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1 axis, consistent with observations of "lumpy coexistence".
2 e tropics affect processes mediating species coexistence.
3 nvironmental filtering would mediate species coexistence.
4  competitive interactions to promote spatial coexistence.
5 rformance, which may help facilitate spatial coexistence.
6 orhombic-hexagonal (o-h) morphotrophic phase coexistence.
7 rol's ability to support liquid-liquid phase coexistence.
8 ocal and regional patterns and mechanisms of coexistence.
9  membrane do not require liquid-liquid phase coexistence.
10 stochasticity, and this further destabilises coexistence.
11 gion of liquid-ordered and liquid-disordered coexistence.
12 o single best competitor, may ensure species coexistence.
13  its design and selection to avoid polymorph coexistence.
14 p-down forcing reduces competition, allowing coexistence.
15 environmental variability to promote species coexistence.
16 stem, which oppose the hypothesis of neutral coexistence.
17 fluences C. albicans biofilm development and coexistence.
18  microbiota impact plant fitness and species coexistence.
19 teractions into our understanding of species coexistence.
20 , thus limiting our ability to link NDisD to coexistence.
21 e range of conditions necessary for feasible coexistence.
22 hich can then be tuned to achieve multiphase coexistence.
23 ree pathways by which this variation affects coexistence: (1) changes in competitive dynamics because
24  association between energy availability and coexistence across an entire vertebrate class (Aves).
25 tion and promotes sustainable human-wildlife coexistence across large multiple-use landscapes.
26 indings provide an explanation for bacterial coexistence alongside an activate neutrophil infiltrate.
27 in terms of energetic constraints, such that coexistence among competing species is limited in low pr
28                We show that the incidence of coexistence among sister species increases with overall
29 ent shade tolerances and the second axis for coexistence among species with the same shade tolerance.
30 elowground strategies in relation to species coexistence and abundance, we assessed four key belowgro
31 d niche differentiation to influence species coexistence and community structure.
32                                          The coexistence and competition between superconductivity an
33                               Explaining the coexistence and distribution of species in time and spac
34  of nonuniform intraspecific competitions on coexistence and find that a wider spectrum of coexistenc
35 g how environmental fluctuations can promote coexistence and maintain biodiversity.
36 n breast cancer, yet an understanding of the coexistence and regulation of various tumor cell subpopu
37 ts and their variation mediate plant species coexistence and spatial distribution.
38 roviding a new microscopic mechanism for the coexistence and strong coupling between ferroelectricity
39 s an important role in species adaptation to coexistence and that niche segregation takes place at th
40 ulting from hydraulic lift affect tree-grass coexistence and the range of environmental conditions in
41 t exhibit phase competition, order parameter coexistence, and emergent order parameter topologies con
42  phase during immiscible liquid-liquid phase coexistence, and the contrast persisted through the crit
43 ms, their impact on species interactions and coexistence are largely ignored in traditional coexisten
44 an important role, as long-term quasi-stable coexistence arises spontaneously in most populations, an
45 work, we propose a mechanism for maintaining coexistence at the resistance locus: linkage to a second
46 r; and, character displacement enables their coexistence at two sites in which the species are known
47 ations can also lead to an undesirable phase coexistence between crystal polymorphs.
48 f fitness in microbial communities, allowing coexistence between function-performing helpers and func
49                      The results demonstrate coexistence between lo and liquid-disordered (ld) phases
50 adox of enrichment': as light increases, the coexistence between the acquired phototroph and its prey
51 We show that acquired phototrophy stabilises coexistence, but that the nature of this coexistence exh
52 ps can both stabilise or destabilise species coexistence, but the strength and importance of intransi
53        Here we shed light on this surprising coexistence by systematically investigating the impact o
54 or, Pilea pumila, may affect their long-term coexistence, by testing the competitive effects of popul
55                               Alternatively, coexistence can be maintained by specialization to explo
56       We also show how fluctuation-dependent coexistence can buffer ecosystem functioning against inc
57                            Understanding the coexistence, competition and/or cooperation between supe
58 mpirical networks, we show that the range of coexistence conditions in mutualistic systems can be ana
59 uid organelles formed by intracellular phase coexistence could provide an additional means of sequent
60            We have previously shown that the coexistence curve of an antibody solution can be readily
61 rystal solubility line and the liquid-liquid coexistence curve, of IgG antibodies.
62 ronments such as those encountered along the coexistence curve.
63  measure the molecular interactions and full coexistence curves (binodals), which quantify the protei
64                        It than predicts full coexistence curves, osmotic compressibilities, and secon
65 tibodies with respect to their liquid-liquid coexistence curves.
66                                While species coexistence depends on both local and regional mechanism
67  relating to a proposed state of three-phase coexistence, due to the difficulty in clearly distinguis
68 ses coexistence, but that the nature of this coexistence exhibits a 'paradox of enrichment': as light
69 develop a model to study spatial patterns of coexistence, focusing on predator-prey and host-parasite
70            The isotropic and nematic (I + N) coexistence for rod-like colloids is a signature of the
71            Herein, we demonstrate the stable coexistence, from 180 K to 800 K, of the unexpected soli
72       Niche partitioning facilitates species coexistence in a world of limited resources, thereby enr
73 ites and illustrates the role of mixed-phase coexistence in achieving large changes in physical prope
74 te that energy availability promotes species coexistence in closely related lineages, providing a key
75 hesis need to be refined to account for this coexistence in drylands.
76 tively control the DWs associated with AF/FM coexistence in FeRh thin films we must fully understand
77 ssessing the ecological mechanisms promoting coexistence in hyperdiverse rainforests remains a consid
78 misleading conclusions about competition and coexistence in LMH assemblages, and that LMH diversity m
79 there is no explicit demonstration of such a coexistence in mathematical and simulation studies.
80 ronmental conditions compatible with species coexistence in mutualistic systems, also known as struct
81 k is an important driver of biodiversity and coexistence in natural communities.
82 owledge needed to judge their importance for coexistence in nature.
83  temperature for diversification and species coexistence in plant and animal communities.
84 ydraulic lift in the stability of tree-grass coexistence in savannas.
85                                          The coexistence in some patients of cancer cells and T cells
86 after human arrival, with shorter periods of coexistence in some regions.
87 cial debonding, which is compatible with the coexistence in the composite of both, strong and weak ce
88                    Percolation of such phase coexistence in the vicinity of MIT leads to first-order
89 e change, could increase the opportunity for coexistence in this community.
90 ow rocky soils and trees, as well as species coexistence in this mixed forest, where oak facilitates
91 quences of intraspecific trait variation for coexistence in two- and multispecies competitive communi
92 coexistence of predator and virus, and where coexistence, in return, lowered intraspecific diversity
93 ible consequences of long-term BQ-stabilized coexistence, including sympatric speciation and the evol
94          Therefore, employing RSFs and their coexistence is a promising route in defect engineering o
95 ts to population health, and their potential coexistence is an alarming prospect.
96           For two species, the likelihood of coexistence is in general reduced by intraspecific varia
97 e partitioning and the mechanisms of species coexistence is largely restricted to modern time-scales
98   Mathematical modeling predicts that stable coexistence is only possible when antibiotic resistance
99 mic model for A. bipunctata and H. axyridis, coexistence is predicted between the native and invasive
100 the niche differences that stabilize species coexistence is rare.
101               One mechanism that may explain coexistence is the degree to which a species tolerates h
102 mated to apply to phospholipids, equilibrium coexistence is typically registered, but metastable anti
103 ase transitions of POPE brings a three-phase coexistence line when the two transitions overlap.
104                    Existing theories explain coexistence mainly as an effect of competitive relations
105 Failure to account for fluctuation-dependent coexistence may explain deviations from the expected neg
106         Eco-evolutionary analyses of classic coexistence mechanisms are yielding new insights into th
107 e, as this is the defining feature of stable coexistence mechanisms.
108      First, it is possible to engineer phase coexistence mediated by a first-order phase transition b
109             We examine fluctuation-dependent coexistence models, identifying communities that are bot
110 el niche differentiation, both of which make coexistence more difficult.
111 ies have been carried out to investigate the coexistence of a few competitive species and in most cas
112 ehavior can be tuned from a mixed state to a coexistence of a liquid-crystalline and a gel, or a liqu
113                                          The coexistence of abnormal GLS/abnormal LAVi was associated
114 l implications, as we conclude patients with coexistence of adverse lesions and hyperdiploidy should
115                                          The coexistence of all these interests and their cross-ferti
116                                    Increased coexistence of Alzheimer disease (AD) and type 2 diabete
117 thy multiple myeloma is characterised by the coexistence of an active multiple myeloma clone and a be
118 ed spectral variation is consistent with the coexistence of an electronic supermodulation with struct
119 e evolutionary processes allowing the robust coexistence of antibiotic sensitive and resistant strain
120 Srn+1TinO3n+1 thin films, we demonstrate the coexistence of antiferroelectric, ferroelectric and new
121 particularly pronounced when considering the coexistence of asthmalike and oculonasal symptoms.
122 he age of onset and initial treatment of AF, coexistence of atrial tachyarrhythmia and (2) progressio
123 ed at the austenite/martensite interface via coexistence of B19 and 9R martensites.
124 y of preferential allocation likely leads to coexistence of beneficial and nonbeneficial symbionts.
125           This result is consistent with the coexistence of both "irreversible" and reversible transi
126 ility and, confirming our hypothesis, robust coexistence of both bacterial species.
127 re structure, with some samples exhibiting a coexistence of both cluster structures.
128                                          The coexistence of both conditions results in a higher risk
129 D overlap syndrome (ACOS) was defined as the coexistence of both COPD and current asthma.
130 investigations in acetonitrile indicated the coexistence of both helix types.
131                             Furthermore, the coexistence of both LGI1 and CASPR2 antibodies in an ind
132 easurements are used to show that there is a coexistence of both tetragonal and orthorhombic phases t
133                                  The unusual coexistence of bound and continuum excitations observed
134 thrombogenic atrial substrate and the common coexistence of cardiac and extracardiac stroke risk fact
135 is-by-behavior interactions), supporting the coexistence of categorical mechanisms of ASD.
136 planation for the role of disturbance in the coexistence of climax and colonist species.
137       This revealed the frequent within-host coexistence of clonally descended cells that differed in
138                   Chimera states, namely the coexistence of coherent and incoherent behavior, were pr
139                                          The coexistence of coherent and incoherent singlet fission m
140 , we found that spatial separations make the coexistence of competing species more likely.
141                                  We observed coexistence of conventional fractional quantum Hall effe
142 ther, other factors such as imitation or the coexistence of coordinating and anticoordinating agents
143  Under DME reaction conditions at 1 bar, the coexistence of Cu(0) in the active catalyst core togethe
144                              XANES indicated coexistence of Cu(I) and Cu(II) in control and Cu-expose
145                                          The coexistence of dANM and normal migration was characteriz
146                Recent studies have suggested coexistence of different cancer stem cell populations wi
147 creasing pressure towards globalisation, the coexistence of different cultures is a distinctive featu
148 MS) can often be interpreted in terms of the coexistence of different isomeric species.
149 t population dynamics generally leads to the coexistence of different metabolic types.
150 d predators can either promote or reduce the coexistence of different plant functional groups in trop
151                    The first axis allows for coexistence of different shade tolerances and the second
152 rane water transport can be modulated by the coexistence of different tetrameric species and by intra
153                                          The coexistence of different yeasts in a single vineyard rai
154                             Here we show the coexistence of distinct breast cancer stem-like cells (B
155 mate fluctuations are able to (i) induce the coexistence of dynamic behaviors that would be incompati
156                                          The coexistence of dysplastic nevus syndrome and a BAP1 germ
157 or on the Arabian Peninsula and to the brief coexistence of early-domesticated and wild individuals.
158       Theoretical studies have revealed that coexistence of even three or four species can be extreme
159                                          The coexistence of Fe(III) (hydr)oxide, characteristic 15N a
160 ography (FA) may be challenging owing to the coexistence of features related to the primary diagnosis
161 tion spectroscopy analysis indicate that the coexistence of ferromagnetic regions, superparamagnetic
162 ulator transition (MIT) that may result from coexistence of ferromagnetic, metallic and insulating ph
163 ion mobility peak widths associated with the coexistence of fewer conformations and possible conforma
164 growth favour a facultative strategy and the coexistence of fixers and non-fixers.
165                             In the region of coexistence of fluid and gel-like domains, the micropipe
166 xtent we agree with Burkart et al. about the coexistence of general intelligence and modular cognitiv
167 n dies down locally, often leading to stable coexistence of genetically distinct lineages.
168 orphic reinforcement systems can explain the coexistence of gregariousness and monogamy.
169 del posited in mammalian cells, in which the coexistence of H3K4me3 and H3K27me3 at developmental pro
170  Specifically, in the ternary composite, the coexistence of HA and bacteria inhibits Cd adsorption, s
171 semiconductor FeBi2Se4 enables unprecedented coexistence of high n-type electrical conduction and fer
172 nts, including for transmissible strains the coexistence of highly divergent lineages acquired by pat
173                                          The coexistence of humans and microbes throughout evolution
174                                              Coexistence of hyperdense middle cerebral artery sign an
175 IX study (ISRCTN68454111) and shown that the coexistence of hyperdiploidy or t(11;14) does not abroga
176                  Our results reveal that the coexistence of hypoxia along with free fatty acids exace
177 creased conformational heterogeneity and the coexistence of inactive, intermediate, and active states
178 allenge in ecology lies in understanding the coexistence of intraguild species, well documented at th
179      However, much of this work examines the coexistence of just pairs of competitors.
180                 Inhomogeneity along with the coexistence of Li-rich and Li-poor phases are broadly ob
181 ly provide an explanation for the "peaceful" coexistence of ligand and receptor of a representative m
182 or Cr(6+) formation is 800 degrees C for the coexistence of lime and eskolaite; (2) upon addition of
183 ifficult problem of explaining the long-term coexistence of many serotypes of major- and minor-group
184                 Our results demonstrate that coexistence of many species becomes possible by the minu
185               It has been suggested that the coexistence of many species has been achieved by the fin
186 fects decorate titanium diselenides with the coexistence of metal-Ti-atom incorporation and Se-anion
187                                          The coexistence of metastable derivative structural polytype
188 e acquired data show a temperature-dependent coexistence of monomers, dimers, and higher-order aggreg
189                                              Coexistence of more than one cTnT variant results in a t
190 iation between the rs1786814 GG genotype and coexistence of more than one TNNT2 splicing variant (90.
191  to overcome this limitation and demonstrate coexistence of multi-user QKD and full power data traffi
192 es local diversity so that understanding the coexistence of multiple adaptive phenotypes requires dec
193 d cancer clone mixing, as exemplified by the coexistence of multiple cancer lineages harboring distin
194 a multivalued current is possible due to the coexistence of multiple convective states.
195 ounced kinetic heterogeneity, suggesting the coexistence of multiple docked and undocked RNA conforma
196              SCIFIO is structured to support coexistence of multiple domain-specific open exchange fo
197 ted globally via weak-to-moderate dispersal, coexistence of multiple genotypes can occur.
198  is frequently required due to the potential coexistence of multiple populations, existence of substa
199  as rotational stacking fault (RSF), but the coexistence of multiple RSFs with different rotational a
200 f food resources hypothesized to explain the coexistence of multiple sympatric granivores.
201                                          The coexistence of multiple types of carriers and inhomogene
202  DNA (mtDNA) mutations, but heteroplasmy-the coexistence of mutant and wild-type mtDNA-complicates th
203 stic simulations, we explain this surprising coexistence of neutral/charged species as resulting from
204 nally, other case reports have described the coexistence of NSCLC and SCLC, further challenging the c
205 f cobalt cardiomyopathy seems to require the coexistence of one or more cofactors, particularly a low
206                                              Coexistence of organisms in nature is more likely when p
207 ity for thrombin, which is unaffected by the coexistence of other proteins.
208 ually transmitted infection, arises from the coexistence of over 200 genetically distinct types.
209 ed as one mechanism that might allow for the coexistence of overstory woody plants and understory gra
210 For intermediate interactions, we observed a coexistence of phases.
211  interspecific competition and promoting the coexistence of plant sister species.
212 redient in the classical hypothesis that the coexistence of plant species is enabled via differentiat
213 ed partial switch of polarization due to the coexistence of polarizations along both the a-axis and c
214 em, where host-virus coevolution facilitated coexistence of predator and virus, and where coexistence
215                                              Coexistence of predators that share the same prey is com
216  to domatia and GPM availability favored the coexistence of predatory mites at a low density of the i
217                                We report the coexistence of pseudogaped and anisotropic Dirac-like el
218                             Up until now the coexistence of QKD with data has been limited to bandwid
219 ndergoing lumen formation to demonstrate the coexistence of seamless transcellular lumens and single
220 of carriage is a partial explanation for the coexistence of sensitive and resistant strains and that
221  competing views of LFC by demonstrating the coexistence of sensory specialization and MD functionali
222 ity of identifying treatable diseases or the coexistence of several disease-causing variants, using e
223 cts of the vibration dynamics arise from the coexistence of several nonlinearly coupled modes.
224 riegation in the absence of antagonists, and coexistence of short- and long-term memory at loci with
225 cific competition, in order to enable stable coexistence of species [3].
226 m, we provide a possible explanation for the coexistence of such variation.
227                                          The coexistence of sulfate and DMA ions within the pores pla
228 2, representing the freestanding case of the coexistence of superconductivity and ferromagnetism in o
229                            Consequently, the coexistence of superconductivity and ferromagnetism is u
230                                              Coexistence of the abnormal size or echostructure of the
231                    However, we also observed coexistence of the cubic and tetragonal phases over a ra
232 tes of TI is very challenging because of the coexistence of the highly conducting bulk states.
233                                              Coexistence of the low-symmetry phases results in extens
234                                          The coexistence of the T790M resistance mutation with anothe
235 y-dependent selection that leads to a stable coexistence of the two cell types.
236       The tomograms unambiguously reveal the coexistence of the two enantiomeric forms of opposite ha
237 ered phase, the liquid-disordered phase, and coexistence of the two phases are simulated for each mix
238 ediate concentration between them causes the coexistence of the two superlattices.
239  common genetic background could explain the coexistence of these three anomalies.
240 mensional differentiation allows the spatial coexistence of these two dense populations in the study
241               To quantify the prevalence and coexistence of these two forms of ICU-acquired weakness
242                                              Coexistence of these two mechanisms strongly depends on
243           In triangular-lattice magnets, the coexistence of third-neighbor antiferromagnetic and near
244 nce, whereas further lithiation leads to the coexistence of three distinct phases within single nanop
245           In this report, we demonstrate the coexistence of three RSFs with three different rotationa
246                                  We show the coexistence of time-locked, glutamate receptor and GABA
247                                          The coexistence of topological order and other unusual prope
248 e sample of participants, we demonstrate the coexistence of transient and sustained effects of mixing
249               In regions with rainy summers, coexistence of tropical ectothermic species may be deter
250            Coevolution can promote long-term coexistence of two competing species if selection acts t
251  Based on these observations, we propose the coexistence of two distinct activity-dependent systems o
252                    These finding suggest the coexistence of two distinct activity-dependent systems o
253  from one patient sputum sample revealed the coexistence of two genetically diverged, recombining lin
254 lline phase were found and attributed to the coexistence of two groups of triglycerides.
255 of the photoelectron spectrum discovered the coexistence of two isomers in the ion beam, including th
256 re gradient in conditions where they exhibit coexistence of two liquid phases.
257   The neutron diffraction data also reveal a coexistence of two magnetic phases that further highligh
258                                              Coexistence of two or three simulated spin probe populat
259 However, the striking syndrome similarities, coexistence of two otherwise rare antibodies and molecul
260  from host heterogeneity, promotes long-term coexistence of two pathogen types in simulations of a po
261 CM), unlike the BCM, are able to explain the coexistence of two stable final opinions, often observed
262 or and the radial distribution function, the coexistence of two structurally distinct domains is obse
263 ps to the substrate enable and stabilize the coexistence of unexpected phases.
264 efits of multicellularity promote the stable coexistence of unicellular and multicellular genotypes,
265 cornerstone of quantum mechanics, limits the coexistence of wave and particle behaviours of quantum s
266                                          The coexistence of woody plants and grasses in savannas is d
267 e an important mechanism responsible for the coexistence of woody plants and grasses in savannas.
268      Integrating evolution into the study of coexistence offers new insights, while enriching our und
269  differences through time that could promote coexistence on a limiting resource.
270  lead to a transition from regional to local coexistence or it may lead directly to extinction, depen
271 pes can perturb and eventually destroy their coexistence over longer time scales.
272 ng was limited, coculture trends changed yet coexistence persisted under both homogenous and heteroge
273 lloids, including arbitrarily wide gas-solid coexistence, reentrant melting, and even reversible tran
274 is characterized by an extensive three-phase coexistence region of fluid (ld-phospholipid enriched)/l
275 ition, leading to a large Lbeta/Lalpha phase coexistence region where gel-phase domains contain appro
276 hase is increased, leading to a larger lo/ld coexistence region.
277 he role of energetic constraints in limiting coexistence remains largely unknown.
278 k models stabilizes dynamics, making species coexistence robust to the perturbation of both populatio
279 d reaction-diffusion analysis of approach-to-coexistence simulation data from Aragones et al..
280 oexistence and find that a wider spectrum of coexistence states can emerge and persist.
281 itions imposes a limitation on the resulting coexistence states, leading to only selective types of s
282 cts with more traditional drivers of species coexistence such as niche partitioning.
283    This approach ignores those mechanisms of coexistence that emerge only in diverse competitive netw
284  traditionally ignored in studies of species coexistence, the magnitude of intraspecific variation in
285 ions and found that despite their history of coexistence, the vast majority formed distinct boundarie
286                                              Coexistence theory has been developed with an almost exc
287 To integrate intransitivity into traditional coexistence theory, we developed a metric of growth rate
288 existence are largely ignored in traditional coexistence theory.
289 e to seed-size variation and promote species coexistence through a tolerance-fecundity trade-off.
290       We also observe the expected two-phase coexistence throughout the entire charging process.
291  on MacArthur's classic model of competitive coexistence to investigate such community-level competit
292 ences in the evolutionary time available for coexistence to occur.
293 al properties from ice, through liquid-vapor coexistence, to the critical point.
294 roecology from a killer-prey relationship to coexistence using two different non-motile Escherichia c
295 biota, can potentially mediate plant species coexistence via negative feedbacks.
296 use a consumer-resource model to explore how coexistence via the temporal storage effect and relative
297                                        Their coexistence was promoted more by increases in stabilizin
298 r's integration into the community and their coexistence with native species.
299 unctions, e.g., communication signals during coexistence with other microorganisms, virulence factors
300 sticity in foraging traits helps to maintain coexistence within this guild and whether foraging modal

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