Related references
Note: Only part of the references are listed.Inhibitors of Human ABCG2: From Technical Background to Recent Updates With Clinical Implications
Yu Toyoda et al.
FRONTIERS IN PHARMACOLOGY (2019)
Identification of hepatic NPC1L1 as an NAFLD risk factor evidenced by ezetimibe-mediated steatosis prevention and
Yu Toyoda et al.
FASEB BIOADVANCES (2019)
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients
Blanka Stiburkova et al.
ARTHRITIS RESEARCH & THERAPY (2019)
An update on the genetics of hyperuricaemia and gout
Tanya J. Major et al.
NATURE REVIEWS RHEUMATOLOGY (2018)
Clinically relevant mutations in the ABCG2 transporter uncovered by genetic analysis linked to erythrocyte membrane protein expression
Boglarka Zambo et al.
SCIENTIFIC REPORTS (2018)
Identification of ABCG2 as an Exporter of Uremic Toxin Indoxyl Sulfate in Mice and as a Crucial Factor Influencing CKD Progression
T. Takada et al.
SCIENTIFIC REPORTS (2018)
Polymorphisms of the Multidrug Pump ABCG2: A Systematic Review of Their Effect on Protein Expression, Function, and Drug Pharmacokinetics
Niall Heyes et al.
DRUG METABOLISM AND DISPOSITION (2018)
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
Akiyoshi Nakayama et al.
ANNALS OF THE RHEUMATIC DISEASES (2017)
Identification of Febuxostat as a New Strong ABCG2 Inhibitor: Potential Applications and Risks in Clinical Situations
Hiroshi Miyata et al.
Frontiers in Pharmacology (2017)
Clinical and Molecular Evidence of ABCC11 Protein Expression in Axillary Apocrine Glands of Patients with Axillary Osmidrosis
Yu Toyoda et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2017)
Structure of the human multidrug transporter ABCG2
Nicholas M. I. . Taylor et al.
NATURE (2017)
Functional non-synonymous variants of ABCG2 and gout risk
Blanka Stiburkova et al.
RHEUMATOLOGY (2017)
Multiple common and rare variants of ABCG2 cause gout
Toshihide Higashino et al.
RMD OPEN (2017)
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes
Hirotaka Matsuo et al.
ANNALS OF THE RHEUMATIC DISEASES (2016)
Novel dysfunctional variant in ABCG2 as a cause of severe tophaceous gout: biochemical, molecular genetics and functional analysis
Blanka Stiburkova et al.
RHEUMATOLOGY (2016)
Regulation of the Axillary Osmidrosis-Associated ABCC11 Protein Stability by N-Linked Glycosylation: Effect of Glucose Condition
Yu Toyoda et al.
PLOS ONE (2016)
Halogenated hydrocarbon solvent-related cholangiocarcinoma risk: biliary excretion of glutathione conjugates of 1,2-dichloropropane evidenced by untargeted metabolomics analysis
Yu Toyoda et al.
SCIENTIFIC REPORTS (2016)
Identification of residues in ABCG2 affecting protein trafficking and drug transport, using co-evolutionary analysis of ABCG sequences
Ameena J. Haider et al.
BIOSCIENCE REPORTS (2015)
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese
Changgui Li et al.
NATURE COMMUNICATIONS (2015)
Ethnic Differences in ATP-binding Cassette Transporter, Sub-family G, Member 2 (ABCG2/BCRP): Genotype Combinations and Estimated Functions
Masayuki Sakiyama et al.
DRUG METABOLISM AND PHARMACOKINETICS (2014)
Complex Analysis of Urate Transporters SLC2A9, SLC22A12 and Functional Characterization of Non-Synonymous Allelic Variants of GLUT9 in the Czech Population: No Evidence of Effect on Hyperuricemia and Gout
Olha Hurba et al.
PLOS ONE (2014)
ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload
Hirotaka Matsuo et al.
SCIENTIFIC REPORTS (2014)
Common dysfunctional variants of ABCG2 have stronger impact on hyperuricemia progression than typical environmental risk factors
Akiyoshi Nakayama et al.
SCIENTIFIC REPORTS (2014)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Anna Koettgen et al.
NATURE GENETICS (2013)
Common dysfunctional variants in ABCG2 are a major cause of early-onset gout
Hirotaka Matsuo et al.
SCIENTIFIC REPORTS (2013)
Decreased extra-renal urate excretion is a common cause of hyperuricemia
Kimiyoshi Ichida et al.
NATURE COMMUNICATIONS (2012)
Ubiquitin-Mediated Proteasomal Degradation of ABC Transporters: a New Aspect of Genetic Polymorphisms and Clinical Impacts
Hiroshi Nakagawa et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2011)
Membrane transporters in drug development
Kathleen M. Giacomini et al.
NATURE REVIEWS DRUG DISCOVERY (2010)
ABCG2: A perspective
Robert W. Robey et al.
ADVANCED DRUG DELIVERY REVIEWS (2009)
Earwax, osmidrosis, and breast cancer: why does one SNP (538G > A) in the human ABC transporter ABCC11 gene determine earwax type?
Yu Toyoda et al.
FASEB JOURNAL (2009)
Disruption of N-linked glycosylation enhances ubiquitin-mediated proteasomal degradation of the human ATP-binding cassette transporter ABCG2
Hiroshi Nakagawa et al.
FEBS JOURNAL (2009)
Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout
Owen M. Woodward et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Common Defects of ABCG2, a High-Capacity Urate Exporter, Cause Gout: A Function-Based Genetic Analysis in a Japanese Population
Hirotaka Matsuo et al.
SCIENCE TRANSLATIONAL MEDICINE (2009)
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations
Melanie Kolz et al.
PLOS GENETICS (2009)
Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
Hirotaka Matsuo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
Abbas Dehghan et al.
LANCET (2008)
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout
Veronique Vitart et al.
NATURE GENETICS (2008)
SLC2A9 Is a High-Capacity Urate Transporter in Humans
Mark J. Caulfield et al.
PLOS MEDICINE (2008)
Functional analysis of SNPs variants of BCRP/ABCG2
C Kondo et al.
PHARMACEUTICAL RESEARCH (2004)
Molecular identification of a renal urate-anion exchanger that regulates blood urate levels
A Enomoto et al.
NATURE (2002)
TEXtopo:: shaded membrane protein topology plots in LATEX2ε
E Beitz
BIOINFORMATICS (2000)
Share Paper
