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

Por Langer, Henning Tim, Afzal, Shoaib, Kempa, Stefan, Spuler, Simone
Publicado no Sci Rep (2020)

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

Por Spuler, Simone, Stroux, Andrea, Kuschel, Franziska, Kuhlmey, Adelheid, Kendel, Friederike
Publicado em 2011

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

Por Escobar, Helena, Schöwel, Verena, Spuler, Simone, Marg, Andreas, Izsvák, Zsuzsanna
Publicado no Mol Ther Nucleic Acids (2016)

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

Por Zacharias, Ute, Purfürst, Bettina, Schöwel, Verena, Morano, Ingo, Spuler, Simone, Haase, Hannelore
Publicado em 2011

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

Por Philippi, Susanne, Bigot, Anne, Marg, Andreas, Mouly, Vincent, Spuler, Simone, Zacharias, Ute
Publicado em 2012

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

Por Kufeld, Markus, Escobar, Helena, Marg, Andreas, Pasemann, Diana, Budach, Volker, Spuler, Simone
Publicado no Ann Transl Med (2017)

A Molecular Signature of Myalgia in Myotonic Dystrophy 2

Por Moshourab, Rabih, Palada, Vinko, Grunwald, Stefanie, Grieben, Ulrike, Lewin, Gary R., Spuler, Simone
Publicado no EBioMedicine (2016)

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

Por Biedasek, Katrin, Andres, Janin, Mai, Knut, Adams, Stephanie, Spuler, Simone, Fielitz, Jens, Spranger, Joachim
Publicado em 2011

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

Por Malatras, Apostolos, Michalopoulos, Ioannis, Duguez, Stéphanie, Butler-Browne, Gillian, Spuler, Simone, Duddy, William J.
Publicado no BMC Med Genomics (2020)

Loss of Ptpn11 (Shp2) drives satellite cells into quiescence

Por Griger, Joscha, Schneider, Robin, Lahmann, Ines, Schöwel, Verena, Keller, Charles, Spuler, Simone, Nazare, Marc, Birchmeier, Carmen
Publicado no eLife (2017)

Dysferlin-Peptides Reallocate Mutated Dysferlin Thereby Restoring Function

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

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

Por Kim, Minchul, Franke, Vedran, Brandt, Bettina, Lowenstein, Elijah D., Schöwel, Verena, Spuler, Simone, Akalin, Altuna, Birchmeier, Carmen
Publicado no Nat Commun (2020)

Human satellite cells have regenerative capacity and are genetically manipulable

Por Marg, Andreas, Escobar, Helena, Gloy, Sina, Kufeld, Markus, Zacher, Joseph, Spuler, Andreas, Birchmeier, Carmen, Izsvák, Zsuzsanna, Spuler, Simone
Publicado em 2014

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

Por Langer, Henning T., Senden, Joan M. G., Gijsen, Annemie P., Kempa, Stefan, van Loon, Luc J. C., Spuler, Simone
Publicado no Front Physiol (2018)

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

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

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

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

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

Por Blaszczyk, Edyta, Grieben, Ulrike, von Knobelsdorff-Brenkenhoff, Florian, Kellman, Peter, Schmacht, Luisa, Funk, Stephanie, Spuler, Simone, Schulz-Menger, Jeanette
Publicado no 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...

Por Blaszczyk, Edyta, Grieben, Ulrike, von Knobelsdorff-Brenkenhoff, Florian, Kellman, Peter, Schmacht, Luisa, Funk, Stephanie, Spuler, Simone, Schulz-Menger, Jeanette
Publicado no J Cardiovasc Magn Reson (2019)

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

Por Schmacht, Luisa M, Traber, Julius, Grieben, Ulrike I, Utz, Wolfgang, Dieringer, Matthias A, Kellman, Peter, Spuler, Simone, Schulz-Menger, Jeanette
Publicado no J Cardiovasc Magn Reson (2015)

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

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