Mass spectrometry for congenital disorders of glycosylation, CDG
- 21 June 2006
- journal article
- review article
- Published by Elsevier BV in Journal of Chromatography B
- Vol. 838 (1), 3-8
- https://doi.org/10.1016/j.jchromb.2006.02.028
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporterBlood, 2005
- Hydrophilic Affinity Isolation and MALDI Multiple-Stage Tandem Mass Spectrometry of Glycopeptides for GlycoproteomicsAnalytical Chemistry, 2004
- Mass spectrometry of oligosaccharidesMass Spectrometry Reviews, 2004
- Apolipoprotein C-III Isofocusing in the Diagnosis of Genetic Defects in O-Glycan BiosynthesisClinical Chemistry, 2003
- Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiencyBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1999
- Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.Archives of Disease in Childhood, 1994
- Site-specific carbohydrate identification in recombinant proteins using MALD-TOF MSAnalytical Chemistry, 1993
- Electrospray Ionization for Mass Spectrometry of Large BiomoleculesScience, 1989
- Laser desorption ionization of proteins with molecular masses exceeding 10,000 daltonsAnalytical Chemistry, 1988
- Electrospray interface for liquid chromatographs and mass spectrometersAnalytical Chemistry, 1985