A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
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SLC transporters as therapeutic targets: emerging opportunitiesHomozygous SLC2A9 mutations cause severe renal hypouricemia.A case of renal hypouricemia and a G774A gene mutation causing acute renal injury that was improved by hemodialysis.Xenobiotic, bile acid, and cholesterol transporters: function and regulation.Serum uric acid distribution according to SLC22A12 W258X genotype in a cross-sectional study of a general Japanese population.Gout: a review of nonmodifiable and modifiable risk factors.Uric acid level has a U-shaped association with loss of kidney function in healthy people: a prospective cohort study.Analysis of mutations in the urate transporter 1 (URAT1) gene of Japanese patients with hypouricemia in northern Japan and review of the literature.Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.Prevalence and possible causes of hypouricemia at a tertiary care hospital.Effect of dietary control of urinary uric acid excretion in calcium oxalate stone formers and non-stone-forming controlsPharmGKB summary: uric acid-lowering drugs pathway, pharmacodynamics.Prevalence of URAT1 allelic variants in the Roma population.URAT1 gene polymorphisms influence uricosuric action of losartan in hypertensive patients with hyperuricemia.What lies behind serum urate concentration? Insights from genetic and genomic studies.High-resolution melting analysis for the rapid detection of an intronic single nucleotide polymorphism in SLC22A12 in male patients with primary gout in China.Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease.Absence of SLC22A12 gene mutations in Greek Caucasian patients with primary renal hypouricaemia.High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction.Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.Acute kidney injury due to rotavirus gastroenteritis-associated obstructive uric acid stones in a Japanese infant harboring a heterozygous W258X mutation.A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1.A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia.Multiple Membrane Transporters and Some Immune Regulatory Genes are Major Genetic Factors to GoutLarge-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levelsLong-term effects of the SLC2A9 G844A and SLC22A12 C246T variants on serum uric acid concentrations in childrenRenal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review
P2860
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P2860
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@ast
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@en
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@nl
type
label
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@ast
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@en
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@nl
prefLabel
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@ast
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@en
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@nl
P2093
P1433
P1476
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
@en
P2093
Hitoshi Endou
Makoto Hosoyamada
Naoharu Iwai
Naomi Tago
Yoshihiro Kokubo
Yukari Mino
P304
P356
10.1111/J.1523-1755.2004.00839.X
P407
P577
2004-09-01T00:00:00Z
P5875
P6179
1006034159