A pharmacological characterization of GABA, THIP and DS2 at binary α4β3 and β3δ receptors: GABA activates β3δ receptors via the β3(+)δ(-) interface von Lee, HJ, Absalom, N.L, Hanrahan, J.R, van Nieuwenhuijzen, P, Ahring, P.K, Chebib, M

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GABAA α5 subunit-containing receptors do not contribute to reversal of inflammatory-induced spinal sensitization as indicated by the unique selectivity profile of the GABAA recepto... von de Lucas, A. Garcia, Ahring, P.K., Larsen, J.S., Rivera-Arconada, I., Lopez-Garcia, J.A., Mirza, N.R., Munro, G.

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Electrophysiological characterization of NS9283, a novel positive allosteric modulator of α4β2 nicotinic receptors von Grupe, M., Grunnet, M., Christensen, J.K., Jensen, A.A., Ahring, P.K.

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In vitro pharmacological profile of a novel α4β2 positive allosteric modulator NS9283 (A-969933) von Malysz, J., Dyhring, T., Ahring, P.K., Olsen, G.M., Peters, D., Gronlien, J.H., Wetterstrand, C., Ween, H., Haakerud, M., Thorin-Hagene, K., Andersen, E., Anderson, D.J., Hu, M., Kroeger, P.E., Lee, C.-H.L., Gopalakrishnan, M., Timmermann, D.B.

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Modulation of the Ca 2+ -dependent K + Channel, hslo , by the Substituted Diphenylurea NS 1608, Paxilline and Internal Ca 2 von STRØBÆK, D., CHRISTOPHERSEN, P., HOLM, N.R., MOLDT, P., AHRING, P.K., JOHANSEN, T.E., OLESEN, S.-P.

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