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1 the role played by ethylene in the ripening receptacle.
2 d by this gene during the development of the receptacle.
3 iral pattern on the subtending stem tip, the receptacle.
4 ffect sperm movement into the female storage receptacle.
5 to galactose in a microdialysis hollow fiber receptacle.
6 that AGL15 binds the HAE promoter in floral receptacles.
7 ise to eugenol production in ripe strawberry receptacles.
8 2 expression is almost restricted to the red receptacles.
9 sed in stamen filaments, anthers, and flower receptacles.
15 active GAs made in the stamens and/or flower receptacles are transported to petals to promote their g
16 e levels of PhETR1 and PhETR2 in pistils and receptacles are unaffected by self-pollination or treatm
17 al expression analysis of the achene and the receptacle at four stages of fruit ripening, and of the
20 he sepals, petals, and stamens attach to the receptacle, at the base of pedicels, and at the base of
22 red either intravenous cocaine or water to a receptacle (controls), followed by 30 d of enforced abst
23 revealed differences between the achene and receptacle development program, and reinforced the role
24 f ions (e.g. K+) throughout the cells of the receptacle during potentiation, which then move into the
25 increases greatly in floral organ-supporting receptacles during the development and maturation of sil
26 ripe strawberry (Fragaria x ananassa) fruit receptacles, eugenol is biosynthesized by eugenol syntha
30 roduced from the achene is essential for the receptacle fruit set, a paradigm for studying crosstalk
31 f Hibiscus sabdariffa (petals), Rosa canina (receptacles), Ginkgo biloba (leaves), Cymbopogon citratu
32 e's primary sperm-storage organ, the seminal receptacle, has undergone rapid divergence within the Dr
33 hey increased their head entries to the food receptacle in a pattern that was consistent with conditi
34 phosphorylated through development in floral receptacles in a MITOGEN-ACTIVATED PROTEIN KINASE KINASE
36 UGT71K3 transcript expression in strawberry receptacles led to a significant reduction in the level
37 elations between additive effects of seminal receptacle length and thorax length in both experiments.
38 gevity, female egg productivity, and seminal receptacle length did not show consistent correlated res
40 Quantitative genetic analysis of seminal receptacle length was carried out on two laboratory stra
43 tion), and gamete expulsion from potentiated receptacles of Pelvetia compressa began about 2 min afte
45 significant increase in whole berry R(h) and receptacle R(h) in the latter stages of ripening (80-100
46 rom tomato in that the fruit is derived from receptacle rather than ovary tissue and strawberry is no
47 o the sepals, stigmas, anther filaments, and receptacles, reaching a peak when the stigma was recepti
48 nous ABA application to the RNAI-transformed receptacle reversed most defects caused by FaGAMYB down-
49 e to FaGAMYB in the initiation of strawberry receptacle ripening and acting upstream of the known reg
53 on of FaEOBII was ripening related and fruit receptacle specific, although high expression values wer
54 importance is the discovery of a developing receptacle-specific module exhibiting similar molecular
55 pts were detected by RT PCR at all stages of receptacle swelling (auxin-dependent) and ripening (inhi
56 ggregate fruit consisting of a fleshy floral receptacle that bears a cluster of real dry fruits (ache
57 lants, MAP kinase activity is reduced in the receptacle, the part of the stem that holds the floral o
58 distributed into each of four blood culture receptacles: the Isolator tube (Wampole Laboratories, Cr
60 pening process, and fruit flesh derived from receptacle tissues rather than the ovary wall which is m
62 bsequent decrease in eugenol content in ripe receptacles was also observed, confirming the involvemen
64 emature release of gametes in the light when receptacles were incubated with inhibitors of slow-type
66 ibited sperm depletion only from the seminal receptacle, whereas absence of both OA and TA perturbed
67 ed in the replums, funiculi, and the silique receptacles, whereas the other GA3ox genes are only expr
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