A. Eriksson

发表

In Vivo and Ex Vivo Inhibition of Spinal Nerve Ligation-Induced Ectopic Activity by Sodium Channel Blockers Correlate to In Vitro Inhibition of NaV1.7 and Clinical Efficacy: A Pharmacokinetic-Pharmacodynamic Translational Approach

P. Lund, S. Visser, T. Bueters, 2013, Pharmaceutical Research.

Phenethyl nicotinamides, a novel class of Na(V)1.7 channel blockers: structure and activity relationship.

P. Lund, Jonas Malmborg, A. Minidis, 2012, Bioorganic & medicinal chemistry letters.

Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship.

P. Lund, P. Arvidsson, L. Sandberg, 2011, Bioorganic & medicinal chemistry letters.

3-Oxoisoindoline-1-carboxamides: potent, state-dependent blockers of voltage-gated sodium channel Na(V)1.7 with efficacy in rat pain models.

P. Lund, P. Arvidsson, L. Sandberg, 2012, Journal of medicinal chemistry.

In Vivo and Ex Vivo Inhibition of Spinal Nerve Ligation-Induced Ectopic Activity by Sodium Channel Blockers Correlate to In Vitro Inhibition of NaV1.7 and Clinical Efficacy: A Pharmacokinetic-Pharmacodynamic Translational Approach

P. Lund, S. Visser, T. Bueters, 2013, Pharmaceutical Research.

Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A.

Mohamed Chahine, J. Krupp, L. Dahllund, 2008, Journal of neurophysiology.

A stop codon mutation in SCN9A causes lack of pain sensation.

P. Lund, J. Krupp, G. Rouleau, 2007, Human molecular genetics.

by Toggling an Amino Acid in the First S3-S4 Linker Alternative Splicing Modulates Inactivation of Type 1 Voltage-gated Sodium Channels

James O. Jackson, D. Johnston, R. Gray, 2015 .

Linkage analysis and functional evaluation of inherited clinical pain conditions.

J. Krupp, D. Hellgren, A. Eriksson, 2010, Methods in molecular biology.

In vitro characterization of AR-A000002, a novel 5-hydroxytryptamine(1B) autoreceptor antagonist.

C. Ahlgren, Charlotte Ahlgren, Anders Eriksson, 2004, European journal of pharmacology.

Structure and activity relationship in the (S)-N-chroman-3-ylcarboxamide series of voltage-gated sodium channel blockers.

P. Lund, L. Sandberg, T. Bueters, 2012, Bioorganic & medicinal chemistry letters.

Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A.

J. Krupp, L. Dahllund, M. Chahine, 2008, Journal of neurophysiology.