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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.                                      
  
     9 psis thaliana and Arabidopsis halleri during self-pollination and interspecific pollination and durin
  
  
    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
  
    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
  
  
  
    25     In plants, the shift from outcrossing to self-pollination is common, providing the opportunity fo
  
  
    28 lysis of segregating F2 progeny derived from self-pollination of F1 hybrids from four crosses (B73 x 
  
  
  
    32 in pistils and receptacles are unaffected by self-pollination or treatment with 1 micro/l ethylene th
  
  
    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
  
    38     The transition from cross-pollination to self-pollination was accompanied, not by a change in the
  
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