Neuromuscular synaptic function in mice lacking major subsets of gangliosides von Zitman, F.M.P, Todorov, B, Jacobs, B.C, Verschuuren, J.J, Furukawa, K, Willison, H.J, Plomp, J.J

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P5.18 Human anti-MuSK IgG4 autoantibodies cause myasthenia gravis in immunodeficient mice von Klooster, R, Plomp, J.J, Straasheijm, K.R, Huijbers, M.G, Niks, E.H, Detmers, F.J, Hermans, P.W, Sleijpen, K, Losen, M, de Baets, M.H, van der Maarel, S.M, Verschuuren, J.J

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α-Neurexins are required for efficient transmitter release and synaptic homeostasis at the mouse neuromuscular junction von Sons, M.S., Busche, N., Strenzke, N., Moser, T., Ernsberger, U., Mooren, F.C., Zhang, W., Ahmad, M., Steffens, H., Schomburg, E.D., Plomp, J.J., Missler, M.

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Gene dosage-dependent transmitter release changes at neuromuscular synapses of Cacna1a R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle wea... von Kaja, S., van de Ven, R.C.G., Broos, L.A.M., Veldman, H., van Dijk, J.G., Verschuuren, J.J.G.M., Frants, R.R., Ferrari, M.D., van den Maagdenberg, A.M.J.M., Plomp, J.J.

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Characterization of acetylcholine release and the compensatory contribution of non-Cav2.1 channels at motor nerve terminals of leaner Cav2.1-mutant mice von KAJA, S, VAN DE VEN, R. C. G, BROCS, L. A. M, FRANTS, R. R, FERRARI, M. D, VAN DEN MAAGDENBERG, A. M. J. M, PLOMP, J. J

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A bioassay for neuromuscular junction-restricted complement activation by myasthenia gravis acetylcholine receptor antibodies von Plomp, J.J., Huijbers, M.G.M., Verschuuren, J.J.G.M., Borodovsky, A.

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Characterization of acetylcholine release and the compensatory contribution of non-Ca v2.1 channels at motor nerve terminals of leaner Ca v2.1-mutant mice von Kaja, S., van de Ven, R.C.G., Broos, L.A.M., Frants, R.R., Ferrari, M.D., van den Maagdenberg, A.M.J.M., Plomp, J.J.

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Advances in the understanding of disease mechanisms of autoimmune neuromuscular junction disorders von Huijbers, M.G., Marx, A., Plomp, J.J., Panse, R. le, Phillips, W.D.

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Development of the mouse neuromuscular junction in the absence of regulated secretion von Heeroma, J.H, Plomp, J.J, Roubos, E.W, Verhage, M

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Neuromuscular synapse electrophysiology in myasthenia gravis animal models von Plomp, J.J., Huijbers, M.G.M., Verschuuren, J.J.G.M.

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Development and characterization of agonistic antibodies targeting the Ig-like 1 domain of MuSK von Lim, J.L., Augustinus, R., Plomp, J.J., Roya-Kouchaki, K., Vergoossen, D.L.E., Fillie-Grijpma, Y., Struijk, J., Thomas, R., Salvatori, D., Steyaert, C., Blanchetot, C., Vanhauwaert, R., Silence, K., Maarel, S.M. van der, Verschuuren, J.J., Huijbers, M.G.

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Characterization of acetylcholine release and the compensatory contribution of non-Cav 2.1 channels at motor nerve terminals of leaner Cav 2.1-mutant mice von Kaja, S, van de Ven, R.C.G, Broos, L.A.M, Frants, R.R, Ferrari, M.D, van den Maagdenberg, A.M.J.M, Plomp, J.J

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IgG4-mediated autoimmune diseases: a niche of antibody-mediated disorders von Huijbers, M.G., Plomp, J.J., Maarel, S.M. van der, Verschuuren, J.J.

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Functional monovalency amplifies the pathogenicity of anti-MuSK IgG4 in myasthenia gravis von Vergoossen, D.L.E., Plomp, J.J., Gstottner, C., Fillie-Grijpma, Y.E., Augustinus, R., Verpalen, R., Wuhrer, M., Parren, P.W.H.I., Dominguez Vega, E., Maarel, S.M. van der, Verschuuren, J.J., Huijbers, M.G.

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Simvastatin treatment does not ameliorate muscle pathophysiology in a mouse model for Duchenne muscular dystrophy von Verhaart, I.E.C., Cappellari, O., Tanganyika-de Winter, C.L., Plomp, J.J., Nnorom, S., Wells, K.E., Hildyard, J.C.W., Bull, D., Aartsma-Rus, A., Wells, D.J.

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Low dystrophin levels are insufficient to normalize the neuromuscular synaptic abnormalities of mdx mice von Pijl, E.M. van der, Putten, M. van, Niks, E.H., Verschuuren, J.J.G.M., Aartsma-Rus, A., Plomp, J.J.

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Optogenetic termination of ventricular arrhythmias in the whole heart: towards biological cardiac rhythm management von Nyns, E.C.A., Kip, A., Bart, C.I., Plomp, J.J., Zeppenfeld, K., Schalij, M.J., Vries, A.A.F. de, Pijnappels, D.A.

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Natural disease history of the dy(2J) mouse model of laminin alpha 2 (merosin)-deficient congenital muscular dystrophy von Pasteuning-Vuhman, S., Putker, K., Tanganyika-de Winter, C.L., Boertje-van der Meulen, J.W., Vliet, L. van, Overzier, M., Plomp, J.J., Aartsma-Rus, A., Putten, M. van

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Upregulation of quantal content at endplates of α-bungarotoxin-treated rats: a study on the role of NO, arachidonic acid metabolites and protein kinases von Plomp, J.J., Molenaar, P.C.

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Passive transfer models of myasthenia gravis with muscle-specific kinase antibodies von Verschuuren, J.J.G.M., Plomp, J.J., Burden, S.J., Zhang, W., Fillie-Grijpma, Y.E., Stienstra-van Es, I.E., Niks, E.H., Losen, M., Maarel, S.M. van der, Huijbers, M.G.

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