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1 ophenyl ring whose 5-substituent is N-methyl-p-aminobenzoic acid).
2 zed poly(3,4-ethylenedioxythiopene) and poly(p-aminobenzoic acid).
3                          With [3H]benzidine, p-aminobenzoic acid, a NAT1-specific substrate, increase
4                    After derivatisation with p-aminobenzoic acid and sodium cyanoborohydride, the sam
5 human NAT1 acetylates the sunscreen additive p-aminobenzoic acid and tobacco smoke carcinogen 4-amino
6  immobilized with the carboxyl group of poly(p-aminobenzoic acid) and served as the probe, a target D
7                                              p-Aminobenzoic acid beta-D-glucopyranosyl ester esterase
8 s and other nutrients (inositol, adenine, or p-aminobenzoic acid) in the transformation medium to dev
9 phosphate, N-acetyl glucosamine, putrescine, p-aminobenzoic acid, L-cysteine and L-glutamine, and hor
10 rotonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methyl ester (PABAOMe) occurs at the
11 s that creates a specific binding pocket for p-aminobenzoic acid, one of the two DHPS substrates.
12 he assay medium, by predepositing N-biotinyl-p-aminobenzoic acid onto the standard sample collection
13  folate methanopterin is the condensation of p-aminobenzoic acid (pAB) and 5-phospho-alpha-D-ribosyl-
14 tead of an N-riboside in the condensation of p-aminobenzoic acid (pABA) and 5-phospho-alpha-D-ribosyl
15                               Protonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methy
16 endent behavior of the zwitterionic molecule p-aminobenzoic acid (PABA) at a Ag(111) electrode surfac
17 on the observation that exogenously supplied p-aminobenzoic acid (PABA) can antagonize the action of
18 lasmodia species, unlike humans, can utilize p-aminobenzoic acid (PABA) for the de novo generation of
19 starter unit p-nitrobenzoic acid (pNBA) from p-aminobenzoic acid (pABA) in the biosynthesis of antibi
20  0.22 nM, indicating that replacement of the p-aminobenzoic acid (pABA) moiety does not diminish cyto
21 nthesis of aromatic amino acids (AroAAs) and p-aminobenzoic acid (PABA) was demonstrated in M. maripa
22 uctural analog and competitive antagonist to p-aminobenzoic acid (PABA), which is a precursor of fola
23 ically active v-tPA, which in turn cleaves a p-aminobenzoic acid (PABA)-peptide adduct to release fre
24     Studies revealed that PABA/NO's N-methyl-p-aminobenzoic acid substituent is bound to the dinitrob
25 osides, including a compound that features a p-aminobenzoic acid subunit.
26 3-1.71 g S/d) and 0.17-0.27 g inorganic S/d; p-aminobenzoic acid-validated 24-h urine samples (n = 47
27 in biosynthesis, namely, the condensation of p-aminobenzoic acid with phosphoribosylpyrophosphate to

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