Biology:SLC4A7
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Solute carrier family 4, sodium bicarbonate cotransporter, member 7, also known as SLC4A7, is a human gene.[1]
See also
References
Further reading
- "Molecular cloning of a new sodium bicarbonate cotransporter cDNA from human retina.". Biochem. Biophys. Res. Commun. 246 (2): 535–8. 1998. doi:10.1006/bbrc.1998.8658. PMID 9610397.
- "Mapping of the human NBC3 (SLC4A7) gene to chromosome 3p22.". Genomics 57 (2): 321–2. 1999. doi:10.1006/geno.1999.5781. PMID 10198178.
- "Cloning, tissue distribution, genomic organization, and functional characterization of NBC3, a new member of the sodium bicarbonate cotransporter family.". J. Biol. Chem. 274 (23): 16569–75. 1999. doi:10.1074/jbc.274.23.16569. PMID 10347222.
- "NBC3 expression in rabbit collecting duct: colocalization with vacuolar H+-ATPase.". Am. J. Physiol. 277 (6 Pt 2): F974–81. 2000. PMID 10600945.
- "The cystic fibrosis transmembrane conductance regulator interacts with and regulates the activity of the HCO3- salvage transporter human Na+-HCO3- cotransport isoform 3.". J. Biol. Chem. 277 (52): 50503–9. 2003. doi:10.1074/jbc.M201862200. PMID 12403779.
- "Structural and functional characterization of the human NBC3 sodium/bicarbonate co-transporter carboxyl-terminal cytoplasmic domain.". Mol. Membr. Biol. 20 (4): 307–17. 2004. doi:10.1080/0968768031000122520. PMID 14578046.
- "Regulation of the human NBC3 Na+/HCO3- cotransporter by carbonic anhydrase II and PKA.". Am. J. Physiol., Cell Physiol. 286 (6): C1423–33. 2004. doi:10.1152/ajpcell.00382.2003. PMID 14736710.
- "Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry.". Anal. Chem. 76 (10): 2763–72. 2004. doi:10.1021/ac035352d. PMID 15144186.
- "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization.". Curr. Biol. 14 (16): 1436–50. 2004. doi:10.1016/j.cub.2004.07.051. PMID 15324660.
- "Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.". Hum. Mol. Genet. 14 (24): 3933–43. 2006. doi:10.1093/hmg/ddi417. PMID 16301216.
- "Large-scale mapping of human protein–protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. 2007. doi:10.1038/msb4100134. PMID 17353931.
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