Characterization of a Mutation in the Reduced Folate Carrier in a Transport Defective L1210 Murine Leukemia Cell Line
Kevin E. Brigle(Virginia Cancer Institute), I. David Goldman(Albert Einstein College of Medicine)
Cited by 129
Related Papers
Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues
|Expert Reviews in Molecular Medicine|2009|384
Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1
|Blood Advances|2018|22
Random Mutagenesis of the Proton-coupled Folate Transporter (SLC46A1), Clustering of Mutations, and the Bases for Associated Losses of Function
|Journal of Biological Chemistry|2011|19
Substitutions that lock and unlock the proton-coupled folate transporter (PCFT-SLC46A1) in an inward-open conformation
|Journal of Biological Chemistry|2019|9
Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function
|American Journal of Physiology-Cell Physiology|2016|8