Molecular Pharmacology: 67 (4)

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About the Cover Computer model for the binding of the RTG molecule within the pore region of the Kv7.2 (KCNQ2) channel. See the article by Wuttke et al. on page 1009 of this issue.

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SB-431542 Is a Potent and Specific Inhibitor of Transforming Growth Factor-β Superfamily Type I Activin Receptor-Like Kinase (ALK) Receptors ALK4, ALK5, and ALK7
The G-Protein-Coupled Receptors in the Human Genome Form Five Main Families. Phylogenetic Analysis, Paralogon Groups, and Fingerprints
Pharmacological Properties of Y-27632, a Specific Inhibitor of Rho-Associated Kinases
Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.
The Orphan Human Pregnane X Receptor Mediates the Transcriptional Activation of CYP3A4 by Rifampicin through a Distal Enhancer Module

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