ライフサイエンスコーパス: at @3 phase of

1 jecting excitatory neurons, on average, fire at a specific phase of a local 30 Hz network rhythm.

2 ees of postcolumn (bio)molecular specificity at the detection phase of a separation.

3 igger memory reactivation when they occurred at the optimal phase of a slow oscillation.

4 ter defibrillation shocks and shocks applied at the plateau phase of a normal action potential produc

5 alpha activity that biases TC cells to fire at certain phases of alpha, offering a pathway for corti

6 sating for an sAPPalpha deficit taking place at the early asymptomatic phase of Alzheimer disease.

7 ate that neonates are biased to Th2 function at all phases of an immune response.

8 s indicate that ICOS exerts distinct effects at different phases of an immune response: ICOS can inhi

9 rst spikes evoked by a stimulus would appear at different phases of an oscillation, depending on the

10 gamma radiation (GR) induced JNK activities at the early phase of apoptosis in Jurkat T-cells.

11 g immunity, enzymes, and structural proteins at all phases of atresia.

12 eter Delta(t) showed much higher sensitivity at the initial phase of Au-protein and protein-protein i

13 activity in various brain regions increases at specific phases of brain oscillations.

14 sion levels of carbohydrate metabolism genes at different phases of bud dormancy.

15 socioemotional orientation than individuals at earlier phases of career development.

16 of CD8+ T cells are differentially expressed at different phases of CD8+ T-cell responses.

17 By isolating complexes at different phases of cell growth and manipulating nucl

18 ormal spirochaete growth and morphology even at early phases of cell division.

19 DBM was found to arrest TRAMP-C1 cells at G(2)-M phase of cell cycle and suppressed phosphoryla

20 chievable concentrations, by arresting cells at G0/G1 phase of cell cycle and without any induction o

21 rd4 did not bind to genes that are expressed at later phases of cell cycle.

22 ed corresponding changes in mitotic activity at the early log phase of cell growth.

23 lly caused BL cells to undergo growth arrest at the G1 phase of cell cycle before their entry into ap

24 es cell proliferation in DU145 and PC3 cells at the G1 phase of cell cycle.

25 ion for most melanoma cells is growth arrest at the G2-M phase of cell cycle.

26 phoma cells underwent apoptosis and arrested at the G2/M phase of cell cycle.

27 ive stress arrested a population of C6 cells at the G2/M phase of cell cycle.

28 pressed genomic instability-associated genes at distinct phases of cellular transformation, exhibited

29 At least three phases of change in gene expression could

30 the basis of the time course of expression, at least three phases of change in gene expression could

31 These fusion proteins, which are at present in different phases of clinical development,

32 At the middle phase of CMV replication in RPE cells, a l

33 c FGF, FGF20, is the likely ligand for FGFR1 at this sensory specification phase of cochlear developm

34 IgM Ab's in the initial stage and IgG2a Ab's at the effector phase of collagen-induced arthritis.

35 However, diaphragmatic abnormalities at the initial phase of critical illness remain poorly d

36 etween USP8, AIP4, and the ESCRT-0 machinery at the early sorting phase of CXCR4 and underscore the v

37 Mitochondrial proteomic analysis at the initial phase of degeneration in the model detect

38 l fluid may affect the dentin caries process at the early phases of demineralization.

39 to P80 varies markedly in different tissues, at different phases of development, and regionally withi

40 dual overexpression during regeneration and at least one phase of development.

41 ean regulatory state specification functions at upstream phases of development of the body plan.

42 and 1044 genes significantly down-regulated at acidogenic and solventogenic phase of DG-8052, respec

43 ly increased in the retinas of animal models at the vasodegenerative phase of diabetic retinopathy.

44 ease that represented uptake by pagetic foci at different pathologic phases of disease.

45 y extrahepatic biliary tissues from patients at early phases of disease.

46 , EPCs were recruited into inflamed synovium at the acute phase of disease and formed de novo blood v

47 At the clinical phase of disease, brain PrP(Sc) levels i

48 severe deficit in mitochondrial respiration at the clinical phase of disease.

49 ic imaging in detecting the cell infiltrates at the early phase of disease onset.

50 se activity, we examined the effect of IL-27 at the effector phase of disease using adoptive transfer

51 he ventral tegmental area (VTA) are involved at early phases of drug addiction.

52 und that children can be included in studies at the early phases of drug development and should be an

53 tribution, metabolism, excretion/toxicology) at very early phases of drug development, thereby enabli

54 found that the muscles appear to be excited at a particular phase of each locomotor body bend.

55 ight control of excitatory inputs that arise at a specific phase of each theta cycle.

56 e evoked by mechanical perturbations applied at various phases of each task.

57 Platelet depletion at the effector-inflammatory phase of EAE in mice result

58 isms time their cellular activities to occur at distinct phases of Earth's solar day, not through the

59 ontrol of amplitude and timing of expression at different phases of embryogenesis, and control of spa

60 Thus, synaptophysin regulates at least two phases of endocytosis to ensure vesicle ava

61 a significant decrease in cell proliferation at the erythropoietin-dependent phase of erythropoiesis.

62 cialists are now entrusted with patient care at different phases of evaluation and treatment.

63 Inhibition of monocyte infiltration at the induction phase of experimental autoimmune uveiti

64 ow that they control different sets of genes at distinct phases of flower development.

65 ubset of CD8(+)PD-1(+)FOXP3(+) T lymphocytes at the earliest phase of functional differentiation afte

66 rity of REM theta phase-shifting cells fired at the ascending phase of gamma oscillations during waki

67 nhibitory concentrations, excision can occur at all phases of growth.

68 oncentrations (sub-MICs) were added to cells at an early stationary phase of growth; this was followe

69 ous DNA damage than isogenic wild-type cells at any phase of growth.

70 We show that at the postexponential phase of growth, the LetA/S an

71 solated from the serotype M6 GAS strain JRS4 at different phases of growth and transcript levels were

72 refore fails to secrete normal levels of Hla at early phases of growth.

73 e discovered that cells of Bacillus subtilis at the mid-exponential phase of growth are a mixed popul

74 ted GMSM-K cells displayed cell cycle arrest at the S phase of growth and double-strand DNA damage wa

75 these important virulence factor transcripts at this phase of growth.

76 mainly from the cleared specimens, showed that at the early phase of healing, ePTFE membranes interf

77 ation preceded detectable adipocyte necrosis at the early phase of HFD.

78 rent therapies or to select the right target at the right phase of illness for future drug developmen

79 ies, the vascular lesion was visualized only at the arterial phase of image acquisition; the other ni

80 ells to APCs, a role that might be important at the preadaptive phase of immune responses to some mic

81 At late phase of infection, enhanced bacterial counts in

82 Mice were euthanized at the early phase of infection (21 hours) or during the

83 ively present M84-specific epitopes starting at the early phase of infection.

84 anine kidney cells were treated with MbetaCD at the late phase of infection for a short duration, bud

85 bicistronic viral RNA, which is transcribed at the late phase of infection, is responsible for expre

86 its protein level is substantially increased at the late phases of infection cycle.

87 At the mid-acute phase of infection (14 weeks), resoluti

88 d 2 (V1-V2) from multiple sequences isolated at the primary phase of infection to those isolated arou

89 suggest a mechanism of viral immune evasion at the very earliest phase of infection.

90 rammed death receptor 1 expression also seen at this phase of infection.

91 matory cytokine/chemokine release from BMDMs at the initial phase of infections.

92 ing opposite regulatory roles of IkappaBzeta at initial and resolution phases of inflammation.

93 ration and macrophage function occurred only at the postacute/chronic phase of inflammation and was a

94 derstood, particularly at higher frequencies at which the relative phase of inhibition and excitation

95 Then interventions were timed at earlier and later phases of intermediate-stage diseas

96 er intensive lowering of blood pressure (BP) at the acute phase of intracerebral haemorrhage (ICH) is

97 r data support the hypothesis that there are at least two distinct phases of involution: an initial p

98 At the very early phase of ischemia, high-resolution res

99 s a major cause of renal failure, especially at the early phase of kidney transplant when ischemia-re

100 At this late phase of learning, the BLA effect occurred

101 ential expressions of the B1-containing RNAs at the early phase of Leishmania-macrophage interaction

102 interaction between Fgfr and Bmp7 signaling at the induction phases of lens development.

103 ene and gene groups that play critical roles at different phases of liver development and regeneratio

104 hp2 tyrosine phosphatase is a critical event at the early phase of liver regeneration.

105 The molecular events that occur at the early phase of many demyelinating neurodegenerati

106 a phenomenon that separates ribosomal types at a critical phase of maturation.

107 ay be regulated by TNF (probably indirectly) at different phases of maturation and/or differentiation

108 e purified and separated into subpopulations at different phases of maturation.

109 n, proliferation, and cell cycle progression at the G0/G1 phase of MCL cells.

110 demonstrate that in vivo, mTORC1 activation at the early phase of mechanical overload in skeletal mu

111 ent membrane disruption, it is not effective at stopping the initial phase of membrane disruption bef

112 ay 10, the SAAs of both Adelta- and C-fibers at the "ascending" phase of microcontractions were signi

113 the recruitment of the polo-like kinase Plk1 at defined phases of mitosis.

114 ers and that the kinetics of exchange varies at different phases of mitosis.

115 survivin has separable checkpoint functions at multiple phases of mitosis and in the control of mito

116 Brd4 binding to M/G1 genes increased at telophase, the end phase of mitosis, coinciding with

117 to determine how mitochondrial S-nitrosation at the reperfusion phase of myocardial infarction is car

118 studies on the roles of various immune cells at different phases of obesity and discuss molecular mec

119 igation of therapeutically tractable targets at distinct phases of PDA development and progression.

120 Proteinases are important at several phases of physiological and pathological infl

121 tion and the generation of a myocyte progeny at all phases of prenatal life and up to one day after b

122 ceptor D1 (Drd1), and substance P expression at different phases of prenatal development was associat

123 or controversy about orientation selectivity at later phases of processing and gives a mechanistic vi

124 218 showed differential transcript abundance at various phases of R. typhi intracellular growth.

125 Targeting therapy at this phase of RA to break the cycles of recurrent inf

126 IVRT was decreased in the post-ASO patients at each phase of recovery compared with normal data (p <

127 ody-mediated disruption of netrin-1 function at the peak phase of recruitment increased OPC numbers.

128 criptionally to accommodate shifting demands at each phase of regeneration for NF heteropolymers of d

129 study aimed to investigate neuroinflammation at different phases of relapsing-remitting (RR) experime

130 f IL-27 subunits and its receptor in the CNS at the effector phases of relapsing-remitting EAE includ

131 e oxygen species (p < .05), and increased NO at a later phase of reperfusion (p < .01).

132 ial action potential at the plateau, but not at the terminal phase of repolarization, which led to ra

133 rties were lost with continued decomposition at later phases of ripening.

134 The frequency at which the phase of rotation relative to deflection of

135 rt a signaling role for proteoglycans during at least two distinct phases of skeletal development.

136 and molecular evidence that LEC functions in at least two phases of snRNA transcription: an initiatio

137 At the early phase of STEMI, the risk of prehospital SCA

138 Therapeutic intervention at the earliest phase of symptom exacerbation in schizop

139 ssion of the reporter gene was downregulated at S-phase of synchronized cells.

140 Tcf-1 is required at the earliest phase of T-cell determination for progre

141 eased systemic blood pressure, CBF and PbrO2 at the hyperacute phase of TBI.

142 The greatest improvement potential occurs at the early phases of technology development; therefore

143 s in the suppression of IFN-gamma expression at the two phases of Th1 responses.

144 althy adult participants were studied: women at 2 different phases of the menstrual cycle (early foll

145 Young women were scanned at 2 discrete phases of the menstrual cycle (midcycle an

146 ttern (bounce) and in a nonreturning pattern at 3 different phases of the SPECT acquisition (early, m

147 ctions in a signal sequence-dependent manner at a critical, early phase of the translocation process.

148 in target tissues for mitochondrial function at a distinct phase of the cellular growth cycle.

149 omplex, binding to both VEGFR2 and PI3K p85, at a late phase of the VEGF response, and that this lead

150 an additional tailored escort electron beam at a later phase of the acceleration, when the witness b

151 e in the response to UV were mediated by ATM at a later phase of the response.

152 proliferation was not associated with arrest at a particular phase of the cell cycle nor was it assoc

153 d that the c-MYB-dependent release of Pol II at a specific phase of the cell cycle is facilitated by

154 Further, neurons fired action potentials at a specific theta phase of the LFP, and the insertion

155 H autoantibodies induce neutralization of FH at acute phase of the disease, leading to an overall imp

156 llowing initiation of differentiation occurs at all phases of the cell cycle instead of only those ce

157 hronized populations revealed that PGE2 acts at all phases of the cell cycle to delay normal progress

158 reatment with vinblastine alone and occurred at all phases of the cell cycle.

159 hase arrest-the increase in p27Kip1 occurred at all phases of the cell cycle.

160 ory protocol, wherein subjects ate and slept at all phases of the circadian cycle-achieved by schedul

161 However, GTR and GSAT were present at all phases of the cycle.

162 The ccgs peaked in mRNA accumulation at all phases of the day, with the majority peaking in t

163 ical regulator of the CD8 T-cell homeostasis at all phases of the T-cell response to an acute viral i

164 lative to that observed in the control cells at all three phases of the growth curve.

165 hich multiple interventions were implemented at an early phase of the epidemic also showed a trend to

166 hich multiple interventions were implemented at an early phase of the epidemic had peak death rates a

167 and DNA and that this reduction is occurring at an early phase of the process.

168 e following folding mechanism for protein A: At an early precollapse phase of the process, a few nati

169 These data place Blimp-1 at an important phase of the CD8 T cell effector respons

170 y of inducible perfusion abnormalities occur at an intermediate phase of the stress test, without wal

171 climbing-fiber-driven Purkinje cell learning at arbitrary phases of the vestibular input.

172 that spiking of single neurons often occurs at certain phases of the global oscillation.

173 rently prevents them from changing direction at critical phases of the cell cycle.

174 A window of anabolic potential exists at defined early phases of the disease trajectory (>90 d

175 ecify the destruction of particular proteins at different phases of the cell cycle are controlled by

176 Using oligonucleotide arrays to assay mRNAs at different phases of the cell cycle in BCR/ABL-transfo

177 distinct roles for these checkpoint kinases at different phases of the cell cycle.

178 cells to CD95 (Fas; APO-1)-induced apoptosis at different phases of the cell cycle.

179 in Synechococcus and that they are expressed at different phases of the circadian cycle.

180 the cell cycle; instead, apoptosis can occur at different phases of the cycle depending on the apopto

181 utations affect the function of each complex at different phases of the cycle.

182 displayed distinct properties and phenotype at different phases of the disease course and remained r

183 iming in fast and slow interneurons occurred at different phases of the EPSPs of simultaneously activ

184 metabolism in human and mouse skin collected at different phases of the hair cycle; in hamster melano

185 rom both the Th1 and Th17-mediated responses at different phases of the inflammatory process.

186 TMS was applied unexpectedly at different phases of the movement cycle.

187 g to coding of different odorants and active at different phases of the respiratory cycle.

188 lder abduction motion in a self-paced manner at different phases of the sway.

189 ceptors (VSRs) by injecting rhythmic current at different phases of the swim cycle and determined int

190 asma membrane proteins from promoters active at different phases of the symbiosis, we show that polar

191 premature atrial complexes (PACs) delivered at different phases of the tachycardia cycle: when a PAC

192 r feeding-related activity, making them fire at distinct phases of the gamma oscillation.

193 hythmic columnar-specific motorneuron bursts at distinct phases of the locomotor cycle.

194 urbs metabolic functions of specific tissues at distinct phases of the sleep/wake cycle.

195 istribution of the traction forces generated at each phase of the cycle (protrusion, contraction, ret

196 Strategies for timely access to CR at each phase of the process are important given the neg

197 We found at early phase of the infection, PFOS inhibited the expa

198 r anchoring ability, and premature hair loss at early telogen phase of the hair cycle, resulting in c

199 At either end, phasing of the boxes with respect to the

200 vities of CDK2 and completely arrested cells at G(1) phase of the cell cycle by p27(Kip1) and at G(1)

201 Compound 1 blocks the growth of cancer cells at G0/G1 phase of the cell cycle.

202 ng RNA interference resulted in hESCs arrest at G1 phase of the cell cycle and differentiation to ext

203 growth inhibition is due to an accumulation at G1 phase of the cell cycle and is paralleled by a los

204 Tachpyridine arrested cells at G2, a radiosensitive phase of the cell cycle, and enh

205 In contrast, cells arrested at G2/M phase of the cell cycle were almost devoid of te

206 ovirus infection are arrest of the host cell at G2/M phase of the cell cycle with continuing viral DN

207 ithin the hinge domain occurs preferentially at G2/M phase of the cell cycle.

208 eradication is to take place at all, renders at least one phase of the dynamics essentially stochasti

209 would have continued through the Archean to at least the early phases of the Great Oxidation Event,

210 ignificant upregulation of chloride currents at M phase of the cell cycle.

211 The step responses were measured at many spatial phases of the grating stimulus.

212 y-1,2,3,4-tetrahydro-naphthalene (8-OH-DPAT) at midday advanced the phase of the free-running circadi

213 endent, and it associates with cyclin A/Cdk2 at multiple phases of the cell cycle.

214 ntal metastasis models, a role for autophagy at nearly every phase of the metastatic cascade has been

215 perform replication is divided into stages that occur at distinct phases of the cell cycle.

216 in (Timeless-interacting protein) accumulate at OriP during S phase of the cell cycle.

217 e identified may be important for regulation at other phases of the cell cycle.

218 ations in real time and trigger measurements at particular phases of the movement cycle.

219 In both groups, cell firing occurred at progressively earlier phases of the theta rhythm as t

220 for viability and is expressed specifically at S phase of the cell cycle.

221 ssion of targets that regulate proliferation at several distinct phases of the cell cycle.

222 e life-history traits may be more beneficial at some phase of the parasite's developmental process th

223 een signaling molecules and actin organizers at specific phases of the cell cycle.

224 ation, we triggered inhibition of dorsal CA1 at specific phases of the endogenous theta rhythm in fre

225 hmically amplify and attenuate the responses at specific phases of the rhythm (prominent for frequenc

226 ne such "firing field," spikes tend to occur at successively earlier theta phases of the local field

227 HJs in S phase, with SLX-MUS and GEN1 acting at temporally distinct phases of the cell cycle.

228 hemolytic uremic syndrome patients collected at the acute phase of the disease.

229 h experimental autoimmune encephalitis (EAE) at the chronic phase of the disease in search of an alte

230 f recombination intermediates showed defects at the cleavage phase of the reaction.

231 The mutagenic responses at the different phases of the reduction reaction were u

232 se PCR indicated expression of these kinases at the early mid phase of the developmental cycle.

233 tion of brain serotonin transporter function at the early phase of the disease.

234 bles an application of C-H functionalization at the early phase of the synthesis during the construct

235 ues could be exploited to overcome obstacles at the effector phase of the antitumor immune response a

236 r naive Treg can suppress antitumor immunity at the effector phase of the immune response induced by

237 is required at the inductive phase, but not at the effector phase, of the Th1 response within the in

238 Moreover, RSK2(-/-) MEFs accumulated at the G(1) phase of the cell cycle under normal cell cu

239 ls exposed to DETA-NONOate remained arrested at the G(1) phase of the cell cycle whereas untreated co

240 and thymidine incorporation and halted cells at the G(1) phase of the cell cycle.

241 hat IFN-tau induced hepatocyte growth arrest at the G0/G1 phase of the cell cycle and that the majori

242 on system resulted in a stable growth arrest at the G0/G1 phase of the cell cycle, preventing tumor c

243 nic fibroblasts and arrested both cell lines at the G0/G1 phase of the cell cycle.

244 xpression leads to the accumulation of cells at the G0/G1 phase of the cell cycle.

245 es PCD in peripheral blood mononuclear cells at the G0/G1 phase of the cell cycle.

246 s expressing PARP antisense RNA were blocked at the G0/G1 phase of the cell cycle.

247 DNA cleavage by RAG occurs only at the G1 phase of the cell cycle and generates two hair

248 inhibitor GGTI-298 arrests human tumor cells at the G1 phase of the cell cycle and increases the prot

249 anisms: prolonging the time that cells spend at the G1 phase of the cell cycle due to an increase in

250 factor beta (TGF-beta) causes growth arrest at the G1 phase of the cell cycle in most cell types.

251 ed inhibition of E7 phosphorylation occurred at the G1 phase of the cell cycle.

252 pstream of genes with peak transcript levels at the G1 phase of the cell cycle.

253 kinase inhibitors (CDKIs) which cause arrest at the G1 phase of the cell cycle.

254 helial cells (VEC) and arrested their growth at the G1 phase of the cell cycle.

255 opic expression of RPL23a resulted in arrest at the G1 phase of the cell cycle.

256 l line blocked by hydroxyurea or aphidicolin at the G1/S phase of the cell cycle or by nocodazole at

257 Cells arrested at the G1/S phase of the cell cycle showed similar level

258 ction of HOX11 into Xenopus oocytes arrested at the G2 phase of the cell cycle promoted progression t

259 ugs are known to induce Bcl2 phosphorylation at the G2-M phase of the cell cycle, with concomitant ap

260 stabilizing agent, is known to arrest cells at the G2/M phase of the cell cycle and induce apoptosis

261 lower concentrations of paclitaxel to arrest at the G2/M phase of the cell cycle and undergo apoptosi

262 V-1 accessory protein Vpr arrests host cells at the G2/M phase of the cell cycle by interacting with

263 hat stabilizes microtubules and blocks cells at the G2/M phase of the cell cycle in a manner similar

264 ule-interfering agents is an arrest of cells at the G2/M phase of the cell cycle, other effects may a

265 s, Cdk1 induced FOXO1 Ser249 phosphorylation at the G2/M phase of the cell cycle, resulting in FOXO1-

266 perature 32 degrees C leads to growth arrest at the G2/M phase of the cell cycle.

267 nsin complex concentrates in the rDNA region at the G2/M phase of the cell cycle.

268 rotubule assembly, results in mitotic arrest at the G2/M phase of the cell cycle.

269 itive mutations or depletion leads to arrest at the G2/M phase of the cell cycle.

270 reased apoptosis, and induced partial arrest at the G2M phase of the cell cycle.

271 otes), the procyclic promastigotes collected at the logarithmic phase of the culture displayed a stri

272 strain of P. falciparum and arrest parasites at the ring phase of the asexual stage and also gametocy

273 ream regions of genes whose expression peaks at the same phase of the cell cycle.

274 x 10(8) Transformants/mug DNA) was obtained at the stationary growth phase of the bacterium (OD 6.0)

275 arily inactivate the dorsal hippocampus (DH) at three different phases of the procedure, which produc

276 The maximum expression of these genes occurs at two different phases of the day and may depend on a p

277 ch mark the posterior of each segment, arise at two different phases of the primary pattern.

278 he DREAM (DP, RB-like, E2F and MuvB) complex at two distinct phases of the cell cycle.

279 d in cisplatin-resistant cells, cells halted at various phases of the cell cycle, and in different ca

280 ctivity, inducing a level of exercise driven at various phases of the light-dark cycle.

281 r, requiring that motor neurons be recruited at various phases of the locomotor cycle.

282 discriminate among spatial memories encoded at different circadian phases of their activity.

283 travel between specialized microenvironments at different phases of their development while interacti

284 t, however, lymphoid lineages rely on Ikaros at distinct phases of their development.

285 he glomerular mesangium also participates in at least the early phase of these diseases.

286 ng the phase of maximal gamma power to occur at later phases of theta.

287 Rather, CD4(+) T cells appeared to act at the effector phase of tumor rejection and responded t

288 bjects held in short-term memory is enhanced at specific phases of underlying oscillatory population

289 The new peptides acted at an early phase of viral infection, and, when combined

290 At an early phase of viral infection, contact and cooper

291 and the viral and cellular proteins required at each phase of viral DNA replication so that it can be

292 arget of antiviral therapy, has an impact on at least two distinct phases of viral replication.

293 y protein named T-antigen which is expressed at the early phase of viral lytic infection and plays a

294 s, revealing two distinct proteomic profiles at two phases of virus replication.

295 volution of the dynamic shear strength, with at least two phases of weakening separated by strengthen

296 exception of acute upregulation of miR-200c at the early phase of wound healing in aged skin.

297 was observed only when the slope of the PRC at a phase of zero, corresponding to spike initiation, w