- SLC46A1
Proton-coupled folate transporter, also known as PCFT, is a human
gene .cite web | title = Entrez Gene: PCFT proton-coupled folate transporter| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=113235| accessdate = ]PBB_Summary
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summary_text =References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Subramanian VS, Marchant JS, Said HM |title=Apical membrane targeting and trafficking of the human proton-coupled transporter in polarized epithelia. |journal=Am. J. Physiol., Cell Physiol. |volume=294 |issue= 1 |pages= C233–40 |year= 2008 |pmid= 18003745 |doi= 10.1152/ajpcell.00468.2007
*cite journal | author=Nakai Y, Inoue K, Abe N, "et al." |title=Functional characterization of human proton-coupled folate transporter/heme carrier protein 1 heterologously expressed in mammalian cells as a folate transporter. |journal=J. Pharmacol. Exp. Ther. |volume=322 |issue= 2 |pages= 469–76 |year= 2007 |pmid= 17475902 |doi= 10.1124/jpet.107.122606
*cite journal | author=Zhao R, Min SH, Qiu A, "et al." |title=The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption. |journal=Blood |volume=110 |issue= 4 |pages= 1147–52 |year= 2007 |pmid= 17446347 |doi= 10.1182/blood-2007-02-077099
*cite journal | author=Sharma S, Dimasi D, Bröer S, "et al." |title=Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epithelium. |journal=Exp. Cell Res. |volume=313 |issue= 6 |pages= 1251–9 |year= 2007 |pmid= 17335806 |doi= 10.1016/j.yexcr.2007.01.019
*cite journal | author=Latunde-Dada GO, Takeuchi K, Simpson RJ, McKie AT |title=Haem carrier protein 1 (HCP1): Expression and functional studies in cultured cells. |journal=FEBS Lett. |volume=580 |issue= 30 |pages= 6865–70 |year= 2007 |pmid= 17156779 |doi= 10.1016/j.febslet.2006.11.048
*cite journal | author=Qiu A, Jansen M, Sakaris A, "et al." |title=Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption. |journal=Cell |volume=127 |issue= 5 |pages= 917–28 |year= 2007 |pmid= 17129779 |doi= 10.1016/j.cell.2006.09.041
*cite journal | author=Shayeghi M, Latunde-Dada GO, Oakhill JS, "et al." |title=Identification of an intestinal heme transporter. |journal=Cell |volume=122 |issue= 5 |pages= 789–801 |year= 2005 |pmid= 16143108 |doi= 10.1016/j.cell.2005.06.025
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899PBB_Controls
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