Sereda, Michael W.
Universitätsmedizin Göttingen · Max Planck Institute of Experimental Medicine
6 papers on CoChatORCID 0000-0003-3837-6575
Most cited papers
- Verified
Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity
Fünfschilling, U., Supplie, L. M., Mahad, D., Boretius, S., Saab, A. S., Edgar, J., Brinkmann, B. G., Kassmann, C. M., Tzvetanova, I. D., Möbius, W., et al. (2012) · Nature
Neurogenesis and neuroplasticity mechanismsMultiple Sclerosis Research Studies
Cited by 1,523
- Verified
Microglia facilitate repair of demyelinated lesions via post-squalene sterol synthesis
Berghoff, S. A., Spieth, L., Sun, T., Hosang, L., Schlaphoff, L., Depp, C., Düking, T., Winchenbach, J., Neuber, J., Ewers, D., et al. (2021) · Nature Neuroscience
Multiple Sclerosis Research StudiesNeuroinflammation and Neurodegeneration Mechanisms
Cited by 307
- Verified
Rho kinase inhibition modulates microglia activation and improves survival in a model of amyotrophic lateral sclerosis
Tönges, L., Günther, R., Suhr, M., Jansen, J., Balck, A., Saal, K., Barski, E., Nientied, T., Götz, A. A., Koch, J., et al. (2014) · Glia
Amyotrophic Lateral Sclerosis ResearchNeuroinflammation and Neurodegeneration Mechanisms
Cited by 121
- Verified
A role for myelin-associated peroxisomes in maintaining paranodal loops and axonal integrity
Kassmann, C. M., Quintes, S., Rietdorf, J., Möbius, W., Sereda, M. W., Nientiedt, T., Saher, G., Baes, M., & Nave, K.-A. (2011) · FEBS Letters
Hereditary Neurological DisordersMultiple Sclerosis Research Studies
Cited by 52
- Verified
Rho Kinase Inhibition with Fasudil in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis—Symptomatic Treatment Potential after Disease Onset
Günther, R., Balck, A., Koch, J. C., Nientiedt, T., Sereda, M., Bähr, M., Lingor, P., & Tönges, L. (2017) · Frontiers in Pharmacology
Amyotrophic Lateral Sclerosis ResearchNeurogenetic and Muscular Disorders Research
Cited by 47
- Verified
Peroxisomal dysfunctions cause lysosomal storage and axonal Kv1 channel redistribution in peripheral neuropathy
Kleinecke, S., Richert, S., de Hoz, L., Brügger, B., Kungl, T., Asadollahi, E., Quintes, S., Blanz, J., McGonigal, R., Naseri, K., et al. (2017) · eLife
Hereditary Neurological DisordersLysosomal Storage Disorders Research
Cited by 46
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