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Simone Spuler

Showing results (21-30 of 98) with videos related to

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Human Molecular Genetics|April 24, 2015
Dysferlin rescue by spliceosome-mediated pre-mRNA trans-splicing targeting introns harbouring weakly defined 3' splice sitesSusanne Philippi, Stéphanie Lorain, Cyriaque Beley, et al.
BMC Medical Genomics|May 13, 2020
MyoMiner: explore gene co-expression in normal and pathological muscleApostolos Malatras, Ioannis Michalopoulos, Stéphanie Duguez, et al.
Molecular Therapy. Nucleic Acids|March 3, 2023
Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutationStefanie Müthel, Andreas Marg, Busem Ignak, et al.
International Journal of Molecular Sciences|February 26, 2022
Statins Aggravate the Risk of Insulin Resistance in Human MuscleStefanie A Grunwald, Stefanie Haafke, Ulrike Grieben, et al.
Traffic (Copenhagen, Denmark)|June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|November 8, 2021
Progressive myocardial injury in myotonic dystrophy type II and facioscapulohumeral muscular dystrophy 1: a cardiovascular magnetic resonance follow-up studyEdyta Blaszczyk, Carolin Lim, Peter Kellman, et al.
Elife|May 3, 2017
Loss of Ptpn11 (Shp2) drives satellite cells into quiescenceJoscha Griger, Robin Schneider, Ines Lahmann, et al.
Scientific Reports|May 9, 2022
Myofibrillar protein synthesis rates are increased in chronically exercised skeletal muscle despite decreased anabolic signalingHenning T Langer, Daniel West, Joan Senden, et al.
Critical Care Medicine|July 23, 2009
Nonexcitable muscle membrane predicts intensive care unit-acquired paresis in mechanically ventilated, sedated patientsSteffen Weber-Carstens, Susanne Koch, Simone Spuler, et al.
Journal of Neuromuscular Diseases|December 3, 2016
FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular DystrophyEsma Ziat, Kamel Mamchaoui, Maud Beuvin, et al.
Pageof 10

Showing results (21-30 of 98) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|April 24, 2015
Dysferlin rescue by spliceosome-mediated pre-mRNA trans-splicing targeting introns harbouring weakly defined 3' splice sitesSusanne Philippi, Stéphanie Lorain, Cyriaque Beley, et al.
BMC Medical Genomics|May 13, 2020
MyoMiner: explore gene co-expression in normal and pathological muscleApostolos Malatras, Ioannis Michalopoulos, Stéphanie Duguez, et al.
Molecular Therapy. Nucleic Acids|March 3, 2023
Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutationStefanie Müthel, Andreas Marg, Busem Ignak, et al.
International Journal of Molecular Sciences|February 26, 2022
Statins Aggravate the Risk of Insulin Resistance in Human MuscleStefanie A Grunwald, Stefanie Haafke, Ulrike Grieben, et al.
Traffic (Copenhagen, Denmark)|June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|November 8, 2021
Progressive myocardial injury in myotonic dystrophy type II and facioscapulohumeral muscular dystrophy 1: a cardiovascular magnetic resonance follow-up studyEdyta Blaszczyk, Carolin Lim, Peter Kellman, et al.
Elife|May 3, 2017
Loss of Ptpn11 (Shp2) drives satellite cells into quiescenceJoscha Griger, Robin Schneider, Ines Lahmann, et al.
Scientific Reports|May 9, 2022
Myofibrillar protein synthesis rates are increased in chronically exercised skeletal muscle despite decreased anabolic signalingHenning T Langer, Daniel West, Joan Senden, et al.
Critical Care Medicine|July 23, 2009
Nonexcitable muscle membrane predicts intensive care unit-acquired paresis in mechanically ventilated, sedated patientsSteffen Weber-Carstens, Susanne Koch, Simone Spuler, et al.
Journal of Neuromuscular Diseases|December 3, 2016
FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular DystrophyEsma Ziat, Kamel Mamchaoui, Maud Beuvin, et al.
Pageof 10