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Cellular and Molecular Life Sciences : CMLS|August 25, 2022
The phospho-landscape of the survival of motoneuron protein (SMN) protein: relevance for spinal muscular atrophy (SMA)Nora Tula Detering, Tobias Schüning, Niko Hensel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 21, 2024
The spinal muscular atrophy gene product regulates actin dynamicsTobias Schüning, Andre Zeug, Katharina Strienke, et al.
Cell Transplantation|March 17, 2020
In Vivo and In Vitro Evaluation of a Novel Hyaluronic Acid-Laminin Hydrogel as Luminal Filler and Carrier System for Genetically Engineered Schwann Cells in Critical Gap Length Tubular Peripheral Nerve Graft in RatsNina Dietzmeyer, Zhong Huang, Tobias Schüning, et al.
Human Molecular Genetics|March 10, 2025
Aggregates associated with amyotrophic lateral sclerosis sequester the actin-binding protein profilin 2Sabrina Kubinski, Luisa Claus, Tobias Schüning, et al.
Human Molecular Genetics|May 5, 2024
From data to discovery: AI-guided analysis of disease-relevant molecules in spinal muscular atrophy (SMA)Ines Tapken, Daniela Kuhn, Nico Hoffmann, et al.
Human Molecular Genetics|November 17, 2025
Alterations along the neuroendocrine axis of leptin homeostasis: white adipose tissue and hypothalamus in a severe SMA mouse modelInes Bünermann, Nora Detering, Ines Tapken, et al.
Cells|November 6, 2020
A Single Amino Acid Residue Regulates PTEN-Binding and Stability of the Spinal Muscular Atrophy Protein SMNSebastian Rademacher, Nora T Detering, Tobias Schüning, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2021
Impairment of the neurotrophic signaling hub B-Raf contributes to motoneuron degeneration in spinal muscular atrophyNiko Hensel, Federica Cieri, Pamela Santonicola, et al.
Brain : a Journal of Neurology|August 25, 2024
The systemic complexity of a monogenic disease: the molecular network of spinal muscular atrophyInes Tapken, Theresa Schweitzer, Martina Paganin, et al.
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