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1 of the reaction of human serum albumin with homocysteine thiolactone.
2 es results in the formation of the thioester homocysteine thiolactone.
3 results in formation of a cyclic thioester, homocysteine thiolactone.
4 me, edits homocysteine by converting it into homocysteine thiolactone.
5 ves of methionine is as fast as formation of homocysteine thiolactone.
6 d carboxyl group forming a cyclic thioester, homocysteine thiolactone.
7 d carboxyl group forming a cyclic thioester, homocysteine thiolactone.
8 nce at 240 nm, a maximum in a UV spectrum of homocysteine-thiolactone.
12 ther thiol-containing compounds, including l-homocysteine thiolactone and DTT, induced VEGF expressio
13 The metabolic conversion of homocysteine to homocysteine thiolactone and the reactivity of the thiol
14 sitive assay for the determination of plasma homocysteine-thiolactone and demonstrate its utility wit
15 ted directly with D,L-homocysteine or with L-homocysteine thiolactone, and a dose response was establ
16 ned product of the non-natural N-hexanoyl- l-homocysteine thiolactone at 1.3 A resolution is also det
21 ts in approximately 40% of survivors or with homocysteine thiolactone in combination with each of a s
24 ionine by methionine synthase), produce more homocysteine thiolactone, in addition to homocysteine, t
25 ation of rapid electrophoretic monitoring of homocysteine thiolactone-induced protein oligomerization
26 Substrate specificity studies suggest that homocysteine thiolactone is a likely natural substrate o
28 potentially harmful, the ability to detoxify homocysteine thiolactone is essential for biological int
35 ins by homocysteine and its cyclic congener, homocysteine thiolactone, is emerging as an area of grea
36 29 of the 60 human plasma samples analyzed, homocysteine-thiolactone levels were below the detection
37 ne hydrolase is not involved because neither homocysteine thiolactone nor an S-adenosylhomocysteine h
38 ic dose (200 mM D,L-homocysteine or 100 mM L-homocysteine thiolactone) on incubation days 0, 1, and 2
40 duced by the addition of homoserine lactone, homocysteine thiolactone, pyruvate, Casamino Acids, or a
45 ocess of neural tube closure with sufficient homocysteine thiolactone to induce NC and NT defects in
48 servations for the aminolysis of N-acetyl-dl-homocysteine thiolactone with n-butylamine in THF and CH
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