SLC2A9 gene

Known as: SLC2A9, solute carrier family 2 member 9, urate voltage-driven efflux transporter 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2018
0102020002018

Papers overview

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2011
2011
Renal hypouricemia is a heterogeneous inherited disorder characterized by impaired uric acid handling in the renal tubules… (More)
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2010
2010
Hereditary hypouricemia may result from mutations in the renal tubular uric acid transporter URAT1. Whether mutation of other… (More)
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Highly Cited
2008
Highly Cited
2008
Renal hypouricemia is an inherited disorder characterized by impaired renal urate (uric acid) reabsorption and subsequent low… (More)
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Highly Cited
2008
Highly Cited
2008
Uric acid is the end product of purine metabolism in humans and great apes, which have lost hepatic uricase activity, leading to… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Serum uric acid levels in humans are influenced by diet, cellular breakdown, and renal elimination, and correlate with… (More)
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Highly Cited
2008
Highly Cited
2008
Hyperuricemia is a significant factor in a variety of diseases, including gout and cardiovascular diseases. Although renal… (More)
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Highly Cited
2008
Highly Cited
2008
Many common diseases are accompanied by disturbances in biochemical traits. Identifying the genetic determinants could provide… (More)
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Highly Cited
2008
Highly Cited
2008
Genetically encoded FRET glucose nanosensors have proven to be useful for imaging glucose flux in HepG2 cells. However, the… (More)
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Highly Cited
2007
Highly Cited
2007
High serum uric acid levels elevate pro-inflammatory-state gout crystal arthropathy and place individuals at high risk for… (More)
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Highly Cited
2004
Highly Cited
2004
The recently cloned human GLUT9 gene, which maps to chromosome 4p15.3-p16, consists of 12 exons coding for a 540-amino acid… (More)
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