ライフサイエンスコーパス: -dependent

1 induce pyroptosis, as measured by caspase-1-dependent interleukin-1beta release, though this phenoty

2 nction protein expression through an IL-10RA-dependent mechanism.

3 rophysiological recordings show that Sema-1a-dependent R axon lamination is required for preventing t

4 ation of an erythroid-specific, protein 4.1R-dependent membrane skeleton is an important feature not

5 ne potential, facilitates downstream Ca(2+) -dependent pathways and becomes concentrated in specific

6 This is well exemplified by the Ca(2+)-dependent inactivation of L-type Ca(2+) channels, whose

7 A group of "plant-like" Ca(2+)-dependent protein kinases (CDPKs) transduces cytosolic C

8 27 suppressed osteoclastogenesis in an Egr-2-dependent manner that up-regulates Id2, the repressor of

9 on inflammation in a CC-chemokine receptor 2-dependent manner, and the nonclassical blood resident mo

10 hymic ILCs improved thymopoiesis in an IL-22-dependent fashion.

11 f these cytokines, inhibiting interleukin-23-dependent production of interleukin-17.

12 1-CXCR2 signaling axis identified HIF-2alpha-dependent neutrophil recruitment as an essential mechani

13 e findings suggest a new paradigm where IL-4-dependent up-regulation of Cox-1 expression may play a k

14 cytotoxic T-lymphocyte-associated protein 4-dependent (CTLA4-dependent) manner.

15 us, and this coincides with TCP20 and NLP6&7-dependent up-regulation of nitrate assimilation and sign

16 at they contain a highly conserved sortase A-dependent cell wall-anchored C terminus, whereas the sur

17 gand increased markers of tricarboxylic acid-dependent and -independent energy biogenesis and oxygen

18 GBPs inhibit actin-dependent motility and cell-to-cell spread of bacteria b

19 ion and inhibition of a broad range of actin-dependent functions, including phagocytosis, granule exo

20 telomeres after damage in an ATM activation-dependent manner.

21 Activity-dependent pruning also occurs at embryonic Drosophila ne

22 el RT neurons are predisposed to an activity-dependent switch from GABA-mediated inhibition to excita

23 n the synapse, where well-described activity-dependent mechanisms are known to play a key role in lea

24 ory protein required for efficient, activity-dependent AMPAR endocytosis.

25 By modifying rules that govern activity-dependent synaptic plasticity, addictive drugs can derai

26 a crucial role for this pathway in activity-dependent long-term depression (LTD) at hippocampal Scha

27 ne rapidly with age, culminating in activity-dependent, non-apoptotic cell death.

28 By inducing activity-dependent plasticity in the visual cortex of adult rats

29 Application of this method, activity-dependent proximity ligation (ADPL), to serine hydrolase

30 Using a novel activity-dependent technology called CANE developed in our labora

31 inally, we describe a novel form of activity-dependent intrinsic plasticity that persistently elimina

32 ess the spatiotemporal changes of actomyosin-dependent force and stiffness along the antero-posterior

33 these cellular phenotypes in a dose- and age-dependent manner in cortex and striatum of mice.

34 haviorally tested mice revealed distinct age-dependent patterns of accumulation in multiple oligomeri

35 aphy of a cuticular drusen distribution; age-dependent variations in cuticular drusen phenotypes, inc

36 However, the primary causes of age-dependent EFA remain largely elusive.

37 e changes in follicle populations showed age-dependent decreases in total follicles and percentages o

38 The accumulation of AGO4-dependent het-siRNAs also requires several factors known

39 iously that Rab8a recruits PI3Kgamma for Akt-dependent signaling during TLR4 activation to limit the

40 s as well as alcohol expectancies in alcohol-dependent patients and healthy controls and assessed tre

41 olite that can competitively inhibit alphaKG-dependent enzymes.

42 A selective peptide inhibitor of AMPH-dependent trafficking of the neuronal excitatory amino a

43 romoting AMP-activated protein kinase (AMPK)-dependent trafficking of KATP and Kv2.1 channels to the

44 orthogonal to the rips, inducing an angular-dependent change in the reversal mechanism.

45 reversal characteristics captured by angular-dependent first order reversal curve measurements indica

46 EFL mutations eliminated off-target antibody-dependent monocyte phagocytosis of cynomolgus monkey pla

47 ly induced by vaccines, can trigger antibody-dependent cellular effector functions, through engagemen

48 re is growing interest in utilizing antibody-dependent cellular cytotoxicity (ADCC) to eliminate infe

49 sed approach to specifically mislocalize APC-dependent RNAs suggests that localization of the APC-dep

50 t RNAs suggests that localization of the APC-dependent RNA subgroup is functionally important for cel

51 hoice of the appropriate tool is application-dependent.

52 Furthermore, DDX21 is both an ATP-dependent and ATP-independent helicase, and both ATPase

53 ndependent helicase, and both ATPase and ATP-dependent helicase activities are inhibited by Rev in a

54 erstanding of the proteasome's multistep ATP-dependent mechanism, its biochemical and structural feat

55 ce of glibenclamide, an inhibitor of the ATP-dependent potassium (KATP)-channels, thus suggesting a p

56 gests that the asymmetry of the three ATPase-dependent 120 degrees power strokes imposed by the relat

57 s of auxin-induced SAUR expression and auxin-dependent elongation growth were closely correlated.

58 lls and involved a switch from BCL2 to BCLXL-dependent cell survival.

59 DAC) PAR2 protein is necessary for TGF-beta1-dependent cell motility.

60 nization of RNA synthesis and ligand binding-dependent conformational refolding.

61 d as a moonlighting protein, with two biotin-dependent cytosolic metabolic roles and a distinct bioti

62 TAZ promoter in a CC(A/T-rich)6GG (CArG) box-dependent manner and induced TAZ protein expression.

63 This mechanism is distinct from the BRCA2-dependent fork protection pathway, in which stable RAD51

64 n, acting to drive immune escape via a C3/C5-dependent pathway.Significance: This provocative study s

65 ors (BKIs) of Cryptosporidium parvum calcium-dependent protein kinase 1 (CpCDPK1) are leading candida

66 es of auditory nerve firing, or that calcium-dependent processes involved in release are altered with

67 ) H]ryanodine binding and Ca(2+) /calmodulin-dependent protein kinase II (CaMKII) phosphorylation of

68 re, we show that activated Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) strongly interacts

69 Scaffolding the calcium/calmodulin-dependent phosphatase 2B (PP2B, calcineurin) focuses and

70 In contrast, when the calcium/calmodulin-dependent protein kinase II (CaMKII) was blocked with KN

71 n recruited calcium/calmodulin (Ca(2+)/CaMK)-dependent protein kinase II (CaMKII) to the hippocampal

72 wide association study data on 2080 cannabis-dependent cases and 6435 cannabis-exposed controls of Eu

73 -independent mechanism that involves caspase-dependent T cell apoptosis and upregulation of inhibitor

74 e ability of HMGA1 to stimulate beta-catenin-dependent transcription, suggesting that interactions be

75 acellular protein that enhances beta-catenin-dependent Wnt signaling and has previously been shown to

76 Alterations in the Cdk/Cdc14-dependent phosphorylation status of Spc110, or its inact

77 quires both cyclin-dependent kinase 1 (CDK1)-dependent phosphorylation and its autophosphorylation at

78 molecular link between the processes of Cdk1-dependent priming and self-priming of Plk1 substrates.

79 Cell-dependent minimal to no toxicity of Inh2-B1, and its abi

80 high-avidity epitope provided strong, T cell-dependent protection against viruses or tumors.

81 he mother centriole mediates most centrosome-dependent processes, the role of the daughter remains po

82 perturbing S phase and by blocking the Chk1-dependent response to replication fork damage.

83 Ch25h deficiency results in cholesterol-dependent reduced mitochondrial respiratory capacity and

84 cted in MKs and platelets, the impact of CK2-dependent signaling on MK/platelet (patho-)physiology ha

85 ative stress, and this upregulation is CLOCK-dependent.

86 tes in vivo, GsD is expressed and allows CNO-dependent cAMP signaling and glycogen breakdown.

87 ti-proliferation gene transcripts in a Cnot3-dependent manner, and promoted their degradation.

88 Here, we identify several novel CO2-dependent changes in the NF-kappaB pathway.

89 roposed to be formed using CysS, a cobalamin-dependent radical S-adenosylmethionine (SAM) methyltrans

90 or-specific antibody (DSA) causes complement-dependent endothelial cell injury in kidney transplants,

91 ivo evidence for contributions of complement-dependent membrane perturbations to prothrombotic TF act

92 topoisomerase II activity in a concentration-dependent manner.

93 ionic substituents and shows a concentration-dependent, tunable transition temperature in aqueous sol

94 ts activity was both time- and concentration-dependent.

95 Notably, 12 was able to cause concentration-dependent inhibition of cell proliferation, yielding an

96 Thus, LIS1 exerts concentration-dependent effects on dynein motility and can synergize w

97 od mononuclear cells elicited a cell contact-dependent expansion of MDSCs.

98 alcified PFP, purified DNA triggered contact-dependent thrombin generation (TG) and amplified TG init

99 In summary, ARID1A has context-dependent tumor-suppressive and oncogenic roles in cance

100 subtilis causes strand- and sequence-context-dependent GC --> AT transitions.

101 sis of the decoy effect could be the context-dependent activation of the valuation area.

102 Plants use context-dependent information to calibrate growth responses to t

103 In this study, we generated Zwitch, a Cre-dependent invertible gene-trap cassette, enabling the es

104 aintaining proper neddylation levels for CRL-dependent proteostasis.

105 hocyte-associated protein 4-dependent (CTLA4-dependent) manner.

106 Cyclin-dependent kinases 4 and 6 (CDK4/6) are fundamental drive

107 ontaining 4 (BRD4) with NF-kappaB and cyclin-dependent kinase 9 (CDK9).

108 totic activation of Gwl requires both cyclin-dependent kinase 1 (CDK1)-dependent phosphorylation and

109 lar, to THZ1, a covalent inhibitor of cyclin-dependent kinase 7 (CDK7).

110 is strictly controlled by a number of cyclin-dependent kinases (CDKs) and CDK inhibitors (CKIs), the

111 ibitors of mTOR and inhibitors of the cyclin-dependent kinases CDK4 and CDK6 substantially improve pr

112 we further validate its detection with data-dependent acquisition and targeted analyses.

113 -nucleotide polymorphisms, considering depth-dependent behavior of similarity metrics for identical a

114 marker that is reliable, cheap, less device-dependent, and can be easily and repeatedly used on a la

115 e previously showed that the differentiation-dependent cellular transcription factors KLF4 and BLIMP1

116 ion of MutLalpha endonuclease, PCNA- and DNA-dependent activation of MutLalpha ATPase, and MutLalpha

117 TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of IFN-regulatory factors (DAI) that

118 in vivo (using rainbow trout fry) in a dose-dependent and time-dependent manner.

119 Furthermore, there was a dose-dependent association between the prevalence of low VA a

120 in kinase (MAPK) cascade and triggers a dose-dependent differentiation response.

121 decompensation, mortality, and HCC in a dose-dependent manner (P for trend <0.0001, <0.0001, and 0.00

122 asma levels of fitusiran increased in a dose-dependent manner and showed no accumulation with repeate

123 se activities are inhibited by Rev in a dose-dependent manner, although ATP-independent helicase acti

124 amphetamine-induced hyperactivity in a dose-dependent manner, similar to the atypical antipsychotic,

125 y initiation of liver regeneration in a dose-dependent manner, without modifying the peak regenerativ

126 Patients who received inclisiran had dose-dependent reductions in PCSK9 and LDL cholesterol levels

127 We found that PEGylation prevented dose-dependent hemolysis in the concentrations studied (0-10

128 oactive component of cannabis, produced dose-dependent conditioned place aversion and a reduction in

129 we observed that 1B6 displayed a rapid dose-dependent clearance (t(1/2) 10-60 h) in contrast to 1F11

130 n A small but statistically significant dose-dependent T1-weighted signal enhancement was observed in

131 verexpression results in a significant, dose-dependent increase in EGFR tyrosine phosphorylation, par

132 Temporal, dose-dependent and specific disruption of the TJ-associated Z

133 e-induced apoptosis occurring in a Bax, Drp1-dependent manner.

134 We have recently reported that HPV E7-dependent promoter hypermethylation leads to downregulat

135 ase C- and Gbetagamma-metalloproteinase/EGFR-dependent MAPK/ERK signaling cascades.

136 hus constitute a common endpoint of both EMT-dependent and EMT-independent cancer dissemination progr

137 stress, associated impairment of endothelium-dependent vasorelaxation, and preserves endothelial Sirt

138 antibodies reduced tau uptake in an epitope-dependent manner: N-terminal (Tau13) and middomain (6C5

139 Our results point to an EsRalpha-dependent, reciprocal interaction between IP3 and ryanod

140 active targets for the treatment of estrogen-dependent diseases like endometriosis and breast cancer.

141 Thus, ETR1 and ETR2 have both ethylene-dependent and -independent roles in plant cells that aff

142 an early developmental time when experience-dependent plasticity shapes such circuits.

143 ocaine CPP extinction and lack of extinction-dependent changes in hippocampal PSD CaMKII expression a

144 NQO1 is a FAD-dependent, two-domain multifunctional stress protein act

145 ss if FANCI is also involved in these FANCD2-dependent mechanisms, we generated isogenic FANCI-, FANC

146 superlattice period-, temperature- and field-dependent evolution of these structures, we observe seve

147 Flavin-dependent halogenases are useful enzymes for providing h

148 epresents a new class of zinc-binding flavin-dependent halogenases and provides new insights into a p

149 ls, we show that B cells primarily use force-dependent extraction and resort to enzymatic liberation

150 suggest that 5-HT neurons exert a frequency-dependent, cell-type-specific control over BA circuitry

151 this equilibrium is determined by frequency-dependent selection.

152 implementing GBAi in vivo, we show that GBA-dependent signaling modulates phenotypes during Xenopus

153 Thus, GCK-dependent glycolysis regulates Treg cell migration.

154 Suc affects the circadian oscillator in a GI-dependent manner was unknown.

155 induce GRalpha nuclear translocation and GRE-dependent GILZ expression.

156 quantitative proteomics to characterize Hat1-dependent changes in the composition of nascent chromati

157 tion of the ALOX5 is responsible for the Hcy-dependent worsening of the AD phenotype in a relevant mo

158 ing an infrared laser, for reproducible heat-dependent gene expression in small sublineages (one to f

159 are known to generate a directional helicity-dependent photocurrent in three-dimensional topological

160 ing of the mechanism underlying HBoV1 helper-dependent AAV2 replication may also provide insights int

161 pocampal CA1 pyramidal cells and hippocampal-dependent cognitive function.

162 cking PRMT8 also exhibit reduced hippocampus-dependent memory.

163 a subset of odor combinations, this history-dependent processing was useful in helping to identify t

164 Sse1sbd was fully competent to support Hsp90-dependent signaling through heterologously expressed glu

165 Together, our data reveal an HSPG-dependent pathway that specifically allows dendrites of

166 ceruleus is associated with decreased 5-HT2A-dependent noradrenergic transmission.

167 onses through the initiation of a type I IFN-dependent DDR.

168 d humoral immune responses that included IgE-dependent basophil activation and measurement of serum i

169 resenting cells and we aimed at studying IgE-dependent antigen presentation in both cell types.

170 lecting system development requires integrin-dependent cell-extracellular matrix interactions.

171 ol efflux do not necessarily represent inter-dependent events, but MafB is broadly involved in both t

172 l ion and ligand binding sites and metal ion-dependent RNA stabilities.

173 Both IR68a- and IR40a-dependent pathways drive hygrosensory behavior: each is

174 In root cells, HS triggered an iron-dependent cell death pathway that was characterized by d

175 The phosphorylation of STAT5B on the JAK2-dependent Y699 site is significantly reduced in the live

176 as well as nuclear factor kappaB (NF-kappaB)-dependent cell survival.

177 through a synergistic induction of NF-kappaB-dependent MMP1 expression in cancer cells.

178 gesting a possible mechanism underlying KCC2-dependent insulin release.

179 ification increases receptor tyrosine kinase-dependent activation of RAS more potently in colorectal

180 nal theory calculations, show distinct layer-dependent semiconductor-to-semimetal evolution of 2D lay

181 in network parameters arising from learning-dependent synaptic plasticity.

182 e epilepsy, alpha-related blood oxygen level-dependent signal changes demonstrated lower decreases re

183 licit greatly exaggerated blood-oxygen-level-dependent (BOLD) responses in the anterior insular corte

184 obular proteins, such as mCherry, in a light-dependent manner.

185 me 2 (CRY2) can simultaneously undergo light-dependent CRY2-CRY2 homo-oligomerization and CRY2-CIB1 h

186 Stat3-phosphorylation/activation in an LKB1-dependent manner, preventing its recruitment to canonica

187 we demonstrate that key RQC activities-Ltn1p-dependent ubiquitination and Rqc2p-mediated Carboxy-term

188 Our results show that m6A-dependent RNA structural alterations can promote direct

189 However, the mGluR-dependent reduction in ICa was not mimicked by Gbetagamm

190 In an in vitro and cell-based model of MMP-dependent breast cancer cellular invasiveness, this N-TI

191 of endotoxin-induced inflammation in an MPO-dependent manner.

192 able RAD51 filament formation prevents MRE11-dependent degradation of the newly synthesized DNA at st

193 ans for interrogating mechanisms of mutation-dependent drug response, which will have a significant i

194 gical means as a potential treatment for MYC-dependent tumors.

195 se that phosphorylates MyD88, promoted MyD88-dependent signaling and mediates dermatosis in Ptpn6(spi

196 rameter combinations, which represent myosin-dependent contractility, a characteristic viscosity-adhe

197 ucture of many mineral soils could undergo N-dependent changes as atmospheric CO2 concentrations rise

198 tuin 1 (SIRT1), a conserved mammalian NAD(+)-dependent protein deacetylase, senses environmental stre

199 We assessed neuronal-dependent and -independent contributions by activating o

200 uses on recent progress on the roles of NFIC-dependent and NFIC-independent signaling pathways in too

201 Nicotine-dependent smokers and nonsmokers completed a probabilist

202 red 35 proteins mainly related to nucleotide-dependent processes and lipid metabolism.

203 m Toxoplasma gondii is hydroxylated by an O2-dependent prolyl-4-hydroxylase (PhyA), and the resulting

204 ed one substitution severely impaired OGFOD1-dependent hydroxylation of a neighboring proline residue

205 -helical domains in a position- and organism-dependent manner.

206 We report a new distance- and orientation-dependent, all-atom statistical potential derived from s

207 is a member of the Fe (II)- and oxoglutarate-dependent AlkB dioxygenase family and is linked to both

208 Here, oxygen-dependent changes in C. jejuni physiology were studied a

209 s and caused only a minor inhibition of P2X1-dependent Ca(2+) entry.

210 e majority of sequences examined display p53-dependent enhancer activity during the DNA damage respon

211 ied that these proteins induce TREM-1 in p65-dependent manner.

212 Unexpectedly, we identified PABPN1-dependent ALYREF binding near the 3' end of the mRNA.

213 istance, and although expression of the Pap1-dependent genes still relied on stress induction, anothe

214 alpha interaction with PCNA, as well as PCNA-dependent activation of MutLalpha endonuclease, PCNA- an

215 o a cholesterol-rich diet and uncover a PDL1-dependent mechanism through which MZB cells use their in

216 Model-predicted deficits in PEEP-dependent lung recruitment correlate with altered lung l

217 Thus, we demonstrated peptide-dependent binding of the activating NK cell receptor KIR

218 resistance of the DeltagpsB mutant was PgdA-dependent and OatA-independent.

219 Electrochemical analysis revealed a pH-dependent and remarkably high Fe(III)-OH/Fe(II)-OH2 redu

220 sed by hydrogen bonding to water, where a pH-dependent excitation energy appears to be an intrinsic p

221 Because of its position and pH-dependent reduction potential, N2 has long been consider

222 significantly inhibited both phosphoantigen-dependent and -independent activation of Vgamma9Vdelta2

223 erse biological processes by phosphorylation-dependent protein-protein interactions.

224 Inhibition of PI3K-dependent exocytosis of TRPC6 is thought to be the under

225 stimulation also elicited a Ca(2+)- and PKC-dependent reduction in synaptojanin1 recruitment to clat

226 Calcium/PKCalpha-dependent activation of NUAK1 supports engagement of the

227 Position-dependent effects on peptide retention for different res

228 cell division pattern indicating a position-dependent patterning mechanism may be in place.

229 inactivates dopamine D2 receptors in a PRDX6-dependent manner.

230 event occurring in the airways of prednisone-dependent asthmatic patients with increased eosinophil a

231 alters species stoichiometry and proteasome-dependent turnover of nuclear MAF1.

232 ACD11) in planta and promotes the proteasome-dependent turnover of ACD11 in cell-free degradation ass

233 ides enriched in lipid rafts to inhibit raft-dependent PI3K signaling.

234 trols lysosome positioning through Ragulator-dependent, but mTORC1-independent, modulation of BORC.

235 e that Rap1 contains an AD required for Rap1-dependent gene transcription.

236 Our current studies show that K-Ras-dependent cells are refractive to PKCdelta-driven apopto

237 t lung cancer cell lines classified as K-Ras-dependent or -independent for co-dependency on protein k

238 ing as an on-off switch controlling an RbohD-dependent mechanism in response to different stresses, s

239 aint that is mediated by muscarinic receptor-dependent regulation of mitochondrial function via AMPK.

240 iatric risk gene TCF4 enhances NMDA receptor-dependent early network oscillations.

241 ed miRNA expression, we used Cre recombinase-dependent miRNA tagging and affinity purification in mic

242 Further, this reconsolidation-dependent updating process appears to reorganize the neu

243 er-range interactions connecting replication-dependent histone genes on chromosome 6, potentially rep

244 ontal sensorimotor control and rapid, reward-dependent reorganization of control dynamics.

245 ctivity, supporting the conclusion that RIMA-dependent nuclear IYO accumulation triggers cell differe

246 rt a versatile S-adenosyl-l-methionine (SAM)-dependent enzyme, LepI, that can catalyse stereoselectiv

247 On the one hand, models of scale-dependent feedbacks, whereby plants facilitate neighbour

248 ape this restriction, Gag promotes secretase-dependent cleavage of APP, resulting in the overproducti

249 is a major factor, which determines sequence-dependent behavior of peptides in HILIC.

250 The local sequence-dependent features of DNA found in high-resolution struc

251 rcoming its decoy activity and seed sequence-dependent gene silencing activity.

252 me proliferator-activated receptor signaling-dependent switch from glycolysis to fatty acid oxidation

253 inflammatory cytokines via a Wnt5a signaling-dependent mechanism.

254 properties while the latter results in size-dependent mechanical properties at the nanometer scales.

255 est migration in Xenopus embryos in a Snail1-dependent manner, indicating that the mechanism of actio

256 al tubule by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2

257 Interestingly, in the absence of sodium-dependent Pi transport activity, the PiT1-PiT2 heterodim

258 Thus sortilin-dependent as well as sortilin-independent sorting mechan

259 Thus, species-dependent regulation of PlexA1 expression may have been

260 formed synapses via dendritic calcium spike-dependent mechanisms.

261 nd parabolic barrier approximation) and spin-dependent drift-diffusion model.

262 vated smooth muscle gene promoters in an SRF-dependent manner.

263 a rich extracellular environment in a stage-dependent manner producing complex microstructural patte

264 rate how sensory information regulates state-dependent reflexes in the lower urinary tract and contri

265 distinct signalling mechanisms direct stress-dependent versus homeostatic regeneration, and highlight

266 , but remains poorly understood in substrate-dependent cells.

267 s as a molecular linker between the synapsin-dependent reserve pool and the presynaptic endocytosis m

268 erogeneously in terms of responsiveness to T-dependent stimuli.

269 tion of ERalpha, which in turn increases TAM-dependent anti-estrogen chemosensitivity in vitro and in

270 s are examined through time- and temperature-dependent transport measurements.

271 esults could be accounted for by temperature-dependent changes in both Km and kcat (three substitutio

272 The study of temperature-dependent sex determination (TSD) in vertebrates has att

273 tly activated to bind GPIbalpha in a tension-dependent manner.

274 Time-dependent Cox regression models were used to calculate h

275 Time-dependent leukocyte density and diversity and the magnit

276 on of pre-change exposure, suggesting a time-dependent decision threshold.

277 Taurocholate induced a time-dependent increase in LPC proliferation and expression o

278 itis B in China, we propose an age- and time-dependent discrete model and use the method of non-linea

279 nbow trout fry) in a dose-dependent and time-dependent manner.

280 Dose- and time-dependent tumor uptake was studied in nude BALB/c mice b

281 can be ascribed to an interplay between time-dependent many-particle scattering and phase-space filli

282 n of pressure to the complex causes its time-dependent dissociation and the loss of both DHO and ATC

283 we were able to identify several major time-dependent phenotypic changes in blood immune cell subset

284 nt work by Ezawa; on the calculation of time-dependent gap length distributions in pairwise alignment

285 a distinct meaning for the encoding of time-dependent signals.

286 e on S. cerevisiae through the device's time-dependent frequency shift and motional resistance.

287 95% confidence intervals (CI), for the time-dependent risk related to ENE positivity.

288 -level risk factors were analysed using time-dependent Cox regression to examine their potential infl

289 ed that autophagy in NP cells was not TonEBP-dependent; hyperosmolarity did not upregulate autophagy

290 ed skin cancer development in mice in a TSLP-dependent manner.

291 ors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and d

292 implicated in mediating several forms of use-dependent plasticity, but the mechanisms by which it con

293 xyketone rearrangement catalysed by vanadium-dependent haloperoxidases to account for these discrepan

294 ing kidney dysfunction in a vasopressinergic-dependent manner.

295 base of the lamellipodium, where a vinculin-dependent clutch couples actin to previously positioned

296 ene) electrochemical devices exhibit voltage-dependent heterogeneous swelling consistent with device

297 reduced functional expression of the voltage-dependent potassium channel subunit Kv1.1 substantially

298 The wavelength-dependent conversion of two rapid photoinduced ligation

299 ranscriptome gene expression analyses on WNT-dependent KDR(+)CD235a(-) definitive hematopoietic mesod

300 k controlling phosphate accumulation in zinc-dependent manner.