戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.
10 erm in two types of organs, a single seminal receptacle and a pair of spermathecae.
11 AMYB caused an arrest in the ripening of the receptacle and inhibited colour formation.
12 orrelated with eugenol content in both fruit receptacle and petals.
13           We find innervation of the seminal receptacle and spermathecae by octopaminergic-tyraminerg
14 e and before storage of sperm in the seminal receptacles and spermathecae.
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
18  exhibited more approaches to the reinforcer receptacle at nonreinforcement times.
19  in the achene at the green stage and in the receptacle at the red stage.
20 he sepals, petals, and stamens attach to the receptacle, at the base of pedicels, and at the base of
21 onoids were quantitatively assessed in fresh receptacles by HPLC-PDA analysis.
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
27  a motorized XY stage, which functioned as a receptacle for 96-well microtiter plates.
28        Humic lakes and pools are the primary receptacles for terrigenous carbon in these meta-ecosyst
29 d seed coat coordinate seed, ovary wall, and receptacle fruit development.
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
35                               Therefore, the receptacle is an integral part of the strawberry flower
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
39 he correlated evolution of sperm and seminal receptacle length is discussed.
40     Quantitative genetic analysis of seminal receptacle length was carried out on two laboratory stra
41 ied as hub genes operating in the developing receptacle network.
42                                          The receptacle of the strawberry (Fragaria x ananassa) fruit
43 tion), and gamete expulsion from potentiated receptacles of Pelvetia compressa began about 2 min afte
44 iable increase in head entries in the dipper receptacle on nicotine versus saline sessions.
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
50 uit are the numerous dry achenes dotting the receptacle's surface.
51                 The ethanolic extract of the receptacles showed no sign of cytotoxicity when tested i
52 d X-linked genes affect female ventral sperm receptacle size.
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
59 n that the edible flesh is actually enlarged receptacle tissue.
60 pening process, and fruit flesh derived from receptacle tissues rather than the ovary wall which is m
61 l, the amount of eugenol in FaMYB10-silenced receptacles was also diminished.
62 bsequent decrease in eugenol content in ripe receptacles was also observed, confirming the involvemen
63                                          Its receptacles were eaten by shepherds in Valais (Switzerla
64 emature release of gametes in the light when receptacles were incubated with inhibitors of slow-type
65                           In ripe strawberry receptacles, where the expression of FaEOBII was silence
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
68 d with deposition of gels or solutes in many receptacle xylem conduits.

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。