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1 sence or presence of a methyl group at the 4-amino nitrogen.
2 n active site potassium ion with the epsilon-amino nitrogen.
3 rance and suppress oxidation of BBT at the 1-amino nitrogen.
4 starch liquefaction time and increased free amino nitrogen.
5 ble nitrogen, viscosity, friability and free-amino nitrogen.
6 inding the oxazolidines together at their 3'-amino nitrogens.
7 ises from slow on-off proton exchange of the amino nitrogen, a process influenced by solution tempera
8 an index of collagen accumulation) and alpha-amino nitrogen (alpha-AN, mmol/cm, an index of total pro
9 In each polypeptide chain, the free alpha-amino nitrogen and carbonyl oxygen of the amino-terminal
10 nally, the internuclear distance between the amino nitrogens and the extent of modulation of basal [3
13 Hg(II) with two thioether sulfur atoms, two amino nitrogen atoms, and a phenol oxygen atom arranged
14 utylsalicylidenimine) chelate built onto two amino nitrogens attached to the pz periphery; R is a sol
16 f reducing sugars, ethanol, acetic acid, and amino nitrogen did not differ significantly (p<0.05) bet
19 ing their synthesis, a broad spectrum of the amino nitrogen is actively loaded into the phloem of lea
20 icyclo[3.2.1]octanes and demonstrate that an amino nitrogen is not required for binding to the DAT.
21 SAM and orient the lone pair orbital on the amino nitrogen (N) of Gly toward the donor methyl group
22 vy atom isotope effects at C-2, C-3, and the amino nitrogen of aspartate were determined for the reac
23 An (15)N R1rho NMR experiment targeting the amino nitrogen of guanine (dG-N2) provides direct eviden
27 opy with selective 15N-labeling of exocyclic amino nitrogens on bases of interest, we are able to res
33 re found to form more readily with secondary amino nitrogens than primary amino nitrogens tethered to
35 e accessibility for formaldehyde of cytosine amino nitrogens within WC base pairs adjacent to HG base
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