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Annals of the New York Academy of Sciences|June 16, 2005
Identification of binding sites with differing affinity and potency for relaxin analogues on LGR7 and LGR8 receptorsMichelle L Halls, Ross A Bathgate, Satoko Sudo, et al.
Chemical Communications (Cambridge, England)|July 4, 2017
Garlic-inspired trisulfide linkers for thiol-stimulated H2S releaseFrancesca Ercole, Michael R Whittaker, Michelle L Halls, et al.
Biochemical Pharmacology|September 10, 2018
Glucagon-like peptide-1 receptor internalisation controls spatiotemporal signalling mediated by biased agonistsMadeleine M Fletcher, Michelle L Halls, Peishen Zhao, et al.
Annals of the New York Academy of Sciences|May 7, 2009
RXFP1 couples to the Galpha-Gbetagamma-PI3K-PKCzeta pathway via the final 10 amino acids of the receptor C-terminal tailMichelle L Halls, Maria Papaioannou, John D Wade, et al.
Journal of Cell Science|September 15, 2012
A key phosphorylation site in AC8 mediates regulation of Ca(2+)-dependent cAMP dynamics by an AC8-AKAP79-PKA signalling complexDebbie Willoughby, Michelle L Halls, Katy L Everett, et al.
Annals of the New York Academy of Sciences|May 7, 2009
Roles of the receptor, the ligand, and the cell in the signal transduction pathways utilized by the relaxin family peptide receptors 1-3Roger J Summers, Ross A D Bathgate, John D Wade, et al.
Annals of the New York Academy of Sciences|May 7, 2009
Relaxin activates multiple cAMP signaling pathway profiles in different target cellsMichelle L Halls, Tim D Hewitson, Xiao-Lei Moore, et al.
Biomacromolecules|December 15, 2015
Macromolecular Hydrogen Sulfide Donors Trigger Spatiotemporally Confined Changes in Cell SignalingFrancesca Ercole, Friederike M Mansfeld, Maria Kavallaris, et al.
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