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1 deletion or ssDNA-binding mutant, suggesting competition for a common binding site.
2 pH 8 than at pH 4, consistent with substrate competition for a common ion-binding site.
3           The data strongly suggest there is competition for a common pool of Und-P, whose proper dis
4 due to climate change will increase top-down competition for a dwindling biomass of prey, potentially
5      It has recently been suggested that the competition for a finite pool of microRNAs (miRNA) gives
6  suggest a CP-independent mechanism based on competition for a host-limiting factor, which operates a
7                      This balance depends on competition for a limited amount of homeostatic cytokine
8  receptor (TCR) ligands and is controlled by competition for a limited developmental niche, but the t
9 etworks are usually investigated separately, competition for a limited pool of actin monomers (G-acti
10  the quantity and size of organelles through competition for a limited supply of components is quickl
11 nism controlling virulence thresholds may be competition for a viral receptor.
12 ught to have arisen due to intense male-male competition for access to females.
13 s suggest that the optimal trade may reflect competition for access to mutualistic partners among pla
14              These observations predict that competition for access to Myo2 may be a common mechanism
15 n benefits acquired versus given and between competition for access to partners (competitive ability)
16 efit from being seen as generous if there is competition for access to partners and if generosity is
17 F-actin networks are in homeostasis, whereby competition for actin monomers (G-actin) is critical for
18 these results are consistent with a model of competition for activating and inactivating cleavages ca
19 cal model of GlnB and GlnK that incorporates competition for active and allosteric sites, as well as
20                     Anticorrelation suggests competition for active Cdc42 or for its effectors.
21                      These dynamics indicate competition for active Cdc42 or its regulators and the p
22  times faster, respectively, suggesting that competition for active sites on the electrode surface is
23     The theory further includes metal-proton competition for adsorption at cell-surface binding sites
24 II) sorption between the two solids types or competition for adsorption sites in the presence of sili
25 plasmic reticulum-associated degradation nor competition for Ag between class I and class II molecule
26 reasing rural resource scarcity, principally competition for agricultural land.
27                    In a second approach, the competition for aptamer binding takes place off-strip, a
28  Fc-d E1E2-immunized mice exhibited stronger competition for AR3B and AR5A than the WT, whereas the l
29 sions interfered with the task, indicating a competition for attentional resources between the task a
30 al) targets in the visual scene will win the competition for attentional resources.
31                                              Competition for available axon space by myelinating olig
32 esence of the coffee matrix, possibly due to competition for available carbon sources.
33  X are activated coincident with each other, competition for available membrane binding sites masks t
34 p mathematical models to investigate whether competition for benefits alone can allow the persistence
35                                 We find that competition for benefits alone is sufficient to promote
36                      The key finding is that competition for benefits provides a biologically-realist
37 een miRNAs and lncRNAs and that this creates competition for binding between the miRNA, a lncRNA and
38 lity; removal of the polyubiquitin chains or competition for binding by addition of free polyubiquiti
39                                              Competition for binding DNA between SsoDnaG and SsoMCM c
40 raction network, suggesting the existence of competition for binding sites or partners by genes of di
41 eric state of the transposase, mediated by a competition for binding sites.
42 y due to crowding on the vesicle surface and competition for binding sites.
43                               Unidirectional competition for binding to E2 was observed between HC33
44 ive of (R)-PFI-2 demonstrated dose-dependent competition for binding to endogenous SETD7 in MCF7 cell
45 m responsible for this phenotype relies upon competition for binding to HA on the surface of infected
46 nd that an incoherent feedforward loop, from competition for binding to kappaB motifs, could provide
47  wild-type PAX5, resulting in DN activity by competition for binding to PAX5-target sites.
48 ylation/deacetylation, respectively, through competition for binding to Sp1, and suggest that p300 mo
49  G-proteins and beta-arrestins are in steric competition for binding to the cytoplasmic surface of ei
50 ion of (unlabeled) RRM2, no doubt reflecting competition for binding to the i-motif DNA.
51 solution, indicating that there is metal-ion competition for binding to the plant roots.
52 ian period are proposed to rely primarily on competition for binding with coactivators on an alpha-he
53 e shipping sector, due to limited supply and competition for bioenergy from other energy sectors.
54  had the strongest effect on the strength of competition for both species, and few observed compariso
55 ppocampal CaM binding proteins, we find that competition for CaM binding serves as a tuning mechanism
56         In contrast, DIPs that interfere via competition for capsids have the potential to be evoluti
57                               This may limit competition for cellular and viral helper factors and, h
58           This situation inevitably leads to competition for cellular resources.
59 irschman Index, a standard measure of market competition for centers within the OPO donor service are
60 otons; together, these two factors eliminate competition for charge and space during ion formation.
61  affected the TC electrooxidation because of competition for CNT sorption and electrooxidation sites.
62 sticity of axonal arbors combined with their competition for collicular resources can deeply remodel
63          Our data provide evidence of active competition for colonization niches in the C. elegans gu
64                  Staphylococcus aureus is in competition for colonization with the normal respiratory
65  better adapted to their environment win the competition for common resources from less well-adapted
66 n" a swarm of individual small tasks tempers competition for CPU time in the shared HPC environment,
67 gamma on the Abca1 promoter, suggesting that competition for CREB-binding protein may contribute to S
68                              This suggests a competition for CRIP1a and beta-arrestin binding to the
69 t prevent VWF D4-CK binding, suggesting that competition for CUB-domain binding to the spacer domain
70 rations were described in a PK/PD model, and competition for d-serine sites on NMDA receptors was dem
71        This study provides clear evidence of competition for different arginine methylation types on
72 nds not only on DO concentration but also on competition for dissolved gas.
73                 Here, we show that a dynamic competition for DNA binding between nucleosome-forming h
74                 Factors leading to increased competition for donor allografts are associated with poo
75             Such sequestration combined with competition for each phosphosite provides an intuitive e
76  and VC), their survival requires successful competition for electron donor within the entire organoh
77                                              Competition for electrons among different steps of denit
78 nditions typical of islands, such as reduced competition for embedded prey and low predation risk.
79  the capacity of the BM LLPC compartment and competition for entry to it.
80  H2Bub1 levels and SAGA DUB activity through competition for ENY2 binding.
81  to determine cross-reactivity, avidity, and competition for epitope binding; Western blot analysis w
82            The nanopolymer allows for direct competition for epitopes on proteins of interest, thus f
83                           Here we argue that competition, for example between heterotrophic and ferme
84 excess interneurons are eliminated through a competition for extrinsically derived trophic signals.
85                                              Competition for FABPs may in part or wholly explain the
86 rachiopods have overlapping niches such that competition for food and space may occur.
87  from individuals of the same species due to competition for food and space) and increases population
88  Adelie penguin populations, suggesting that competition for food may exacerbate the Adelie penguin d
89          Climate-driven sympatry may lead to competition for food resources between species.
90                                              Competition for food resources is a strong ecological fo
91 o; bats selected for more dilute nectar when competition for food was higher.
92                          Aggression mediates competition for food, mating partners, and habitats and,
93                          To avoid the fierce competition for food, South African ball-rolling dung be
94 ting bats adaptively jam conspecifics during competitions for food.
95 re a limited number of academic jobs and the competition for funding and space in competitive journal
96 tin concentration in a cell is critical, and competition for G-actin helps regulate the proper amount
97  charr ecomorphs, suggests the importance of competition for generating and maintaining polymorphism,
98 n is neither cell-autonomous nor mediated by competition for generic trophic factors, but regulated b
99  resulting in somatic chimeras and stem cell competitions for gonadal niches.
100 nitiate strong SO(4)(2-) reduction only when competition for H(2) inside the biofilm was relieved by
101        Long-term exposure to sulfides and/or competition for H(2) may have been responsible for the c
102   To explore the reductant flux and possible competition for H(2) production in vivo, T. kodakarensis
103 affect nitrate and perchlorate removals: (1) competition for H(2), (2) promotion of PRB growth due to
104 us use of nitrate and perchlorate by PRB and competition for H(2), the same resources in PRB, and spa
105                                  The kinetic competition for H2O2 within bacteria is complex, which s
106  and AR5A than the WT, whereas the levels of competition for HC84.26 and AR4A were similar.
107            We predicted that by intensifying competition for help, our manipulation would force domin
108 y, such as seasonal declines in fecundity or competition for high-quality mates.
109 olutionary response to greater intraspecific competition for higher quality food.
110                              Consistent with competition for histidine, high extracellular concentrat
111 sion and contraction and are associated with competition for homeostatic cytokines.
112                       Many models describing competition for hosts between non-interacting pathogen s
113                           Existing theory on competition for hosts between pathogen strains has propo
114 nge of BMP signaling in an in vitro assay by competition for HSPG-binding.
115 salts further enhance this enrichment due to competition for hydration in the bulk.
116 ralizing properties are the result of direct competition for IFN-alpha2A binding to the IFN receptor
117 ously encountered pathogens as the result of competition for IL-15.
118 with NK cells inhibit their proliferation by competition for IL-2 but not for IL-15.
119 reg modulation of differentiation occurs via competition for IL-2 during the late expansion period, a
120 ularly concerning during times of increasing competition for increasingly limited funds.
121 accounts for clone diversity as arising from competition for interleukins.
122                 Instead, it is determined by competition for interleukins.
123 r VTE biosynthesis and overcoming endogenous competition for intermediates.
124  classical experiment as being the result of competition for intrathymic niches specifically supporti
125 it, so that the significance of interference competition for invasion ecology remains uncertain.
126 ry are complicated by high sample diversity, competition for ionization among peptides, and mass redu
127                                              Competition for iron influences host-pathogen interactio
128                                              Competition for iron is a critical component of successf
129      Collectively these results suggest that competition for iron via siderophore piracy and species-
130             However, in regions with intense competition for iron, some microbes optimize iron acquis
131  of MDM2 modulates interactions with p53 via competition for its binding cleft, exchanging slowly bet
132 recent theory, which suggests that increased competition for krill is one of the major drivers of Ade
133 ginases were expressed by stimulated Ms, but competition for L-Arg with NOS2 was excluded.
134 olving at least several mechanisms: there is competition for ligands or for the formation of heterodi
135 ng increased fine root biomass and increased competition for light driving increased allocation to wo
136 ight is abundant are especially sensitive to competition for light from neighboring vegetation.
137                                              Competition for light has profound effects on plant perf
138 cies-interaction that may be affected is the competition for light in deciduous forests, where early
139  formed in exclosures, and may indicate that competition for light led to the decrease in H. uninervi
140                                              Competition for light triggers numerous developmental ad
141 s common to all vegetation-height-structured competition for light under a prevailing disturbance reg
142 -vascular land plants not only faced intense competition for light, as vascular land floras grew tall
143 evolution: although often thought to reflect competition for light, light limitation is unlikely for
144 rives plant species loss through intensified competition for light, whereas herbivores prevent compet
145 d defensive weapon used against neighbors in competition for light.
146 ciated only with photosynthetic capacity and competition for light.
147       During early development, the level of competition for limited (maternally provided) resources
148 y that family dynamics, specifically sibling competition for limited household resources (e.g. food,
149                      Moreover, together with competition for limited niche access, such models may pr
150 several mechanisms including direct killing, competition for limited nutrients, and enhancement of im
151 that relatives should help each other, while competition for limited resources may select for harming
152             Theoretical studies predict that competition for limited resources reduces biodiversity t
153 ed site creates an environment that leads to competition for limited resources within the synovium, r
154 in the animal kingdom that is used to settle competition for limited resources.
155 ess of morphological divergence that reduces competition for limited resources.
156        It has been shown experimentally that competition for limited translational resources by upstr
157                These results explain how the competition for limiting DDK kinase and CDK targets at o
158 nfluences their rate, perhaps as a result of competition for limiting factors.
159 es in biophysical processes to intraspecific competition for limiting resources manifested at the pop
160 -native plants should often benefit from low competition for limiting resources that define niches.
161 nizes BMP signaling in HFSCs but not through competition for limiting Smad4-coactivator.
162 vation interfere with one another because of competition for lipid rafts, revealing how frequent memb
163 , our data show that deposits are due to CFH competition for lipoprotein binding sites in Bruch's mem
164                    In open ocean ecosystems, competition for low availability of essential nutrients
165 d highlights the importance of SAP and SHP-1 competition for Ly108 ITSM binding as a rheostat for the
166 eas that already had a PCI program with more competition for market share, near populations with high
167 iased, the more numerous sex faces increased competition for mates and is more likely to yield to the
168                              Adult male-male competition for mates in this species is supported by en
169 s is unlikely to be due to greater male-male competition for mates on islands.
170 ntional sex roles (female care and male-male competition for mates) to be reversed (male care and fem
171                Sexual selection is driven by competition for mates, and the advantage of a competitor
172 g the surge of novel TOAMs to increase price competition for Medicare beneficiaries.
173 ese findings are consistent with there being competition for metabolically available hepatocyte selen
174                  These results indicate that competition for miRNAs may indeed provide an elementary
175 erent species attack the same host, there is competition for monopolization of host resources.
176                              Although strong competition for N between the plant and soil microbes wa
177 cements by decreasing SIRT1 activity through competition for NAD supplies.
178 tion-induced forgetting effect" is caused by competition for neural resources between the processes o
179            These results are consistent with competition for niche space limiting species accumulatio
180                               Interestingly, competition for nitrate did not lead to exclusion of one
181 rogen ratios among macroalgae suggested that competition for nitrogen also shaped interactions among
182 fine root allocation strategies for trees in competition for nitrogen and light as a function of CO2
183           These findings support mycorrhizal competition for nitrogen as an independent driver of soi
184 at soil carbon respiration may be reduced by competition for nitrogen between symbiotic ectomycorrhiz
185 rediction is a consequence of both increased competition for nitrogen driving increased fine root bio
186 study, we apply our theoretical framework to competition for nutrients among differently sized phytop
187                              Cooperation and competition for nutrients among its constituents only pa
188 exist because dispersal reduces interference competition for nutrients among kin, at the cost of a sl
189 lements of interspecific antagonism, such as competition for nutrients and its ability to cause a los
190 th cholesterol-lipid concentrate, suggesting competition for nutrients as one of the possible mechani
191 m virulence, providing new insights into the competition for nutrients at the host-pathogen interface
192 bal scales, suggesting that plant-decomposer competition for nutrients exerts a fundamental control o
193                                              Competition for nutrients is a key factor controlling pa
194 trol plots, AM roots may intensify microbial competition for nutrients.
195  impede soil C losses by enhancing microbial competition for nutrients.
196 er, iron lies at the center of host-pathogen competition for nutritional resources and recent trials
197 llations were found to result from a kinetic competition for O2 between Hmp and respiratory cytochrom
198  posits that the trade-off arises because of competition for one or more limiting resources, and we h
199 thin the same animal, these data reveal that competition for, or availability of, Ag at the level of
200 ication, involving acetate cross-feeding and competition for organic carbon and oxygen.
201                    This allowance may create competition for organs between stable LVAD-supported reg
202                       Although not excluding competition for peptide/MHC complexes as an explanation,
203                          In the latter case, competition for pollinator services and costs of hybridi
204 hosphorylation through a mechanism involving competition for PP1 molecules within the same macromolec
205 AD) falls, at least in part due to metabolic competition for precursors.
206 ifferent labs and in the first international competition for predicting peptide:MHC-I binding, their
207 gers, forming colonies can lead to extensive competition for prey around breeding areas and a zone of
208 ense breeding aggregations result in intense competition for prey in surrounding waters, whereas non-
209 urces in the soil, besides increasing fungal competition for progressively limited resources.
210    Many viruses degrade host mRNAs to reduce competition for proteins/ribosomes and promote viral gen
211                                              Competition for PRPF8 availability alters the transcript
212 on with time of illumination might be due to competition for reduced ferredoxins between ferredoxin-N
213 rmation for detailed processing by resolving competition for representation among stimuli in retinoto
214 the lack of practical discoveries, increased competition for research funds, uncertainties on the rep
215                 Root system interactions and competition for resources are active areas of research t
216      Density-dependent mass change suggested competition for resources in both winter and summer but
217 populations, while others predict that local competition for resources inhibits cooperation.
218 to impose selection to increase WUE, whereas competition for resources may select for decreased WUE t
219 erspective of classical population dynamics, competition for resources seems to be at odds with the o
220 ly set by niche filling (that is, ecological competition for resources), rather than by the rate of a
221 en post-reproductive demise, thus decreasing competition for resources, they are also likely to harm
222 nd the costs of defence may be higher due to competition for resources.
223 ent has an equally important role because of competition for resources.
224 enol metabolites did not exhibit significant competition for resveratrol and thyroxine preferential b
225                  Our main findings are that: competition for ribosomes, rather than tRNAs, limits glo
226  model that aims to understand how small RNA competition for RISC-formation affects target gene repre
227                                     However, competition for scarce Mg(2+) and topological constraint
228 tion and suggests that the production of and competition for secondary fermentation byproducts, such
229 tosynthesis were not affected by nitrogen or competition for seedlings in full sunlight, but they res
230 iRNA-mediated gene repression; and (iii) the competition for shared miRNAs leading to the cross-regul
231 s can drive protocell membrane growth during competition for single-chain lipids.
232 eochemical models that simulate simultaneous competition for soil N substrates by multiple processes
233 e this, we made direct measurements of plant competition for soil nitrogen (N).
234 sion experiments, and this likely occurs via competition for soil nitrogen, an effect larger than 2 d
235 ric allocation patterns affected the plants' competition for soil nutrient supply.
236  and partial support for Grime's theory that competition for soil nutrients is greater under potentia
237 e found no evidence for Tilman's theory that competition for soil nutrients is stronger at low, compa
238 new mechanistic model that accounts for both competition for soil water in the shallow soil and fire-
239 ences in the sorption kinetics and degree of competition for sorption sites between the contaminants
240                                 In addition, competition for sorption sites was never observed in mul
241 prevent colonization with MDROs through both competition for space and resources and the complex immu
242                        In areas with intense competition for space and resources, evaluation of the e
243 predators and is likely to result in greater competition for space between faster-growing palatable s
244 we show a clear latitudinal trend in contest competition for space in nearshore marine environments,
245 rons and possibly reductase enzymes, and (4) competition for space in the biofilm.
246                  Further, there is no direct competition for space or antigenic stimulation in the mo
247 tree allometries, random placement of trees, competition for space, and mortality.
248 d spatial proximity influence the outcome of competition for space, and provide a general framework f
249 s in constrained environments and requires a competition for space.
250                                              Competition for substrates is a ubiquitous selection pre
251                                          The competition for sugar acquisition at the plant-pathogen
252        However, TCR gene transfer results in competition for surface expression and inappropriate pai
253 onomously or through a population-autonomous competition for survival signals derived from other inte
254 a critical mechanism governing developmental competition for survival.
255 versity based on a network representation of competition for systems with large numbers of competitor
256 ing the possibility that Ag presentation and competition for T cell help, rather than Ag-dependent si
257  rates of reactivity with enzymes, such that competition for target engagement with reversible inhibi
258 tional evidence demonstrating that interaxon competition for target space is necessary to establish t
259 from the two eyes undergo activity-dependent competition for territory in the dorsal lateral genicula
260 n platelet-rich hemophilia A plasma revealed competition for TF, which potentially could reduce the e
261 d seed tannin extraction and that there is a competition for the adsorption sites between anthocyanin
262 uccess is pollinator limited, due to intense competition for the attention of a specialized pollinato
263 they fail to fuse normally, leading to their competition for the autophagy machinery with damaged pat
264 thought to be largely shaped by interspecies competition for the available resources, but cooperative
265                              Cooperation and competition for the benefits of multicellularity promote
266                  Empirical data suggest that competition for the benefits provided by mutualistic par
267                  Our data reveal a three-way competition for the CaM-binding element, whereby phospho
268  regulated pertinent endothelial targets via competition for the coactivator p300.
269 nfirm that, as a consequence of inter-colony competition for the diffusing nutrients and of cell deat
270 ractions need to be considered beyond simple competition for the drug transporter itself and may expl
271 enced dynamics in systems with interspecific competition for the entire duration of the experiment wh
272 dentify candidates that increase or decrease competition for the FSC niche.
273 nd neuroendocrine clones suggests a possible competition for the ligand Stem cell factor and offers t
274 nts revealed an existence of Rho-NusA direct competition for the overlappingnut(NusA-binding site) an
275 ynthase are spatially separated to eliminate competition for the proton motive force.
276 d mechanisms across the primates to mitigate competition for the sake of cooperation.
277 iferatoxin-induced activation likely through competition for the same binding sites.
278 e protective effect of IgG responses through competition for the same Env binding sites.
279 containing populations shifted toward direct competition for the same limiting catabolic electron don
280 cribed regulating homeostasis, which involve competition for the same niche by cells having overlappi
281 between OT-I and F5 T cells, consistent with competition for the same resource(s) required for homeos
282  may experience a rarity disadvantage due to competition for the services of pollinators.
283 idence that splicing improves due to reduced competition for the splicing machinery.
284 licle stem cells (FSCs) that undergo neutral competition for the stem cell niche.
285                            The efficiency of competition for the stop codon between release factors (
286       Fitness-related costs (or benefits) of competition for the winning parasitoid reveal that time
287 /S18-2, to study mechanisms of the predicted competition for their incorporation into ribosomes.
288 affect each other's expression level through competition for their microRNA (miRNA) coregulators.
289 r high-value fed aquaculture products grows, competition for these crops will also rise, as will the
290 f the regulation is a result of the inherent competition for this docking site.
291                             It predicts that competition for trading partners will affect the value o
292 elated to nonoperon genes, consistent with a competition for transcriptional resources.
293 t the first evidence, to our knowledge, that competition for trophic resources and phylogeny are pivo
294 r increased transpiration because of reduced competition for water and increased light availability,
295 ere we focus on the role of individual-level competition for water and light in forest carbon allocat
296 riments can be explained by individual-based competition for water and light within a continuously va
297 cations of carbon storage when it alleviates competition for water by incentivizing competitive plant
298 dry out as a result of rapid evaporation and competition for water increases between coexisting tree
299 ylation and the differential effects of this competition for wild-type CFTR and the major F508del mut
300 t and nonoverlapping, suggesting that direct competition for xol-1 binding is not how XSEs counter AS

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