A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis

This publication has 39 references indexed in Scilit:

• Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig
  Biochemical Journal, 2002
• Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase
  Published by Elsevier ,2002
• Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
  Journal of Clinical Investigation, 2002
• Intracellular Functions of N-Linked Glycans
  Science, 2001
• Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.
  Journal of Clinical Investigation, 1998
• Phosphomannomutase deficiency is a cause of carbohydrate‐deficient glycoprotein syndrome type I
  FEBS Letters, 1995
• SUC1 and SUC2: two sucrose transporters from Arabidopsis thaliana; expression and characterization in baker's yeast and identification of the histidine‐tagged protein
  The Plant Journal, 1994
• The N‐oligosaccharyltransferase complex from yeast
  FEBS Letters, 1994
• Biosynthesis of asparagine-linked oligosaccharides in Saccharomyces cerevisiae: the alg2 mutation
  Glycobiology, 1993
• Solubilization and Characterization of the Initial Enzymes of the Dolichol Pathway from Yeast
  European Journal of Biochemistry, 1982