Nerve damage induced skeletal muscle atrophy is associated with increased accumulation of intramuscular glucose and polyol pathway intermediates

Tekijä Langer, Henning Tim, Afzal, Shoaib, Kempa, Stefan, Spuler, Simone
Julkaisussa Sci Rep (2020)

Delay in diagnosis of muscle disorders depends on the subspecialty of the initially consulted physician

Tekijä Spuler, Simone, Stroux, Andrea, Kuschel, Franziska, Kuhlmey, Adelheid, Kendel, Friederike
Julkaistu 2011

Full-length Dysferlin Transfer by the Hyperactive Sleeping Beauty Transposase Restores Dysferlin-deficient Muscle

Tekijä Escobar, Helena, Schöwel, Verena, Spuler, Simone, Marg, Andreas, Izsvák, Zsuzsanna
Julkaisussa Mol Ther Nucleic Acids (2016)

Ahnak1 abnormally localizes in muscular dystrophies and contributes to muscle vesicle release

Tekijä Zacharias, Ute, Purfürst, Bettina, Schöwel, Verena, Morano, Ingo, Spuler, Simone, Haase, Hannelore
Julkaistu 2011

Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy

Tekijä Philippi, Susanne, Bigot, Anne, Marg, Andreas, Mouly, Vincent, Spuler, Simone, Zacharias, Ute
Julkaistu 2012

Localized irradiation of mouse legs using an image-guided robotic linear accelerator

Tekijä Kufeld, Markus, Escobar, Helena, Marg, Andreas, Pasemann, Diana, Budach, Volker, Spuler, Simone
Julkaisussa Ann Transl Med (2017)

A Molecular Signature of Myalgia in Myotonic Dystrophy 2

Tekijä Moshourab, Rabih, Palada, Vinko, Grunwald, Stefanie, Grieben, Ulrike, Lewin, Gary R., Spuler, Simone
Julkaisussa EBioMedicine (2016)

Skeletal Muscle 11beta-HSD1 Controls Glucocorticoid-Induced Proteolysis and Expression of E3 Ubiquitin Ligases Atrogin-1 and MuRF-1

Tekijä Biedasek, Katrin, Andres, Janin, Mai, Knut, Adams, Stephanie, Spuler, Simone, Fielitz, Jens, Spranger, Joachim
Julkaistu 2011

MyoMiner: explore gene co-expression in normal and pathological muscle

Tekijä Malatras, Apostolos, Michalopoulos, Ioannis, Duguez, Stéphanie, Butler-Browne, Gillian, Spuler, Simone, Duddy, William J.
Julkaisussa BMC Med Genomics (2020)

Loss of Ptpn11 (Shp2) drives satellite cells into quiescence

Tekijä Griger, Joscha, Schneider, Robin, Lahmann, Ines, Schöwel, Verena, Keller, Charles, Spuler, Simone, Nazare, Marc, Birchmeier, Carmen
Julkaisussa eLife (2017)

Dysferlin-Peptides Reallocate Mutated Dysferlin Thereby Restoring Function

Tekijä Schoewel, Verena, Marg, Andreas, Kunz, Severine, Overkamp, Tim, Siegert Carrazedo, Romy, Zacharias, Ute, Daniel, Peter T., Spuler, Simone
Julkaistu 2012

Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells

Tekijä Kim, Minchul, Franke, Vedran, Brandt, Bettina, Lowenstein, Elijah D., Schöwel, Verena, Spuler, Simone, Akalin, Altuna, Birchmeier, Carmen
Julkaisussa Nat Commun (2020)

Human satellite cells have regenerative capacity and are genetically manipulable

Tekijä Marg, Andreas, Escobar, Helena, Gloy, Sina, Kufeld, Markus, Zacher, Joseph, Spuler, Andreas, Birchmeier, Carmen, Izsvák, Zsuzsanna, Spuler, Simone
Julkaistu 2014

Muscle Atrophy Due to Nerve Damage Is Accompanied by Elevated Myofibrillar Protein Synthesis Rates

Tekijä Langer, Henning T., Senden, Joan M. G., Gijsen, Annemie P., Kempa, Stefan, van Loon, Luc J. C., Spuler, Simone
Julkaisussa Front Physiol (2018)

Linking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers

Tekijä Raith, Marianne, Valencia, Rocio G, Fischer, Irmgard, Orthofer, Michael, Penninger, Josef M, Spuler, Simone, Rezniczek, Günther A, Wiche, Gerhard
Julkaistu 2013

Cardiac involvement of the systemic disorder myotonic dystrophy type II - detection by CMR

Tekijä Grosse, Luisa, Traber, Julius, Grieben, Ulrike I, Utz, Wolfgang, Dieringer, Matthias A, Kellman, Peter, Spuler, Simone, Schulz-Menger, Jeanette
Julkaistu 2014

Subclinical myocardial injury in patients with Facioscapulohumeral muscular dystrophy 1 and preserved ejection fraction – assessment by cardiovascular magnetic resonance

Tekijä Blaszczyk, Edyta, Grieben, Ulrike, von Knobelsdorff-Brenkenhoff, Florian, Kellman, Peter, Schmacht, Luisa, Funk, Stephanie, Spuler, Simone, Schulz-Menger, Jeanette
Julkaisussa J Cardiovasc Magn Reson (2019)

Correction to: Subclinical myocardial injury in patients with Facioscapulohumeral muscular dystrophy 1 and preserved ejection fraction – assessment by cardiovascular magnetic reson...

Tekijä Blaszczyk, Edyta, Grieben, Ulrike, von Knobelsdorff-Brenkenhoff, Florian, Kellman, Peter, Schmacht, Luisa, Funk, Stephanie, Spuler, Simone, Schulz-Menger, Jeanette
Julkaisussa J Cardiovasc Magn Reson (2019)

Cardiac involvement of myotonic dystrophy type II in patients with preserved ejection fraction - Detection by CMR

Tekijä Schmacht, Luisa M, Traber, Julius, Grieben, Ulrike I, Utz, Wolfgang, Dieringer, Matthias A, Kellman, Peter, Spuler, Simone, Schulz-Menger, Jeanette
Julkaisussa J Cardiovasc Magn Reson (2015)

Risk factors in critical illness myopathy during the early course of critical illness: a prospective observational study

Tekijä Weber-Carstens, Steffen, Deja, Maria, Koch, Susanne, Spranger, Joachim, Bubser, Florian, Wernecke, Klaus D, Spies, Claudia D, Spuler, Simone, Keh, Didier
Julkaistu 2010