Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Association between SLC22A12 rs1529909 and rs7929627 polymorphism and hyperuricemia].

Wei sheng yan jiu = Journal of hygiene research - 1 Jul 2017

Zhang Yadi, Zhang Fandi, Zhao Li, Du Jiancai, Wang Yun, Guo Zhongqin

Abstract excerpt

OBJECTIVE: To investigate the relationship between SLC22A12 gene rs1529909 and rs7929627 polymorphism and hyperuricemia of residents in Yinchuan, Ningxia province. METHODS: Through retrospective analysis in healthy subjects from April to November in 2014, 365 patients with hyperuricemia were selected. 1∶ 1 matched casecontrol study was carried out, matched with age( ± 5 years old), gender, race, and selected 365...

Topics

Join the communities discussing this publication.

Case-Control Studies
Child, Preschool
China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Organic Anion Transporters

Organic Cation Transport Proteins

Source

Identifiers

PMID: 29903181

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Association between SLC22A12 rs1529909 and rs7929627 polymorphism and hyperuricemia].PMID 29903181Read ↗

[The associations between adenosine triphosphate binding cassette subfamily G member-2 single nucleotide polymorphism and hyperuricemia in a Chinese tertiary hospital faculty cohort].Semantic proximity Read ↗

[Polymorphisms of SLC17A1 gene and their interaction with alcohol drinking among Uygur patients with hyperuricemia].Semantic proximity Read ↗

[Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].Semantic proximity Read ↗

ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort.Semantic proximity Read ↗

Association of ABCG2 rs2231142 Allele and BMI With Hyperuricemia in an East Asian PopulationSemantic proximity Read ↗

The rs13129697 polymorphism of the SLC2A9 gene, but not rs7442295 is associated with impaired glucose tolerance/impaired fasting glucose complicated with hyperuricaemia in Han Chinese malesSemantic proximity Read ↗

Prevalence of hyperuricemia among the Chinese population of the southeast coastal region and association with single nucleotide polymorphisms in urate‑anion exchanger genes: SLC22A12, ABCG2 and SLC2A9.Semantic proximity Read ↗

Association of an Exon SNP of SLC2A9 Gene with Hyperuricemia Complicated with Type 2 Diabetes Mellitus in the Chinese Male Han Population.Semantic proximity Read ↗

Genotype and Phenotype of Renal Hypouricemia: A Single-Center Study from China.Semantic proximity Read ↗

Prevalence of hypouricaemia and SLC22A12 mutations in healthy Korean subjects.Semantic proximity Read ↗

T6092C polymorphism of SLC22A12 gene is associated with serum uric acid concentrations in Korean male subjects.Semantic proximity Read ↗

URAT1 gene polymorphisms influence uricosuric action of losartan in hypertensive patients with hyperuricemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.