Metabolic manipulation of glycosylation disorders in humans and animal models
- 31 August 2010
- journal article
- review article
- Published by Elsevier BV in Seminars in Cell & Developmental Biology
- Vol. 21 (6), 655-662
- https://doi.org/10.1016/j.semcdb.2010.03.011
Abstract
No abstract availableKeywords
This publication has 69 references indexed in Scilit:
- Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type IbJournal of Medical Genetics, 2002
- Conditional control of selectin ligand expression and global fucosylation events in mice with a targeted mutation at the FX locusThe Journal of cell biology, 2002
- Sialylation is essential for early development in miceProceedings of the National Academy of Sciences of the United States of America, 2002
- Studies of mannose metabolism and effects of long-term mannose ingestion in the mouseBiochimica et Biophysica Acta (BBA) - General Subjects, 2001
- The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyNature Genetics, 2001
- Phosphomannose Isomerase Deficiency: A Carbohydrate-Deficient Glycoprotein Syndrome with Hepatic-Intestinal PresentationAmerican Journal of Human Genetics, 1998
- Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.JCI Insight, 1998
- A Bifunctional Enzyme Catalyzes the First Two Steps inN-Acetylneuraminic Acid Biosynthesis of Rat LiverPublished by Elsevier BV ,1997
- Human Fibroblasts Prefer Mannose over Glucose as a Source of Mannose for N-GlycosylationPublished by Elsevier BV ,1997
- Oral Ingestion of Mannose Elevates Blood Mannose Levels: A First Step toward a Potential Therapy for Carbohydrate-Deficient Glycoprotein Syndrome Type IBiochemical and Molecular Medicine, 1997