ライフサイエンスコーパス: Vicia faba

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1 sion and sieve plate occlusion in fava bean (Vicia faba).

2 g epidermal peels from leaves of broad bean (Vicia faba).

3 ning cc , and we tested these predictions in Vicia faba.

4 e domain (CDPK) in guard cell protoplasts of Vicia faba.

5 psis thaliana proteins with high homology to Vicia faba AKIP1 and other heterogeneous nuclear ribonuc

6 r transpiration rate (90% RH) in broad bean (Vicia faba), an apoplastic phloem loader.

7 mbranes of guard cells in epidermal peels of Vicia faba and Commelina communis can be made accessible

8 Samples of soil, the broad bean plant, Vicia faba and irrigation water were collected from the

9 prephloem pathways of the apoplasmic loader Vicia faba and Nicotiana tabacum showed, to our knowledg

10 in desalted leaf extracts of the C(3) plants Vicia faba and rice (Oryza sativa).

11 onging to the galegoid clade (Pisum sativum, Vicia faba and Vicia hirsuta).

12 glaucum, Pinus elliottii, Selaginella apoda, Vicia faba and Vicia narbonensis.

13 cotyledonous plant species (Hordeum vulgare, Vicia faba, and Nicotiana tabacum).

14 the roots of maize (Zea mays) and faba bean (Vicia faba) are characterized.

15 mined surface area for intact guard cells of Vicia faba as they underwent changes in volume in respon

16 of this research was the characterisation of Vicia faba (broadbean) protein isolates and related frac

17 ide sequence information was used to clone a Vicia faba complementary DNA, AAPK, encoding a guard cel

18 Fava beans (Vicia faba) contain dihydroxyphenylalanine (dopa), and t

19 to mesophyll cell protoplasts of fava bean (Vicia faba cv Long Pod) plants and demonstrated ABA inhi

20 risome subunits in e.g. Medicago truncatula, Vicia faba, Dipteryx panamensis and Canavalia gladiata w

21 ea mays) flour enriched with 30% broad bean (Vicia faba) flour and 20% of quinoa (Chenopodium quinoa)

22 fied and recombinant kinases were applied to Vicia faba guard cell vacuoles during patch-clamp experi

23 g the whole-vacuole mode of patch-clamp with Vicia faba guard cell vacuoles, three distinct cation cu

24 fied the [Ca(2+)](i) dynamics of I(anion) in Vicia faba guard cells, measuring channel current under

25 (ABA) responses in Arabidopsis thaliana and Vicia faba guard cells.

26 ing the patch clamp technique on broad bean (Vicia faba) guard cells we demonstrate that both steady-

27 resulting from 30 d of supplementation with Vicia faba L.

28 Faba bean (Vicia faba L.) provides environmental and health benefit

29 Two faba bean (Vicia faba L.) subspecies major and minor and lentil see

30 We have isolated a gene from bean (Vicia faba L.), called Vein1, that encodes a novel prote

31 Unlike uninfected leaves, stomatal pores of Vicia faba leaves infected with S. sclerotiorum are open

32 We have isolated two distinct Vicia faba MT genes that belong to the type 1 group of p

33 cer arietinum, Glycine max, Lupinus alba and Vicia faba, nonlegume dicots Brassica napus and Helianth

34 without bundle sheath extensions, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nic

35 e purification of several immunophilins from Vicia faba plants.

36 s attenuate the BBMV spreading in inoculated Vicia faba plants.

37 larly methyl salicylate, making bean plants, Vicia faba, repellent to aphids but attractive to aphid

38 patch clamping of guard-cell protoplasts of Vicia faba revealed that 1,2-dihexanoylglycerol and 1-ol

39 We show in Vicia faba that O(3) inhibits (i) guard cell K(+) channe

40 and characterized a gene encoding FKBP12 in Vicia faba (VfFKBP12).

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