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Argente-Escrig, H., Schultheis, D., Kamm, L., Schowalter, M., Thiel, C., Tuerk, M., Clemen, C. S., Muelas, N., Castanon, M. J., Wiche, G., Herrmann, H., Vilchez, J. J. and Schroeder, R. . Plectin-related scapuloperoneal myopathy with treatment-responsive myasthenic syndrome. Neuropathol. Appl. Neurobiol.. HOBOKEN: WILEY. ISSN 1365-2990
Diermeier, S., Buttgereit, A., Clemen, C. S., Schroeder, R. and Friedrich, O. (2016). Aging-related progressive skeletal muscle weakness in mutant DesR349P muscles: a matter of compromised cytoarchitecture. Acta Physiol., 216. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716
Diermeier, S., Buttgereit, A., Winter, L., Clemen, C. S., Schroeder, R. and Friedrich, O. (2015). Structure-related force deficit predicted by quantitative multiphoton microscopy of single skeletal muscle fibers from an animal model of human desminopathy. Acta Physiol., 213. S. 189 - 190. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716
Diermeier, S., Buttgereit, A., Winter, L., Clemen, C. S., Schroeder, R. and Friedrich, O. (2015). Structure-related force deficit predicted by quantitative multiphoton microscopy of single skeletal muscle fibers from an animal model of human desminopathy. Acta Physiol., 213. S. 189 - 190. HOBOKEN: WILEY-BLACKWELL. ISSN 1748-1716
Diermeier, S., Haug, M., Reischl, B., Buttgereit, A., Schuermann, S., Spoerrer, M., Goldmann, W. H., Fabry, B., Elhimine, F., Stehle, R., Pfitzer, G., Winter, L., Clemen, C., Schroeder, R. and Friedrich, O. (2016). DesR349P Mutation Results in Ultrastructural Disruptions and Compromise of Skeletal Muscle Biomechanics Already at Preclinical Stages in Young Mice before the Onset of Protein Aggregation. Biophys. J., 110 (3). S. 303A - 304. CAMBRIDGE: CELL PRESS. ISSN 1542-0086
Diermeier, S., Iberl, J., Vetter, K., Haug, M., Reischl, B., Buttgereit, A., Schuermann, S., Spoerrer, M., Goldmann, W. H., Fabry, B., Elhimine, F., Stehle, R., Pfitzer, G., Winter, L., Clemen, C., Schroeder, R. and Friedrich, O. (2015). DesR349P mutation results in ultrastructural disruptions and compromise of skeletal muscle biomechanics already at preclinical stages in young mice before the onset of protein aggregation. Mol. Biol. Cell, 26. BETHESDA: AMER SOC CELL BIOLOGY. ISSN 1939-4586
Heckmann, M. B., Bauer, R., Jungmann, A., Winter, L., Rapti, K., Strucksberg, K-H, Clemen, C. S., Li, Z., Schroeder, R., Katus, H. A. and Mueller, O. J. (2016). AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice. Gene Ther., 23 (8-9). S. 673 - 680. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5462
Ruppert, T., Heckmann, M. B., Rapti, K., Schultheis, D., Jungmann, A., Katus, H. A., Winter, L., Frey, N., Clemen, C. S., Schroeder, R. and Mueller, O. J. (2020). AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies. Gene Ther., 27 (10-11). S. 516 - 525. LONDON: SPRINGERNATURE. ISSN 1476-5462
Sprinkart, A. M., Block, W., Traeber, F., Meyer, R., Paulin, D., Clemen, C. S., Schroeder, R., Gieseke, J., Schild, H. and Thomas, D. (2012). Characterization of the failing murine heart in a desmin knock-out model using a clinical 3 T MRI scanner. Int. J. Cardiovasc. Imaging, 28 (7). S. 1699 - 1706. DORDRECHT: SPRINGER. ISSN 1573-0743
Winter, L., Unger, A., Berwanger, C., Spoerrer, M., Tuerk, M., Chevessier, F., Strucksberg, K. -H., Schloetzer-Schrehardt, U., Wittig, I., Goldmann, W. H., Marcus, K., Linke, W. A., Clemen, C. S. and Schroeder, R. (2019). Imbalances in protein homeostasis caused by mutant desmin. Neuropathol. Appl. Neurobiol., 45 (5). S. 476 - 495. HOBOKEN: WILEY. ISSN 1365-2990