Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: Relationship to clinical severity and indications on the role of intracellular sulfate production

1998/10/01 by Antonio Rossi, Ilkka Kaitila, William R. Wilcox +5 · 53 citations
Biochemistry, Genetics and Molecular Biology · Chemistry · #Anatomy #Biochemistry #Biology #Cartilage #Chemistry #Chondroitin sulfate #Connective tissue disorders research #Disaccharide #Extracellular matrix #Genetics #Glucosamine #Glycosaminoglycan #Glycosylation and Glycoproteins Research #In vivo #Keratan sulfate #Proteoglycan #Proteoglycans and glycosaminoglycans research #Sulfation

paper · doi:10.1016/s0945-053x(98)90088-9

published in Matrix Biology 17(5), 361-369 (Elsevier BV)

crossref issued 1998/10/01 · crossref published 1998/10/01 · crossref published-print 1998/10/01 · openalex publication_date 1998/10/01 · crossref created 2002/10/17 · crossref deposited 2021/05/29 · openalex created_date 2025/10/10 · crossref indexed 2026/05/12 · openalex updated_date 2026/08/01

Citations

• Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene
• The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping

Cited by

• Multiple Roles of the SO42−/Cl−/OH− Exchanger Protein Slc26a2 in Chondrocyte Functions
• Homozygosity for a novel DTDST mutation in a child with a ‘broad bone‐platyspondylic’ variant of diastrophic dysplasia
• Physiological Roles and Regulation of Mammalian Sulfate Transporters
• A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia
• Autosomal recessive multiple epiphyseal dysplasia with homozygosity for C653S in the DTDST gene: Double‐layer patella as a reliable sign
• Sulfate transporter [wikipedia]