Graeme Bilbe

Novartis, Basel, Basel-Stadt, France 
"Graeme Bilbe"
Mean distance: 17.01 (cluster 11)
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Feuerbach D, Pezous N, Weiss M, et al. (2015) AQW051, a novel, potent and selective α7 nicotinic ACh receptor partial agonist: pharmacological characterization and phase I evaluation. British Journal of Pharmacology. 172: 1292-304
Vranesic I, Ofner S, Flor PJ, et al. (2014) AFQ056/mavoglurant, a novel clinically effective mGluR5 antagonist: identification, SAR and pharmacological characterization. Bioorganic & Medicinal Chemistry. 22: 5790-803
Conti B, Maier R, Barr AM, et al. (2007) Region-specific transcriptional changes following the three antidepressant treatments electro convulsive therapy, sleep deprivation and fluoxetine. Molecular Psychiatry. 12: 167-89
Hoyer D, Thakker DR, Natt F, et al. (2006) Global down-regulation of gene expression in the brain using RNA interference, with emphasis on monoamine transporters and GPCRs: implications for target characterization in psychiatric and neurological disorders. Journal of Receptor and Signal Transduction Research. 26: 527-47
Bowler WB, Buckley KA, Gartland A, et al. (2001) Extracellular nucleotide signaling: a mechanism for integrating local and systemic responses in the activation of bone remodeling. Bone. 28: 507-12
Dixon CJ, Bowler WB, Littlewood-Evans A, et al. (1999) Regulation of epidermal homeostasis through P2Y2 receptors. British Journal of Pharmacology. 127: 1680-6
Mosbacher J, Maier R, Fakler B, et al. (1998) P2Y receptor subtypes differentially couple to inwardly-rectifying potassium channels. Febs Letters. 436: 104-10
Hipskind RA, Bilbe G. (1998) MAP kinase signaling cascades and gene expression in osteoblasts. Frontiers in Bioscience : a Journal and Virtual Library. 3: d804-16
Bowler WB, Gallagher JA, Bilbe G. (1998) G-protein coupled receptors in bone. Frontiers in Bioscience : a Journal and Virtual Library. 3: d769-80
Kellenberger S, Muller K, Richener H, et al. (1998) Formoterol and isoproterenol induce c-fos gene expression in osteoblast-like cells by activating beta2-adrenergic receptors. Bone. 22: 471-8
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