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Reinhard, J. R., Lin, S., McKee, K. K., Meinen, S., Crosson, S. C., Sury, M., Hobbs, S., Maier, G., Yurchenco, P. D. and Rüegg, M. A. (2017) ‘Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice’, Science Translational Medicine, 9(396), p. eaal4649. 10.1126/scitranslmed.aal4649.   edoc | Open Access
McKee, K. K., Crosson, S. C., Meinen, S., Reinhard, J. R., Rüegg, M. A. and Yurchenco, P. D. (2017) ‘Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype’, Journal of Clinical Investigation, 127(3), pp. 1075–1089. 10.1172/JCI90854.   edoc | Open Access
Meinen, S., Barzaghi, P., Lin, S., Lochmuller, H. and Ruegg, M. A. (2007) ‘Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stages’, The Journal of cell biology, Vol. 176, H. 7, pp. 979–993. 10.1083/jcb.200611152.   edoc | Open Access
Moll, J., Barzaghi, P., Lin, S., Bezakova, G., Lochmuller, H., Engvall, E., Muller, U. and Ruegg, M. A. (2001) ‘An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy’, Nature, 413(6853), pp. 302–307. 10.1038/35095054.   edoc