Results 11 to 20 of about 2,667 (184)
Clinical and functional characterization of URAT1 variants. [PDF]
Idiopathic renal hypouricaemia is an inherited form of hypouricaemia, associated with abnormal renal handling of uric acid. There is excessive urinary wasting of uric acid resulting in hypouricaemia.
Velibor Tasic +8 more
doaj +6 more sources
Molecular basis of the urate transporter URAT1 inhibition by gout drugs
Hyperuricemia is a condition when uric acid, a waste product of purine metabolism, accumulates in the blood. Untreated hyperuricemia can lead to crystal formation of monosodium urate in the joints, causing a painful inflammatory disease known as gout ...
Yang Suo +10 more
doaj +5 more sources
Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1 [PDF]
Objectives Human urate transporter 1 (URAT1) is a member of the organic anion transporter family (SLC22A12) that primarily regulates the renal tubular reabsorption of uric acid. This case–control study was designed to analyse whether hURAT1 might also be a candidate gene for hyperuricaemia or hypouricaemia.
Cho, Sung Kweon +3 more
openaire +5 more sources
The relationship of uric acid with macrophages has not been fully elucidated. We investigated the effect of uric acid on the proinflammatory ability of human macrophages and then examined the possible molecular mechanism involved. Primary human monocytes
Camilo P. Martínez-Reyes +8 more
doaj +2 more sources
Gout is caused by elevated serum urate levels, which can be treated using inhibitors of the uric acid transporter, URAT1. Here, we characterize verinurad (RDEA3170), which is currently under evaluation for gout therapy.
Philip K. Tan +3 more
doaj +2 more sources
Molecular mechanism of drug inhibition of URAT1
Hyperuricemia, characterized by elevated serum urate levels, is a key factor in the pathogenesis of gout. URAT1 is essential for renal urate reabsorption and has emerged as a critical therapeutic target for managing hyperuricemia.
Zhuoya Yu +12 more
doaj +3 more sources
This work aimed to investigate the effect of fucoidan (FPS) on urate transporters induced by uric acid (UA). The results showed that UA stimulated the expression of glucose transporter 9 (GLUT9) and urate transporter 1 (URAT1) in HK-2 cells, and FPS ...
Yu Zhang +8 more
doaj +2 more sources
URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews [PDF]
Hereditary renal hypouricemia may be complicated by nephrolithiasis or exercise-induced acute renal failure. Most patients described so far are of Japanese origin and carry the truncating mutation W258X in the uric acid transporter URAT1 encoded by SLC22A12. Recently, we described severe renal hypouricemia in Israeli patients with uric acid transporter
Dinour, Dganit +10 more
openaire +4 more sources
Objective Previous studies have revealed associations between hyperuricemia and microvascular diseases, but the association between hyperuricemia and abdominal aortic aneurysm (AAA) remains unclear. The aim of this study was to elucidate the pathogenesis
Jen-Chun Wang +4 more
doaj +2 more sources
Effects of Osthol Isolated from Cnidium monnieri Fruit on Urate Transporter 1
(1) Background: Crude drugs used in traditional Japanese Kampo medicine or folk medicine are major sources of new chemical entities for drug discovery.
Yuusuke Tashiro +7 more
doaj +2 more sources

