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NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels

PloS one, 2011-03, Vol.6 (3), p.e17963-e17963

2011

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Modulation of Microglia by Voluntary Exercise or CSF1R Inhibition Prevents Age-Related Loss of Functional Motor Units

Cell reports (Cambridge), 2019-11, Vol.29 (6), p.1539-1554.e7

2019

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High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome

Journal of biomolecular screening, 2015-10, Vol.20 (9), p.1101-1111

2015

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Engineering circuits of human iPSC-derived neurons and rat primary glia

Frontiers in neuroscience, 2023-05, Vol.17, p.1103437-1103437

2023

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Transmission-selective muscle pathology induced by the active propagation of mutant huntingtin across the human neuromuscular synapse

Frontiers in molecular neuroscience, 2024-01, Vol.16, p.1287510-1287510

2024

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Preferential amplification of a human mitochondrial DNA deletion in vitro and in vivo

Scientific reports, 2018-01, Vol.8 (1), p.1799-10, Article 1799

2018

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Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse

Neuromuscular disorders : NMD, 2004-10, Vol.14 (10), p.675-682

2004

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Effect of calpain and proteasome inhibition on Ca²⁺-dependent proteolysis and muscle histopathology in the mdx mouse

The FASEB journal, 2008-12, Vol.22 (12), p.4190-4200

2008

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Utrophin is a calpain substrate in muscle cells

Muscle & nerve, 2006-06, Vol.33 (6), p.753-759

2006

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Orally available selective melanocortin-4 receptor antagonists stimulate food intake and reduce cancer-induced cachexia in mice

PloS one, 2009-03, Vol.4 (3), p.e4774-e4774

2009

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A Multidisciplinary Evaluation of the Effectiveness of Cyclosporine A in Dystrophic Mdx Mice

The American journal of pathology, 2005-02, Vol.166 (2), p.477-489

2005

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Receptor clustering and pathogenic complement activation in myasthenia gravis depend on synergy between antibodies with multiple subunit specificities

Acta neuropathologica, 2022-11, Vol.144 (5), p.1005-1025

2022

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CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency

Science (American Association for the Advancement of Science), 2016-03, Vol.351 (6278), p.1199-1203

2016

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Topologically controlled circuits of human iPSC-derived neurons for electrophysiology recordings

Lab on a chip, 2022-03, Vol.22 (7), p.1386-143

2022

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Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance

European heart journal, 2009-01, Vol.30 (1), p.116-124

2009

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Identification of Small Molecules Which Induce Skeletal Muscle Differentiation in Embryonic Stem Cells via Activation of the Wnt and Inhibition of Smad2/3 and Sonic Hedgehog Pathways

Stem cells (Dayton, Ohio), 2016-02, Vol.34 (2), p.299-310

2016

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Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients

Laboratory investigation, 2004-10, Vol.84 (10), p.1271-1278

2004

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Novel cell-penetrating α-keto-amide calpain inhibitors as potential treatment for muscular dystrophy

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5176-5181

2005

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Glucocorticoid-mediated regulation of utrophin levels in human muscle fibers

Neuromuscular disorders : NMD, 2002-10, Vol.12, p.S95-S104

2002

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Omigapil Ameliorates the Pathology of Muscle Dystrophy Caused by Laminin-α2 Deficiency

The Journal of pharmacology and experimental therapeutics, 2009-12, Vol.331 (3), p.787-795

2009

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Effect of calpain and proteasome inhibition on Ca 2+ ‐dependent proteolysis and muscle histopathology in the mdx mouse

The FASEB journal, 2008-12, Vol.22 (12), p.4190-4200

2008

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Detection of glucocorticoid-like activity in traditional Chinese medicine used for the treatment of Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2003-11, Vol.13 (9), p.699-704

2003

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Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency

The Journal of pharmacology and experimental therapeutics, 2009-12, Vol.331 (3), p.787

2009

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Bank- und Kapitalmarktrecht

5, 2019

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NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels

Modulation of Microglia by Voluntary Exercise or CSF1R Inhibition Prevents Age-Related Loss of Functional Motor Units

High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome

Engineering circuits of human iPSC-derived neurons and rat primary glia

Transmission-selective muscle pathology induced by the active propagation of mutant huntingtin across the human neuromuscular synapse

Preferential amplification of a human mitochondrial DNA deletion in vitro and in vivo

Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse

Effect of calpain and proteasome inhibition on Ca²⁺-dependent proteolysis and muscle histopathology in the mdx mouse

Utrophin is a calpain substrate in muscle cells

Orally available selective melanocortin-4 receptor antagonists stimulate food intake and reduce cancer-induced cachexia in mice

A Multidisciplinary Evaluation of the Effectiveness of Cyclosporine A in Dystrophic Mdx Mice

Receptor clustering and pathogenic complement activation in myasthenia gravis depend on synergy between antibodies with multiple subunit specificities

CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency

Topologically controlled circuits of human iPSC-derived neurons for electrophysiology recordings

Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance

Identification of Small Molecules Which Induce Skeletal Muscle Differentiation in Embryonic Stem Cells via Activation of the Wnt and Inhibition of Smad2/3 and Sonic Hedgehog Pathways

CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations

Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients

Novel cell-penetrating α-keto-amide calpain inhibitors as potential treatment for muscular dystrophy

Glucocorticoid-mediated regulation of utrophin levels in human muscle fibers

Omigapil Ameliorates the Pathology of Muscle Dystrophy Caused by Laminin-α2 Deficiency

Effect of calpain and proteasome inhibition on Ca 2+ ‐dependent proteolysis and muscle histopathology in the mdx mouse

Detection of glucocorticoid-like activity in traditional Chinese medicine used for the treatment of Duchenne muscular dystrophy

Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency

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