Functional non-synonymous variants of ABCG2 and gout risk

Genetic background of uric acid metabolism in a patient with severe chronic tophaceous gout

(2016) Lenka Petru et al.   CLINICA CHIMICA ACTA

Severe tophaceous gout and disability: changes in the past 15 years

(2016) Carlos Omar López López et al.   CLINICAL RHEUMATOLOGY

Jump into a New Fold—A Homology Based Model for the ABCG2/BCRP Multidrug Transporter

(2016) Laura László et al.   PLoS One

Replication of association of the apolipoprotein A1-C3-A4 gene cluster with the risk of gout

(2016) Humaira Rasheed et al.   RHEUMATOLOGY

Hyperuricemia in acute gastroenteritis is caused by decreased urate excretion via ABCG2

(2016) Hirotaka Matsuo et al.   Scientific Reports

The Molecular Physiology of Uric Acid Homeostasis

(2015) Asim K. Mandal et al.   Annual Review of Physiology

Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response

(2015) CC Wen et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Novel dysfunctional variant inABCG2as a cause of severe tophaceous gout: biochemical, molecular genetics and functional analysis

(2015) Blanka Stiburkova et al.   RHEUMATOLOGY

Functional Polymorphisms of the ABCG2 Gene Are Associated with Gout Disease in the Chinese Han Male Population

(2014) Danqiu Zhou et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Joint Effects of Alcohol Consumption and ABCG2 Q141K on Chronic Tophaceous Gout Risk

(2014) H.-P. Tu et al.   JOURNAL OF RHEUMATOLOGY

ABCG2 Dysfunction Increases Serum Uric Acid by Decreased Intestinal Urate Excretion

(2014) Tappei Takada et al.   NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS

Metabolic Syndrome, Alcohol Consumption and Genetic Factors Are Associated with Serum Uric Acid Concentration

(2014) Blanka Stibůrková et al.   PLoS One

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

(2013) Hirotaka Matsuo et al.   Scientific Reports

Effects of the lipid environment, cholesterol and bile acids on the function of the purified and reconstituted human ABCG2 protein

(2012) Ágnes Telbisz et al.   BIOCHEMICAL JOURNAL

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

(2012) Kimiyoshi Ichida et al.   Nature Communications

Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I

(2011) Blanka Stiburkova et al.   CLINICA CHIMICA ACTA

Frequency and risk factors of gout flares in a large population-based cohort of incident gout

(2011) D. Rothenbacher et al.   RHEUMATOLOGY

A strong role for the ABCG2 gene in susceptibility to gout in New Zealand Pacific Island and Caucasian, but not Māori, case and control sample sets

(2010) Amanda J. Phipps-Green et al.   HUMAN MOLECULAR GENETICS

The rs2231142 variant of the ABCG2 gene is associated with uric acid levels and gout among Japanese people

(2010) K. Yamagishi et al.   RHEUMATOLOGY

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

(2009) O. M. Woodward et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

(2009) Melanie Kolz et al.   PLoS Genetics

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

(2008) Abbas Dehghan et al.   LANCET