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Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption

The proton-coupled folate transporter (PCFT-SLC46A1) mediates intestinal folate absorption and folate transport across the choroid plexus, processes defective in hereditary folate malabsorption (HFM). This paper characterizes the functional defect, and the roles of two mutated PCFT residues, associa...

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Bibliografski detalji
Glavni autori: Shin, Daniel Sanghoon, Zhao, Rongbao, Fiser, Andras, Goldman, David I.
Format: Artigo
Jezik:Inglês
Izdano: American Physiological Society 2012
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3469714/
https://ncbi.nlm.nih.gov/pubmed/22843796
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00171.2012
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