A Deficiency in Dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl α3-Glucosyltransferase Defines a New Subtype of Congenital Disorders of Glycosylation
Open Access
- 1 March 2003
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 278 (11), 9962-9971
- https://doi.org/10.1074/jbc.m211950200
Abstract
No abstract availableKeywords
This publication has 63 references indexed in Scilit:
- Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl MannosyltransferasePublished by Elsevier ,2002
- A strategy for disease gene identification through nonsense-mediated mRNA decay inhibitionNature Biotechnology, 2001
- Human Glycosylation Disorders and Sugar Supplement TherapyBiochemical and Biophysical Research Communications, 1999
- Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.Journal of Clinical Investigation, 1998
- Diseases of abnormal protein glycosylation: an emerging area.Journal of Clinical Investigation, 1998
- Phosphomannomutase deficiency is a cause of carbohydrate‐deficient glycoprotein syndrome type IFEBS Letters, 1995
- Growth-related coordinate regulation of the early N-glycosylation genes in yeastGlycobiology, 1994
- Reversible forskolin‐induced impairment of sucrase‐isomaltase mRNA levels, biosynthesis, and transport to the brush border membrane in Caco‐2 cellsJournal of Cellular Physiology, 1989
- A simple method for displaying the hydropathic character of a proteinJournal of Molecular Biology, 1982
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979