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1 e form of galactosyl- and glucosylgalactosyl-hydroxylysine.
2 ase in hydroxylysine and glucosyl-galactosyl hydroxylysine.
3 ylation and subsequently by glycosylation of hydroxylysine.
4 w that a sulfilimine bond (-S=N-) crosslinks hydroxylysine-211 and methionine-93 of adjoining protome
5 xyproline (61-73 residues/1000 residues) and hydroxylysine (5-6 residues/1000 residues) and were iden
6 ng cancer by increasing the amount of stable hydroxylysine aldehyde-derived collagen cross-links (HLC
7 sues, tumor stroma contains higher levels of hydroxylysine aldehyde-derived collagen cross-links (HLC
8 ctivity and is critical for the formation of hydroxylysine-aldehyde derived intermolecular collagen c
10 y in folding and secretion and a decrease in hydroxylysine and glucosyl-galactosyl hydroxylysine.
11 esults indicate that the slight increases in hydroxylysine and hexose content observed occasionally i
15 The final Fmoc-protected (2S,5R)-6-azido-5-hydroxylysine derivative can be used in solid-phase pept
16 process and treated with copper sulfate and hydroxylysine, either alone or in combination, following
17 nal collagen-modifying enzyme possessing LH, hydroxylysine galactosyltransferase (GT), and galactosyl
18 ce of significant amounts of hydroxyproline, hydroxylysine, glycine, and carbohydrate suggesting the
19 cantly improved when a degree of theoretical hydroxylysine glycosylation was applied, showing for the
22 was no significant increase in the amount of hydroxylysine, hydroxyproline, or in the hydroxylysine-l
24 glycan structure Glc(alpha1-2)Gal linked to hydroxylysine in animals, the functional significance of
26 roline and/or the increased glycosylation of hydroxylysine in type I collagen disturbs the lateral gr
27 howed that glycosylation of non-cross-linked hydroxylysine is different from that involved in cross-l
28 of hydroxylysine, hydroxyproline, or in the hydroxylysine-linked glycoside glucosyl-galactose in the
30 lating glycine, proline, hydroxyproline, and hydroxylysine, peaking 1 h after the supplement was give
31 ommonly conjugated to a serine, threonine or hydroxylysine residue of the polypeptide, the chemical n
32 N) that covalently cross-link methionine and hydroxylysine residues at the interface of adjoining tri
34 oxidative deamination of peptidyl-lysine and hydroxylysine residues in collagens and lysine residues
35 yridinoline collagen crosslinks derived from hydroxylysine residues in the collagen telopeptide domai
36 limine bonds between opposing methionine and hydroxylysine residues to structurally reinforce the col
38 deamination of epsilon-amines of lysine and hydroxylysine residues within collagen and elastin, gene
43 ata elucidate the role of copper sulfate and hydroxylysine toward improving the biomechanical propert
44 ecursor to the modified amino acid (2S,5R)-5-hydroxylysine was developed on the basis of the use of a
46 edium with copper sulfate and the amino acid hydroxylysine would enhance the activity of lysyl oxidas
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