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1 monosaccharide components when treated with nasturtium beta-D-galactosidase, followed by alternation
3 with the highest sequence similarity to the nasturtium CSL gene, is coordinately expressed with othe
6 different sidechains of pea cell wall XG and nasturtium seed storage XG affect their binding to cellu
7 he enhanced ability of pea cell wall XG over nasturtium seed storage XG to associate with cellulose i
8 nalyses of SlXTH2, a Group 2 tomato XTH, and nasturtium seed TmXTH1 revealed a spectrum of modes of a
9 xyloglucan endo transglycosylase (tXET) and nasturtium seed xyloglucanase (nXGase) were produced het
10 nly one member of Group 3 has been reported: nasturtium TmXH1, which has a highly specialized functio
11 omogeneity from the cotyledons of germinated nasturtium (Tropaeolum majus L.) seedlings during the mo
14 DNA sequences were generated from developing nasturtium (Tropaeolum majus) seeds, which produce large
15 zyme had similar catalytic properties to the nasturtium (Tropaeolum majus) xyloglucanase1 responsible
16 ntially divergent from a previously isolated nasturtium XET (NXG1) expressed in germinating seed coty
17 r oligosaccharides representative of pea and nasturtium XG can adopt a hypothesized cellulose-binding
18 In contrast, the relatively low ability of nasturtium XG to bind cellulose is consistent with the n
23 D-galactosidase, followed by alternations of nasturtium xyloglucan-specific alpha-xylosidase and this
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