C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany
- 31 March 2011
- journal article
- research article
- Published by Elsevier in Neurobiology of Aging
- Vol. 32 (3) , 548.e1-548.e4
- https://doi.org/10.1016/j.neurobiolaging.2009.11.017
Abstract
No abstract availableKeywords
Funding Information
- Deutsche Forschungsgemeinschaft (SFB581)
This publication has 13 references indexed in Scilit:
- Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutationNeurobiology of Aging, 2009
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral SclerosisScience, 2009
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral SclerosisScience, 2008
- Molecular biology of amyotrophic lateral sclerosis: insights from geneticsNature Reviews Neuroscience, 2006
- TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spinesJournal of Cell Science, 2005
- Kinesin Transports RNANeuron, 2004
- From charcot to lou gehrig: deciphering selective motor neuron death in alsNature Reviews Neuroscience, 2001
- Characterization of Two Evolutionarily Conserved, Alternatively Spliced Nuclear Phosphoproteins, NFAR-1 and -2, That Function in mRNA Processing and Interact with the Double-stranded RNA-dependent Protein Kinase, PKRJournal of Biological Chemistry, 2001
- The staden sequence analysis packageMolecular Biotechnology, 1996
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993