Associated Papers
Investigation of rs11568476 Polymorphism in the SLC13A2 Gene in Turkish Patients with Hypocitraturia and Calcium-Containing Kidney Stones.
Başaran E et al.
Biomedicines, 2025
Cryo-EM structures of the human NaS1 and NaDC1 transporters revealed the elevator transport and allosteric regulation mechanism.
Chi X et al.
Science Advances, 2024
Genetic polymorphisms as prognostic factors for recurrent kidney stones: A systematic review and meta-analysis.
Atmoko W et al.
Plos One, 2021
rs11567842 SNP in SLC13A2 gene associates with hypocitraturia in Thai patients with nephrolithiasis.
Udomsilp P et al.
Genes & Genomics, 2018
Evidence for epistatic interaction between VDR and SLC13A2 genes in the pathogenesis of hypocitraturia in recurrent calcium oxalate stone formers.
Rendina D et al.
Journal of Nephrology, 2017
Single nucleotide polymorphisms in the human Na+-dicarboxylate cotransporter affect transport activity and protein expression.
Pajor AM et al.
American Journal of Physiology. Renal Physiology, 2010
Associations between renal sodium-citrate cotransporter (hNaDC-1) gene polymorphism and urinary citrate excretion in recurrent renal calcium stone formers and normal controls.
Okamoto N et al.
International Journal of Urology : Official Journal of the Japanese Urological Association, 2007
Polymorphisms in the human homologue of the drosophila Indy (I'm not dead yet) gene.
Lee P et al.
Mechanisms of Ageing and Development, 0
SLC13 family of Na⁺-coupled di- and tri-carboxylate/sulfate transporters.
Bergeron MJ et al.
Molecular Aspects of Medicine, 0
Select a paper to view details