The retention and cellular internalization of drug delivery systems and theranostics for
cancer therapy can be improved by targeting molecules. Since an increased uptake of …

Riboflavin transporter (RFT) 2 has recently been identified as a transporter that may be,
mainly based on the functional characteristics of its rat ortholog (rRFT2), involved in the …

Brown–Vialetto–Van Laere syndrome (BVVLS) is a genetic condition caused by a mutation
in the C20orf54 gene, which also codes for an intestinal riboflavin transporter. We report the …

Riboflavin is an essential cofactor in many enzymatic processes and in the production of
flavin adenine dinucleotide (FAD). Here, we report that the partial depletion of riboflavin …

Abstract Human riboflavin transporter 2 (RFT2, also termed as SLC52A3) was recently
identified as a susceptibility gene to esophageal squamous cell carcinoma (ESCC) …

Transport of riboflavin (RF) across both the brush border membrane (BBM) and basolateral
membrane (BLM) of the polarized enterocyte occurs via specific carrier-mediated …

Riboflavin (Rf) receptors bind and translocate Rf and its phosphorylated forms (eg flavin
mononucleotide, FMN) into cells where they mediate various cellular metabolic pathways …

Riboflavin deficiency can cause a variety of metabolic problems that lead to skin and
mucosal disorders. Limited evidence suggests that high intake of riboflavin may reduce …

Background/Aim: Riboflavin transport in enterocytes is mediated by three translocators:
RFVT3 located on the apical membrane, and RFVT1 and RFVT2 on the basolateral …

Inborn errors of Riboflavin (Rf) transport and metabolism have been recently related to
severe human neuromuscular disorders, as resulting in profound alteration of human …