Genetic selection of activatory mutations in KcsA. by Paynter, J, Sarkies, P, Andres-Enguix, I, Tucker, S

Erratum: The pore structure and gating mechanism of K2P channels (The EMBO Journal (2011) 30 (3607-3619) doi:10.1038/emboj.2011.268) by Piechotta, P, Rapedius, M, Stansfeld, P, Bollepalli, M, Ehrlich, G, Andres-Enguix, I, Fritzenschaft, H, Decher, N, Sansom, M, Tucker, S, Baukrowitz, T

The pore structure and gating mechanism of K2P channels (vol 30, pg 3607, 2011) by Piechotta, P, Rapedius, M, Stansfeld, P, Bollepalli, M, Ehrlich, G, Andres-Enguix, I, Fritzenschaft, H, Decher, N, Sansom, M, Tucker, S, Baukrowitz, T

The pore structure and gating mechanism of K2P channels by Piechotta, P, Rapedius, M, Stansfeld, P, Bollepalli, M, Erhlich, G, Andres-Enguix, I, Fritzenschaft, H, Decher, N, Sansom, M, Tucker, S, Baukrowitz, T

Structural and Mechanistic Insights into Gating of K2P Channels by Rapedius, M, Piechotta, P, Stansfeld, P, Bollepalli, M, Ehrlich, G, Andres-Enguix, I, Fritzenschaft, H, Decher, N, Sansom, M, Tucker, S, Baukrowitz, T

Functional complementation and genetic deletion studies of KirBac channels: activatory mutations highlight gating-sensitive domains. by Paynter, J, Andres-Enguix, I, Fowler, P, Tottey, S, Cheng, W, Enkvetchakul, D, Bavro, V, Kusakabe, Y, Sansom, MS, Robinson, N, Nichols, C, Tucker, S

Functional complementation and genetic deletion studies of KirBac channels: Activatory mutations highlight gating-sensitive domains by Paynter, J, Andres-Enguix, I, Fowler, P, Tottey, S, Cheng, W, Enkvetchakul, D, Bavro, V, Kusakabe, Y, Sansom, M, Robinson, N, Nichols, C, Tucker, S

The pore structure and gating mechanism of K2P channels. by Piechotta, P, Rapedius, M, Stansfeld, P, Bollepalli, M, Ehrlich, G, Erhlich, G, Andres-Enguix, I, Fritzenschaft, H, Decher, N, Sansom, MS, Tucker, S, Baukrowitz, T

Functional analysis of missense variants in the TRESK (KCNK18) K channel by Andres-Enguix, I, Shang, L, Stansfeld, P, Morahan, J, Sansom, M, Lafrenière, R, Roy, B, Griffiths, L, Rouleau, G, Ebers, G, Cader, Z, Tucker, S

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. by Lafrenière, R, Cader, M, Poulin, J, Andres-Enguix, I, Simoneau, M, Gupta, N, Boisvert, K, Lafrenière, F, McLaughlan, S, Dubé, M, Marcinkiewicz, M, Ramagopalan, S, Ansorge, O, Brais, B, Sequeiros, J, Pereira-Monteiro, J, Griffiths, L, Tucker, S, Ebers, G, Rouleau, G