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1  stable above 200 GPa, and LaH8 a C2/m space group structure.
2 or by individuals paying attention to global group structure.
3  construction of ideologies that rationalize group structure.
4  magnitude and were strongly influenced by R-group structure.
5 these traits may be related to our ancestral group structure.
6 nd do not require kin selection or a special group structure.
7 terol side chain structure, and sterol polar group structure.
8 tributes to the evolution of variable social group structure.
9 ff setting while taking into account a given group structure.
10  punishment and cooperation under a range of group structures.
11 ly correlating with the differences in ketal group structures.
12 uting heteroaromatic subunits into the donor group structures.
13 enzodioxocin (5-5), and cinnamyl alcohol end-group structures.
14 rences in institutional make-up and interest group structures.
15 ches for molecular data analysis ignore such group structures.
16 estigated the species traits related to this grouping structure.
17 t isochronous beat and slower metrical (beat grouping) structures.
18 lations of network robustness show that this group structure affects cancer-specific response to chap
19 sional and large data, and by leveraging the group structure among the lagged temporal variables acco
20 cted an important aspect of the problem--the group structure among the lagged temporal variables natu
21                                              Group structures among genes encoded in functional relat
22 (G(2,1)-norm), to incorporate the biological group structures among SNPs induced from their genetic a
23 PLS) that utilizes biological information on group structures among variables and performs group sele
24 One key feature of DNA methylation data is a grouped structure among CpG sites from a gene that are p
25 ddition, the proposed method can exploit any grouping structure among features, while alternative met
26 ude of social functions in order to regulate group structure and hierarchy.
27                In a cross-sectional study of group structure and kinship we found that belugas formed
28 yields a detailed picture of the polymer end-group structure and microstructure.
29 zed particles and vary known features of the group structure and motion via a class of generative mod
30                    The effect of substituent group structure and position on biodegradation potential
31  size, and the communication topology affect group structure and response to perturbation.
32 tor effects have been shown to affect social group structure and social behaviour as well as individu
33 ge cultural F ST values provide evidence for group structure and therefore scope for group selection.
34 ouble-exponential distribution, to integrate group structures and to adaptively shrink the effects of
35 characterized the prepared films' functional groups, structure, and morphology.
36                 In contrast, the Lewis blood group structures are receptors for many strains of Helic
37 eal the importance of tightly bound toroidal group structures as an intermediate state prior to the e
38 fically incorporates genome and/or phenotype grouping structures, as well as phenotype correlation st
39                                Latent social group structure-based allyship estimates, in contrast, r
40 eals novel superlattices composed of lattice groups structured by four-atomic layers of alternating P
41 rates that, as in the genetic case, apparent group structure can be a consequence of geographic cline
42                                              Group structure can be modeled using social network anal
43 networks, we provide further evidence of how group structure can foster group cohesion.
44                             We highlight how group-structured cultural selection shapes the scale and
45                         Because biofilm cell group structure depends on initial cell distributions at
46 sion of labour-depending upon details of the group structure, division of labour can be favoured for
47 model two types of prior knowledge: one as a group structure (e.g. linkage disequilibrium blocks amon
48 sed to receive either standard care or a 6-h group structured education programme with an annual refr
49 terns of dispersal can generate variation in group structure, even within the same species or populat
50                 Demographic factors (age and group structure) explained SSB variation only marginally
51 ure anti-B, which require the complete blood group structure for binding.
52              Our finding of the unusual side group structures for two well-known cell wall polysaccha
53 with broad consequences for sociality (e.g., group structure, functioning), ecology (e.g., response t
54  parameters for the emergence of farming are group structuring, group size, conservatism, and farming
55  Furthermore, by investigating heterogeneous group structures, I demonstrate a potential influence of
56 ed dispersal patterns influence variation in group structure in the plural breeding superb starling (
57 omics technologies have introduced a two-way grouping structure in multiple testing, as seen in singl
58 erg (2dGBH) procedure to harness the two-way grouping structure in omics data, extending the traditio
59 sures in combination with metrics describing group structure, including different proximity, social,
60 ntraspecific, within-population variation in group structure, including variation in kin structure of
61                   Furthermore, incorporating group structures increased robustness of the feature sel
62 confirmed oligomer series with different end group structures, indicating that the applied HPLC metho
63                                       Social group structure is highly variable and can be important
64                                   Within the group structure itself we find that the most gregarious
65 have limited ability to exploit such two-way grouping structure, leading to potential power loss.
66 ndings demonstrate that while complex social group structures may be unnecessary for the evolution of
67                         Total relatedness in group-structured models can be partitioned into two comp
68           This paper examines relatedness in group structured modes, in which a trait affects the fit
69     Previous work has informally argued that group-structure must favour pro-social punishment.
70 l responses as required in the highly social group structure observed in the African wild dog.
71                            Although the head group structure of acyl chain-labeled NBD phospholipids
72 iciency Virus (HIV), is affected by the risk group structure of the infected population.
73                                      The end-group structure of the polysaccharide fragments allowed
74 ture of master transcription factors and the group structure of their simultaneous regulatory effects
75  detecting associated genes by incorporating group structures of biological pathways.
76 d by anion-exchange chromatography, the side group structures of both polysaccharides are modified fu
77 e incorporated biological information on the group structures of the methylation CpG sites when integ
78  such cases, applying TDC while ignoring the group structure often yields imbalanced lists of discove
79 t the observed algorithms accurately predict group structure over development.
80 , the evolution of anti-social punishment in group-structured populations has not been formally addre
81            We develop a theoretical model of group-structured populations in which individuals are as
82                         Because evolution in group-structured populations is governed by the balance
83  of pro-social punishment and cooperation in group-structured populations should be re-evaluated.
84 trated that equitable offers could evolve in group-structured populations when there is a cost (i.e.,
85 iable measured on each sample and the latent group structure represented by some given tree.
86  order parameters describing the macroscopic group structure, revealing the existence of at least thr
87 n processes, and opens the study of adaptive group-structured systems.
88                   This view is equivalent to grouping structures that are connected by free-energy ba
89 population imbalance, the complexity of cell group structures, the proportion and the similarity of n
90 adaptive hypergraphs, our method reveals how group structure unlocks new dynamical regimes and enable
91 ystem trade-offs, which can be achieved with group-structured versions of Price's equation.
92 iables in neural network, over no or uniform group structure, which is more favorable in smaller stud
93  integrate clustering approaches to identify group structures within such datasets.
94 lation studies also show a robustness to the grouping structure within the clinical space.