Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lidia I. Stoykova"'
Autor:
Lidia I. Stoykova, Thomas Scanlin
Publikováno v:
Current Organic Chemistry. 12:900-910
Publikováno v:
Current Organic Chemistry. 8:385-394
Activity of fucosyltransferases and altered glycosylation in cystic fibrosis airway epithelial cells
Publikováno v:
Biochimie. 83:743-747
Cystic fibrosis (CF) glycoconjugates have a glycosylation phenotype of increased fucosylation and/or decreased sialylation when compared with non-CF. A major increase in fucosyl residues linked alpha 1,3 to antennary GlcNAc was observed when surface
Publikováno v:
Journal of Neuroscience Research. 66:497-505
As oligodendrocytes mature they progress through a series of distinct differentiation steps characterized by the expression of specific markers. One such marker, polysialic acid found on the neural cell adhesion molecule (NCAM), is detected by antibo
Publikováno v:
European Journal of Biochemistry. 225:159-166
Terminal glycosylation may be a mechanism to control the function of specific biologically active glycoproteins. The biosynthesis of terminal sialyl and fucosyl residues on certain glycoproteins has been linked to the expression of the respective gly
Publikováno v:
Comparative Biochemistry and Physiology Part B: Comparative Biochemistry. 98:397-402
1. 1. The liver tissue from nine species of amphibians, reptiles and birds were tested for dolichol concentration and isoprenologue distribution of dolichol family by high-performance liquid chromatography. In the case of chicken ( Gallus domesticus
Publikováno v:
Biochimie. 85(3-4)
Cystic fibrosis (CF) has a glycophenotype of aberrant sialylation and/or fucosylation. The CF glycophenotype is expressed on membrane glycoconjugates of CF airway epithelial cells as increased fucosyl residues in alpha1,3/4 linkage to N-acetyl glucos
Autor:
Arvind J. Trindade, Mary Catherine Glick, Lidia I. Stoykova, Thomas F. Scanlin, Andrew D. Rhim
Publikováno v:
Journal of Cystic Fibrosis. :95-96
Altered terminal glycosylation, with increased fucosylation and decreased sialylation, is a hallmark of the cystic fibrosis (CF) glycosylation phenotype. The glycosylation phenotype of CF airway epithelial cells has been modulated by the expression o