysosomal Ca(2+) rel

296 activity of Apt-Au NPs/BiOCl nanocomposites is suppressed by vascular endothelial growth factor-A165

297 of tyrosine 845 on unliganded EGFR monomers is suppressed by vesicular recycling through perinuclear

298 se cells and tissues, and their activity may be suppressed by vitamin D.

299 fects revealed active bone resorption, which is suppressed by Wnt activation in osteoblast and osteoc

300 Mn(2+) and Co(2+) and the cleavage activity was suppressed by Zn(2+).