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

Genetic Variation in Human Vitamin C Transporter Genes in Common Complex Diseases.

Advances in nutrition (Bethesda, Md.) - 1 Mar 2016

Shaghaghi Mandana Amir, Kloss Olena, Eck Peter

Abstract excerpt

Adequate plasma, cellular, and tissue vitamin C concentrations are required for maintaining optimal health through suppression of oxidative stress and optimizing functions of certain enzymes that require vitamin C as a cofactor. Polymorphisms in the vitamin C transporter genes, compromising genes encoding sodium-dependent ascorbate transport proteins, and also genes encoding facilitative transporters of...

Read the complete abstract on PubMed

Topics

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

Share to Chronic Disease
Share to Genetic Association Studies
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucose Transport Proteins, Facilitative

Share to Nutrigenomics

Share to Oxidative Stress

Share to Polymorphism, Single Nucleotide

Share to Protein Isoforms

Source

Open in PubMed Open full text

Identifiers

PMID: 26980812
DOI: 10.3945/an.115.009225
PMCID: PMC4785466

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Variation in Human Vitamin C Transporter Genes in Common Complex Diseases.PMID 26980812Read ↗

Human genetic variation influences vitamin C homeostasis by altering vitamin C transport and antioxidant enzyme function.Semantic proximity Read ↗

Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2.Semantic proximity Read ↗

Genetic Variants Influencing Individual Vitamin D StatusSemantic proximity Read ↗

Genetic variation at the SLC23A1 locus is associated with circulating concentrations of L-ascorbic acid (vitamin C): evidence from 5 independent studies with >15,000 participants.Semantic proximity Read ↗

Vitamin Pharmacogenomics: New Insight into Individual Differences in Diseases and Drug Responses.Semantic proximity Read ↗

Vitamin C transporter gene polymorphisms, dietary vitamin C and serum ascorbic acid.Semantic proximity Read ↗

An update on vitamin B12-related gene polymorphisms and B12 statusSemantic proximity Read ↗

Polymorphisms Contributing to Calcium Status: A Systematic Review.Semantic proximity Read ↗

Variation in the sodium-dependent vitamin C transporter 2 gene is associated with risk of acute coronary syndrome among women.Semantic proximity Read ↗

Common Genetic Determinants of Vitamin D Insufficiency: A Genome-Wide Association StudySemantic proximity Read ↗

Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents.Semantic proximity Read ↗

Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans.Semantic proximity Read ↗

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