Related references
Note: Only part of the references are listed.Elevated serum uric acid in nondiabetic people mark pro-inflammatory state and HDL dysfunction and independently predicts coronary disease
Altan Onat et al.
CLINICAL RHEUMATOLOGY (2013)
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis
Blanka Stiburkova et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Changes in Serum Urate and Urate Excretion With Age
Blanka Stiburkova et al.
ADVANCES IN CHRONIC KIDNEY DISEASE (2012)
Genome-Wide Association of Serum Uric Acid Concentration: Replication of Sequence Variants in an Island Population of the Adriatic Coast of Croatia
Rebekah Karns et al.
ANNALS OF HUMAN GENETICS (2012)
Uric acid level as a risk marker for metabolic syndrome: A Chinese cohort study
Tsan Yang et al.
ATHEROSCLEROSIS (2012)
Alcohol intake and the risk of hyperuricaemia: A 6-year prospective study in Japanese men
K. Nakamura et al.
NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES (2012)
Uric Acid Is More Strongly Associated with Impaired Glucose Regulation in Women than in Men from the General Population: The KORA F4-Study
Christa Meisinger et al.
PLOS ONE (2012)
Acute kidney injury in two children caused by renal hypouricaemia type 2
Blanka Stiburkova et al.
PEDIATRIC NEPHROLOGY (2012)
Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia
Blanka Stiburkova et al.
MOLECULAR GENETICS AND METABOLISM (2011)
The SLC2A9 nonsynonymous Arg265His variant and gout: evidence for a population-specific effect on severity
Jade E. Hollis-Moffatt et al.
ARTHRITIS RESEARCH & THERAPY (2011)
Associations of a non-synonymous variant in SLC2A9 with gouty arthritis and uric acid levels in Han Chinese subjects and Solomon Islanders
Hung-Pin Tu et al.
ANNALS OF THE RHEUMATIC DISEASES (2010)
Association between GLUT9 and gout in Japanese men
Wako Urano et al.
ANNALS OF THE RHEUMATIC DISEASES (2010)
Variation in the uric acid transporter gene (SLC2A9) and memory performance
Lorna M. Houlihan et al.
HUMAN MOLECULAR GENETICS (2010)
A strong role for the ABCG2 gene in susceptibility to gout in New Zealand Pacific Island and Caucasian, but not M(a)over-barori, case and control sample sets
Amanda J. Phipps-Green et al.
HUMAN MOLECULAR GENETICS (2010)
The rs2231142 variant of the ABCG2 gene is associated with uric acid levels and gout among Japanese people
Kazumasa Yamagishi et al.
RHEUMATOLOGY (2010)
Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity
K. G. M. M. Alberti et al.
CIRCULATION (2009)
Significant association between methylenetetrahydrofolate reductase 677T allele and hyperuricemia among adult Japanese subjects
Simon Itou et al.
NUTRITION RESEARCH (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)
Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
Hirotaka Matsuo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Gout and the Risk of Parkinson's Disease: A Cohort Study
Mary De Vera et al.
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH (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 influences uric acid concentrations with pronounced sex-specific effects
Angela Doering et al.
NATURE GENETICS (2008)
SLC2A9 Is a High-Capacity Urate Transporter in Humans
Mark J. Caulfield et al.
PLOS MEDICINE (2008)
Genome scan for determinants of serum uric acid variability
Subrata D. Nath et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)
Association of methylenetetrahydrofolate reductase (C677T) polymorphism with hyperuricemia
Jamal Golbahair et al.
NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES (2007)
Role of uric acid in hypertension, renal disease, and metabolic syndrome
Marcelo Heinig et al.
CLEVELAND CLINIC JOURNAL OF MEDICINE (2006)
Serum uric acid is a determinant of metabolic syndrome in a population-based study
Altan Onat et al.
AMERICAN JOURNAL OF HYPERTENSION (2006)
Metabolic syndrome - a new world-wide definition. A consensus statement from the international diabetes federation
KGMM Alberti et al.
DIABETIC MEDICINE (2006)
Polymorphism of methylenetetrahydrofolate reductase gene (C677T MTHFR) is not a confounding factor of the relationship between serum uric acid level and the prevalence of hypertension in Japanese men
H Lwin et al.
CIRCULATION JOURNAL (2006)
Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart Study
Q Yang et al.
METABOLISM-CLINICAL AND EXPERIMENTAL (2005)
The C677 mutation in methylene tetrahydrofolate reductase gene: Correlation with uric acid and cardiovascular risk factors in elderly Korean men
YS Hong et al.
JOURNAL OF KOREAN MEDICAL SCIENCE (2004)
Beer, liquor, and wine consumption and serum uric acid level: The Third National Health and Nutrition Examination Survey
HK Choi et al.
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH (2004)
Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion
K Ichida et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2004)
Genetic variants of homocysteine metabolizing enzymes and the risk of coronary artery disease
B Janosíková et al.
MOLECULAR GENETICS AND METABOLISM (2003)
Linkage analysis of a composite factor for the multiple metabolic syndrome - The National Heart, Lung, and Blood Institute Family Heart Study
WH Tang et al.
DIABETES (2003)
An association of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and common carotid atherosclerosis
R Kawamoto et al.
JOURNAL OF HUMAN GENETICS (2001)
The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men
M Zuo et al.
JOURNAL OF HUMAN GENETICS (2000)
Segregation analysis of serum uric acid in the NHLBI family heart study
JB Wilk et al.
HUMAN GENETICS (2000)
Share Paper
