Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1Srinivas Aluri, I. David Goldman|Blood Advances|2018Cited by 22
Substitutions that lock and unlock the proton-coupled folate transporter (PCFT-SLC46A1) in an inward-open conformationSrinivas Aluri, I. David Goldman|Journal of Biological Chemistry|2019Cited by 9
Substituted-cysteine accessibility and cross-linking identify an exofacial cleft in the 7th and 8th helices of the proton-coupled folate transporter (SLC46A1)Srinivas Aluri, I. David Goldman|American Journal of Physiology-Cell Physiology|2017Cited by 7