4. Shin DS, Zhao R, Fiser A, Goldman DI
Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption.
Am J Physiol Cell Physiol (2012) 303(8) : C834-42
PMID: 22843796     PMCID: PMC3469714

3. Zhao R, Shin DS, Fiser A, Goldman ID
Identification of a functionally critical GXXG motif and its relationship to the folate binding site of the proton-coupled folate transporter (PCFT-SLC46A1).
Am J Physiol Cell Physiol (2012) 303(6) : C673-81
PMID: 22785121     PMCID: PMC3468349

2. Lakshmanan V, Rhee K, Wang W, Yu Y, Khafizov K, Fiser A, Wu P, Ndir O, Mboup S, Ndiaye D, Daily J
Metabolomic analysis of patient plasma yields evidence of plant-like alpha-linolenic acid metabolism in Plasmodium falciparum.
J Infect Dis (2012) ,
PMID: 22566569     PMCID: PMC3490690

1. Shin DS, Zhao R, Yap EH, Fiser A, Goldman ID
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.
Am J Physiol Cell Physiol (2012) ,
PMID: 22345511     PMCID: PMC3361945