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

Novel riboflavin transporter family RFVT/SLC52: identification, nomenclature, functional characterization and genetic diseases of RFVT/SLC52.

Molecular aspects of medicine - 1 Jan 2000

Yonezawa Atsushi, Inui Ken-ichi

Abstract excerpt

Riboflavin, a water-soluble vitamin also known as vitamin B2, is essential for normal cellular functions. Riboflavin transporters play important roles in its homeostasis. Recently, three novel riboflavin transporters were identified, and designated as RFT1, RFT2 and RFT3. Because the RFTs did not...

Read the complete abstract on PubMed

Topics

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

Share to Absorption
Share to Cloning, Molecular
Share to Hearing Loss, Sensorineural

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Transport Proteins

Share to Molecular Structure

Share to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Share to Receptors, G-Protein-Coupled

Share to Riboflavin

Source

Identifiers

PMID: 23506902
DOI: 10.1016/j.mam.2012.07.014

Genes

RFT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23506902-2026-09-04.2. 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

Novel riboflavin transporter family RFVT/SLC52: identification, nomenclature, functional characterization and genetic diseases of RFVT/SLC52.PMID 23506902Read ↗

Recent advances in riboflavin transporter RFVT and its genetic disease.Semantic proximity Read ↗

Complete Deletion of Slc52a2 Causes Embryonic Lethality in Mice.Semantic proximity Read ↗

Clinical presentation and outcome of riboflavin transporter deficiency: mini review after five years of experience.Semantic proximity Read ↗

An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.Semantic proximity Read ↗

Impaired riboflavin transport due to missense mutations in <i>SLC52A2</i> causes Brown‐Vialetto‐Van Laere syndromeSemantic proximity Read ↗

Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2.Semantic proximity Read ↗

SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters.Semantic proximity Read ↗

Systematic analysis of the role of SLC52A2 in multiple human cancersSemantic proximity Read ↗

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.Semantic proximity Read ↗

Polymorphism of Riboflavin Transporter (RFVT) Gene in Patients with Esophageal Cancer in Hakka Population in Southern ChinaSemantic proximity Read ↗

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.Semantic proximity Read ↗

Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency.Semantic proximity Read ↗

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