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

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

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

5 40%, and the osteoclasts and bone resorption were suppressed by 50% in NTAP-Ti in vivo.

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

7 seed peaked at 48 h after fertilization and was suppressed by 96 h after fertilization, correspondin

8 ular and molecular psoriasis characteristics are suppressed by a clinically relevant dose/schedule of

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

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

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

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

13 activity during calcium stimulation can only be suppressed by a high degree of phosphorylation in mul

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

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

16 ated modeling revealed that phase separation is suppressed by a "magic-number effect" which occurs if

17 , we show that NLRP3 inflammasome activation is suppressed by a centrosomal protein Spata2.

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

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

20 n between a stimulus and an aversive outcome is suppressed by a new association with an appetitive or

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

22 cy of abnormal calcium release events, which was suppressed by a cell-permeable form of AIP.

23 The induction was suppressed by a p53 inhibitor and marginal in a p53-

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

25 ciated with cytoplasmic chaperonins that can be suppressed by ADAT2 overexpression.

26 e show that TNF-alpha-mediated NGF induction is suppressed by adiponectin-directed therapeutics such

27 otubule depolymerase whose activity in vitro is suppressed by alpha-tubulin detyrosination-a posttran

28 tic-like effects in TMT-stressed rats, which were suppressed by AM630.

29 The salt sensitivity phenotype could be suppressed by amino acid substitutions in the transgl

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

31 ins in a SM and cholesterol-rich leaflet can be suppressed by an opposite leaflet containing unsatura

32 illouin zone, the bandwidth of the flat band is suppressed by an order of magnitude compared to the D

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

34 , CXCR2, IL-6, ICAM-1, P-selectin, and C5aR) was suppressed by anti-G-CSFR, as was the level of circu

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

36 tion of the phthalocyanine ligand, which can be suppressed by appending electron-donating amino subst

37 tructures known as infection cushions, which was suppressed by application of exogenous cAMP and domi

38 icagrelor pretreatment, platelet aggregation was suppressed by approximately 80%.

39 -6 messenger RNA expression within the liver was suppressed by ARA 290 treatment.

40 spatial frequencies, the majority of boutons were suppressed by arousal.

41 ase of JNK activation, and this ROS response was suppressed by arrestin-dependent activation of the M

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

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

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

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

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

47 Growth of fibrils can be suppressed by blocking fibril ends from their interac

48 ugh antibody-dependent enhancement [ADE]) or was suppressed by both DENV and ZIKV immunity.

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

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

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

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

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

54 vs. 0.16 +/- 0.05 APs/min, p = 0.004); these were suppressed by CaMKII inhibition.

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

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

57 Overgrowth by active TOR signaling is suppressed by CCT RNAi.

58 nt of venous thrombo-inflammation, which can be suppressed by CD39.

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

60 S reactivity against self-DNA in the nucleus is suppressed by chromatin tethering.

61 brain, adult hippocampal neurogenesis (AHN) is suppressed by chronic stress, primarily at the ventra

62 Hydrogen evolution is suppressed by CO(2) reduction as all protons at the e

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

64 ipose expression of the DNA demethylase TET1 is suppressed by cold and other stimulators of beige adi

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

66 ical prediction that such instability should be suppressed by confinement.

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 This was suppressed by constitutively active RagB, an activat

70 ear forces, while mitosis and the cell cycle are suppressed by constricted migration, consistent with

71 Indeed, aging phenotypes were suppressed by continued expression of Hey in ECs, s

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

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

74 y molecular absorption of PO molecular bands is suppressed by correction model using least squares ba

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

76 when insulin-induced somatostatin secretion is suppressed by dapagliflozin (an inhibitor of sodium-g

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

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

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

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

81 ncreased Taf1 occupancy upon Kin28 depletion is suppressed by depletion of TBP, while depletion of TB

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

83 RTKs), RPTP activities have been reported to be suppressed by dimerization, which may prevent RPTPs f

84 AtSAL1 phosphatase activity is suppressed by dimerization, intramolecular disulfide

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

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

87 o-called Frohlich exciton phonon interaction is suppressed by doping.

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

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

90 dative stress and aminoglycosides, which can be suppressed by eamA overexpression.

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

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

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

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

95 ctron charge and h Planck's constant), which is suppressed by exceptionally small in-plane magnetic f

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

97 tem cell lineage tracing, a process that can be suppressed by exogenous gastrin treatment.

98 combination, possibly mediated by helicases, are suppressed by exonucleases ExoI and RecJ.

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

100 log of CDK19, causes larval lethality, which is suppressed by expression of human CDK19 reference cDN

101 te-dependent expression of behavior that can be suppressed by external inputs conveying a competing b

102 Contralateral invasion is suppressed by extracellular matrix (ECM) and programm

103 lls were stimulus-driven by novel images but were suppressed by familiar stimuli and showed ramping a

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

105 c enhancement, and this increased inhibition is suppressed by fear learning but is not restored by ex

106 ll death in Mtb-infected macrophage cultures was suppressed by ferrostatin-1 (Fer-1), a well-characte

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

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

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

110 Li dendrite growth of metallic lithium anode is suppressed by forming a lithium fluoride (LiF)-enrich

111 regation of the conjugated organic molecules is suppressed by functionalization with sterically deman

112 ysis reveals cytoskeleton related genes that are suppressed by Galpha(13), identifying Galpha(13) as

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

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

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

116 These sensitivities are suppressed by genetically eliminating Ku nonhomologo

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

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

119 cell division that facilitates mutation and is suppressed by GPCR signaling.

120 The TaRca1 gene was induced, whereas TaRca2 was suppressed by heat stress.

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

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

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

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

125 e show that the activity of Siah1/2 can also be suppressed by host cell factor 1 (HCF1), and the hith

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

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

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

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

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

131 egative regulator of osteoclastogenesis that is suppressed by hypoxia.

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

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

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

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

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

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

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

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

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

141 Electrical excitability is suppressed by increased vacuolar Ca(2+) levels.

142 um in helical chiral nanowire structures can be suppressed by inhibiting electron transport in a heli

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

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

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

146 eptide enhanced neurite outgrowth that could be suppressed by inhibitors of the estrogen receptors al

147 Migration was suppressed by inhibitors of the prolyl isomerase Pin

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

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

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

151 FoxO transcription factors are suppressed by insulin and thus are key mediators of

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

153 chaotic flows in non-rotating active fluids-is suppressed by intrinsic rotation of chiral active par

154 Consequently, if circulation of VZV is suppressed by introduction of chickenpox vaccination,

155 ndicate that mutant p53 gain-of-function can be suppressed by IRP2 and FDXR deficiency, both of which

156 In the dark, PDE6 activity is suppressed by its inhibitory gamma-subunit (Pgamma).

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 othelial migration and T cell entry into LNs were suppressed by Lama5 through the receptors alpha6 in

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

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

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

165 ermore, we show that BCL11A mRNA translation is suppressed by LIN28B through direct interactions, ind

166 known to be detrimental to the TADF process, are suppressed by linking the PTZ units to form a cyclop

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

168 several 8-nm forward and backward steps that were suppressed by loads.

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

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

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

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

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

174 h multimodal signaling, but rather M current was suppressed by M(1)R stimulation in these cells, simi

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

176 and ultimately on MERVL regulation could all be suppressed by manipulating U7 RNA levels.

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

178 cells is a major driver to autoimmunity and is suppressed by mechanisms of regulation.

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

180 larvae are hypersensitive to hypoxia, which is suppressed by miR-274 expression in glia or by increa

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

182 ation acquisition, quinone reductase 2 (QR2) is suppressed by miRNA-182 (miR-182) in the CA1 region o

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

184 ns were identified: small-loop hairpins that were suppressed by MRE11, SAE2, SLX1, and YKU80 and larg

185 n peripheral blood mononuclear cells (PBMCs) were suppressed by MSC bioreactor culture confirmed by a

186 ll-intrinsic manner in nonneuronal cells and is suppressed by multiple, independent viral functions t

187 that defects caused by changing residue E86 are suppressed by mutations altering either LPS structur

188 export of La due to mutation of the NRE can be suppressed by mutations in RRM1, but the mechanism by

189 Mating-induced death is suppressed by mutations in cell fusion genes ( FUS1,

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

191 rophosphatases is lethal, but this lethality is suppressed by mutations of CPF subunits Ppn1, Swd22,

192 In vivo defects in cse4-R37A were suppressed by mutations in OKP1 and AME1, and bioch

193 the bon mutants in osmotic stress responses were suppressed by mutations in the NLR gene SNC1 or the

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

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

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

197 displayed enhanced osteoclastogenesis, which was suppressed by Notch2 ASOs.

198 Importantly, iAs-induced transformation was suppressed by NRF2 knockdown.

199 ruent with self-motion during locomotion but are suppressed by other directions and contrasts.

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

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

202 dysregulated positive feedback loop, and can be suppressed by overexpression of the housekeeping sigm

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

204 It was suppressed by P2Y12 receptor antagonists, which also

205 These AHL4-DNA interactions were suppressed by PA species that bound to AHL4.

206 Disintegration can be suppressed by paclitaxel treatment.

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

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

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

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

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

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

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

214 utes to early transcriptional responses that are suppressed by PiSFI3.

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

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

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

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

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

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

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

222 responses are typically short-lived and can be suppressed by proteins that act post-translationally,

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

224 and cellularization defects in Drp1 mutants are suppressed by reducing mitochondrial fusion and incr

225 Further, Vps29 phenotypes are suppressed by reducing Rab7 or overexpressing the GT

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

227 ion, suggesting that selfish centromeres can be suppressed by regulating meiotic timing.

228 ors in an MHC class II-dependent fashion and are suppressed by regulatory T cells.

229 ular protein degradation in lysosomes, which were suppressed by restoring full-length APC.

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

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

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

233 somal instability (CIN) and these phenotypes are suppressed by RNH1 overexpression in hpr1Delta strai

234 While the CDW-SRO is suppressed by SC, it is partially transformed into th

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

236 innate immune induction in fly Adar mutants is suppressed by silencing of Dicer-2, which has a RNA h

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

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

239 n both osteosarcoma and breast cancer, which is suppressed by siRNA-mediated MALT1 knockdown, suggest

240 92593 as well as when its protein expression was suppressed by siRNA in both Melan-a and B16-F10 cell

241 rom loss of repressors such as microRNAs can be suppressed by slow metabolism.

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

243 JNK was suppressed by SP600125 or Jnk siRNA.

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 pappaa mutants' enhanced hair cell loss can be suppressed by stimulation of IGF1 availability and th

248 h sound-evoked responses of auditory neurons are suppressed by stimuli outside their receptive field,

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

250 ibed during vegetative growth, their effects are suppressed by strong and constitutive silencing by m

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

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

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

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

255 All toxicity features, however, are suppressed by the coexpression of PI3K.

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

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

258 PGE2 was able to upregulate many genes that are suppressed by the profibrotic cytokine TGF-beta, whe

259 A resulting in cytokine release, which could be suppressed by the addition of a corticosteroid in vit

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

261 to enable ripening initiation and this could be suppressed by the ET perception inhibitor 1-MCP.

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

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

264 Viral replication is suppressed by the adaptive immune response; when thes

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

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

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

274 Here we examined how APC/C activity is suppressed by the small pseudosubstrate inhibitor Acm

275 uclear retained in mESCs, and its processing is suppressed by the splicing factor PPIE, which is high

276 The killing of tumor cells by CD8(+) T cells is suppressed by the tumor microenvironment, and increas

277 gainst Kallithea virus infection but that it is suppressed by the virus.

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

279 astasis of orthotopic BT474-TtzmR xenografts was suppressed by the combination.

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

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

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

283 accumulation of 8-oxo-dG and gammaH2AX-which was suppressed by the NADPH oxidase inhibitor diphenylen

284 ed by activated form of PARP, caspases-3 and was suppressed by the pan-caspase inhibitor Z-VAD-FMK.

285 c neurons projecting to the NAc medial shell were suppressed by the MOR agonists DAMGO and morphine,

286 e states, where quasiparticle backscattering is suppressed by time-reversal symmetry (TRS).

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

288 ignaling and IL-6 production, an effect that is suppressed by TRAF5.

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

290 Furthermore, desensitization can be suppressed by trapping the linker in the resting stat

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

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

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 rthermore, undesired uptake into liver cells was suppressed by using l-deoxygalactosyl modified carbo

297 esult of polar surface relaxation, which can be suppressed by varying the lattice symmetry breaking u

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

299 tion, inflammatory responses are believed to be suppressed by Y. pestis virulence factors in order to

300 SLX1, and YKU80 and large-loop hairpins that were suppressed by YEN1, TEL1, SWR1, and MRC1.