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IL-1α reversibly inhibits skeletal muscle ryanodine receptor. a novel mechanism for critical illness myopathy?
Friedrich O, Yi B, Edwards JN, Reischl B, Wirth-Hücking A, Buttgereit A, Lang R, Weber C, Polyak F, Liu I, von Wegner F, Cully TR, Lee A, Most P, Völkers M. Friedrich O, et al. Among authors: reischl b. Am J Respir Cell Mol Biol. 2014 Jun;50(6):1096-106. doi: 10.1165/rcmb.2013-0059OC. Am J Respir Cell Mol Biol. 2014. PMID: 24400695 Free PMC article.
The desmin mutation R349P increases contractility and fragility of stem cell-generated muscle micro-tissues.
Spörrer M, Kah D, Gerum RC, Reischl B, Huraskin D, Dessalles CA, Schneider W, Goldmann WH, Herrmann H, Thievessen I, Clemen CS, Friedrich O, Hashemolhosseini S, Schröder R, Fabry B. Spörrer M, et al. Among authors: reischl b. Neuropathol Appl Neurobiol. 2022 Apr;48(3):e12784. doi: 10.1111/nan.12784. Epub 2021 Dec 10. Neuropathol Appl Neurobiol. 2022. PMID: 34850968
Early signs of architectural and biomechanical failure in isolated myofibers and immortalized myoblasts from desmin-mutant knock-in mice.
Diermeier S, Iberl J, Vetter K, Haug M, Pollmann C, Reischl B, Buttgereit A, Schürmann S, Spörrer M, Goldmann WH, Fabry B, Elhamine F, Stehle R, Pfitzer G, Winter L, Clemen CS, Herrmann H, Schröder R, Friedrich O. Diermeier S, et al. Among authors: reischl b. Sci Rep. 2017 May 3;7(1):1391. doi: 10.1038/s41598-017-01485-x. Sci Rep. 2017. PMID: 28469177 Free PMC article.
The MyoRobot technology discloses a premature biomechanical decay of skeletal muscle fiber bundles derived from R349P desminopathy mice.
Haug M, Meyer C, Reischl B, Prölß G, Vetter K, Iberl J, Nübler S, Schürmann S, Rupitsch SJ, Heckel M, Pöschel T, Winter L, Herrmann H, Clemen CS, Schröder R, Friedrich O. Haug M, et al. Among authors: reischl b. Sci Rep. 2019 Jul 24;9(1):10769. doi: 10.1038/s41598-019-46723-6. Sci Rep. 2019. PMID: 31341183 Free PMC article.
44 results