Functional polymorphisms of the ABCG2 gene are associated with gout disease in the Chinese Han male population (Q33755969)

29 July 2017

title

Functional polymorphisms of the ABCG2 gene are associated with gout disease in the Chinese Han male population (English)

1 reference

29 July 2017

Danqiu Zhou

1

1 reference

29 July 2017

Yunqing Liu

2

1 reference

29 July 2017

Xinju Zhang

3

1 reference

29 July 2017

Xiaoye Gu

4

1 reference

29 July 2017

Hua Wang

5

1 reference

29 July 2017

Xinhua Luo

6

1 reference

29 July 2017

Jin Zhang

7

1 reference

29 July 2017

Hejian Zou

8

1 reference

29 July 2017

Ming Guan

9

1 reference

29 July 2017

language of work or name

English

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publication date

22 May 2014

1 reference

International Journal of Molecular Sciences

29 July 2017

published in

1 reference

29 July 2017

volume

15

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29 July 2017

issue

5

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29 July 2017

page(s)

9149-9159

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

22 May 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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

21 June 2018

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Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study

21 June 2018

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Gout-causing Q141K mutation in ABCG2 leads to instability of the nucleotide-binding domain and can be corrected with small molecules

21 June 2018

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Polymorphisms in the presumptive promoter region of the SLC2A9 gene are associated with gout in a Chinese male population

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

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

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The effect of ABCG2 V12M, Q141K and Q126X, known functional variants in vitro, on the disposition of lamivudine

21 June 2018

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21 June 2018

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21 June 2018

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Single nucleotide polymorphisms result in impaired membrane localization and reduced atpase activity in multidrug transporter ABCG2.

21 January 2018

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https://api.crossref.org/works/10.3390%2FIJMS15059149

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

21 January 2018

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https://api.crossref.org/works/10.3390%2FIJMS15059149

Urate transport across the apical membrane of renal proximal tubules

21 January 2018

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https://api.crossref.org/works/10.3390%2FIJMS15059149

Association of an intronic SNP of SLC2A9 gene with serum uric acid levels in the Chinese male Han population by high-resolution melting method

21 January 2018

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https://api.crossref.org/works/10.3390%2FIJMS15059149

High-resolution melting analysis for the rapid detection of an intronic single nucleotide polymorphism in SLC22A12 in male patients with primary gout in China

21 January 2018

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Eight novel single nucleotide polymorphisms in ABCG2/BCRP in Japanese cancer patients administered irinotacan

21 January 2018

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https://api.crossref.org/works/10.3390%2FIJMS15059149

Functional assessment of ABCG2 (BCRP) gene polymorphisms to protein expression in human placenta.

21 January 2018

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Gout in ambulatory care settings in the United States

21 January 2018

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Sex differences in uric acid and risk factors for coronary artery disease

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24857923

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24857923

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of gout and hyperuricemia in the US general population: the National Health and Nutrition Examination Survey 2007-2008

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24857923

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3390/IJMS15059149

1 reference

29 July 2017

1 reference

29 July 2017

1 reference