Research Output per year
Fingerprint Dive into the research topics where Wilfried Rossoll is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 8 Similar Profiles
Motor Neurons
Medicine & Life Sciences
Spinal Muscular Atrophy
Medicine & Life Sciences
Axons
Medicine & Life Sciences
Messenger RNA
Medicine & Life Sciences
Proteins
Medicine & Life Sciences
Growth Cones
Medicine & Life Sciences
Genes
Medicine & Life Sciences
Carrier Proteins
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects
Spinal muscular atrophy: a novel role of SMN in axonal ribonucleoprotein complexe
Project: Research project
Spinal Muscular Atrophy: Cell-based drug screens for treatment of axonal defects
Project: Research project
RNA Processing Defects in SMA and Their Contribution to the Disease Phenotype
Project: Research project
Research Output 1997 2019
1
Citation
(Scopus)
Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites
Rossol, W. & Bassell, G. J., Jan 16 2019, In : Neuron. 101, 2, p. 204-206 3 p.Research output: Contribution to journal › Short survey
Dendrites
Axons
Mitochondria
Endosomes
Protein Biosynthesis
9
Citations
(Scopus)
MRNP assembly, axonal transport, and local translation in neurodegenerative diseases
Khalil, B., Morderer, D., Price, P. L., Liu, F. & Rossol, W., Jan 1 2018, (Accepted/In press) In : Brain Research.Research output: Contribution to journal › Article
Axonal Transport
Neurodegenerative Diseases
Axons
Maintenance
Spinal Muscular Atrophy
2
Citations
(Scopus)
RNP assembly defects in spinal muscular atrophy
Price, P. L., Morderer, D. & Rossol, W., Jan 1 2018, Advances in Neurobiology. Springer New York LLC, p. 143-171 29 p. (Advances in Neurobiology; vol. 20).Research output: Chapter in Book/Report/Conference proceeding › Chapter
Spinal Muscular Atrophy
Small Nuclear Ribonucleoproteins
Spliceosomes
Multiprotein Complexes
Motor Neuron Disease
65
Citations
(Scopus)
TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD
Chou, C. C., Zhang, Y., Umoh, M. E., Vaughan, S. W., Lorenzini, I., Liu, F., Sayegh, M., Donlin-Asp, P. G., Chen, Y. H., Duong, D. M., Seyfried, N. T., Powers, M. A., Kukar, T., Hales, C. M., Gearing, M., Cairns, N. J., Boylan, K. B., Dickson, D. W., Rademakers, R. V., Zhang, Y. & 5 others, , Feb 1 2018, In : Nature Neuroscience. 21, 2, p. 228-239 12 p.Research output: Contribution to journal › Article
Nuclear Pore
Cell Nucleus Active Transport
DNA-Binding Proteins
Pathology
Nuclear Pore Complex Proteins
18
Citations
(Scopus)
Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALS
Coyne, A. N., Lorenzini, I., Chou, C. C., Torvund, M., Rogers, R. S., Starr, A., Zaepfel, B. L., Levy, J., Johannesmeyer, J., Schwartz, J. C., Nishimune, H., Zinsmaier, K., Rossol, W., Sattler, R. & Zarnescu, D. C., Oct 3 2017, In : Cell Reports. 21, 1, p. 110-125 16 p.Research output: Contribution to journal › Article
Synaptic Vesicles
Amyotrophic Lateral Sclerosis
Neurons
Dynamins
Motor Neurons