Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laura Ruschkies"'
Autor:
André T Lopes, Torben J Hausrat, Frank F Heisler, Kira V Gromova, Franco L Lombino, Timo Fischer, Laura Ruschkies, Petra Breiden, Edda Thies, Irm Hermans-Borgmeyer, Michaela Schweizer, Jürgen R Schwarz, Christian Lohr, Matthias Kneussel
Publikováno v:
PLoS Biology, Vol 18, Iss 8, p e3000820 (2020)
Mutations in the gene encoding the microtubule-severing protein spastin (spastic paraplegia 4 [SPG4]) cause hereditary spastic paraplegia (HSP), associated with neurodegeneration, spasticity, and motor impairment. Complicated forms (complicated HSP [
Externí odkaz:
https://doaj.org/article/fd94a10cc9314b0d9d95e7c1e309a73e
Autor:
Sabine A. H. Hoffmeister-Ullerich, Michael R. Kreutz, Laura Ruschkies, Jessica E. M. Dunleavy, Melanie Richter, Monika S. Brill, Thomas Misgeld, Franco L. Lombino, Edda Thies, Michael Frotscher, André T. Lopes, Torben J. Hausrat, David Lutz, Froylan Calderon de Anda, Mary Muhia, Francis J. McNally, Jeffrey Lopez-Rojas, Irm Hermans-Borgmeyer, Matthias Kneussel
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Scientific Reports
Scientific reports, 9:15940
Scientific reports, vol 9, iss 1
Scientific Reports
Scientific reports, 9:15940
Scientific reports, vol 9, iss 1
Microtubule severing regulates cytoskeletal rearrangement underlying various cellular functions. Katanin, a heterodimer, consisting of catalytic (p60) and regulatory (p80) subunits severs dynamic microtubules to modulate several stages of cell divisi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166efaa6b8e3f7367fa7a47152ee290b
http://link.springer.com/article/10.1038/s41598-019-52367-3
http://link.springer.com/article/10.1038/s41598-019-52367-3
Autor:
Jürgen R. Schwarz, Michaela Schweizer, Kira V. Gromova, Timo Fischer, Frank F. Heisler, Torben J. Hausrat, Franco L. Lombino, Christian Lohr, Irm Hermans-Borgmeyer, André T. Lopes, Petra Breiden, Edda Thies, Laura Ruschkies, Matthias Kneussel
Publikováno v:
PLoS Biology
PLoS Biology, Vol 18, Iss 8, p e3000820 (2020)
PLoS Biology, Vol 18, Iss 8, p e3000820 (2020)
Mutations in the gene encoding the microtubule-severing protein spastin (spastic paraplegia 4 [SPG4]) cause hereditary spastic paraplegia (HSP), associated with neurodegeneration, spasticity, and motor impairment. Complicated forms (complicated HSP [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9608091febc3d2e75111043496b5d754
https://doi.org/10.1371/journal.pbio.3000820
https://doi.org/10.1371/journal.pbio.3000820
Autor:
Torben J. Hausrat, Mengzhe Wang, Laura Ruschkies, Tatjana Kleele, Matthias Kneussel, Emily Weigand, Stefan Engelhardt, Matthew Fisher, Miriam S. Reuter, Andrea Ahles, Thomas Misgeld, Natalia A. Marahori, Monika S. Brill, Derron L. Bishop
Publikováno v:
Neuron
Neuron 92(4), 845-856 (2016). doi:10.1016/j.neuron.2016.09.049
Neuron 92(4), 845-856 (2016). doi:10.1016/j.neuron.2016.09.049
Summary Developmental axon remodeling is characterized by the selective removal of branches from axon arbors. The mechanisms that underlie such branch loss are largely unknown. Additionally, how neuronal resources are specifically assigned to the bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf965582f3c572f2a15258b4d8c6ed2
https://pubmed.ncbi.nlm.nih.gov/27773584
https://pubmed.ncbi.nlm.nih.gov/27773584