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 lyze the conversion of UDP-D-xylose to UDP-D-apiose.
2 selectively from di-O-isopropylidene-alpha-D-apiose.
3 discernible amounts of cell wall-associated apiose.
4 ermit insights into the mechanism by which d-apiose and other branched monosaccharides are formed.
5 n of UDP-d-glucuronate to a mixture of UDP-d-apiose and UDP-d-xylose with a turnover number of 0.3 mi
8 nts of aqueous methanol-acetonitrile-soluble apiose but did not result in discernible amounts of cell
13 to provide evidence that the ability to form apiose existed prior to the appearance of rhamnogalactur
17 ed that uridine 5'-diphospho-d-apiose (UDP-d-apiose) is formed from UDP-d-glucuronate by decarboxylat
19 r-bound galacturonate, xylose, arabinose and apiose residues (all produced via UDP-glucuronate) stemm
20 turonan-II (RG-II) via boron bridges between apiose residues is essential for normal plant growth and
24 have established that uridine 5'-diphospho-d-apiose (UDP-d-apiose) is formed from UDP-d-glucuronate b
27 estral enzyme of UDP-xylose synthase and UDP-apiose/UDP-xylose synthase was diverged to two distinct
30 etyl-protected phosphonate analogue of UDP-D-apiose was synthesized and used in an in situ HPLC assay
31 up d-[U-(14) C]apiose; therefore, exogenous apiose would block only apoplastic RG-II dimerization in