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1 elatives, Arabidopsis thaliana is capable of self-pollination.
2  ecological and genetic conditions favouring self-pollination.
3 lects changes in the extent of geitonogamous self-pollination.
4 e propagated through multiple generations by self-pollination.
5  ethylene production and petal abscission as self-pollination.
6 NA hypomethylation mutant, ddm1, by repeated self-pollination.
7 nalysis of compatibility classes of in vitro self-pollinations.
8                              Higher rates of self-pollination and increased tetraploid advantage incr
9 psis thaliana and Arabidopsis halleri during self-pollination and interspecific pollination and durin
10 ion of these factors with different rates of self-pollination and tetraploid advantage.
11 es the positive impact of any given level of self-pollination and tetraploid advantage.
12 ween years, these conditions likewise favour self-pollination, and this can result in a mixture of se
13  of infrequent pollinator visits, autonomous self-pollination boosted seed output per flower, the key
14 ese probes increased slightly in response to self-pollination, but the degree of accumulation in resp
15 ry morphological innovations associated with self-pollination can evolve rapidly after the inactivati
16 lant species that autonomously reproduce via self-pollination consistently have larger geographic ran
17 ollinator visitation as well as among-flower self-pollination (geitonogamy) in self-compatible specie
18 yle length) associated with the evolution of self-pollination in cultivated tomatoes.
19 ns and the evolution of nearly cleistogamous self-pollination in others may reflect local pollinator-
20 ents demonstrate that pollen sampling during self-pollination in pea conforms to the binomial distrib
21 its will evolve towards increased autonomous self-pollination in plant populations experiencing unrel
22       Darwin proposed an adaptive benefit of self-pollination in providing reproductive assurance whe
23                            The inhibition of self-pollination in self-incompatible Brassicaceae is ba
24                                              Self-pollination is common in plants, and limited seed a
25     In plants, the shift from outcrossing to self-pollination is common, providing the opportunity fo
26                                 The shift to self-pollination is one of the most prevalent evolutiona
27                                              Self-pollination of diploid zonal geranium (Pelargonium
28 lysis of segregating F2 progeny derived from self-pollination of F1 hybrids from four crosses (B73 x
29                                              Self-pollination of heterozygous ospal4 mutant lines pro
30                                              Self-pollination of individual KanR plants from these fa
31                                              Self-pollination of these partially fertile F(1) plants
32 in pistils and receptacles are unaffected by self-pollination or treatment with 1 micro/l ethylene th
33                                    In pines, self-pollination rates can be as high as 34% yet only 5%
34                                              Self pollination resulted in lower seed set, germination
35 tes of rates of recombination, mutation, and self-pollination, show that LD is more extensive than ex
36 istils had exserted stigmas, thus preventing self-pollination, similar to wild-type pistils treated w
37       After two generations of inbreeding by self-pollination, the ddm1/ddm1 lines became nonfluoresc
38     The transition from cross-pollination to self-pollination was accompanied, not by a change in the
39                                     In vitro self-pollinations were analysed and recorded and plants

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