A 'complexity' of urate transporters (Q37770954)

22 August 2017

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title

A 'complexity' of urate transporters (English)

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22 August 2017

2

Igor Rudan

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Harry Campbell

series ordinal

4

object named as

Harry Campbell

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22 August 2017

Alan F Wright

1

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PubMed ID

20613716

22 August 2017

Nicholas D Hastie

series ordinal

3

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PubMed ID

20613716

22 August 2017

language of work or name

English

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publication date

7 July 2010

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22 August 2017

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22 August 2017

78

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22 August 2017

5

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22 August 2017

446-452

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https://scigraph.springernature.com/pub.10.1038/ki.2010.206

22 August 2017

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cites work

Recent developments in our understanding of the renal basis of hyperuricemia and the development of novel antihyperuricemic therapeutics

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7 January 2021

Uric acid, evolution and primitive cultures

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Lessons from comparative physiology: could uric acid represent a physiologic alarm signal gone awry in western society?

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Molecular identification of a renal urate anion exchanger that regulates blood urate levels

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7 January 2021

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

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7 January 2021

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

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7 January 2021

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects

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7 January 2021

The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review)

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7 January 2021

SLC2A9 is a high-capacity urate transporter in humans

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7 January 2021

Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans

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7 January 2021

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia

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Mouse GLUT9: evidences for a urate uniporter.

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Solute carrier family 2, member 9 and uric acid homeostasis

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Identification and characterization of human glucose transporter-like protein-9 (GLUT9): alternative splicing alters trafficking.

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Mutations in the SLC2A9 gene cause hyperuricosuria and hyperuricemia in the dog

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7 January 2021

Glut9 is a major regulator of urate homeostasis and its genetic inactivation induces hyperuricosuria and urate nephropathy

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Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

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7 January 2021

Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout

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Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population

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Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

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p-aminohippuric acid transport at renal apical membrane mediated by human inorganic phosphate transporter NPT1.

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New insights into renal transport of urate.

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Relationship between resistance to insulin-mediated glucose uptake, urinary uric acid clearance, and plasma uric acid concentration.

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The multivalent PDZ domain-containing protein PDZK1 regulates transport activity of renal urate-anion exchanger URAT1 via its C terminus

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7 January 2021

Uric acid and serum antioxidant capacity: a reaction to atherosclerosis?

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Uric acid: the oxidant-antioxidant paradox

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Adverse effects of the classic antioxidant uric acid in adipocytes: NADPH oxidase-mediated oxidative/nitrosative stress

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7 January 2021

Uric acid and cardiovascular risk

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7 January 2021

Molecular identification of a danger signal that alerts the immune system to dying cells

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7 January 2021

Gout-associated uric acid crystals activate the NALP3 inflammasome

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The inflammasomes: guardians of the body

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Uric acid: a novel mediator and marker of risk in chronic kidney disease?

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7 January 2021

Hyperuricemia and associated diseases

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Prevalence of the metabolic syndrome in individuals with hyperuricemia

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7 January 2021

Serum concentrations of uric acid and the metabolic syndrome among US children and adolescents

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7 January 2021

The conundrum of hyperuricemia, metabolic syndrome, and renal disease.

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7 January 2021

A role for uric acid in the progression of renal disease

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7 January 2021

Homozygous SLC2A9 mutations cause severe renal hypouricemia

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7 January 2021

Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum

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7 January 2021

Tamm-Horsfall glycoprotein: biology and clinical relevance

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Ins and outs of major facilitator superfamily antiporters.

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7 January 2021

Case of anakinra as a steroid-sparing agent for gout inflammation

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7 January 2021

Febuxostat compared with allopurinol in patients with hyperuricemia and gout

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7 January 2021

What lies behind serum urate concentration? Insights from genetic and genomic studies

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7 January 2021

Identifiers

DOI

10.1038/KI.2010.206

1 reference

22 August 2017

1 reference

PubMed ID

20613716