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1 cts, but are fixed across subgenomes through self pollination.
2 elatives, Arabidopsis thaliana is capable of self-pollination.
3  ecological and genetic conditions favouring self-pollination.
4 lects changes in the extent of geitonogamous self-pollination.
5 e propagated through multiple generations by self-pollination.
6 he blocking of pollen production, to prevent self-pollination.
7  ethylene production and petal abscission as self-pollination.
8 NA hypomethylation mutant, ddm1, by repeated self-pollination.
9 iated outcross pollen deposition rather than self-pollination.
10 nalysis of compatibility classes of in vitro self-pollinations.
11                              Higher rates of self-pollination and increased tetraploid advantage incr
12 psis thaliana and Arabidopsis halleri during self-pollination and interspecific pollination and durin
13 ion of these factors with different rates of self-pollination and tetraploid advantage.
14 es the positive impact of any given level of self-pollination and tetraploid advantage.
15  during domestication and involves crossing, self-pollination, and clonal propagation for its cultiva
16 ween years, these conditions likewise favour self-pollination, and this can result in a mixture of se
17  including those involved in optimization of self-pollination, attraction of animal pollinators, and
18  of infrequent pollinator visits, autonomous self-pollination boosted seed output per flower, the key
19  We found that stigmatic ROS increased after self-pollination but decreased after compatible(CP)- pol
20 ese probes increased slightly in response to self-pollination, but the degree of accumulation in resp
21 ry morphological innovations associated with self-pollination can evolve rapidly after the inactivati
22 lant species that autonomously reproduce via self-pollination consistently have larger geographic ran
23 ollinator visitation as well as among-flower self-pollination (geitonogamy) in self-compatible specie
24              The exceptionally high level of self-pollination (>99%) in B. tectorum has contributed t
25 yle length) associated with the evolution of self-pollination in cultivated tomatoes.
26 ns and the evolution of nearly cleistogamous self-pollination in others may reflect local pollinator-
27 ents demonstrate that pollen sampling during self-pollination in pea conforms to the binomial distrib
28 its will evolve towards increased autonomous self-pollination in plant populations experiencing unrel
29       Darwin proposed an adaptive benefit of self-pollination in providing reproductive assurance whe
30                            The inhibition of self-pollination in self-incompatible Brassicaceae is ba
31 ating can cause an increase or a decrease in self-pollination in sympatric populations.
32  increase in yields due to the efficiency of self-pollination in the domesticated grapevine (Vitis vi
33                     One method of preventing self-pollination in the female plants is to apply a chem
34                                              Self-pollination is common in plants, and limited seed a
35     In plants, the shift from outcrossing to self-pollination is common, providing the opportunity fo
36                                 The shift to self-pollination is one of the most prevalent evolutiona
37 (female) S-determinants that control whether self-pollination is successful or not.
38 ltered pollen tube morphology (in vitro) and self-pollination led to fewer seeds and shorter siliques
39                                              Self-pollination of diploid zonal geranium (Pelargonium
40 lysis of segregating F2 progeny derived from self-pollination of F1 hybrids from four crosses (B73 x
41                                              Self-pollination of heterozygous ospal4 mutant lines pro
42                                              Self-pollination of individual KanR plants from these fa
43                                              Self-pollination of these partially fertile F(1) plants
44 in pistils and receptacles are unaffected by self-pollination or treatment with 1 micro/l ethylene th
45                                    In pines, self-pollination rates can be as high as 34% yet only 5%
46                                              Self pollination resulted in lower seed set, germination
47 tes of rates of recombination, mutation, and self-pollination, show that LD is more extensive than ex
48 istils had exserted stigmas, thus preventing self-pollination, similar to wild-type pistils treated w
49       After two generations of inbreeding by self-pollination, the ddm1/ddm1 lines became nonfluoresc
50     The transition from cross-pollination to self-pollination was accompanied, not by a change in the
51                                     In vitro self-pollinations were analysed and recorded and plants