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Molecular Pharmacology|December 4, 2003
Selective antimicrotubule activity of N1-phenyl-3,5-dinitro-N4,N4-di-n-propylsulfanilamide (GB-II-5) against kinetoplastid parasitesKarl A Werbovetz, Dan L Sackett, Dawn Delfín, et al.Molecular Pharmacology|December 4, 2003
Soluble guanylyl cyclase activator YC-1 inhibits human neutrophil functions through a cGMP-independent but cAMP-dependent pathwayTsong-Long Hwang, Hsiu-Wen Hung, Shu-Hui Kao, et al.Molecular Pharmacology|December 4, 2003
A new principle for tight junction modulation based on occludin peptidesStaffan Tavelin, Kei Hashimoto, John Malkinson, et al.Molecular Pharmacology|December 4, 2003
Pharmacological and genetic analysis of 90-kDa heat shock isoprotein-aryl hydrocarbon receptor complexesMarc B Cox, Charles A MillerMolecular Pharmacology|December 4, 2003
Allosteric enhancers of A1 adenosine receptors increase receptor-G protein coupling and counteract Guanine nucleotide effects on agonist bindingHeidi Figler, Ray A Olsson, Joel LindenMolecular Pharmacology|December 4, 2003
Serine 447 in the carboxyl tail of human VPAC1 receptor is crucial for agonist-induced desensitization but not internalization of the receptorJean-Claude Marie, Christiane Rouyer-Fessard, Alain Couvineau, et al.Molecular Pharmacology|October 24, 2003
Different affinities of inhibitors to the outwardly and inwardly directed substrate binding site of organic cation transporter 2Christopher Volk, Valentin Gorboulev, Thomas Budiman, et al.Molecular Pharmacology|October 24, 2003
Acquired cellular resistance to flavopiridol in a human colon carcinoma cell line involves up-regulation of the telomerase catalytic subunit and telomere elongation. Sensitivity of resistant cells to combination treatment with a telomerase inhibitorChristopher M Incles, Christoph M Schultes, Lloyd R Kelland, et al.Molecular Pharmacology|October 24, 2003
beta2-Adrenergic signaling in human heart: shift from the cyclic AMP to the arachidonic acid pathwayCatherine Pavoine, Niloufar Behforouz, Chantal Gauthier, et al.Molecular Pharmacology|October 24, 2003
An N-terminal histidine is the primary determinant of alpha subunit-dependent Cu2+ sensitivity of alphabeta3gamma2L GABA(A) receptorsHeejeong Kim, Robert L MacdonaldPageof 1,019