Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research interests include Biology, Medicine, Pathology, Skeletal muscle, Immunology, and Neuroscience.
Weight loss with GLP-1 medicines does not result in a disproportionate loss of muscle mass or function in obese mice and humans
Mitochondrial damage is associated with an early immune response in inclusion body myositis
Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoids
Complement profiling of sural nerves in chronic-inflammatory demyelinating polyneuropathy
Serglycin und Periostin als potenzielle neue Serum-Biomarker für die GNE-Myopathie
Brain malformations and seizures by impaired chaperonin function of TRiC
Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathy
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 2
Highly sensitive therapeutic drug monitoring of infliximab in serum by targeted mass spectrometry in comparison to ELISA data
Novel Genetic and Biochemical Insights into the Spectrum of <i>NEFL</i> -Associated Phenotypes
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study
Dysregulation of FLVCR1a-dependent mitochondrial calcium handling in neural progenitors causes congenital hydrocephalus
Proteomic studies in <i>VWA1</i>‐related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkers
Post-COVID exercise intolerance is associated with capillary alterations and immune dysregulations in skeletal muscles
Periostin as a blood biomarker of muscle cell fibrosis, cardiomyopathy and disease severity in myotonic dystrophy type 1
Skeletal muscle provides the immunological micro-milieu for specific plasma cells in anti-synthetase syndrome-associated myositis
Endoplasmic reticulum‐stress and unfolded protein response‐activation in immune‐mediated necrotizing myopathy
New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1
Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)
Simple Targeted Assays for Metabolic Pathways and Signaling: A Powerful Tool for Targeted Proteomics
RhoA regulates translation of the Nogo-A decoy SPARC in white matter-invading glioblastomas