A G Protein-coupled Receptor for UDP-glucose*
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J. Chambers | L. Macdonald | H. Sarau | R. Ames | K. Freeman | J. Foley | Yuan-E Zhu | M. Mclaughlin | P. Murdock | L. Mcmillan | J. Trill | Ann Swift | N. Aiyar | P. Taylor | L. Vawter | S. Naheed | P. Szekeres | G. Hervieu | C. Scott | Jeanette Watson | A. Murphy | E. Duzic | C. Klein | D. Bergsma | Shelagh Wilson | G. P. Livi | Sajda Naheed
[1] L. Yip,et al. Effects of uridine diphosphoglucose (UDPG) infusion on 5-phosphoribosyl pyrophosphate (PRPP) levels of mouse tissues. , 1987, Biochemical pharmacology.
[2] R. Mulligan,et al. Two dominant-acting selectable markers for gene transfer studies in mammalian cells. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[3] J. Thorner,et al. The STE2 gene product is the ligand-binding component of the alpha-factor receptor of Saccharomyces cerevisiae. , 1988, The Journal of biological chemistry.
[4] E. Kieff,et al. Epstein-Barr virus-induced genes: first lymphocyte-specific G protein-coupled peptide receptors , 1993, Journal of virology.
[5] M. Simon,et al. Gα15 and Gα16 Couple a Wide Variety of Receptors to Phospholipase C (*) , 1995, The Journal of Biological Chemistry.
[6] Paul J. Harrison,et al. Structure‐activity relationship of a pyrimidine receptor in the rat isolated superior cervical ganglion , 1995, British journal of pharmacology.
[7] J. Broach,et al. Yeast alpha mating factor structure-activity relationship derived from genetically selected peptide agonists and antagonists of Ste2p , 1996, Molecular and cellular biology.
[8] H. Herzog,et al. Intron 17 of the human retinoblastoma susceptibility gene encodes an actively transcribed G protein-coupled receptor gene. , 1996, Genome research.
[9] M. Spedding,et al. X. International Union of Pharmacology recommendations for nomenclature of new receptor subtypes. , 1996, Pharmacological reviews.
[10] D. Middlemiss,et al. GR127935 acts as a partial agonist at recombinant human 5-HT1Dα and 5-HT1Dβ receptors , 1996 .
[11] G. Burnstock. The past, present and future of purine nucleotides as signalling molecules , 1997, Neuropharmacology.
[12] T. K. Harden,et al. Direct Demonstration of Mechanically Induced Release of Cellular UTP and Its Implication for Uridine Nucleotide Receptor Activation* , 1997, The Journal of Biological Chemistry.
[13] T. Kendall Harden,et al. An examination of deoxyadenosine 5′(α‐thio)triphosphate as a ligand to define P2Y receptors and its selectivity as a low potency partial agonist of the P2Y1 receptor , 1997, British journal of pharmacology.
[14] R. Duman,et al. The isolation and characterization of a novel G protein-coupled receptor regulated by immunologic challenge , 1997, Brain Research.
[15] M. Colbert,et al. A genetic selection for isolating cDNAs encoding secreted proteins. , 1997, Gene.
[16] R. Nicholas,et al. HEK293 human embryonic kidney cells endogenously express the P2Y1 and P2Y2 receptors , 1997, Neuropharmacology.
[17] J. Broach,et al. Identification of surrogate agonists for the human FPRL-1 receptor by autocrine selection in yeast , 1998, Nature Biotechnology.
[18] Jilly F. Evans,et al. Receptor for motilin identified in the human gastrointestinal system. , 1999, Science.
[19] J. Chambers,et al. Melanin-concentrating hormone is the cognate ligand for the orphan G-protein-coupled receptor SLC-1 , 1999, Nature.
[20] J. Chambers,et al. Identification, molecular cloning, expression, and characterization of a cysteinyl leukotriene receptor. , 1999, Molecular pharmacology.
[21] H. Sarau,et al. Human urotensin-II is a potent vasoconstrictor and agonist for the orphan receptor GPR14 , 1999, Nature.
[22] H. Heng,et al. Discovery of three novel orphan G-protein-coupled receptors. , 1999, Genomics.