Advancing drug discovery through assay development: a survey of tool compounds within the human solute carrier superfamily by Digles, D, Ingles-Prieto, A, Dvorak, V, Mocking, TAM, Goldmann, U, Garofoli, A, Homan, EJ, Di Silvio, A, Azzollini, L, Sassone, F, Fogazza, M, Bärenz, F, Pommereau, A, Zuschlag, Y, Ooms, JF, Tranberg-Jensen, J, Hansen, JS, Stanka, J, Sijben, HJ, Batoulis, H, Bender, E, Martini, R, IJzerman, AP, Sauer, DB, Huber, KVM

Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies. by Auer-Grumbach, M, Toegel, S, Schabhüttl, M, Weinmann, D, Chiari, C, Bennett, D, Beetz, C, Klein, D, Andersen, P, Böhme, I, Fink-Puches, R, Gonzalez, M, Harms, M, Motley, W, Reilly, M, Renner, W, Rudnik-Schöneborn, S, Schlotter-Weigel, B, Themistocleous, A, Weishaupt, J, Ludolph, A, Wieland, T, Tao, F, Abreu, L, Windhager, R, Zitzelsberger, M, Strom, T, Walther, T, Scherer, S, Züchner, S, Martini, R, Senderek, J