Associated Papers
A genome-wide association analysis reveals new pathogenic pathways in gout.
Major TJ et al.
Nature Genetics, 2024
Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families.
Hebbar P et al.
Scientific Reports, 2023
Effects of genetic and nongenetic factors on hyperuricemia in Chinese patients with coronary artery disease.
Zhang W et al.
Pharmacogenomics, 2021
The genetics of hyperuricaemia and gout.
Reginato AM et al.
Nature Reviews. Rheumatology, 2012
Apical voltage-driven urate efflux transporter NPT4 in renal proximal tubule.
Jutabha P et al.
Nucleosides, Nucleotides & Nucleic Acids, 2011
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations.
Zhang G et al.
Human Genomics, 2011
Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia.
Stiburkova B et al.
Molecular Genetics and Metabolism, 2011
Functional analysis of human sodium-phosphate transporter 4 (NPT4/SLC17A3) polymorphisms.
Jutabha P et al.
Journal of Pharmacological Sciences, 2011
Functional Analysis of Human Sodium-Phosphate Transporter 4 (NPT4/SLC17A3) Polymorphisms.
Jutabha P et al.
Journal of Pharmacological Sciences, 2011
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