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RFT2 encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin.
C20orf54 rs13042395 polymorphism was significantly associated with decreased ESCC and GCA (show NPR1 ELISA Kits) risk especially for the subjects with under-weight or normal.
A close association exists between functional SNP rs3746804 in C20orf54 and susceptibility to esophageal squamous cell carcinoma
the single-nucleotide polymorphism rs13042395 in C20orf54 showed a significantly lower risk of esophageal squamous cell carcinoma in the younger age group but no significant association in the older group in a Korean population.
Binding of Sp1 (show PSG1 ELISA Kits) to the minimal SLC52A3 promoter.
Increase in methylation of CpG 2 and CpG 3 in hRFT2gene promoter region is associated with the genesis of cervical squamous cell carcinoma.
Results suggest that RFT2 contributes to esophageal squamous cell carcinoma tumorigenesis and may serve as a potential therapeutic target.
C20orf54 expression were significantly up-regulated in CSCC (show CYP11A1 ELISA Kits).
data suggest that MMND is a distinct clinical subgroup of childhood onset MND (show CLN8 ELISA Kits) patients where the known genetic defects are so far negative.
These results strongly suggest that RFVT3 would functionally be involved in riboflavin absorption in the apical membranes of intestinal epithelial cells
summary of recent findings on the cloning, nomenclature, functional characterization and genetic diseases of RFVT1/SLC52A1 (show GPR172B ELISA Kits), RFVT2/SLC52A2 (show GPR172A ELISA Kits) and RFVT3/SLC52A3 [review]
the RFVT-3 system is the main transporter involved in carrier-mediated riboflavin uptake in the native mouse small and large intestine
This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease.
riboflavin transporter 2
, solute carrier family 52 member 3
, solute carrier family 52, riboflavin transporter, member 3