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1 rsicon esculentum (Mill cv. Ailsa Craig) and Nicotiana plumbaginifolia.
2 RNA from N. alata styles but not to RNA from Nicotiana plumbaginifolia, a species known to lack one o
3 ollen rejection and rejection of pollen from Nicotiana plumbaginifolia also require additional stylar
4 viously been cloned by transposon tagging in Nicotiana plumbaginifolia and maize respectively.
5  in Arabidopsis thaliana, Nicotiana tabacum, Nicotiana plumbaginifolia and Zea mays.
6 roxide dismutase (Fe-SOD) from wild tobacco (Nicotiana plumbaginifolia), Arabidopsis, and potato (Sol
7             We have selected 143 independent Nicotiana plumbaginifolia cell lines that survive in the
8  in epidermal strips of a transgenic line of Nicotiana plumbaginifolia expressing aequorin (the prote
9 en reading frame very similar to that in the Nicotiana plumbaginifolia gene PMA1.
10  N-terminus was isolated and used to probe a Nicotiana plumbaginifolia genomic library.
11                   Two new allelic mutants of Nicotiana plumbaginifolia have been isolated which displ
12 s following transient expression in tobacco (Nicotiana plumbaginifolia) leaves.
13 xhibits high sequence similarity to tobacco (Nicotiana plumbaginifolia) pectin glucuronyltransferase.
14 he tomato (Lycopersicon esculentum) yg-2 and Nicotiana plumbaginifolia pew1 photomorphogenic mutants
15 nalysis of expression in seeds of transgenic Nicotiana plumbaginifolia plants showed that whereas a p
16     When Agrobacterium was used to transform Nicotiana plumbaginifolia protoplasts and Arabidopsis th
17                             Using transgenic Nicotiana plumbaginifolia seedlings in which the calcium
18                          Transgenic tobacco (Nicotiana plumbaginifolia) seedlings containing the Ca(2
19           The cDNA clone was used to express Nicotiana plumbaginifolia SSU in Escherichia coli.
20                     Transgenic wild tobacco (Nicotiana plumbaginifolia Viv.) plants were produced tha

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