SLC46A1

An Error has occured retrieving Wikidata item for infobox SLC46A1‏ (Solute carrier family 46 member 1) هوَ بروتين يُشَفر بواسطة جين SLC46A1 في الإنسان.

قراءة متعمقة

• Subramanian VS، Marchant JS، Said HM (2008). "Apical membrane targeting and trafficking of the human proton-coupled transporter in polarized epithelia". Am. J. Physiol., Cell Physiol. ج. 294 ع. 1: C233–40. DOI:10.1152/ajpcell.00468.2007. PMID:18003745.
• Nakai Y، Inoue K، Abe N، وآخرون (2007). "Functional characterization of human proton-coupled folate transporter/heme carrier protein 1 heterologously expressed in mammalian cells as a folate transporter". J. Pharmacol. Exp. Ther. ج. 322 ع. 2: 469–76. DOI:10.1124/jpet.107.122606. PMID:17475902.
• Zhao R، Min SH، Qiu A، وآخرون (2007). "The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption". Blood. ج. 110 ع. 4: 1147–52. DOI:10.1182/blood-2007-02-077099. PMC:1939898. PMID:17446347.
• Sharma S، Dimasi D، Bröer S، وآخرون (2007). "Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epithelium". Exp. Cell Res. ج. 313 ع. 6: 1251–9. DOI:10.1016/j.yexcr.2007.01.019. PMID:17335806.
• Latunde-Dada GO، Takeuchi K، Simpson RJ، McKie AT (2007). "Haem carrier protein 1 (HCP1): Expression and functional studies in cultured cells". FEBS Lett. ج. 580 ع. 30: 6865–70. DOI:10.1016/j.febslet.2006.11.048. PMID:17156779.
• Qiu A، Jansen M، Sakaris A، وآخرون (2007). "Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption". Cell. ج. 127 ع. 5: 917–28. DOI:10.1016/j.cell.2006.09.041. PMID:17129779.
• Shayeghi M، Latunde-Dada GO، Oakhill JS، وآخرون (2005). "Identification of an intestinal heme transporter". Cell. ج. 122 ع. 5: 789–801. DOI:10.1016/j.cell.2005.06.025. PMID:16143108.
• Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
• Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
• Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.