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1 bacum) plants expressing a wild-type form of Vigna aconitifolia P5CS and a mutated form of the enzyme
2 ly found in elicited seedlings of Phaseolus, Vigna and Lablab, whereas pterocarpans were mainly obser
3 s, including Triticeae and Paniceae grasses, Vigna beans, Dioscorea opposita yam, and Trichosanthes k
4 Nicotiana, Capsicum, Datura, Trigonella, and Vigna, dicot genera that readily regenerate plants from
5 species of tribe Phaseoleae, i.e. Phaseolus, Vigna, Lablab and Psophocarpus, were investigated for in
7 ne proteinases (Phaseolus vulgaris EP-C1 and Vigna mungo SHEP) which are also involved in seed storag
9 e developmental gradients along a mung bean (Vigna radiata L.) hypocotyl of the growth rate, plasma m
10 were isolated from hypocotyls of mung bean (Vigna radiata L.), and pyrophosphate (PPi)- or ATP-depen
13 main and alternative pathways in mung bean (Vigna radiata) and soybean (Glycine max) following growt
15 e-angle x-ray scattering study of mung bean (Vigna radiata) primary cell walls was combined with publ
16 measuring phytic acid content in green gram (Vigna radiata) seeds was investigated by Fourier Transfo
18 abidopsis and from another plant, mung bean (Vigna radiata), to ascertain if this mechanism is common
20 reover, the de novo assembly of a tetraploid Vigna species (V. reflexo-pilosa var. glabra) provides g
24 of As in hydrated and fresh roots of cowpea (Vigna unguiculata 'Red Caloona') seedlings exposed to 4
25 nts Macroptilium atropurpureum (siratro) and Vigna unguiculata (cowpea) indicate that nolA is require
28 rmation of Zn in various tissues of cowpea ( Vigna unguiculata (L.) Walp.) exposed to ZnO-NPs or ZnCl
30 th limited genomic resources such as cowpea [Vigna unguiculata (L.) Walp.] (2n = 2x = 22), the use of
31 d sections of developing soybean and cowpea (Vigna unguiculata [L.] Walp) nodules revealed localizati
32 in the infected region of nodules of cowpea (Vigna unguiculata [L.] Walpers cv. Queen Anne Blackeye).
34 lerance during seedling emergence of cowpea (Vigna unguiculata L. Walp.) in an additive and independe
36 was validated using the purified recombinant Vigna unguiculata PLD, as well as the PLD from Streptomy
37 study we sought to identify QTLs in cowpea (Vigna unguiculata) consistent across experiments conduct
38 re examined within hydrated roots of cowpea (Vigna unguiculata) exposed to either 20 microM selenite
39 focuses on a diversity panel of 188 cowpea (Vigna unguiculata) genotypes to identify which traits ar
43 indirect perception of herbivory in cowpea (Vigna unguiculata) plants attacked by fall armyworm (Spo
45 h as beans (Phaseolus vulgaris) and cowpeas (Vigna unguiculata), differentiation into bacteroids, whi
47 ed peptides, originally described in cowpea (Vigna unguiculata), was limited even within the Fabaceae
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