1 - 26 of 26
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CtBP1 sustains activity-dependent muscle properties and dampens synaptic, contractile and metabolic changes triggered by denervationSkeletal muscle
accessLevelPublic
2026 1 0
Recent advances in the clinical spectrum and pathomechanisms associated with X-linked myopathy with excessive autophagy and other VMA21-related disordersJournal of neuromuscular diseases
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2025 15 137
Intracellular autofluorescence enables the isolation of viable, functional human muscle reserve cells with distinct Pax7 levels and stem cell statesStem cell research & therapy
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2025 19 9
MuSK is a substrate for CaMK2β but this interaction is dispensable for MuSK activation in vivoScientific reports
accessLevelPublic
2025 19 127
Harnessing distinct tissue-resident immune niches via S100A9/TLR4 improves ketone, lipid, and glucose metabolismEndocrinology
accessLevelPublic
2025 59 244
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type ISkeletal muscle
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2024 190 167
Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesisHuman molecular genetics
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2023 146 159
Back to basics: Optimization of DNA and RNA transfer in muscle cells using recent transfection reagentsExperimental cell research
accessLevelPublic
2022 393 462
Low expression of ANT1 confers oncogenic properties to rhabdomyosarcoma tumor cells by modulating metabolism and death pathwaysCell Death Discovery
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2020 363 195
The TOR pathway at the neuromuscular junction: more than a metabolic player?Frontiers in Molecular Neuroscience
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2020 328 323
mTORC1 and PKB/Akt control the muscle response to denervation by regulating autophagy and HDAC4Nature Communications
accessLevelPublic
2019 398 267
mTORC2 affects the maintenance of the muscle stem cell poolSkeletal Muscle
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2019 371 234
mTOR controls embryonic and adult myogenesis via mTORC1Development
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2019 367 219
Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type IJournal of Clinical Investigation
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2017 405 285
“Get the balance right”: pathological significance of autophagy perturbation in neuromuscular disordersJournal of Neuromuscular Diseases
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2016 323 232
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Autophagy
accessLevelRestricted
2016 331 1
Activation of mTORC1 in skeletal muscle regulates whole-body metabolism through FGF21Science signaling
accessLevelRestricted
2015 1 0
Differential response of skeletal muscles to mTORC1 signaling during atrophy and hypertrophySkeletal muscle
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2013 1 0
Rapamycin Attenuates the Progression of Tau Pathology in P301S Tau Transgenic MicePloS one
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2013 1 1
MTORC1 determines autophagy through ULK1 regulation in skeletal muscleAutophagy
accessLevelPublic
2013 1 2
Sustained Activation of mTORC1 in Skeletal Muscle Inhibits Constitutive and Starvation-Induced Autophagy and Causes a Severe, Late-Onset MyopathyCell metabolism
accessLevelPublic
2013 1 0
Selenoprotein N in skeletal muscle : from diseases to functionJournal of molecular medicine
accessLevelRestricted
2012 1 0
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyHuman molecular genetics online
accessLevelRestricted
2011 1 0
Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse : A Mammalian Model for SEPN1-Related MyopathyPloS one
accessLevelPublic
2011 1 1
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humansThe journal of clinical investigation
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2010 2 0
Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursorsBMC developmental biology
accessLevelPublic
2009 1 0
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