Receptor binding assay for nitric oxide- and heme-independent activators of soluble guanylate cyclase.
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[1] J. Stasch,et al. NO‐ and haem‐independent activation of soluble guanylyl cyclase: molecular basis and cardiovascular implications of a new pharmacological principle , 2002, British journal of pharmacology.
[2] J. Stasch,et al. Pharmacological actions of a novel NO‐independent guanylyl cyclase stimulator, BAY 41‐8543: in vitro studies , 2002, British journal of pharmacology.
[3] B. Mayer,et al. cGMP signalling beyond nitric oxide. , 2001, Trends in pharmacological sciences.
[4] F. Murad,et al. YC-1 activation of human soluble guanylyl cyclase has both heme-dependent and heme-independent components , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[5] J. Stasch,et al. NO-independent stimulators of soluble guanylate cyclase. , 2001, Bioorganic & medicinal chemistry letters.
[6] R. Gerzer,et al. NO-independent regulatory site on soluble guanylate cyclase , 2001, Nature.
[7] A. Hobbs. Soluble guanylate cyclase , 2000 .
[8] Y. Zhao,et al. Interaction of soluble guanylate cyclase with YC-1: kinetic and resonance Raman studies. , 2000, Biochemistry.
[9] G. Schultz,et al. Sensitizing soluble guanylyl cyclase to become a highly CO‐sensitive enzyme. , 1996, The EMBO journal.
[10] S. Kuo,et al. YC‐1 inhibited human platelet aggregation through NO‐independent activation of soluble guanylate cyclase , 1995, British journal of pharmacology.
[11] C. W. Scott,et al. A filtration-based assay to quantitate granulocyte-macrophage colony-stimulating factor binding. , 1995, Analytical biochemistry.
[12] E. Barnard,et al. Solubilization in high yield of opioid receptors retaining high‐affinity delta, mu and kappa binding sites , 1984, FEBS letters.
[13] R. Gerzer,et al. Purified soluble guanylyl cyclase expressed in a baculovirus/Sf9 system: stimulation by YC-1, nitric oxide, and carbon monoxide , 1999, Journal of Molecular Medicine.