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1 odified by whole genome duplication (causing allopolyploidy).
2 tant, especially after chromosomal doubling (allopolyploidy).
3 ompletely homologous (homoeologous) genomes (allopolyploidy).
4 Two of these events were inferred to be allopolyploidy.
5 methods, and explicitly tested scenarios for allopolyploidy.
6 , epigenetic and transcriptomic responses to allopolyploidy.
7 xa for comparing the longer term outcomes of allopolyploidy.
8 d by chromosome doubling, a process known as allopolyploidy.
9 o genomic processes that occur subsequent to allopolyploidy.
10 stem for studying the genome evolution after allopolyploidy.
11 ng the evolutionary dynamics associated with allopolyploidy.
12 uplication associated with hybridization, or allopolyploidy, allows these chromosome sets to persist
13 he species sampled are the result of genetic allopolyploidy and result from 28 distinct tetraploidy e
14 temporal progression of genomic responses to allopolyploidy and the underlying mechanisms, remain poo
15 our understanding of genome evolution after allopolyploidy, and could facilitate crop improvements t
16 Nicotiana section Repandae, which arose via allopolyploidy (approximately 5 million years ago) invol
18 not observed and its short-term responses to allopolyploidy are mainly manifested as a high proportio
21 ana is an excellent system in which to study allopolyploidy because half of the species are allotetra
22 , a prominent genetic consequence of nascent allopolyploidy, can exacerbate, diversify and perpetuate
23 ter and wider corolla tubes, suggesting that allopolyploidy could provide an escape from specialist p
25 yploidy events within Stachys, including one allopolyploidy event underlying the Hawaiian mints and t
30 ults highlight white clover as an example of allopolyploidy-facilitated niche expansion, where two pr
34 v provided conclusive evidence for segmental allopolyploidy in B. decumbens, with strong preferential
35 as well as the effects of recent and ancient allopolyploidy in Brassica napus, on genes implicated in
46 The genomic shock hypothesis suggests that allopolyploidy is associated with genome changes driven
53 explained by autopolyploidy or, if there was allopolyploidy, it happened within the Californian redwo
54 se in net diversification rate; nonetheless, allopolyploidy itself is a major mode of speciation.
55 e, a deeper understanding of the kinetics of allopolyploidy may allow us to better understand both bi
56 nto genome function gained from the study of allopolyploidy may be applicable to hybrids of any type
58 ustness of plant cytonuclear interactions to allopolyploidy may reflect features that are general to
62 his process, we explored the consequences of allopolyploidy on xenobiotic tolerance in the genus Spar
63 awaiian species may reflect the influence of allopolyploidy or of selection and adaptive divergence.
64 ain genomes from different parental species (allopolyploidy) or include multiple sets of the same gen
67 pproximately 60 million years (Myr) ago, and allopolyploidy reuniting divergent Gossypium genomes app
68 ary global expansion was probably enabled by allopolyploidy that accelerated genetic novelty through
69 cal framework for elucidating the underlying allopolyploidy that includes a newly adapted tool (DGS-T
70 vide evidence for the selective advantage of allopolyploidy through the fixation of intergenomic hete
72 ne interspecific hybridization, resulting in allopolyploidy; whereas homoploid hybrid speciation was
73 ften accompanied by nuclear genome doubling (allopolyploidy), which has been hypothesized to perturb
75 k for utilizing transcriptome data to detect allopolyploidy, which is important as it may have differ
76 badense genome advances our understanding of allopolyploidy, which will help improve cotton fiber qua
77 identify evidence for de novo adaptation to allopolyploidy within the A. arenosa sub-genome of A. su