Protein localization of SLC26A2 (DTDST) in rat kidney

2010/04/06 by Jeannie M. Chapman, Lawrence P. Karniski · 3 citations
Biochemistry, Genetics and Molecular Biology · Chemistry · Medicine · Neuroscience · #Apical membrane #Biochemistry #Biology #Cell biology #Chemistry #Distal convoluted tubule #Endocrinology #Ion Transport and Channel Regulation #Kidney #Membrane #Membrane protein #Microvillus #Molecular biology #Neonatal Health and Biochemistry #Nephron #Neuroscience of respiration and sleep #Transport protein #Tubule #Western blot

paper · doi:10.1007/s00418-010-0694-x

crossref issued 2010/04/06 · crossref published 2010/04/06 · crossref published-online 2010/04/06 · openalex publication_date 2010/04/06 · crossref created 2010/04/07 · crossref published-print 2010/05/01 · crossref deposited 2019/05/28 · openalex created_date 2025/10/10 · crossref indexed 2026/05/08 · openalex updated_date 2026/07/23

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
• A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype
• Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells

Cited by

• Solute Carrier Family 26 Member a2 (Slc26a2) Protein Functions as an Electroneutral SO42−/OH−/Cl− Exchanger Regulated by Extracellular Cl−
• Multiple Roles of the SO42−/Cl−/OH− Exchanger Protein Slc26a2 in Chondrocyte Functions
• Regulated transport of sulfate and oxalate by SLC26A2/DTDST
• Sulfate transporter [wikipedia]