Galactosyltransferase I is a gene responsible for progeroid variant of Ehlers-Danlos syndrome: molecular cloning and identification of mutations
- 11 September 2002
- journal article
- review article
- Published by Elsevier BV in Biochimica et Biophysica Acta (BBA) - General Subjects
- Vol. 1573 (3), 377-381
- https://doi.org/10.1016/s0304-4165(02)00406-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Biosynthesis of the Linkage Region of GlycosaminoglycansJournal of Biological Chemistry, 2001
- Molecular Cloning and Expression of Human UDP-d-Xylose:Proteoglycan Core Protein β-d-Xylosyltransferase and its First Isoform XT-IIJournal of Molecular Biology, 2000
- Cloning and Expression of a Proteoglycan UDP-Galactose:β-Xylose β1,4-Galactosyltransferase IJournal of Biological Chemistry, 1999
- Human Homolog of Caenorhabditis elegans sqv-3 Gene Is Galactosyltransferase I Involved in the Biosynthesis of the Glycosaminoglycan-Protein Linkage Region of ProteoglycansJournal of Biological Chemistry, 1999
- sqv mutants of Caenorhabditis elegans are defective in vulval epithelial invaginationProceedings of the National Academy of Sciences, 1999
- Three proteins involved in Caenorhabditis elegans vulval invagination are similar to components of a glycosylation pathwayProceedings of the National Academy of Sciences of the United States of America, 1999
- Molecular Cloning and Expression of Glucuronyltransferase I Involved in the Biosynthesis of the Glycosaminoglycan-Protein Linkage Region of ProteoglycansJournal of Biological Chemistry, 1998
- Developmental Regulation of Neural Response to FGF-1 and FGF-2 by Heparan Sulfate ProteoglycanScience, 1993
- The role of proteoglycans in cell adhesion, migration and proliferationCurrent Opinion in Cell Biology, 1992
- Identification of the full-length coding sequence for human galactosyltransferase (β-N-acetylglucosaminide: β1,4-galactosyltransferase)Biochemical and Biophysical Research Communications, 1988