Results 81 to 90 of about 3,983 (152)
Alignment of the GLUT9 amino acids in the studied allelic variants with chimpanzee, horse, dog, mouse, rat and Xenopus paralogs.
Marketa Pavlikova (5660785) +5 more
core +1 more source
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2
Background: Elevated serum uric acid (UA) is associated with gout, hypertension, cardiovascular and renal disease. Hereditary renal hypouricemia type 1 (RHUC1) is caused by mutations in the renal tubular UA transporter URAT1 and can be complicated by ...
Sawyer, Lindsay +25 more
core +1 more source
Clove, the dried flower bud of Syzygium aromaticum, is a global spice used in various culinary traditions. In the present study, the antihyperuricemic (anti-HUA) effect of a clove water extract (CWE) and its mechanism were investigated using a ...
Fang Wang +14 more
doaj +1 more source
The strongest genetic marker of uric acid levels, the rs734553 SNP in the GLUT9 urate transporter gene, predicts progression to kidney failure in CKD patients and associates with systolic BP and carotid intima media thickness in family-based ...
Rizza, S. +25 more
core +1 more source
Background: Although the intestine substantially contributes to daily urate clearance, intestinal urate-lowering strategies remain limited, particularly interventions that coordinately regulate transport, barrier integrity, inflammation, and microbial ...
Mingyuan Fan +9 more
doaj +1 more source
Characterization of GLUT8 and GLUT9, two novel glucose transporter isoforms
Summary Prevalence of type 2 diabetes is increasing worldwide at alarming rates, probably secondarily to that of obesity. As type 2 diabetes is characterized by blood hyperglycemia, controlling glucose entry into tissues from the bloodstream is key to ...
Widmer, M.
core
Recurrent EIARF and PRES With Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation
Renal hypouricemia (RHU) is a hereditary disease that predisposes affected people to exercise-induced acute renal failure (EIARF). In most patients with RHU, the disorder is caused by loss-of-function mutations in SLC22A12 (solute carrier family 22 ...
Norishige Yoshikawa +8 more
core +1 more source
Background & Aims: Acetaminophen (APAP) overdose is the most common cause of drug-induced liver injury worldwide. Uric acid (UA) is involved in sterile inflammation in many organs, but its role in APAP-induced liver injury remains elusive.
Chenxi Tang +10 more
doaj +1 more source
Hyperuricemia (HUA), a metabolic disease caused by excessive production or decreased excretion of uric acid (UA), has been reported to be closely associated with a variety of UA transporters. Clerodendranthus spicatus (C.
Zheng Zhou +5 more
doaj +1 more source
OBJECTIVES:Hyperuricemia associates with hypertension, but it is uncertain whether this relationship is causal in nature. Glucose transporter 9 (GLUT9) gene is a major genetic determinant of plasma uric acid levels in humans.
Mallamaci Francesca +9 more
core +1 more source

