(Q43995070)

28 November 2017

NPT1/SLC17A1 is a renal urate exporter in humans and its common gain-of-function variant decreases the risk of renal underexcretion gout (English)

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28 November 2017

7

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28 November 2017

13

Mariko Naito

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28 November 2017

Toshinori Chiba

1

1 reference

28 November 2017

Hirotaka Matsuo

2

1 reference

28 November 2017

Yusuke Kawamura

3

1 reference

28 November 2017

Shushi Nagamori

4

1 reference

28 November 2017

Takashi Nishiyama

5

1 reference

28 November 2017

Ling Wei

6

1 reference

28 November 2017

Takahiro Nakamura

8

1 reference

28 November 2017

Masayuki Sakiyama

9

1 reference

28 November 2017

Tappei Takada

10

1 reference

28 November 2017

Yutaka Taketani

11

1 reference

28 November 2017

Shino Suma

12

1 reference

28 November 2017

Takashi Oda

14

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28 November 2017

Hiroo Kumagai

15

1 reference

28 November 2017

Yoshinori Moriyama

16

1 reference

28 November 2017

Kimiyoshi Ichida

17

1 reference

28 November 2017

Toru Shimizu

18

1 reference

28 November 2017

Yoshikatsu Kanai

19

1 reference

28 November 2017

Nariyoshi Shinomiya

20

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28 November 2017

language of work or name

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1 January 2015

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28 November 2017

Arthritis & Rheumatology

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28 November 2017

67

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28 November 2017

1

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28 November 2017

281-287

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Decreased extra-renal urate excretion is a common cause of hyperuricemia

28 November 2017

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Type 1 sodium-dependent phosphate transporter (SLC17A1 Protein) is a Cl(-)-dependent urate exporter

21 January 2018

1 reference

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

21 January 2018

1 reference

Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease

21 January 2018

1 reference

Sodium-dependent phosphate cotransporter type 1 sequence polymorphisms in male patients with gout.

21 January 2018

1 reference

Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

21 January 2018

1 reference

The renal urate transporter SLC17A1 locus: confirmation of association with gout

21 January 2018

1 reference

Preliminary criteria for the classification of the acute arthritis of primary gout

21 January 2018

1 reference

Uric Acid Excretion: Quantitative Assessment from Spot, Midmorning Serum and Urine Samples

21 January 2018

1 reference

A proposal for identifying the low renal uric acid clearance phenotype

21 January 2018

1 reference

Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2q.

21 January 2018

1 reference

Common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility

21 January 2018

1 reference

Common dysfunctional variants in ABCG2 are a major cause of early-onset gout

21 January 2018

1 reference

Common dysfunctional variants of ABCG2 have stronger impact on hyperuricemia progression than typical environmental risk factors

21 January 2018

1 reference

Identification of a novel Na+-independent acidic amino acid transporter with structural similarity to the member of a heterodimeric amino acid transporter family associated with unknown heavy chains

21 January 2018

1 reference

Transport properties of a system y+L neutral and basic amino acid transporter. Insights into the mechanisms of substrate recognition.

21 January 2018

1 reference

High affinity D- and L-serine transporter Asc-1: cloning and dendritic localization in the rat cerebral and cerebellar cortices

21 January 2018

1 reference

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia

21 January 2018

1 reference

Homozygous SLC2A9 mutations cause severe renal hypouricemia

21 January 2018

1 reference

Pathogenic GLUT9 mutations causing renal hypouricemia type 2 (RHUC2).

21 January 2018

1 reference

Population structure and eigenanalysis

21 January 2018

1 reference

Principal components analysis corrects for stratification in genome-wide association studies

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ART.38884

1 reference

28 November 2017

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