ライフサイエンスコーパス: competitive

1 nergetic properties of the new materials are competitive.

2 tuted adamantane ammonium ions by direct and competitive (1)H NMR spectroscopy.

3 However, competitive 5-exo-dig cyclization, beta-elimination of t

4 Do competitive abilities change over hundreds of thousands

5 f invasive/exotic species or by reducing the competitive abilities of native species.

6 er evolutionary timescales, species-specific competitive abilities seem relatively stable, suggesting

7 tualist, implying that the trade-off between competitive ability and mutualistic capacity does not al

8 ts in decreased growth rate, cell viability, competitive ability and significant degradation in cell

9 ironment largely results from their superior competitive ability for dissolved nitrate (NO3(-)).

10 nd N acquisition strategies may increase the competitive ability of N2 fixers relative to non-N2 fixe

11 twork-competitive intransitivity and average competitive ability-to ultimately shape biomass producti

12 ing the imidazo[1,2-a]pyridine class of K(+)-competitive acid blockers (P-CABs), have potential appli

13 aches to treatment of GERD include potassium-competitive acid blockers, reflux-reducing agents, bile

14 The assay is based on the competitive adsorption of the sample and the acceptor-la

15 PAH desorption after addition of toluene by competitive adsorption to high-affinity sorption sites w

16 ffects and the pH-dependence of Mn(II)-metal competitive adsorption, system pH largely controls metal

17 erior competitor to F. occidentalis, but its competitive advantage can be counteracted through differ

18 ivation actually improves the deprived eye's competitive advantage during a subsequent period of bino

19 ikely to give bloom-forming green seaweeds a competitive advantage in mixed communities, and our resu

20 wood species, potentially giving hardwoods a competitive advantage in the future.

21 otential functional mechanism underlying the competitive advantage of large offspring size among Trin

22 efore, Thermococcus that possess fhl1 have a competitive advantage over other Thermococcus species in

23 duction of PVDPf-5 is required to maintain a competitive advantage.

24 uman AATZ (the Z variant of AAT) confers any competitive advantages compared to host cells that could

25 y-long sequence from the Levant demonstrates competitive advantages for commensal mice in long-term s

26 rea of biological surface science, including competitive advantages for probing the shape properties

27 egulation of GPCRs now extends beyond simple competitive agonism or antagonism by ligands interacting

28 A competitive alternative pathway is also found where the

29 ented reaction represents an interesting and competitive alternative to metal catalyzed and classical

30 how optical absorption methods have become a competitive alternative to state-of-the-art isotopic rat

31 benefits of social conformity in general and competitive altruism specifically.

32 Our findings highlight the importance of competitive and allelopathic interactions in regulating

33 Our findings reveal that competitive and cooperative interactions between actin b

34 Competitive and cooperative interactions between organis

35 Statistical network analysis revealed that competitive and cooperative reciprocal interactions are

36 ly dependent on plant patterning mediated by competitive and facilitative plant-plant interactions.

37 rge regions of Africa shows how economically competitive and low-environmental-impact renewable resou

38 Here we identified competitive and noncompetitive OCT1-interacting ligands

39 Examples to date have combined various competitive and sequential Forster resonance energy tran

40 nfall year contributed to the dominance of a competitive annual species in the plant community.

41 Derquantel behaved as a competitive antagonist and distinguished M-nAChRs activa

42 and tetramethylenedisulfotetramine, and the competitive antagonist bicuculline reduced fluorescence

43 nding pocket, thus acting predominantly as a competitive antagonist that inhibits the cyclic-nucleoti

44 Competitive antagonists against N-methyl-D-aspartate (NM

45 ated conformations solved for complexes with competitive antagonists and a lack of understanding of t

46 Functionally, selective competitive antagonists of apelin receptor were shown to

47 the exception of orteronel, can function as competitive AR antagonists.

48 The conventionally applied competitive assay format used for small molecule analysi

49 a double-antigen bridging assay but not on a competitive assay or on an indirect EBOV IgG ELISA.

50 different assays; both were negative on the competitive assay, suggesting that prior infection was u

51 Additive/competitive assays indicate that intracellular signaling

52 een substantial growth in the populations of competitive athletes and highly active people (CAHAP).

53 rtic dimensions are slightly larger in young competitive athletes compared with sedentary controls, b

54 Among the competitive athletes, two deaths were attributed to hype

55 losteric inhibitors (bile salts) into potent competitive Autotaxin inhibitors that do not interact wi

56 ated NR or DOX occurs (1) upon addition of a competitive binder (e.g., adamantane ammonium (ADA)) for

57 toluene below its saturation level revealed competitive binding and resulted in an average increase

58 In addition, a competitive binding assay to detect cardiac Troponin I (

59 These findings are supported by results of competitive binding assays and the similarity of the x-r

60 er and repressor activities, possibly due to competitive binding at similar DNA binding sites.

61 Here, de novo Rosetta modeling and competitive binding experiments show that the acidic tip

62 s slides, and fumonisin B1 was detected in a competitive binding inhibition assay using the antifumon

63 s of the selectivity filter in which to test competitive binding of Na(+) These experiments disclosed

64 calization of GFP-Kif17 to the cilia tip and competitive binding of RP2 and Arl3 with Kif17 complexes

65 Competitive binding of the human monoclonal antibody (mA

66 With this view, we investigate the effect of competitive binding on the dynamics of CaM binding partn

67 Affinity Reagents (MegaSTAR) to identify non-competitive binding pairs of recombinant affinity reagen

68 No product inhibition is observed, and competitive binding studies with nitro-containing additi

69 p and apply a physical model of TF-chromatin competitive binding using chemical reaction rate theory

70 Competitive binding was verified using the same soil wit

71 riplet state of diphenyl sulfide also showed competitive C-S bond cleavage giving phenyl sulfinic aci

72 It is a competitive candidate for numerically studying the wideb

73 represent a new class of highly specific ATP-competitive CDK4/6 inhibitors that induce reversible G1-

74 triplet energy transfer (TET) by suppressing competitive charge transfer from QDs to molecules.

75 their derived catalysts are found to exhibit competitive CO2 capacities (0.67-0.91 mmol g(-1) at 25 d

76 d in species discrimination, reproductive or competitive communication.

77 capturing a gradient from weakly to strongly competitive communities.

78 rresponding to 6pgL(-1) diclofenac, which is competitive compared to other label-free immunosensors.

79 CNNB in terms of NA-selectivity among multi-competitive components, long-term stability during the d

80 These reversible, competitive compounds represent a route toward potential

81 mewhat surprisingly, performed better in the competitive condition.

82 of 1.84 and 26.39, respectively, even under competitive conditions.

83 oxin B1), as well as other aflatoxins, under competitive conditions.

84 We contrasted partners across different competitive contexts to gain insight to the influence of

85 or FACS, with imaging and high throughput at competitive cost.

86 However, in order to be competitive, current biosensor nanotechnologies need sig

87 ng potential using [(11)C]raclopride (a weak competitive D2/3 receptor antagonist), and dopamine rele

88 Compared to a competitive DAT inhibitor indatraline, both SRI-compound

89 This analyte was quantified through a competitive detection procedure with 5-[4-(amino)phenyls

90 space, perhaps stemming from physical and/or competitive differences among local communities.

91 elative state, which is an index of relative competitive (dis)advantage.

92 tuting lethally irradiated mice and a strong competitive disadvantage when cotransplanted with wild-t

93 Competitive dynamics and the presence and abundance of m

94 ow and matrix organization interact to shape competitive dynamics in Pseudomonas aeruginosa biofilms.

95 e rigors of the reef, a crowded and fiercely competitive ecosystem.

96 The finding of only a slight competitive edge of ES over EG in population cages sugge

97 itively correlate with competing substances' competitive effect and negatively correlate with target-

98 agnitude of concentration thresholds and the competitive effect of stormwater DOM and possibly deioni

99 rtmannite and basaluminite and the potential competitive effect of sulfate.

100 ncentrations in the solutions did not show a competitive effect on arsenate sorption capacity but had

101 their long-term coexistence, by testing the competitive effects of populations of varying lengths of

102 After the UP, there were no competitive effects, only target-specific semantic effec

103 equilibrium effects, or (iii) non-negligible competitive effects.

104 tivity in comparison to the state-of-the-art competitive ELISA for their higher affinity towards targ

105 Most inhibitory interactions are competitive, emerge in the close neighbourhood of the in

106 H19 acting as a competitive endogenous RNA sequesters miRNA let-7 to rel

107 e most effective molecule identified by this competitive engraftment screening was cardiotrophin-1, a

108 We let human subjects interact in a competitive environment and find that, in the long run,

109 -type (Nrp1(+/+)) Tregs can be assessed in a competitive environment, we find that a high proportion

110 l be concentrated in particular climatic and competitive environments.

111 site faces of the ring scaffold, evidence of competitive epoxidation pathways, promoted by hydrogen-b

112 cal mechanism that reduces the potential for competitive exclusion more strongly in the tropics than

113 ogical approaches when testing prediction of competitive exclusion.

114 -based approach did not provide evidence for competitive exclusion; however, the morphometric analyse

115 Furthermore; the competitive experiments were carried out to test sensor'

116 INTERPRETATION: Competitive factors, in addition to policies advocating

117 nt against mutations affecting hermaphrodite competitive fitness agree to within two-fold, 0.33-0.5%.

118 AS locus are frequent in cancer and modulate competitive fitness and MEK dependency.

119 al variance (VM) for male mating success and competitive fitness are not significantly different from

120 is 0.17%/generation; that of hermaphrodite competitive fitness is 0.11%/generation.

121 The rate of mutational decay of male competitive fitness is 0.17%/generation; that of herma

122 rent from zero, whereas VM for hermaphrodite competitive fitness is similar to that of non-competitiv

123 BCR(-) lymphoma variants that restore competitive fitness normalize GSK3beta activity after co

124 ompetitive fitness is similar to that of non-competitive fitness.

125 In a competitive format, small-molecule target engagement wit

126 Tomato peels oleoresin, TPO, exhibited competitive free radicals scavenging activity with synth

127 added more advanced features and removed the competitive game elements.

128 eramics on the market lack the aesthetics of competitive glass-ceramics and are therefore somewhat re

129 ihydro-1H-pyrazole-3-carboxylic acid (ACEPC) competitive GluN2 antagonists, of which ST3 has a bindin

130 eactivity among the donors were evaluated in competitive glycosylation reactions, and their relative

131 antibodies, it outgrew wild-type controls in competitive growth experiments.

132 Competitive growth of the escape mutant viruses with the

133 to 82 nm) and stimuli-responsive behavior to competitive guest by binding with CB[8], the turn-on flu

134 We show that our item-based model, competitive guided search, accounts for the empirical pa

135 Competitive homo- and hetero-dimerization of their amino

136 AFM1 detection is carried out by means of a competitive immunoassay using secondary biotinylated ant

137 Results from 5 of 8 biotinylated (63%) competitive immunoassays tested falsely high and results

138 tion to the public cloud, while being highly competitive in accuracy and speed with non-private state

139 e inputs can make deep learning methods more competitive in accuracy, while illustrating their genera

140 In this study, using competitive in vitro and in vivo assays, we show that mo

141 Competitive incorporation into the hydrocarbon chain of

142 abeled nucleotide allows for the kinetics of competitive incorporation reactions by DNA polymerase to

143 Monod kinetics with competitive inhibition are used to describe biodegradati

144 s of root and shoot Se accumulation and less competitive inhibition by sulfate or by high-S pretreatm

145 Competitive inhibition experiments with other pneumococc

146 ction of 17beta-Estradiol (E2) following the competitive inhibition format.

147 that FHR-1 enhances complement activation by competitive inhibition of FH binding to some surfaces an

148 Competitive inhibition of HK2-mitochondrial binding in p

149 x (enzyme production) and K m (indicative of competitive inhibition).

150 rs in the presence of UVM-7-SH suggested non-competitive inhibition, which indicated that the materia

151 vitro in the presence and absence of a known competitive inhibitor (NaClO4).

152 ide derived from beta-neurexin is a powerful competitive inhibitor capable of efficiently blocking su

153 and pharmacological inhibition by the lipid-competitive inhibitor GW4869.

154 Binding studies disclosed that the competitive inhibitor isoeugenol is predominantly in its

155 migration through sequestration of Arpin, a competitive inhibitor of Arp2/3 complex.

156 substrate demonstrated that alpha-PanAm is a competitive inhibitor of Cab1.

157 s a potent and selective DAT inhibitor and a competitive inhibitor of cocaine binding to the DAT.

158 rious cellular stresses converts eIF2 into a competitive inhibitor of eIF2B, which triggers the integ

159 ggest that the C terminus of SPI-1 acts as a competitive inhibitor of target proteases as it remains

160 ehyde and yield tagatose 1,6-bisphosphate, a competitive inhibitor of the enzyme.

161 avathrin." Avathrin is a fast, tight binding competitive inhibitor with an affinity of 545 pM for thr

162 We identified (-)-fenchone as a competitive inhibitor with different potencies at the tw

163 ATP-competitive inhibitors against this complex have been re

164 etic compounds (CD4mc) bind gp120 and act as competitive inhibitors of gp120-CD4 engagement.

165 ion in a program to identify pan-isoform ATP-competitive inhibitors of PDHK.

166 hly selective non-metal chelating, substrate-competitive inhibitors of the JmjC KDMs.

167 n and therefore have the potential to act as competitive inhibitors of this interaction.

168 using more reactive dichlorocarbene, due to competitive insertion of the carbene into the N-N bond.

169 Competitive interactions between species can be mitigate

170 evolution of drug resistance by intensifying competitive interactions between susceptible and resista

171 Sensory deprivation shows competitive interactions between the ipsi/contralateral

172 y, this could be explained by changes in the competitive interactions between the resident species an

173 ans, chimpanzees are only able to do this in competitive interactions but this has rarely been direct

174 Competitive interactions can be modulated by resource av

175 esults suggest that foraging traits modulate competitive interactions that underlie community disasse

176 ctions among climate change, disturbance and competitive interactions to produce range shifts are poo

177 he resulting tension between cooperative and competitive interactions was found to generate a phenome

178 species survive, the nature and intensity of competitive interactions within the network also affect

179 During competitive interactions, humans have to estimate the im

180 During between-group competitive interactions, more cohesive groups (i.e. gro

181 ies are thought to be strongly structured by competitive interactions, with niche partitioning of foo

182 fic soils and had knock-on effects for plant competitive interactions.

183 Functional analyses demonstrate that these competitive intramolecular interactions negatively regul

184 wo key properties of the competitive network-competitive intransitivity and average competitive abili

185 ent with JNK-IN-8, an adenosine triphosphate-competitive irreversible pan-JNK inhibitor, significantl

186 compound was selected and further used in a competitive labelling/enrichment assay against the activ

187 ion of ligand strength and concentrations by Competitive Ligand Exchange Adsorptive Cathodic Strippin

188 obtain large datasets of both allosteric and competitive ligands.

189 Serum antibody responses were assessed by competitive Luminex immunoassay.

190 The development of a competitive magnesium battery is plagued by the existing

191 RIIA and ActRIIB ligand binding domains in a competitive manner at the critical myostatin/activin bin

192 classes locally direct dendrite growth in a competitive manner.

193 r oral tetracylines using the framework of a competitive market and evaluated the impact of these pri

194 19620 (9) (Schild-like analysis) suggested a competitive mechanism between the allosteric modulator a

195 e CNBD associated with cAMP regulation and a competitive mechanism in which TRIP8b and cAMP compete f

196 obenecid all inhibit verinurad binding via a competitive mechanism.

197 es the simulation of various co-operative or competitive mechanisms, where there is either a positive

198 transplantation longer even when listed at a competitive MELD score.

199 d of peptide detectability on which the most competitive methods rely.

200 on of resources through efficient and robust competitive methods.

201 lites with distinct roles in cooperative and competitive microbial interactions.

202 zymatic activity with a nM Kd; has a non-ATP competitive mode of action and a novel putative binding

203 ing the branch point adenosine, suggesting a competitive mode of action.

204 7 microM, and steady-state kinetics reveal a competitive mode of inhibition.

205 tro, yet it was attenuated 4- to 6-fold in a competitive murine infection model in vivo This study su

206 absorption could pave the way for novel and competitive nanoporous-graphene based plasmonic-sensors.

207 different origin populations into different competitive neighborhoods within and beyond their elevat

208 The structure of the competitive network is an important driver of biodiversi

209 Our research suggests that the competitive network may therefore act as a unifying link

210 he inclusion of higher-order interactions in competitive network models stabilizes dynamics, making s

211 These findings demonstrate that competitive network structure can be an important determ

212 As such, the competitive network structure may likewise play an impor

213 s possibility by quantifying the links among competitive network structure, species diversity, and co

214 ity interacts with two key properties of the competitive network-competitive intransitivity and avera

215 s of coexistence that emerge only in diverse competitive networks.

216 Thirty competitive OCT1 ligands, defined as ligands predicted i

217 screening of 29332 metabolites predicted 146 competitive OCT1 ligands, of which an endogenous neuroto

218 eased training volume and intensity and more competitive opportunities.

219 Middle-aged men engaged in competitive or recreational leisure sports underwent a n

220 Can we predict competitive outcomes using phenotypic traits?

221 history differences and asymmetric mating on competitive outcomes.

222 of genes regulating cell development (MAGMA competitive P = 3.5 x 10(-6)).

223 toxin microcystin LR and its selection using competitive panning and two novel panning strategies.

224 We have previously shown that MG is a competitive partial agonist at GABA-A receptors.

225 lenge arises from the existence of different competitive pathways.

226 Compared to organic HTL, a very competitive PCE of 18.51% with long-term stability is ac

227 al-copper-that offers simple fabrication and competitive performance in electrochemical detection.

228 attracting increasing attentions and showing competitive performance in energy storage devices includ

229 GMQ showed competitive performance on a benchmark for quality asses

230 r1-xNbO3, 0.03<x<0.20) were reported to show competitive photocatalytic efficiencies under visible li

231 inhibitors, and uncover inhibitor-dependent competitive PPIs.

232 of the method across datasets argues for its competitive predictive ability (AUC of 0.80+/-0.18, AUPR

233 PRSs from this pathway showed competitive predictive accuracy compared with the whole-

234 of S. horneri was suppressed, likely due to competitive pressure from native algae, resulting from p

235 population density nor is it result of lower competitive pressure.

236 variation may be a consequence of different competitive pressures.

237 that liberates acetophenone by at least two competitive processes, one of which involves a palladium

238 minerals through a series of cooperative or competitive processes: solution complexation, ternary su

239 ndirubins have been identified as potent ATP-competitive protein kinase inhibitors.

240 cated mechanism for optical anion sensing in competitive protic organic and aqueous-organic media.

241 s, the tragedy of the commons manifests as a competitive race to fish that compresses fishing seasons

242 , allowing C(1)-C(5) cyclization to become a competitive reaction channel.

243 otential to offer opportunities in designing competitive reactions especially for using a photophysic

244 acellular signaling pathway rather than as a competitive receptor antagonist.

245 ifferent ligands and can arise directly from competitive receptor-ligand interactions.

246 , these results uncover a mechanism by which competitive recruitment of DNA-binding nuclear receptors

247 The benefits of Share 35 in highly competitive regions may be underestimated when examining

248 ses also uncovered potential cooperative and competitive relationships, even among close relatives.

249 se corepressor complex, severely impairs the competitive repopulation capacity of HSCs.

250 nent of the hematopoietic niche by promoting competitive repopulation following lethal irradiation.

251 Moreover, it gave competitive results even when compared to batch producti

252 ng a Cox model; and tumor recurrence using 2 competitive risk models.

253 for the detection of miRNAs making use of a competitive RNA/RNA hybridization configuration is descr

254 taining a stable co-culture of metabolically competitive Salmonella typhimurium strains in microfluid

255 e high-affinity antibody responses depend on competitive selection of B cells carrying somatically mu

256 s accurate Type I error control and displays competitive sensitivity and improved robustness to batch

257 Competitive serial transplantation assays using Zfp521-d

258 9,511 unique ligands for the allosteric and competitive sets, respectively.

259 not sufficient to create a beauty premium in competitive settings.

260 2 inhibitor, selective S-adenosyl-methionine-competitive small-molecule (GSK126), or the DNA methylat

261 ed soil with and without passive dosing of a competitive sorbate.

262 electrostatic behavior of the interface and competitive sorption between protons and other cations f

263 iotic homogenization, the extinction of less-competitive species and the spread of invasive species.

264 resources and their consumption by the most competitive species that accumulated the bulk of biomass

265 than the kmacs heuristic algorithm at highly competitive speed.

266 ion in a sport; of these, 16 occurred during competitive sports and 58 occurred during noncompetitive

267 tolls due to shifts toward participation in competitive sports at earlier ages, increased training i

268 Exercise and competitive sports should be associated with a wide rang

269 udden cardiac arrest during participation in competitive sports was 0.76 cases per 100,000 athlete-ye

270 he incidence of sudden cardiac arrest during competitive sports was 0.76 cases per 100,000 athlete-ye

271 arrest that occurred during participation in competitive sports were determined to have been potentia

272 disease was uncommon during participation in competitive sports.

273 rved temperature dependence is attributed to competitive stabilization of a pre-reactive complex.

274 s-Alder process and provide no evidence of a competitive stepwise pathway.

275 ge with these acidophiles contributed to the competitive success of the Ca.

276 e factors were interdependently limiting for competitive success of VRC01-class B cells.

277 chanism of inhibition from noncompetitive to competitive, such that the antagonist could be outcompet

278 d cells, and signaling through Nod1 promotes competitive survival of mature B cells.

279 The working principle is based on a competitive switch between electron supply from the elec

280 to switch between multiple capsules was more competitive than those expressing any single capsule exc

281 ults suggest that although PCNA is much more competitive than XPA in binding replication forks, PCNA

282 ons between adults and juveniles switch from competitive to facilitative at upper range limits.

283 MultiFLEXX is competitive to standard triple-axis spectroscopy in term

284 y and exhibited heightened reconstitution in competitive transfer assays.

285 stem/progenitor cells exhibited a long-term competitive transplantation advantage.

286 We conclude that competitive tuning could be an important dynamic process

287 otocin by D-Arg8 led to a potent, stable and competitive V1aR-antagonist ([D-Arg8]-inotocin) with a 3

288 he inorganic subunits properties in the very competitive water environment.

289 erization shows that the best inhibitors are competitive with acetyl coenzyme A and an X-ray cocrysta

290 semiconductors and, in terms of quality, is competitive with atomically thin dichalcogenides and bla

291 le linear classification rules, and are even competitive with belief propagation.

292 gh binding the MTD in an interaction that is competitive with binding to the LRS.

293 onal groups and conditions, making it highly competitive with classical reagents, such as periodic ac

294 This makes chlorination effectively competitive with hydroxylation.

295 r growing almonds with chemical compositions competitive with standard cultivars.

296 nd abnormal phenotypes with results that are competitive with state-of-the-art algorithms and with a

297 ed that the performance of PhosphoPredict is competitive with that of several other popular predictio

298 They are competitive with the best electrocatalysts for this reac

299 educed their radiative lifetimes making them competitive with the best reported Ir complexes.

300 e first time by use of this catalyst, and is competitive with the most effective transition-metal cat