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

Identification and characterization of single nucleotide polymorphisms of SLC22A11 (hOAT4) in Korean women osteoporosis patients.

Molecules and cells - 30 Apr 2008

Lee Woon Kyu, Kwak Jin Oh, Hwang Ji-Sun, Suh Chang Kook, Cha Seok Ho

Abstract excerpt

Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation. Non-synonymous SNPs (nsSNPs) change an amino acid. Organic anion transporters (OATs) play an important role in eliminating or reabsorbing endogenous and exogenous organic anionic compounds. Among OATs, hOAT4 mediates high affinity transport of estrone sulfate and dehydroepiandrosterone sulfate. The rapid bone loss that...

Read the complete abstract on PubMed

Topics

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

Share to Base Composition
Share to Biological Transport

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis, Agar Gel

Share to Oocytes

Share to Organic Anion Transporters, Sodium-Independent

Share to Osteoporosis

Share to Xenopus

Source

Identifiers

PMID: 18414001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification and characterization of single nucleotide polymorphisms of SLC22A11 (hOAT4) in Korean women osteoporosis patients.PMID 18414001Read ↗

Seven novel single nucleotide polymorphisms in the human SLC22A1 gene encoding organic cation transporter 1 (OCT1).Semantic proximity Read ↗

Novel single nucleotide polymorphisms of organic cation transporter 1 (SLC22A1) affecting transport functions.Semantic proximity Read ↗

The Membrane Transporter OAT7 (SLC22A9) Is Not a Susceptibility Factor for Osteoporosis in Europeans.Semantic proximity Read ↗

Identification of High-Risk SNPs in SLC22A transporter Genes: Their Potential Role in PCOS and Metformin uptakeSemantic proximity Read ↗

Genetic variations of the SLC22A4 gene in Chinese and Indian populations of Singapore.Semantic proximity Read ↗

Functional characterization of human organic cation transporter OCTN1 single nucleotide polymorphisms in the Japanese population.Semantic proximity Read ↗

Functional consequences of single nucleotide polymorphisms in the human organic anion transporter hOAT1 (SLC22A6).Semantic proximity Read ↗

Fourteen novel single nucleotide polymorphisms in the SLC22A2 gene encoding human organic cation transporter (OCT2).Semantic proximity Read ↗

In Silico Study to Predict the Structural and Functional Consequences of SNPs on Biomarkers of Ovarian Cancer (OC) and BPA Exposure-Associated OC.Semantic proximity Read ↗

Functional characterization of nonsynonymous single nucleotide polymorphisms in the human organic anion transporter 4 (hOAT4).Semantic proximity Read ↗

Identification of CYP19A1 single-nucleotide polymorphisms and their haplotype distributions in a Korean population.Semantic proximity Read ↗

Rare genetic variants in the sodium-dependent organic anion transporter SOAT (SLC10A6): Effects on transport function and membrane expression.Semantic proximity Read ↗

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