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Number of items: 4.

Journal Article

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

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

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

This list was generated on Mon Mar 1 04:48:24 2021 CET.