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1 and in multilocus microsatellite genotypes (genets).
2 associated with the outward expansion of the genet.
3 y ago, Crow and Kimura and Ohta and Kimura [Genet.
4 st performing genets than in best performing genets.
5 spring) for male genets compared with female genets.
6 ll time points, mushrooms resolve into small genets.
7 form by the fusion of at least two distinct genets.
13 the variation in selfing, differences among genets accounted for 16.1% of the variation, and statist
15 ribute model estimated the influence of host genet and treatment on Symbiodiniaceae community composi
16 growth leads to an expansion in the size of genets and increased fitness because large floral displa
17 erved when considering only sexually derived genets and kinship coefficients were significant up to t
18 esolve multi-locus genotypes of host (called genets) and symbionts (called strains), distinguish host
19 l expansion of the genetic individual (i.e., genet), and this should decrease distances gametes and s
22 size and rate of lateral spread (LS) of the genet can be measured or estimated using morphological t
25 cators of coral and algal health in 40 coral genets exposed to each of these three stressors singly a
26 and fungi, the sexually produced offspring (genet) grows indeterminately by producing iterative modu
30 we report on the formation and structure of genets known as symplasmata produced by Pantoea eucalypt
31 end of the experiment, seven of eight coral genets mainly hosted Cladocopium symbionts, whereas the
32 rack temporal and spatial changes of sampled genets necessary for restoration planning and can be app
33 s study, the transcriptomic dynamics of four genets of outplanted Acropora palmata were assessed over
34 ciations among particular symbionts and host genet performance, as well as weaker associations with t
36 ve propagation) in which parental genotypes (genets) produce vegetative modules (ramets) that are cap
37 ogenetic relationships, 22 S-alleles from 34 genets randomly taken at three Tennessee sites from a ne
39 of these 10 isolates were ramets of a single genet, suggesting a genetic basis underlying the procliv
41 mbiodiniaceae) from eight Acropora millepora genets that thrived under or responded poorly to various
42 ils of the response distribution of 40 coral genets that were exposed to four stress treatments (and
44 We exposed multiple ramets of 26 goldenrod genets to nutrient or shade stress and to oviposition by
46 ed Cladocopium symbionts, whereas the eighth genet was dominated by both Cladocopium and Durusdinium
47 Specifically, four 'best performer' coral genets were analyzed at the end of the experiment becaus
48 ed stressors, whereas four 'worst performer' genets were characterized because they experienced subst
49 ngens (Scrophulariaceae), each consisting of genets with unique combinations of homozygous marker gen