Discover Community Create You

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

Tag polymorphisms of solute carrier family 12 member 3 gene modify the risk of hypertension in northeastern Han Chinese.

Journal of human hypertension - 1 Aug 2014

Wang Y L, Qi Y, Bai J N, Qi Z M, Li J R, Zhao H Y, Wang Y F, Lu C Z, Xiao Y, Jia N, Wang B, Niu W Q

Abstract excerpt

Converging evidence suggests that the gene encoding solute carrier family 12 member 3 (SLC12A3) is a logical candidate involved in the underlying cause of hypertension. We therefore selected four tag polymorphisms (rs2304483, rs5804, rs8063291 and rs6499857) from SLC12A3 gene to investigate their...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Body Mass Index
Share to Case-Control Studies
Share to China
Share to Haplotypes
Share to Hypertension
Share to Polymorphism, Genetic
Share to Risk
Share to Solute Carrier Family 12, Member 3

Source

Identifiers

PMID: 24430698
DOI: 10.1038/jhh.2013.134

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24430698-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Tag polymorphisms of solute carrier family 12 member 3 gene modify the risk of hypertension in northeastern Han Chinese.PMID 24430698Read ↗

Interactions between the FTO and GNB3 genes contribute to varied clinical phenotypes in hypertension.Semantic proximity Read ↗

Association of variants in renal salt reabsorption-related gene SLC12A3 with essential hypertension in a Mongolian population.Semantic proximity Read ↗

Genetic variants of SLC12A3 modulate serum lipid profiles in a group of Mongolian pedigree population.Semantic proximity Read ↗

The GPX3 rs3828599 genotype in combination with alcohol consumption and age helps identify a high-risk hypertension subgroup for antioxidant intervention.Semantic proximity Read ↗

Protective Role of TRPC3 Gene Polymorphism (rs10518289) in Obstructive Sleep Apnea Hypopnea Syndrome Among Hypertensive Patients.Semantic proximity Read ↗

Replication of the top 10 most significant polymorphisms from a large blood pressure genome-wide association study of northeastern Han Chinese East Asians.Semantic proximity Read ↗

The relationship between three X-linked genes and the risk for hypertension among northeastern Han Chinese.Semantic proximity Read ↗

Association between the G-protein β3 subunit C825T polymorphism with essential hypertension: a meta-analysis in Han Chinese population.Semantic proximity Read ↗

Correlation between natriuretic peptide receptor C (NPR3) gene polymorphisms and hypertension in the Dai people of China.Semantic proximity Read ↗

Genetic variants of human urea transporter-2 are associated with metabolic syndrome in Asian population.Semantic proximity Read ↗

Genetic susceptibility to essential hypertension in the Chinese han population: a study on GAB1, GAB2, and GAB3 gene polymorphisms.Semantic proximity Read ↗

Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population.Semantic proximity Read ↗

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