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1 ing fitness to facilitate parental-offspring coadaptation.
2 x-based niche partitioning, and sex-specific coadaptation.
3 t of the host species, indicating virus-host coadaptation.
4 ective forces that generate parent-offspring coadaptation.
5 from the disruption of nuclear-mitochondrial coadaptation.
6 confirmation of synchronous plant-herbivore coadaptation.
7 s that feeding preferences have driven their coadaptation.
8 ssurance (Baker's contention) and multilocus coadaptation (Allard's argument) are two distinct hypoth
9 often coexist in the same host, resulting in coadaptation among several phylogenetically distant geno
10 mutualism has occurred through strict-sense coadaptation and cospeciation between pairs of fig and w
11 bolites underlies adaptive immune microbiota coadaptation and promotes colonic homeostasis and health
12 s on the neo-X indicates a pattern of active coadaptation apparently initiated by X-linked transmissi
13 itation and maternal behaviour show signs of coadaptation as they are negatively correlated between m
14 fication has resulted from a long history of coadaptation between microbes and hosts (heritable facto
15 y the parasite, thus intensifying continuous coadaptation between symbionts in a tripartite arms race
16 s work provides insights into the process of coadaptation between the human immune system and a rapid
21 the presence of gene interactions that favor coadaptation can also favor the evolution of genomic imp
22 I prolyl-tRNA synthetase (ProRS), functional coadaptations have occurred in going from the bacterial
23 oethological correlates underlying fly-yeast coadaptation in two drosophilids with distinct habitats.
24 r, the spread of adaptation (i.e., degree of coadaptation) in tonotopically organized regions of audi
25 complementarily, which is consistent with a coadaptation model of imprinting evolution, a model pred
26 uggest that the two ProRS groups may reflect coadaptations needed to accommodate changes in the opera
28 mediated chromosomal rearrangement, and high coadaptation of both male genes and cis-regulatory seque
29 ust catalytic function in different ways, or coadaptation of different steps' properties in pathways;
30 like properties but are heavily dependent on coadaptation of hosts, which continuously evolve to supp
31 control, showing that there is antagonistic coadaptation of maternal and paternal effects on distinc
34 oning, whereas the latter concentrate on the coadaptation of parental supply and offspring demand.
35 tional RNA code can vary in evolution due to coadaptations of the contacts between aminoacyl-tRNA syn
37 Physiological evidence of ejaculate-female coadaptation, paired with a promiscuous mating system, m
38 ir pups has recently been claimed to support coadaptation rather than the kinship theory of genomic i
40 The sexual antagonism and maternal-offspring coadaptation theories view genomic imprinting as a mecha
41 thermore, as predicted by maternal-offspring coadaptation theory, offspring signaling is negatively g
44 actions often favor the evolution of genetic coadaptation, where beneficially interacting alleles evo
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