↑Song ZH, Modi W, Bonner TI (July 1995). „Molecular cloning and chromosomal localization of human genes encoding three closely related G protein-coupled receptors”. Genomics28 (2): 347–9. DOI:10.1006/geno.1995.1154. PMID8530049.
↑Uhlenbrock K, Gassenhuber H, Kostenis E (November 2002). „Sphingosine 1-phosphate is a ligand of the human gpr3, gpr6 and gpr12 family of constitutively active G protein-coupled receptors”. Cellular Signalling14 (11): 941–53. DOI:10.1016/S0898-6568(02)00041-4. PMID12220620.
↑Tanaka S, Ishii K, Kasai K, Yoon SO, Saeki Y (April 2007). „Neural expression of G protein-coupled receptors GPR3, GPR6, and GPR12 up-regulates cyclic AMP levels and promotes neurite outgrowth”. The Journal of Biological Chemistry282 (14): 10506–15. DOI:10.1074/jbc.M700911200. PMID17284443.
Dodatna literatura
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Song ZH, Modi W, Bonner TI (1996). „Molecular cloning and chromosomal localization of human genes encoding three closely related G protein-coupled receptors.”. Genomics28 (2): 347–9. DOI:10.1006/geno.1995.1154. PMID8530049.
Uhlenbrock K, Huber J, Ardati A, et al. (2003). „Fluid shear stress differentially regulates gpr3, gpr6, and gpr12 expression in human umbilical vein endothelial cells.”. Cell. Physiol. Biochem.13 (2): 75–84. DOI:10.1159/000070251. PMID12649592.
Mungall AJ, Palmer SA, Sims SK, et al. (2003). „The DNA sequence and analysis of human chromosome 6.”. Nature425 (6960): 805–11. DOI:10.1038/nature02055. PMID14574404.
„GPR6”. IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Arhivirano iz originala na datum 2012-09-02.